Plant-derived flavanol (-)epicatechin mitigates anxiety in association with elevated hippocampal monoamine and BDNF levels, but does not influence pattern separation in mice

Abstract

Flavanols found in natural products such as cocoa and green tea elicit structural and biochemical changes in the hippocampus, a brain area important for mood and cognition. Here, we evaluated the outcome of daily consumption of the flavanol (-)epicatechin (4 mg per day in water) by adult male C57BL/6 mice on measures of anxiety in the elevated plus maze (EPM) and open field (OF). Furthermore, pattern separation, the ability to distinguish between closely spaced identical stimuli, considered to be mediated by the hippocampal dentate gyrus (DG), was tested using the touchscreen. To investigate mechanisms through which (-)epicatechin may exert its effects, mice were injected with bromodeoxyuridine (50 mg kg ^-1 ) to evaluate adult hippocampal neurogenesis. In addition, monoaminergic and neurotrophin signaling pathway proteins were measured in tissue derived from subject cortices and hippocampi. Flavanol consumption reduced anxiety in the OF and EPM. Elevated hippocampal and cortical tyrosine hydroxylase, downregulated cortical monoamine oxidase-A levels, as well as increased hippocampal brain-derived neurotrophic factor (BDNF) and pro-BDNF support the flavanol's anxiolytic effects. In addition, elevated pAkt in hippocampus and cortex was observed. (-)Epicatechin ingestion did not facilitate touchscreen performance or DG neurogenesis, suggesting a non-neurogenic mechanism. The concurrent modulation of complementary neurotrophic and monoaminergic signaling pathways may contribute to beneficial mood-modulating effects of this flavanol.

OPEN

Citation: Transl Psychiatry (2015) 5, e493; doi:10.1038/tp.2014.135

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ORIGINAL ARTICLE

Plant-derived avanol ( )epicatechin mitigates anxiety in association with elevated hippocampal monoamine and BDNF levels, but does not inuence pattern separation in mice

TP Stringer, D Guerrieri, C Vivar and H van Praag

Flavanols found in natural products such as cocoa and green tea elicit structural and biochemical changes in the hippocampus, a brain area important for mood and cognition. Here, we evaluated the outcome of daily consumption of the avanol ( )epicatechin (4 mg per day in water) by adult male C57BL/6 mice on measures of anxiety in the elevated plus maze (EPM) and open eld (OF). Furthermore, pattern separation, the ability to distinguish between closely spaced identical stimuli, considered to be mediated by the hippocampal dentate gyrus (DG), was tested using the touchscreen. To investigate mechanisms through which ( )epicatechin may exert its effects, mice were injected with bromodeoxyuridine (50 mg kg1) to evaluate adult hippocampal neurogenesis. In addition, monoaminergic and neurotrophin signaling pathway proteins were measured in tissue derived from subject cortices and hippocampi. Flavanol consumption reduced anxiety in the OF and EPM. Elevated hippocampal and cortical tyrosine hydroxylase, downregulated cortical monoamine oxidase-A levels, as well as increased hippocampal brain-derived neurotrophic factor (BDNF) and pro-BDNF support the avanols anxiolytic effects. In addition, elevated pAkt in hippocampus and cortex was observed. ( ) Epicatechin ingestion did not facilitate touchscreen performance or DG neurogenesis, suggesting a non-neurogenic mechanism. The concurrent modulation of complementary neurotrophic and monoaminergic signaling pathways may contribute to benecial

mood-modulating effects of this avanol.

Translational Psychiatry (2015) 5, e493; doi:10.1038/tp.2014.135; published online 6 January 2015

INTRODUCTIONStudies in humans and animal models have shown that dietary interventions rich in plant polyphenols may alleviate stress or anxiety and mitigate cognitive decline.13 Cocoa, green tea, blueberries and grapes contain avanols, a subclass of plant polyphenols with pleiotropic roles in neuroprotection,47

cognition2,8 and mood.9,10 The active ingredient that confers these benets often remains unclear, as most investigations examine whole foods or multiple avanols1114 in animal models

of aging,15,16 cerebrovascular stress17 or Alzheimers disease.1822 As such, a pure avanol of particular interest is ( )epicatechin (EC), which traverses the bloodbrain barrier and may directly affect brain function.2224 EC consumption improves memory in mice24 and snails.25 Its metabolites enhance long-term potentiation in hippocampal slices derived from Alzheimers disease-modeling mice.22

It is unknown whether this avanol may also affect mood regulation. Indