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Abstract

Abnormal activation of the kynurenine and serotonin pathways of tryptophan metabolism is linked to a host of neuropsychiatric disorders. Concurrently, noninvasive brain stimulation (NIBS) techniques demonstrate high therapeutic efficacy across neuropsychiatric disorders, with indications for modulated neuroplasticity underlying such effects. We therefore conducted a scoping review with meta-analysis of eligible studies, conforming with the PRISMA statement, by searching the PubMed and Web of Science databases for clinical and preclinical studies that report the effects of NIBS on biomarkers of tryptophan metabolism. NIBS techniques reviewed were electroconvulsive therapy (ECT), transcranial magnetic stimulation (TMS), and transcranial direct current stimulation (tDCS). Of the 564 search results, 65 studies were included with publications dating back to 1971 until 2022. The Robust Bayesian Meta-Analysis on clinical studies and qualitative analysis identified general null effects by NIBS on biomarkers of tryptophan metabolism, but moderate evidence for TMS effects on elevating serum serotonin levels. We cannot interpret this as evidence for or against the effects of NIBS on these biomarkers, as there exists several confounding methodological differences in this literature. Future controlled studies are needed to elucidate the effects of NIBS on biomarkers of tryptophan metabolism, an under-investigated question with substantial implications to clinical research and practice.

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1. Introduction

1.1. Rationale

The products of tryptophan (TRP) metabolism have vital physiological roles. These bioactive metabolites include serotonin (5-HT), melatonin, and the kynurenines, all with diverse regulatory functions. Although TRP itself is an essential amino acid, with its availability dependent on dietary intake, only a small amount is used for protein synthesis while most of it is degraded via the 5-HT or kynurenine pathways (Figure 1). The biomarkers of interest in the present review, whose concentrations in various media inform about the activation of TRP metabolism are: TRP, kynurenine (KYN), formylkynurenine, kynurenic acid (KA), quinolinic acid (QA), NAD+, 3-hydroxykynurenine (3-HK), xanthurenic acid (XA), picolinic acid (PA), anthranilic acid (AA), 5-HT, oxitriptan, 5-hydroxytryptamine (5-HT), 5-hydroxyindoleacetic acid (5-HIAA), N-acetylserotonin, and melatonin.

Healthy intake of dietary TRP and production of these metabolic products are linked to cardiovascular health [1], gut-brain homeostasis [2], cognitive and mood regulation [3,4], and immune and inflammation mediation [5]. To reach the central nervous system (CNS), a portion of dietary TRP is absorbed in the small intestine to be released into the blood stream. It then traverses through the bloodstream and is subsequently transported across the blood–brain barrier by the L-type amino acid transporter, which is also expressed by nerve cells within the CNS. This dietary TRP is a vital substrate for 5-HT synthesis by serotonergic neurons in the CNS, which project from the rostral raphe nuclei to the cerebral cortex. These cortices ubiquitously express critical proteins for 5-HT neurotransmission, such as the highly studied receptors 5-HT1A and 5HT2A, and monoamine oxidase-A (MAO-A) [6], among several more receptor subtypes and transporters. Serotonergic neurons also project to limbic and sub-cortical structures, other brain stem regions and the spinal cord—providing an anatomical link between the role of serotonin in behavioral, emotional, cognitive, and motor functions mediated by the nervous system. Activation of the kynurenine pathway generates molecules that are neuroactive and mediate inflammatory response [5,7]. Several highly prevalent neuropsychiatric disorders, such as major depressive disorder (MDD), bipolar disorder, and schizophrenia, present with biomarker concentrations that indicate abnormal activation of these pathways [8,9,10]. Further, there is evidence that the restoration of these abnormal activations coincides with therapeutic effects. For instance, antidepressant effects following anti-inflammatory medication are observed in patients with inflammatory conditions [11] and with depressive disorders [12]. Further, the antidepressant effects of the selective serotonin reuptake inhibitor (SSRI), escitalopram, have been observed to negatively correlate with kynurenic acid (KA) plasma levels, with lower levels predicting greater therapeutic outcomes in patients diagnosed with MDD [13]. In a meta-analysis examining peripheral levels of kynurenines in psychiatric patients compared to healthy controls, Marx et al. [9] observed significantly lower TRP levels in patients with MDD and schizophrenia compared to healthy controls, in addition to elevated kynurenine (KYN) to TRP ratios. This latter observation suggests that the diminished TRP availability may be due to over-activation of the kynurenine pathway. Moreover, compared to healthy controls, KA levels were lower in MDD patients but schizophrenia patients had KA levels comparable to controls [9]. Such unique patterns are proposed to underlie the specific syndromes of these disorders [7], supporting efforts to target these abnormal pathway activations for intervention or to inform treatment selection [5,7]. In further support of these efforts, Haroon et al. [14] assessed the association between blood plasma and cerebrospinal fluid (CSF) biomarkers of immune and kynurenine pathway activation, finding elevations in both mediums in depressed patients compared to healthy controls; these elevations also corresponded to more severe motivation and anhedonia symptoms. As elevated kynurenine pathway activation catabolizes more available TRP, serotonin synthesis is consequently diminished due to lack of substrate. Such findings link over-activation of the kynurenine pathway to psychiatric symptoms that are associated with diminished serotonin activity, such as impaired neuroplasticity [15] and disrupted “re-learning” of appropriate emotion processing in depression [4]. Additionally, disrupted serotonin synthesis following kynurenine pathway over-activation lends further credence to the association between psychiatric symptoms and seemingly distant events that alter TRP degradation toward the kynurenine pathway, such as chronic stress [16] and inflammation [7]. As the authors above, Haroon et al. [14] envisioned using biomarkers of TRP metabolism to guide psychiatric treatment.

Noninvasive brain stimulation (NIBS) techniques have demonstrated therapeutic utility across neuropsychiatric disorders, with varied levels of efficacy and quality of evidence [17]. Those techniques under review here are repetitive transcranial magnetic stimulation (rTMS) [17,18,19,20], transcranial direct current stimulation (tDCS) [17,18], and electroconvulsive therapy (ECT) [17]—each considered non-invasive as no breaching or implantation occurs during treatment [21]. Current efforts are aimed at developing precise protocols for these techniques [22]. However, while elucidating the mechanisms of action of NIBS is critical toward these aims, current theories need to be broadened or supported by molecular evidence to account for the enduring therapeutic effects of brain stimulation [23].

In light of theories predicting a link between improved clinical outcomes and recovered pathway activation, and the need to specify molecular mechanisms of NIBS to optimize protocol selection, efforts to investigate the influence of NIBS on tryptophan metabolism are re-emerging [24]. While there exists reviews relevant to this research question [24,25,26], there is a current need for systematic reviews which assess the effects of NIBS on specific biomarkers of tryptophan metabolism in humans and animal models. This examination is critical to understanding the therapeutic mechanisms of brain stimulation across clinical diagnoses and informing efforts toward precision medicine [22].

1.2. Objective

This scoping review systematically surveys the current literature investigating the effects of therapeutic NIBS on biomarkers of tryptophan metabolism and synthesizes findings by qualitative- and meta-analyses. Our findings are discussed in light of current etiological theories of neuropsychiatric disorders and whether they are supported by the observed therapeutic and biomarker effects of NIBS. Our search criteria and research question are summarized in Table 1. Briefly, we sought published studies utilizing therapeutic NIBS, and which probed levels of kynurenine or serotonin pathway metabolites in healthy or diagnosed humans and animal models. No further restrictions were considered.

2. Methods

This invited review was designed to conform with the Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) [27].

2.1. Eligibility Criteria

Inclusion criteria were (1) treatment with ECT, rTMS, or tDCS; (2) participants were human and non-human species; (3) levels of the following biomarkers were assessed using any form of biological sample collection from NIBS-treated participants: tryptophan (TRP), kynurenine (KYN), formylkynurenine, quinolinic acid (QA), NAD+, 3-hydroxykynurenine (3-HK), xanthurenic acid (XA), picolinic acid (PA), anthranilic acid (AA), serotonin (5-HT), oxitriptan, 5-hydroxytryptamine (5-HT), 5-hydroxyindoleacetic acid (5-HIAA), N-acetyl-5-HT, and melatonin; 4) effects of NIBS on biomarkers of interest levels was assessed by comparing baseline with concurrent or post-NIBS levels, without restriction to timepoints of sampling. Exclusion criteria were (1) no new findings were published or data was previously reported. Otherwise, there were no further restrictions on experimental design, the language the manuscript was written-in, NIBS parameters or targets, participant characteristics such as age or diagnosis, nor restrictions on sampling method were considered. The rationale for these relaxed restrictions was to maximize the number of included studies for this survey, as we anticipated this literature to be sparse.

2.2. Information Sources

We searched the NCBI PubMed and Web of Science databases for studies published from inception until 15 July 2022. Included studies and relevant reviews in our search results were also screened for relevant studies.

2.3. Search Strategy

Search terms for NIBS were initially based on techniques in a recent expert review [22], however we focused our search here to ECT, rTMS, and tDCS because preliminary searches to test the feasibility of this review could not identify relevant studies for other NIBS techniques and these techniques are frequently discussed in reviews on the therapeutic efficacy of NIBS and mechanisms of action, e.g, [17]. The subset of TRP metabolites, and corresponding terms for the products of the serotonin and kynurenine pathways that we reviewed were based on recent expert reviews [5,7]. The search queries used for the PubMed and Web of Science search are shown in Table S1.

2.4. Selection and Data Collection

Two independent reviewers (C.G.G. and T.T.Z.L.) conducted the search and initial screening by title and abstract. Both reviewers independently retrieved the identified potential studies, conducted full-article screening, and then extracted data for review. These results were then merged, with any disagreements settled through discussion with G.S.K. No automation tools were used for screening or data extraction.

2.5. Data Items

A customized form was used to report relevant data from our included studies: study design; NIBS protocol parameters (e.g., stimulation site, session count); participant characteristics (e.g., species, health condition, age); control group characteristics when available; biomarkers of TRP metabolism including metabolite concentration levels, ratios, sampling source, and time points; and significant and non-significant effects of NIBS on biomarkers and direction of effect (Table 1). These significant effects were retrieved from one-group pretest-posttest designs or group differences in parallel or crossover designs. For studies using a parallel design, we preferred to report results based on group*time interaction over group differences in posttests.

For quantitative analysis, we extracted numerical results necessary for the calculation of the standardized mean difference (SMD). If only statistical graphs were provided, we extracted the values using WebPlotDigitizer (https://automeris.io/WebPlotDigitizer/, accessed on 15 July 2022). Clinical measures of human participants (e.g., effects on clinical assessment scales) were also extracted. If there were multiple clinical measures, we sought the primary outcome in the study.

2.6. Qualitative Synthesis Methods

Results from clinical and preclinical studies were visualized as bar charts where the counts for significant changes, in either direction, and nonsignificant changes were stacked to present an overview of the effects of NIBS and biomarkers of TRP metabolism. In this synthesis, we stacked studies assessing the same metabolite and NIBS technique (i.e., ECT, rTMS, or tDCS). That is, we differentiated clinical and preclinical studies and NIBS, but did not perform subgroup analyses of all ways in which these studies vary, for example, dissimilar NIBS parameters. Instead, when patterns suggesting heterogeneity or true effects emerged, we agreed to follow them up by examining the characteristics of the relevant studies.

Studies may report findings from multiple experimental groups, for instance, effects on various health conditions. In these cases, we counted experimental groups instead of the study count towards synthesis. Furthermore, within experimental groups, there may be multiple sampling time points. We determined that the time points associated with significant changes would represent the groups, presuming that those time points were most sensitive to effects by NIBS. Experimental groups with significant changes in opposite directions at different time points would be excluded from the bar charts and followed up specifically. The bar charts and other similar graphs were created using the Python library on Plotly (https://plotly.com/python/, accessed on 15 July 2022).

2.7. Quantitative Synthesis Methods by Bayesian Meta-Analysis

Only clinical studies with calculable SMDs underwent meta-analysis. We used the Robust Bayesian Meta-Analysis (RoBMA) method, which applied to the data variety of models resting on different assumptions about effects, heterogeneity, and publication bias [28]. These models were weighted according to their predictability of the data and averaged to draw final inferences. The Bayesian framework allows quantification of evidence for null findings, while more traditional, frequentist approaches cannot distinguish support for null findings from the absence of evidence (in the case of p > 0.05). The qualitative analysis of significant and nonsignificant effects, as described above, and classical meta-analysis methods are examples of frequentist approaches. Besides the above advantage given by the framework, RoBMA benefits from its model-averaging feature such that it does not require all-or-none decisions about publication bias and works well under high heterogeneity [28], well-suited for this scoping review. The resulting inferences were presented as inclusion Bayes factors (BF10), representing the strength of evidence for the presence of the meta-analytic item relative to the absence. For example, a BF10 of effects equal to three means the data are three times more likely to have occurred if effects exist, or three times less likely when BF10 equals 1/3. Such a BF10 larger than three or less than 1/3 is tentatively interpreted as moderate evidence supporting or against the presence of the meta-analytic item, respectively, as per [29]. Additionally, >10 or <1/10 indicates strong evidence; >30 or <1/30 indicates very strong evidence; >100 or <1/100 indicates extreme evidence. As we expected a substantial number of clinical studies that used a one-group pretest-posttest or crossover design, we decided not to exclude them from this meta-analysis and calculate the SMD as the change or difference divided by the pretest or control standard deviation (SD). Computing the standard error of such SMDs requires the pretest-posttest correlation (r), and as few studies reported this, we adopted Rosenthal’s estimate of r = 0.7 [30], and used r = 0.5 and 0.9 for sensitivity testing. For studies with a parallel design, we preferred to calculate the SMD as the group difference in posttests divided by the pooled SD. Similar to the approach in our qualitative analysis above, when there were multiple SMD values within an experimental group, for example, due to multiple sampling time points, we chose the one with the largest absolute value, assuming it is most sensitive to the change.

Statistics measures other than the mean and SD were converted to them as per the Cochrane Handbook [31], except the median and first and third quartile were converted according to [32]. This quantitative analysis was executed using JASP version 0.16.2 (https://jasp-stats.org/, accessed on 15 July 2022).

3. Results

3.1. Selection of Sources of Evidence

A total of 65 studies (Table 2 and Table 3) [33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97] were included after screening 307 records in PubMed and 257 records in Web of Science, with seven of our included studies identified in the references of studies included from databases. A total of 29 studies could not be retrieved or were excluded for not meeting inclusion criteria during full-text screening (Table S2) [36,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125]. Further details of our screening results are shown in the PRISMA flow diagram (Figure 2). All the included studies were published in English.

3.2. Characteristics of Included Studiess

38 included studies recruited humans (Table 2) [33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70] and 27 studied animal models (Table 3) [71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94,95,96,97]. Clinical assessment outcomes for human participants are available in the supplementary spreadsheets.

A histogram of the study count versus publication year (Figure 3) shows that ECT research, both clinical and preclinical, dominated the 1970s and 1980s. Around the year 2000, there was an emergence of preclinical TMS studies followed by clinical research. In the past decade, there have been no preclinical ECT studies, while the number of clinical ECT and TMS studies have been growing, in addition to the appearance of tDCS studies. Of the 37 clinical studies (excluding case reports [49]), 25 (68%) used ECT, and 11 (30%) used TMS. A lower percentage of preclinical studies (12 of 27, 44%) employed ECT, while more (14, 52%) used TMS. An overview of the effects of NIBS on the concentrations of each biomarker of interest are shown Figure 4.

The clinical and preclinical research on the effects of NIBS on biomarkers of TRP metabolism show overlapping and distinct interests in terms of studied metabolites and sampling sources (Figure 5). Overall, the most frequently investigated were TRP, 5-HT and 5-HIAA. In clinical studies, metabolites in the kynurenine pathway, notably KYN and KA, were frequently studied, but missing in preclinical studies.

Clinical studies generally lacked randomized control designs and included pharmacotherapy-as-usual. Of the 37 clinical studies reporting statistical results (thus excluding case reports [49]), 31 used a one-group pretest-posttest design, while six employed a parallel or crossover design, of which four were randomized, and two were not. Regarding preclinical studies, 25 of the 27 (93%) used a parallel design, and no concurrent pharmacotherapy.

The heterogeneity of NIBS study protocols and participant characteristics were also assessed. Large differences across study protocols was the number of sessions, biomarker sampling time-points and, for TMS, stimuli schedule (see supplementary text). In clinical studies (excluding case reports [49]), 30 of 37 treated patients diagnosed with depression (supplementary text). The majority of clinical studies recruited more females than males (25 of the 35 provided the gender ratio, 71%) or recruited equal amounts (two, 6%), with the age mean or median ranging between 40 and 60 (with 27 of the 36 offering such information, 72%). By contrast, in all but two preclinical studies providing sex ratios, animals were all males. Most preclinical studies used healthy animals (22 of 27, 81%). Of 27 preclinical studies, 24 (89%) used rats, two (7%) mice, and one study used dogs (4%). Lastly, biomarker sampling time points appeared arbitrarily chosen or is vaguely described. For a more detailed discussion of these heterogenous methods of our included studies, see supplementary text.

3.3. Qualitative Synthesis Results

Figure 4a,b and Figure 5a–f visualize results of the counts of experimental groups with significant or nonsignificant changes in biomarkers of TRP metabolism, with the latter organized according to sampling medium. Figure 5a–c show examinations of CSF (a), plasma (b), serum (c) in clinical studies, and Figure 5d–f show brain tissue (d), microdialysis (e), and plasma (f) in preclinical studies. The sampling results of brain tissue and microdialysis involved various regions but are collapsed in Figure 5d and e for brevity; they are shown individually in Figure S1. Moreover, for brevity, only ECT and TMS results are visualized, and readers are referred to the bottom of Table 2 and Table 3 for the single clinical or preclinical tDCS study, respectively. For a more detailed report on the qualitative analysis of the methods and results in clinical and preclinical studies, see supplementary text.

3.4. Quantitative Synthesis Results by Bayesian Meta-Analysis

Table 4 lists the BF10 values of effects, heterogeneity, and publication bias for the changes in the biomarker levels by NIBS, where r is set to 0.5, 0.7, or 0.9, in addition to the counts of experimental groups used for calculation. Here, only the outcomes with at least moderate evidence for effects or null effects (BF10 > 3 or <1/3, respectively) across the three r’s are shown. The rest are available in the supplementary spreadsheets. Consistent with our observations from the qualitative analysis, there was strong evidence of heterogeneity of studies assessing ECT effects on TRP plasma levels (BF10>10 across the three r’s), based on the eight studies with calculable SMDs [35,39,43,48,52,53,56,58]. However, these studies also gave moderate evidence for null effects. Furthermore, the same two studies as in the qualitative analysis provided moderate evidence for TMS increasing serum levels of 5-HT (supplementary text) [62,63].

Null effects on three other biomarkers were also observed. Allen et al. [35] and Ryan et al. [52] gave moderate evidence for no change in plasma KA levels and KA/KYN ratio in response to ECT. Both studies were multi-session and recruited depressed patients, with the timing of post-ECT sampling on the scale of days (4–7 days in Allen et al. [35] and 1–3 days in Ryan et al. [52]). Furthermore, Sibon et al. [67] and Tateishi et al. [68] provided moderate evidence for no effects on plasma levels of TRP in response to TMS. However, while Tateishi et al. [68] applied multiple treatment sessions on depressed patients, Sibon et al. [67] entailed one session with young and healthy volunteers. Neither study offered the timing of post-TMS sampling.

SMDs for changes in the levels of the biomarkers were calculable in 32 of 37 clinical studies (86%, excluding case reports [49]), while SMDs for changes in the clinical measures were calculable for 22 (59%; values available in the supplementary spreadsheets). Compared to the effects of NIBS on biomarker concentrations, the BF10 values for ECT and TMS improving clinical measures were both larger than 100, indicating high probably of therapeutic outcomes in response to NIBS (other data are available in the supplementary spreadsheets).

4. Discussion

We conducted a scoping review, which conformed with the PRISMA-ScR statement [27], with qualitative and meta-analysis to assess effects of therapeutic NIBS on biomarkers of TRP metabolism. We used the RoBMA [28] to synthesize the findings of studies with calculable SMDs (Table 4) and found moderate evidence for no effects on plasma TRP levels following ECT, with strong evidence for heterogeneity of these results. These findings suggest the absence of an effect by ECT on biomarkers of interest, but these results are inconclusive as they are more-than-not likely due to differences between ECT protocols or varied time points of post-ECT biomarker sampling. We found moderate evidence for TMS elevating effects on serum levels of 5-HT [62,63], but no effects on plasma KA levels and KA/KYN ratio post-ECT [35,52], and no effects on plasma TRP following TMS [67,68]—however, these latter findings were based on two studies each. Overall, the outcomes of NIBS on these biomarkers of interest (Figure 1) are highly heterogenous, with most studies finding null effects across biomarkers (Figure 4) and sampling method (Figure 5), and reporting insufficient statistics for quantitative synthesis, characterized by high methodological heterogeneity, with only a small number using adequately randomized controlled designs (supplementary text). In summary, we cannot conclusively claim or rule out the effects of NIBS on TRP metabolism given the current literature. However, taken at face-value, our findings provide preliminary evidence that informs current hypotheses for the mechanism of action by therapeutic NIBS across neuropsychiatric disorders, specifically mechanisms influenced by TRP metabolism and its molecular targets. To wit, below we discuss our findings in the context of evidence of NIBS’s impact on substrate availability and cytokine expression that mediate TRP metabolism, followed by changes to neurotransmitter potency critical to the induction of neuroplasticity.

As many studies on NIBS conclude, its mechanism of action need further investigation, but current evidence suggests that the observed therapeutic effects may be underlined by changes to long-term potentiation (LTP) and long-term depression (LTD) induction throughout the CNS. Evidence for these NIBS effects, in association with effects on TRP metabolism, are findings of stimulation-induced molecular and morphological changes in the CNS. For example, Peng et al. [94] investigated the effects of low to high frequency (HF) rTMS over the vertex of unpredictable-stress treated rats, which elevated prefrontal catecholamine levels and reduced MAO-A activity. HF-rTMS at 5 Hz had the highest elevating effects on prefrontal 5-HT levels, while also reducing 5-HIAA, and MAO-A activity [94]—this latter protein being critical to the degradation of 5-HT to 5-HIAA (Figure 1). Our meta-analysis showed elevated serum 5-HT levels following TMS, with null or mixed findings across NIBS and biomarker sampling methods. Indeed, clinical and preclinical studies that assessed the effects of TMS [62,63,64,65,68,69,83,84,85,86,87,88,89,90,91,92,93,94,95,96] and ECT [44,57,71,72,73,74,75,76,77,78,79,80] on 5-HT concentrations reported mostly heterogenous results, with 61% of comparisons reporting null effects (Figure 4a,b), with similar mixed results when examining effects by biomarker source (Figure 5a–f). ECT did not have a significant effect on 5-HT levels, suggesting that the therapeutic mechanisms of ECT differ from rTMS. Indeed, in a recent PET study examining TRD patients treated with ECT, Baldinger-Melich et al. [25] reported negligible changes to MAO-A expression in the cerebral cortex of patients after compared to before ECT, despite high antidepressant effects. Regarding the kynurenines, a recent pilot study examined the effects of rTMS on inflammatory cytokines, finding no effects; nor did cytokine levels correlate with depression severity, although significant antidepressants effects were observed [126]. Our results are consistent with these findings, as null effects of rTMS on KYN/TRP (Figure 4a), a biomarker for the rate of TRP metabolism toward the kynurenine pathway, were observed. Such findings suggest that the therapeutic effects of rTMS may not involve changes to inflammatory cytokine expression that lead to increased activation of the kynurenine pathway.

An alternative and exploratory link between NIBS and TRP metabolism is the research thread on the stimulation effects on the autonomic nervous system (ANS). Heart rate variability is a proxy of ANS health, with high variability interpreted as indicating abnormal ANS functioning in depressed patients [127,128]. Excitatory stimulation of the left DLPFC, a common therapeutic rTMS protocol, has restorative effects on this variability compared to sham stimulation [129]. As absorption in the small intestine is also a function of the ANS, the therapeutic effects of rTMS may affect TRP absorption. A consequence of this hypothesis is abnormal TRP levels in peripheral circulation following abnormal ANS function. Indeed, peripheral TRP levels are significantly lower in depressed patients compared to healthy controls [9]. Restoration of ANS function in depressed patients by NIBS would hypothetically increase peripheral TRP levels if symptoms and these biomarkers are associated—however, our included studies using rTMS mostly found null effects on TRP levels [59,60,69], with one finding significant elevated levels in plasma [68], and meta-analysis showing moderate evidence for no effects of ECT [35,39,43,48,52,53,56,58], despite the antidepressant efficacy of these techniques. This is an interesting line of research, and more direct experiments testing whether there is an association between ANS functioning and TRP availability are needed. The effects on TRP availability are critical, as this is the main source of substrate for the 5-HT and KYN pathways, critical for neuroplasticity [15], and for immune response mediation [1,2,7].

Despite the ubiquitous distribution and functional roles of 5-HT, most of its TRP substrate that enters the CNS is degraded toward the kynurenines (Figure 1). Various neuroactive metabolites are produced by this pathway, such as KA and QA, as they are not permeable across the blood–brain barrier—although, peripheral KYN may also be a major source for KA and QA in the CNS, as KYN has been observed to be highly permeable to the blood-brain barrier [130]. In the CNS, KA and QA have various roles, including in immune response, as both act on microglia. These have further effects on neuroplasticity, as KA acts as a receptor antagonist on neuronal N-methyl-D-aspartate (NMDA) whereas QA acts as an agonist, and with further mechanisms of each altering glutamate levels differentially. The effects of KA are typically considered neuroprotective, whereas QA effects are neurotoxic [7]. In support of these effects, low levels of the KA/QA ratio, indicating more neurotoxic and less neuroprotective products from the kynurenine pathway, were observed to coincide with more severe anhedonia symptoms and smaller cortical thickness of the right dorsal anterior cingulate cortex (ACC) in untreated depressed patients compared to controls [131]. In patients with bipolar disorder, KA/QA ratio has also been observed to be significantly lower than healthy controls [132]. More recently, a meta-analysis sought to identify which biomarkers of kynurenine pathway activity differentiate psychiatric disorders, finding KA/QA being significantly lower in MDD and bipolar disorder patients compared to healthy controls [9]. However, despite ECT having significant antidepressant effects (in uni- and bipolar patients) [17], two included studies reported null effects of ECT on QA/KA, an inversed form [33,52], but a third reported significant reductions of the QA/KA ratio [54]—suggesting less neurotoxic QA and more neuroprotective KA, and no studies investigating these ratios after tDCS nor rTMS (Figure 4). Consistent with these effects, our meta-analysis indicated no effects on plasma KA levels and KA/KYN ratio following ECT [35,52]. Moreover, two studies using rTMS found null effects on KA levels in plasma and CSF despite antidepressant effects [68,69]. This reinforces the possibility that the antidepressant effects of NIBS may not be associated with changes to the production of these neuroactive kynurenines but may instead target downstream molecular targets of TRP metabolism.

NIBS has been observed to potentiate signaling strength of TRP metabolites. For instance, in a PET study, HF-rTMS had significant antidepressant effects, with changes to symptom severity positively correlated with change in 5-HT2A receptor binding in bilateral DLPFC, but negatively correlated with right hippocampus receptor binding [133]. This receptor is thought to mediate expression of brain derived neurotrophic factor (BDNF), with 5-HT2A agonists decreasing BDNF mRNA expression in the hippocampus, but increasing expression in the rat neocortex [134]. In another PET study on healthy participants, the effects of HF-rTMS over the left DLPFC on limbic serotonin synthesis were assessed with the radioligand [(11)C]-alpha-methyl-tryptophan, thought to approximate the capacity of TRP metabolism toward the 5-HT pathway. Brain stimulation over the left DLPFC, compared to over the left occipital cortex, was followed by increases in 5-HT release in the right posterior cingulate cortex, but not cortical or sub-cortical regions, with the metabolite presumed to be from terminals of dorsal raphe nuclei [67]. Baldinger et al. [135] reviewed the literature on the effects of ECT on 5-HT neurotransmission, reporting mixed effects on 5-HT1A, including no effects [136] and diminished 5-HT1A receptor binding in the right subgenual ACC, orbitofrontal cortex, amygdala, and hippocampus [137]. In a separate PET study, 5-HT2A receptor binding was also found to be globally diminished, including in the bilateral occipital cortex, the medial parietal cortex, the limbic cortex, and the bilateral prefrontal cortex of depressed patients after ECT [138]. Thus, while the effects of NIBS on 5-HT and other biomarkers of TRP metabolism may not be directly observable, as indicated by our findings, modulations of the molecular targets of these metabolites may instead underlie the therapeutic effects of NIBS.

We observed several limitations with our review methods. First, biomarker keywords were not abbreviated in our search, nor were all names for the same metabolite used. Potentially, this may have caused some studies to have been missed. We attempted to mitigate this by screening the references of reviews and included studies. Second, some metabolites that may be relevant were excluded (such as 6-sulfatoxymelatonin, a product of melatonin metabolism—e.g., [105] was excluded; Table S2). We initially aimed to keep this review focused on TRP metabolites commonly discussed in light of their vital physiological roles, such as 5-HT, melatonin, kynurenine, and NAD+ [7]. Likewise for NIBS, not all techniques were considered, such as transcranial electric stimulation, though several more exist beyond those reviewed here [22]. We sought studies using ECT, rTMS, and tDCS as these are frequently discussed in reviews on the therapeutic efficacy of NIBS and mechanisms of action, e.g., [17,139]. Lastly, our univariate focus on biomarker levels may not be sufficient to elucidate the mechanisms of action by NIBS and the relation between TRP metabolism and health condition—this aim will require future studies to utilize cross-domain expertise, including biomarker effects. That is, research on the dynamics within and between multiple levels of analysis are needed to develop etiologies of neuropsychiatric disorders that capture real-world variability of patients [140] and to elucidate the dynamics between adaptive biological architecture and metabolic homeostasis. For instance, whether change in brain activity and noise following successful therapeutic NIBS coincides to changes in biomarker levels is an important research question to be investigated with careful signal analysis approaches, such as [141,142,143].

5. Conclusions

This scoping review investigated the effects of non-invasive brain stimulation on biomarkers of tryptophan metabolism and synthesized relevant studies using qualitative and meta-analyses. Although the amount of evidence for each biomarker in clinical and preclinical studies is sparse, we were able to conduct meta-analyses, although studies eligible for this synthesis were few. In agreement with Bayesian meta-analysis results, qualitative analysis revealed highly heterogenous methods and findings in this literature. Thus, more randomized controlled studies are needed to elucidate the effects of therapeutic non-invasive brain stimulation on tryptophan metabolism and the correspondence between biomarkers and abnormalities observed in several neuropsychiatric disorders. Such findings would inform optimal use of brain stimulation, in concurrence with other therapies. Specifically, as the nervous system functions by electrochemical principles, the optimal application or synergism of electrical (e.g., non-invasive and invasive brain stimulation) and chemical (e.g., antidepressant and anti-inflammatory treatments) therapies need further investigation.

Author Contributions

Conceptualization, C.G.G. and G.S.K.; methodology, C.G.G. and T.T.Z.L.; software, C.G.G. and T.T.Z.L.; validation, C.G.G., T.T.Z.L. and G.S.K.; formal analysis, T.T.Z.L.; investigation, C.G.G., T.T.Z.L. and G.S.K.; resources, G.S.K.; data curation, C.G.G. and T.T.Z.L.; writing—original draft preparation and visualization, C.G.G. and T.T.Z.L.; writing—review and editing, C.G.G., T.T.Z.L., R.L.D.K., B.B.B.Z., S.Y.Y. and G.S.K.; supervision, G.S.K.; project administration, C.G.G. and T.T.Z.L.; funding acquisition, G.S.K. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Available data reviewed in this article is contained within the article or Supplementary Materials.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures and Tables
View Image - Figure 1. Products of tryptophan metabolism via serotonin (red) and kynurenine (blue) pathways. Arrows point toward the direction of metabolism as mediated by different enzymes or other catalysts, with fields showing metabolites produced along these pathways. Double arrows indicate multiple metabolic steps (catalysts not shown). Abbreviations: TPH2: tryptophan hydroxylase, isoenzyme 2; AAAD: aromatic acid decarboxylase; MAO-A: monoamine oxidase A; HIOMT: hydroxyindole O-methyl transferase; SNAT: serotonin-N-acetyltransferase; IDO: indoleamine 2,3-dioxyenase; KAT: kynurenine aminotransferase; KMO: kynurenine 3-monooxygenase; KYNU: kynurinase; ACMS: 2-amino-3-carboxymuconic-6-semialdehyde decarboxylase.

Figure 1. Products of tryptophan metabolism via serotonin (red) and kynurenine (blue) pathways. Arrows point toward the direction of metabolism as mediated by different enzymes or other catalysts, with fields showing metabolites produced along these pathways. Double arrows indicate multiple metabolic steps (catalysts not shown). Abbreviations: TPH2: tryptophan hydroxylase, isoenzyme 2; AAAD: aromatic acid decarboxylase; MAO-A: monoamine oxidase A; HIOMT: hydroxyindole O-methyl transferase; SNAT: serotonin-N-acetyltransferase; IDO: indoleamine 2,3-dioxyenase; KAT: kynurenine aminotransferase; KMO: kynurenine 3-monooxygenase; KYNU: kynurinase; ACMS: 2-amino-3-carboxymuconic-6-semialdehyde decarboxylase.

View Image - Figure 2. PRISMA flowchart. *: for each database in our search; **: no automation tools were used.

Figure 2. PRISMA flowchart. *: for each database in our search; **: no automation tools were used.

View Image - Figure 3. Publication year of included studies. Abbreviations: ECT: electroconvulsive therapy; TMS: transcranial magnetic stimulation; tDCS: transcranial direct current stimulation.

Figure 3. Publication year of included studies. Abbreviations: ECT: electroconvulsive therapy; TMS: transcranial magnetic stimulation; tDCS: transcranial direct current stimulation.

View Image - Figure 4. Summary of (a) clinical and (b) preclinical trials findings, including direction of effects by NIBS and by biomarker. Colors indicate statistical effects on biomarkers by NIBS: red = significant increase; blue = significant decrease; yellow = no significant changes to biomarker levels following NIBS. ↑: Significantly increased or the experimental group levels were significantly larger than the control group; ↓: significantly decreased or the experimental group levels significantly smaller than the control group, *: biomarkers in the serotonin pathway; #: biomarkers in the kynurenine pathway. TRP refers to total TRP when not specified, and for brain tissue and microdialysis the regions are collapsed. Abbreviations: TRP: tryptophan; 5-HT: serotonin; 5-HIAA: 5-hydroxyindoleacetic acid; KYN: kynurenine; KA: kynurenic acid; 3-HK: 3-hydroxykynurenine; QA: quinolinic acid; XA: xanthurenic acid; AA: anthranilic acid; PA: picolinic acid; ECT: electroconvulsive therapy; TMS: transcranial magnetic stimulation; ns: not significant.

Figure 4. Summary of (a) clinical and (b) preclinical trials findings, including direction of effects by NIBS and by biomarker. Colors indicate statistical effects on biomarkers by NIBS: red = significant increase; blue = significant decrease; yellow = no significant changes to biomarker levels following NIBS. ↑: Significantly increased or the experimental group levels were significantly larger than the control group; ↓: significantly decreased or the experimental group levels significantly smaller than the control group, *: biomarkers in the serotonin pathway; #: biomarkers in the kynurenine pathway. TRP refers to total TRP when not specified, and for brain tissue and microdialysis the regions are collapsed. Abbreviations: TRP: tryptophan; 5-HT: serotonin; 5-HIAA: 5-hydroxyindoleacetic acid; KYN: kynurenine; KA: kynurenic acid; 3-HK: 3-hydroxykynurenine; QA: quinolinic acid; XA: xanthurenic acid; AA: anthranilic acid; PA: picolinic acid; ECT: electroconvulsive therapy; TMS: transcranial magnetic stimulation; ns: not significant.

View Image - Figure 5. Count of experimental groups reporting significant increases, decreases, or non-significant changes in the metabolites by NIBS. (a–c) From CSF, plasma, and serum in clinical studies respectively. (d–f) from brain tissue, microdialysis, and plasma in preclinical studies respectively. Colors indicate statistical effects on biomarkers by NIBS: red = significant increase; blue = significant decrease; yellow = no significant changes to biomarker levels following NIBS. *: biomarkers in the serotonin pathway; #: biomarkers in the kynurenine pathway. TRP refers to total TRP when not specified, and for brain tissue and microdialysis the regions are collapsed. Abbreviations: TRP: tryptophan; 5-HT: serotonin; 5-HIAA: 5-hydroxyindoleacetic acid; KYN: kynurenine; KA: kynurenic acid; 3-HK: 3-hydroxykynurenine; QA: quinolinic acid; XA: xanthurenic acid; AA: anthranilic acid; PA: picolinic acid; ECT: electroconvulsive therapy; TMS: transcranial magnetic stimulation; ns: not significant.

Figure 5. Count of experimental groups reporting significant increases, decreases, or non-significant changes in the metabolites by NIBS. (a–c) From CSF, plasma, and serum in clinical studies respectively. (d–f) from brain tissue, microdialysis, and plasma in preclinical studies respectively. Colors indicate statistical effects on biomarkers by NIBS: red = significant increase; blue = significant decrease; yellow = no significant changes to biomarker levels following NIBS. *: biomarkers in the serotonin pathway; #: biomarkers in the kynurenine pathway. TRP refers to total TRP when not specified, and for brain tissue and microdialysis the regions are collapsed. Abbreviations: TRP: tryptophan; 5-HT: serotonin; 5-HIAA: 5-hydroxyindoleacetic acid; KYN: kynurenine; KA: kynurenic acid; 3-HK: 3-hydroxykynurenine; QA: quinolinic acid; XA: xanthurenic acid; AA: anthranilic acid; PA: picolinic acid; ECT: electroconvulsive therapy; TMS: transcranial magnetic stimulation; ns: not significant.

View Image - Figure 5. Count of experimental groups reporting significant increases, decreases, or non-significant changes in the metabolites by NIBS. (a–c) From CSF, plasma, and serum in clinical studies respectively. (d–f) from brain tissue, microdialysis, and plasma in preclinical studies respectively. Colors indicate statistical effects on biomarkers by NIBS: red = significant increase; blue = significant decrease; yellow = no significant changes to biomarker levels following NIBS. *: biomarkers in the serotonin pathway; #: biomarkers in the kynurenine pathway. TRP refers to total TRP when not specified, and for brain tissue and microdialysis the regions are collapsed. Abbreviations: TRP: tryptophan; 5-HT: serotonin; 5-HIAA: 5-hydroxyindoleacetic acid; KYN: kynurenine; KA: kynurenic acid; 3-HK: 3-hydroxykynurenine; QA: quinolinic acid; XA: xanthurenic acid; AA: anthranilic acid; PA: picolinic acid; ECT: electroconvulsive therapy; TMS: transcranial magnetic stimulation; ns: not significant.

Figure 5. Count of experimental groups reporting significant increases, decreases, or non-significant changes in the metabolites by NIBS. (a–c) From CSF, plasma, and serum in clinical studies respectively. (d–f) from brain tissue, microdialysis, and plasma in preclinical studies respectively. Colors indicate statistical effects on biomarkers by NIBS: red = significant increase; blue = significant decrease; yellow = no significant changes to biomarker levels following NIBS. *: biomarkers in the serotonin pathway; #: biomarkers in the kynurenine pathway. TRP refers to total TRP when not specified, and for brain tissue and microdialysis the regions are collapsed. Abbreviations: TRP: tryptophan; 5-HT: serotonin; 5-HIAA: 5-hydroxyindoleacetic acid; KYN: kynurenine; KA: kynurenic acid; 3-HK: 3-hydroxykynurenine; QA: quinolinic acid; XA: xanthurenic acid; AA: anthranilic acid; PA: picolinic acid; ECT: electroconvulsive therapy; TMS: transcranial magnetic stimulation; ns: not significant.

PICO statement.

Patient Human or animal models; can be healthy or with an underlying health condition.
Intervention NIBS techniques: ECT, rTMS, or tDCS
Comparison Biomarkers of interest assessed: tryptophan (TRP), kynurenine (KYN), formylkynurenine, kynurenic acid (KA), quinolinic acid (QA), NAD+, 3-hydroxykynurenine (3-HK), xanthurenic acid (XA), picolinic acid (PA), anthranilic acid (AA), serotonin (5-HT), oxitriptan, 5-hydroxytryptamine (5-HT), 5-hydroxyindoleacetic acid (5-HIAA), N-acetyl-5-HT, or melatonin. Measures of their concentrations must be reported and compared to baseline levels, e.g., measures obtained before and again during or after NIBS, or comparison of animal models that received active versus sham NIBS. Studies without a control group can be included, so long as baseline measures are clearly defined.
Outcome Biomarkers must measure serotonin or kynurenine pathway activation, sampled peripherally or centrally (e.g., CSF, plasma/serum, microdialysis, brain tissue analysis in animal models). Changes in health condition will be collected if available (e.g., in humans, clinical scales; in rodents, task specific performance)

Clinical studies included: characteristics and individual results.

Study Design Protocol Participants Demographics Source Timing of Post-NIBS Sampling Biomarker Result
ECT
Aarsland et al., 2019 [33] pretest-posttest Site: right unilateralSeizure length: *median 50.7 s, IQR 16 sSession N: *max. 20Session freq.: 3/week depression (uni- and bipolar, with and without psychotic symptoms) N: 21M:F: 44:56% *Age: median 46, IQR 21.0 * serum 1–2 weeks after the last session (median 10 days, IQR 6) TRP ns
KYN ns
KA ns
3-HK ns
QA ns
PA
XA ns
AA ns
KYN/TRP ns
KA/KYN ns
KA/3-HK ns
QA/KA ns
XA/3-HK ns
PA/QA
Aberg-Wistedt et al., 1986 [34] pretest-posttest Site: bifrontotemporalSeizure length: 45.0 ± 8.2 s *Session N: 8.0 ± 3.1 *Session freq.: 3/week depression (unipolar, without psychotic symptoms) N: 11M:F: 33:67% *Age: 56 ± 16.2 * CSF 3 weeks after the last session 5-HIAA ns
Allen et al., 2018 [35] pretest-posttest Site: bitemporalSession N: max. 6Session freq.: 2/week TRD (unipolar) N: 18M:F: 33:67%Age: 57.5 ± 14.7 plasma 4–7 days after the last session TRP ns
KYN ns
KA ns
KYN/TRP ns
KA/KYN ns
D’Elia et al., 1977 [36] pretest-posttest Site: nondominant unilateralSession N: mean 6.1, range 3–12 depression (uni- and bipolar) N: 24M:F: 38:63%Age: 48.0 ± 12.5, range 22–64 serum mean of levels sampled before each session from the second to the last. TRP ns
Guloksuz et al., 2015 [37] pretest-posttest Site: bifrontotemporalSeizure length: mean 52 s, range 10–200 sSession N: mean 6.1, range 3–11Session freq.: 2/week TRD (uni- and bipolar) N: 19M:F: 32:68%Age: 52.6 ± 14.4, range 23–74 serum before every other session TRP ns
KYN ns
KA
3-HK ns
5-HIAA ns
KYN/TRP
KA/KYN
KA/3-HK
5-HIAA/KYN ns
Hasani et al., 2019 [38] parallel Site: bifrontotemporalSession N: 6–8Session freq.: every other day TRD (unipolar) Exp. group N: 21Age: 35.24 ± 14.17Control group N: 15Age: 33.26 ± 13.59 plasma 16 days after the first session 5-HT ↑ (posttest)
30 days after the first session ↑ (posttest)
Hoekstra et al., 2001 [39] pretest-posttest Site: unilateral and bifrontotemporalSession N: mean 11Session freq.: 2/week TRD (unipolar, with and without psychotic symptoms) N: 20M:F: 35:65%Age: 52 ± 13.1 plasma the morning after the final session TRP ns
Hoffmann et al., 1985 [40] pretest-posttest Site: bitemporalSession N: mean 11, range 6–19 *Session freq.: 3/week depression (uni- and bipolar, with and without psychotic symptoms) N: 7all maleAge: 46 ± 11.2, range 29–61 CSF 12 days after the last session 5-HIAA ns
Hofmann et al., 1996 [41] pretest-posttest Site: bifrontotemporalSeizure length: 40.48 ± 14.12 sSession N: 1 depression (unipolar) N: 31M:F: 29:71%Age: 37.22 ± 13.98 serum 1 min after the session 5-HIAA ns
1 h after the session
2 h after the session
Jori et al., 1975 [42] pretest-posttest Session N: 4–8 depression (with psychotic symptoms) N: 12M:F: 88:12% *Age: mean 45, range 25–63 * CSF 7 days after the final session 5-HIAA
Kirkegaard, Møller and Bjørum, 1978 [43] pretest-posttest Site: unilateralSession N: 10.5 ± 2.6Session freq.: 2/week depression (uni- and bipolar) N: 10M:F: 30:70%Age: mean 63 CSF - TRP ns
plasma TRP
free TRP ns
free/total TRP
Lestra et al., 1998 [44] pretest-posttest Session N: 5–9Session freq.: every 3 or 4 days depression (unipolar) N: 6M:F: 43:57% *Age: range 27–70 * platelet pellet 10 days after the last session 5-HT ns
Mokhtar et al., 1997 [45] pretest-posttest Site: bilateralSeizure length: 20 s in nine, a mild fit in oneSession N: 1 depression (uni- and bipolar) N: 10M:F: 50:50%Age: mean 48.5, SEM 4.3 serum 15 min after the session TRP ns
30 min after the session ns
45 min after the session
1 h after the session
Nikisch and Mathé, 2008 [46] pretest-posttest Site: unilateralSession N: 8Session freq.: 2/week TRD (unipolar, with and without psychotic symptoms) N: 6M:F: 83:17%Age: 40 ± 8 CSF 1 week after the last session 5-HIAA
Olajossy et al., 2017 [47] pretest-posttest Site: bifrontotemporalSession N: 12Session freq.: 2/week recurrent depressive disorder N: 32M:F: 41:59%Age: 49.41 ± 12.73 serum 30 min after the first, sixth, and 12th sessions KA ns
depression in bipolar disorder N: 11M:F: 36:64%Age: 44.73 ± 13.83 ns
schizoaffective disorder N: 7M:F: 43:57%Age: 33.29 ± 8.56 ns
Palmio et al., 2005 [48] pretest-posttest Site: bilateralSeizure length: 45.7 ± 13.2, range 21–66Session N: 3.8 ± 2.2, range 1–7 depression (unipolar, with and without psychotic symptoms) N: 10M:F: 30:70%Age: 55.6 ± 15.8, range 28–73 plasma 2 h after the last session TRP
6 h after the last session
24 h after the last session
48 h after the last session ns
Rudorfer et al., 1988 [49] pretest-posttest Site: uni- and bilateralSeizure length: at least 25 sSession N: 14.3 ± 1.2, range 13–15 depression (unipolar) N: 3all femaleAge: 48.7 ± 22.0, range 35–74 CSF 4–5 days after the last session 5-HIAA No statistical tests: levels reportedly increased in 2 of 3 patients.
Rudorfer et al., 1991 [50] pretest-posttest Site: uni- and bilateralSeizure length: at least 25 sSession N: 13.6 ± 3.3, range 9–19 TRD (unipolar) N: 8M:F: 25:75%Age: 53.1 ± 13.2, range 35–71 CSF 5–10 days after the last session 5-HIAA ns
Ryan et al., 2020 [51] pretest-posttest Site: unilateral and bitemporalSession N: 7.97 ± 2.46Session freq.: 2/week depression (uni- and bipolar, with and without psychotic symptoms) N: 94M:F: 38:62%Age: 55.48 ± 14.72 plasma 1–3 days after the last session XA/3-HK ns
Ryan et al., 2020 [52] pretest-posttest Site: unilateral and bitemporalSession N: 7.96 ± 2.47Session freq.: 2/week depression (uni- and bipolar, with and without psychotic symptoms) N: 94M:F: 38:62%Age: 55.48 ± 14.72 plasma 1–3 days after the last session TRP ns
KYN ns
KA ns
3-HK ns
QA ns
PA ns
XA ns
AA ns
KYN/TRP ns
KA/KYN ns
QA/KA ns
QA/KYN ns
Sawa, 1981 [53] pretest-posttest Session N: 1 depression (uni- and bipolar) N: 9M:F: 44:56%Age: 40.7 ± 11.8, range 20–52 plasma 1 min after the session TRP ns
free TRP
5 min after the session TRP
free TRP ns
10 min after the session TRP
free TRP ns
30 min after the session TRP ns
free TRP ns
1 h after the session TRP ns
free TRP
Schwieler et al., 2016 [54] pretest-posttest Site: right unilateralSession N: 3 TRD (unipolar) N: 15M:F: 58:42% *Age: median 41.0, IQR 25.0–54.0 * plasma - TRP
KYN ↓ $
KA ns
QA
KYN/TRP ns
QA/KA
Smith and Strömgren, 1981 [55] pretest-posttest Site: nondominant unilateralSession freq.: 4/week depression N: 13M:F: 69:31%Age: 42.7 ± 12.5, range 24–61 serum 9 am on the day after the last session TRP ns
Stelmasiak and Curzon, 1974 [56] pretest-posttest Site: unilateralSession N: 1 depression N: 18M:F: 39:61%Age: mean 48, range 20–70 plasma 1 min after the session TRP ns
free TRP
15 min after the session TRP ns
free TRP
30 min after the session TRP ns
free TRP ns
1 h after the session TRP ns
free TRP ns
Udayakumar et al., 1981 [57] pretest-posttest Site: bitemporalSession N: 1 schizophrenia N: 29M:F: 66:34%Age: 27.4 ± 8.0, range 14–49 CSF 5 min after the session 5-HT
48–72 h after the session ns
Whalley, Yates and Christie, 1980 [58] pretest-posttest Session N: 4–9 * depression (unipolar, without psychotic symptoms) N: 11M:F: 25:75% *Age: 49 ± 13.9 * plasma 10 min after the first session TRP
free TRP ns
immediately before the last session TRP ns #
free TRP ns #
12 weeks after the last session TRP ns $
free TRP ns $
TMS
Leblhuber et al., 2021 [59] pretest-posttest Site: medial frontopolar cortexPulse freq.: 20 HzIntensity: 1.5 TPulse N: 2400Session N: 10Session freq.: 5/week TRD (unipolar) N: 21M:F: 48:52%Age: 59.4 ± 15.7 serum - TRP ns
KYN ns
KYN/TRP ns
Leblhuber, Steiner and Fuchs, 2019 [60] parallel Site: bilateral prefrontal cortexPulse freq.: 3 HzIntensity: 0.08 TPulse N: 30 minSession N: 10Session freq.: 5/week TRD (geriatric) Exp. group N: 19M:F: 45:55% *Age: mean 71.9, SEM 2.92Control group N: 10M:F: 45:55% *Age: mean 73.3, SEM 2.69 serum immediately after the last session TRP ns (group x time)
KYN ns (group x time)
KYN/TRP ns (group x time)
Leblhuber et al., 2018 [61] pretest-posttest Site: bilateral prefrontal cortexPulse freq.: 3 HzIntensity: above 100% MTSession N: 10 TRD (geriatric) N: 10M:F: 40:60%Age: 69 ± 8.78 serum - TRP ns
KYN ns
KYN/TRP ns
Liu et al., 2022 [62] parallel Site: bilateral dorsolateral and ventrolateral prefrontal cortexPulse freq.: 0.5 HzIntensity: 0.70 TSession N: 8Session freq.: 5/week post-stroke depression Exp. group N: 35M:F: 57:43%Age: 55.61 ± 6.84Control group N: 35M:F: 66:34%Age: 50.20 ± 6.28 serum 8 weeks after the last session 5-HT ↑ (posttest)
Lu et al., 2018 [63] pretest-posttest Site: bilateral dorsolateral prefrontal cortexPulse freq.: 1 HzIntensity: 80% MTPulse N: 750Session N: 10Session freq.: 5/week generalized anxiety disorders N: 28M:F: 39:61%Age: 45.5 ± 12.67, range 27–72 serum 1 h after the last session 5-HT
Maestú et al., 2013 [64] parallel Site: 33 stimulation coils distributed evenly across an EEG capPulse freq.: 8 HzIntensity: 43 nTPulse N: 20 minSession N: 8Session freq.: 1/week fibromyalgia Exp. group N: 28all femaleAge: 40.7 ± 6.7 *Control group N: 26all femaleAge: 40.7 ± 6.7 * blood - 5-HT ns (group x time)
Miniussi et al., 2005 [65] pretest-posttest Site: left dorsolateral prefrontal cortexPulse freq.: 17 HzIntensity: 110% MTPulse N: 408Session N: 5Session freq.: 1/day TRD (uni- and bipolar, with and without psychotic symptoms) N: 10M:F: 25:75% *Age: mean 58 plasma the day of the last session 5-HT ns
5-HIAA ns
Pulse freq.: 1 HzPulse N: 400 N: 10M:F: 25:75% *Age: mean 52 5-HT ns
5-HIAA ns
Niimi et al., 2020 [66] parallel Site: primary motor cortex of the unaffected hemispherePulse freq.: 1 HzIntensity: 90% MTPulse N: 1200Session N: 22Session freq.: 2/day stroke Exp. group N: 62M:F: 66:34%Age: 62.3 ± 11.0Control group N: 33M:F: 52:48%Age: 66.2 ± 10.8 serum - TRP ns
KYN ns
KYN/TRP ns
Sibon et al., 2007 [67] crossover Site: left dorsolateral prefrontal cortexPulse freq.: 10 HzIntensity: 90% MTPulse N: 450Session N: 1 healthy N: 10M:F: 50:50%Age: 24.7 ± 5.14, range 18–40 plasma - TRP ns
free TRP ns
Tateishi et al., 2021 [68] pretest-posttest Site: left dorsolateral prefrontal cortexPulse freq.: 10 HzIntensity: 100% MTPulse N: 1600Session N: 30Session freq.: 5/week TRD (unipolar) N: 13M:F: 31:69%Age: 54.9 ± 14.3 plasma - TRP
oxitriptan ns
5-HT
melatonin ns
KYN ns
KA ns
3-HK ns
KYN/TRP ns
Tateishi et al., 2022 [69] pretest-posttest Site: left dorsolateral prefrontal cortexPulse freq.: 10 HzIntensity: 100% MTPulse N: 1600Session N: 30Session freq.: 5/week TRD (unipolar) N: 5Age: 48.0 ± 13.9, range 30–72 CSF - TRP ns
5-HT ns
KYN
KA ns
3-HK ns
tDCS
Hadoush et al., 2021 [70] pretest-posttest Site: bilateral primary motor cortex and bilateral dorsolateral prefrontal cortexPolarity: anodalElectrode size: 25 cm2Intensity: 1 mADuration: 20 minSession N: 10Session freq.: 5/week Parkinson’s disease N: 25M:F: 76:24%Age: mean 61.5, range 30–80 serum - melatonin

↑: significantly increased or the experimental group levels were significantly larger than the control group; ↓: significantly decreased or the experimental group levels were significantly smaller than the control group; ns: non-significantly changed or different; *, #, and $: data not available for the featured group but taken from a larger group it belonged to or a subgroup of it, e.g., who were followed up; -: not applicable or data not available; N: count; freq.: frequency; exp.: experimental. For studies using a parallel design, “(group x time)” denotes the result based on group x time interaction, and “(posttest)” group difference in the posttest. Here TRP refers to total TRP when unspecified.

Preclinical studies included: characteristics and individual results.

Study Design Protocol Subjects Demographics Source Timing of Post-NIBS Sampling Biomarker Result
ECT
Evans et al., 1976 [71] parallel Site: ear clipsSession N: 1 healthy Sprague-Dawley rats Exp. group N: -all maleControl group N: -all male brain tissue 30 min after the session TRP ns (posttest)
5-HT ns (posttest)
5-HIAA ns (posttest)
Exp. group N: 5Control group N: 5 1 h after the session 5-HT ns (posttest)
Exp. group N: 6Control group N: 5 3 h after the session TRP ns (posttest)
Exp. group N: 14Control group N: 14 5-HT ns (posttest) *
5-HIAA ↑ (posttest)
Exp. group N: 3Control group N: 3 6 h after the session 5-HT ns (posttest)
Exp. group N: 4Control group N: 5 24 h after the session TRP ns (posttest)
5-HT ns (posttest)
5-HIAA ns (posttest)
Gur et al., 2002 [72] parallel Site: ear clipsSession N: 10Session freq.: 1/day healthy Albino rats Exp. group N: 13all maleControl group N: 16all male microdialysis (ventral hippocampus) 48 h after the last session 5-HT ns (posttest)
microdialysis (anterior hypothalamus) 24 h after the last session ns (posttest)
Juckel et al., 1999 [73] pretest-posttest Site: left medial prefrontal cortexSession N: 1 healthy, anesthetized Sprague-Dawley rats N: 6all male microdialysis (left amygdala) during the session 5-HT
Site: left medial prefrontal cortex healthy, anesthetized Sprague-Dawley rats N: 6 microdialysis (left ventral hippocampus)
Site: left medial prefrontal cortex healthy, behaving Sprague-Dawley rats N: 3 microdialysis (left ventral hippocampus)
Site: right medial prefrontal cortex healthy, anesthetized Sprague-Dawley rats N: 4 microdialysis (left ventral hippocampus)
Site: right medial prefrontal cortex healthy, anesthetized Sprague-Dawley rats N: 3 microdialysis (right ventral hippocampus)
Karoum et al., 1986 [74] pretest-posttest Site: ear clipsSession N: 10Session freq.: 1/day healthy Sprague-Dawley rats N: 5all male brain tissue (caudate nucleus) 20 h after the last session 5-HT ns
5-HIAA ns
5-HIAA/5-HT ns
1 week after the last session 5-HT ns
5-HIAA ns
5-HIAA/5-HT ns
brain tissue (frontal cortex) 20 h after the last session 5-HT ns
5-HIAA ns
5-HIAA/5-HT ns
1 week after the last session 5-HT
5-HIAA ns
5-HIAA/5-HT ns
urine nights between sessions 5-HIAA
nights in the first week after the last session
Khanna et al.,, 1971 [75] parallel Site: templesSession N: 15Session freq.: 1/day healthy dogs later with ECT-induced cardiac abnormalities Exp. group N: 19Control group N: 10 myocardium tissue the day after the last session 5-HT ↑ (posttest)
healthy dogs later without ECT-induced cardiac abnormalities Exp. group N: 11Control group N: 10 ns (posttest)
Madhav et al., 2000 [76] parallel Site: ear clipsSession N: 5Session freq.: every other day Sprague-Dawley rats with serotonergic lesion in the right cingulum bundle (via which the hippocampus receives serotonergic innervation) Exp. group N: 4all maleControl group N: 4all male brain tissue (right hippocampus) 18 days after the last session 5-HT ns (posttest)
5-HIAA ↑ (posttest)
5-HIAA/5-HT ns (posttest)
McIntyre and Oxenkrug, 1984 [77] parallel Site: ear clipsSeizure length: 20–25 sSession N: 7Session freq.: 1/day healthy Sprague-Dawley rats Exp. group N: 14all maleControl group N: 7all male brain tissue (hypothalamus) 9 pm of the day of the last session TRP ns (posttest)
5-HT ↓ (posttest)
5-HIAA ns (posttest)
Exp. group N: 13Control group N: 7 brain tissue (pineal gland) TRP ns (posttest)
5-HT ↓ (posttest)
5-HIAA ns (posttest)
N-acetyl-5-HT ns (posttest)
melatonin ns (posttest)
Session N: 1 Exp. group N: 8Control group N: 7 brain tissue (hypothalamus) TRP ns (posttest)
5-HT ns (posttest)
5-HIAA ↓ (posttest)
Exp. group N: 7Control group N: 7 brain tissue (pineal gland) TRP ns (posttest)
5-HT ns (posttest)
5-HIAA ns (posttest)
N-acetyl-5-HT ns (posttest)
melatonin ns (posttest)
Shields, 1972 [78] parallel Session N: 8 healthy rats Exp. group N: 8Control group N: 8 brain tissue 24 h after the last session 5-HT ns (posttest)
5-HIAA ns (posttest)
Exp. group N: 8Control group N: 7 5-HT ns (posttest)
5-HIAA ns (posttest)
Session N: 12 Exp. group N: 7Control group N: 8 5-HT ns (posttest)
5-HIAA ns (posttest)
Session N: 16 Exp. group N: 6Control group N: 8 5-HT ns (posttest)
5-HIAA ns (posttest)
Session N: 1 Exp. group N: 8Control group N: 8 3 h after the session TRP ns (posttest)
5-HT ns (posttest)
5-HIAA ↑ (posttest) *
Sugrue, 1983 [79] parallel Site: ear clipsSession N: 10Session freq.: 1/day healthy Sprague-Dawley rats Exp. group N: at least 5all maleControl group N: 40–48all male brain tissue (cortex) 6.5 h after the last session 5-HT ns (posttest)
5-HIAA ↑ (posttest)
Tagliamonte et al., 1972 [80] parallel Site: ear clipsSeizure length: 15 sSession N: 2Session freq.: 30 min interval healthy Wistar rats Exp. group N: 24all maleControl group N: 150all male plasma 1 h after the first session TRP ns (posttest)
brain tissue TRP ↑ (posttest)
5-HT ns (posttest)
5-HIAA ↑ (posttest)
Session N: 1 Exp. group N: 21Control group N: 150 plasma TRP ns (posttest)
brain tissue TRP ↑ (posttest)
5-HT ns (posttest)
5-HIAA ↑ (posttest)
Yoshida et al., 1997 [81] parallel Site: ear clipsSeizure length: 20–25 sSession N: 8Session freq.: 1/day healthy Wistar rats Exp. group N: 6all maleControl group N: 6all male microdialysis (striatum) 0–180 after the first session 5-HIAA ↑ (posttest/pretest)
immediately before the last session ↑ (posttest)
Yoshida et al., 1998 [82] parallel Site: ear clipsSeizure length: 20–25 sSession N: 8Session freq.: 1/day healthy Wistar rats Exp. group N: 6all maleControl group N: 6all male microdialysis (frontal cortex) 0–180 after the first session 5-HIAA ↑ (posttest/pretest)
immediately before the last session ↑ (posttest)
TMS
Ben-Shachar et al., 1997 [83] parallel Pulse freq.: 25 HzIntensity: 2.3 TPulse N: 50Session N: 1 healthy Sprague-Dawley rats Exp. group N: 16–20all maleControl group N: 16–20all male brain tissue (frontal cortex) 10 s after the session 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ns (posttest)
brain tissue (hippocampus) 5-HT ↑ (posttest)
5-HIAA ↑ (posttest)
5-HIAA/5-HT ns (posttest)
brain tissue (striatum) 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ns (posttest)
brain tissue (midbrain) 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ns (posttest)
Ben-Shachar et al., 1999 [84] parallel Pulse freq.: 15 HzIntensity: 2 TPulse N: 52Session N: 10Session freq.: 1/day healthy Sprague-Dawley rats Exp. group N: 18–20all maleControl group N: 18–20all male brain tissue (frontal cortex) 4 h after the last session 5-HT ns (posttest)
brain tissue (hippocampus) ns (posttest)
brain tissue (striatum) ns (posttest)
brain tissue (midbrain) ns (posttest)
El Arfani et al., 2017 [85] parallel Site: prefrontal cortexPulse freq.: 20 HzIntensity: 110% MTPulse N: 1560Session N: 20Session freq.: 5/day healthy Sprague-Dawley rats Exp. group N: 6all maleControl group N: 6all male brain tissue (striatum) the day after the last session 5-HT ns (posttest)
5-HIAA ↓ (posttest)
Gur et al., 2000 [86] parallel Pulse freq.: 15 HzIntensity: 1.12 TPulse N: 600Session N: 10Session freq.: 1/day healthy Albino rats Exp. group N: 10all maleControl group N: 10all male microdialysis (left prefrontal cortex) the morning after the last session 5-HT ns (posttest)
Heath et al., 2018 [87] parallel Site: bifrontal cortexPulse freq.: 10 HzIntensity: 12 mTPulse N: 1800Session N: 20Session freq.: 5/week C57BL/6J mice with olfactory bulbectomy (modelling agitated depression) Exp. group N: 11all maleControl group N: 9all male plasma 24 h after the last session TRP ns (posttest)
plasma 5-HT ns (posttest)
Intensity: 90 mT Exp. group N: 5Control group N: 3 brain tissue (frontal cortex) 5-HT ns (posttest)
Exp. group N: 10Control group N: 9 plasma TRP ns (posttest)
plasma 5-HT ↓ (posttest)
Intensity: 1.2 T Exp. group N: 9Control group N: 9 plasma TRP ns (posttest)
plasma 5-HT ns (posttest)
Kanno et al., 2003 [88] parallel Site: frontal brainPulse freq.: 25 HzIntensity: 0.6 TPulse N: 125Session N: 3Session freq.: 1/day healthy Wistar rats Exp. group N: 8all maleControl group N: 7all male microdialysis (prefrontal cortex) - 5-HT ns (posttest)
Kanno et al., 2003 [89] parallel Site: frontal brainPulse freq.: 25 HzIntensity: 0.6 TPulse N: 500Session N: 1 healthy Wistar rats Exp. group N: 6all maleControl group N: 6all male microdialysis (right prefrontal cortex) during and 0–160 min after the session 5-HT ↓ (posttest)
Kanno et al., 2004 [90] parallel Site: frontal brainPulse freq.: 25 HzIntensity: 0.6 TPulse N: 500Session N: 1 healthy Wistar rats Exp. group N: 6all maleControl group N: 6all male microdialysis (right dorsolateral striatum) during and 0–160 min after the session 5-HT ns (posttest)
Keck et al., 2000 [91] parallel Site: left frontal cortexPulse freq.: 20 HzIntensity: 130% MTPulse N: 1000Session N: 1 healthy Wistar rats Exp. group N: 8all maleControl group N: 6all male microdialysis (right dorsal hippocampus) during and 0–30 and 30–60 min after the session 5-HT ns (group x time)
5-HIAA ns (group x time)
Kim et al., 2016 [92] parallel Site: right prefrontal cortexPulse freq.: 10 HzIntensity: 100% MTPulse N: 1000Session N: 15Session freq.: 5/week SHR/Izm rats (spontaneously hypertensive, modelling ADHD) Exp. group N: 9all maleControl group N: 8all male brain tissue (prefrontal cortex) 7 h 50 min after the last session 5-HT ns (posttest)
Löffler et al., 2012 [93] parallel Site: cerebral cortexPulse freq.: 20 HzIntensity: 130% MTPulse N: 300Session N: 1 healthy Wistar rats Exp. group N: 8all maleControl group N: 6all male microdialysis (nucleus accumbens shell) 0–160 min after the session 5-HT ↑ (posttest/pretest)
5-HIAA ns (posttest/pretest)
Peng et al., 2018 [94] parallel Site: vertexPulse freq.: 1 HzIntensity: 0.84 TSession N: 7Session freq.: 1/day Sprague-Dawley rats with chronic unpredictable stress (modelling depression) Exp. group N: 10all maleControl group N: 10all male brain tissue (prefrontal cortex) 24 h after the last session 5-HT ns (posttest)
5-HIAA ns (posttest)
Intensity: 1.26 T Exp. group N: 10Control group N: 10 5-HT ns (posttest)
5-HIAA ns (posttest)
Pulse freq.: 5 HzIntensity: 0.84 T Exp. group N: 10Control group N: 10 5-HT ↑ (posttest)
5-HIAA ↓ (posttest)
Intensity: 1.26 T Exp. group N: 10Control group N: 10 5-HT ↑ (posttest)
5-HIAA ↓ (posttest)
Pulse freq.: 10 HzIntensity: 0.84 T Exp. group N: 10Control group N: 10 5-HT ↑ (posttest)
5-HIAA ↓ (posttest)
Intensity: 1.26 T Exp. group N: 10Control group N: 10 5-HT ↑ (posttest)
5-HIAA ↓ (posttest)
Poh et al., 2019 [95] parallel Site: lambdaPulse freq.: 10 HzIntensity: 12 mTPulse N: 6000Session N: 1 healthy C57BL/6J mice Exp. group N: 5M:F: 60:40%Control group N: 5M:F: 60:40% brain tissue (cortex) immediately after the session 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ↓ (posttest)
brain tissue (hippocampus) 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ns (posttest)
brain tissue (striatum) 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ns (posttest)
Intensity: 1.2 TPulse N: 3600 Exp. group N: 6M:F: 50:50%Control group N: 5M:F: 60:40% brain tissue (cortex) 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ns (posttest)
brain tissue (hippocampus) 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ns (posttest)
brain tissue (striatum) 5-HT ns (posttest)
5-HIAA ns (posttest)
5-HIAA/5-HT ns (posttest)
Wang et al., 2022 [96] parallel Site: center of skullPulse freq.: 10 HzIntensity: 90% MTPulse N: 1000Session N: 40Session freq.: 5/week Sprague-Dawley rats with spinal cord contusion injury Exp. group N: 10all femaleControl group N: 10all female ventral horn sections of the lumbar spinal cord - 5-HT ns (posttest)
tDCS
Tanaka et al., 2013 [97] parallel Site: cortexPolarity: cathodalElectrode size: 5 mm × 5 mmIntensity: 800 μADuration: 10 minSession N: 1 healthy Sprague-Dawley rats Exp. group N: 7all maleControl group N: 7all male microdialysis (striatum) during and 0–390 min after the session 5-HT ns (posttest/pretest)
Polarity: anodal Exp. group N: 7Control group N: 7 ns (posttest/pretest)

↑: Significantly increased or the experimental group levels were significantly larger than the control group; ↓: significantly decreased or the experimental group levels significantly smaller than the control group; ns: non-significantly changed or different; *: data not available for the featured group but taken from a larger group it belonged to or a subgroup of the majority of it; -: not applicable or data not available; N: count; freq.: frequency; exp.: experimental. For studies using the parallel design, “(group x time)” denotes the result based on group x time interaction, “(posttest)” group difference in the posttest, and “(posttest/pretest)” group difference in the posttest values standardized by the pretest ones. Here TRP refers to total TRP when unspecified.

Outcomes of robust Bayesian meta-analysis.

Metabolite Source Studies r Effect BF10 Heterogeneity BF10 Publication Bias BF10
ECT
TRP plasma N: 8 [35,39,43,48,52,53,56,58] 0.5 0.216 10.191 0.645
0.7 0.278 39.36 0.891
0.9 0.183 >100 7.014
KA plasma N: 2 [35,52] 0.5 0.174 0.568 0.656
0.7 0.174 0.629 0.978
0.9 0.269 2.267 1.015
KA/KYN plasma N: 2 [35,52] 0.5 0.174 0.468 0.461
0.7 0.178 0.46 0.461
0.9 0.309 0.782 0.517
TMS
TRP plasma N: 2 [62,63] 0.5 0.279 0.699 0.633
0.7 0.242 0.732 0.683
0.9 0.197 1.306 1.271
5-HT serum N: 2 [62,63]) 0.5 5.46 0.804 1.598
0.7 5.377 0.777 1.678
0.9 9.232 0.79 1.504

r: pretest-posttest correlation; BF10: inclusion Bayes factor, bolded when >3 or <1/3, suggesting moderate evidence for or against the presence of the meta-analytic item, respectively.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms23179692/s1.

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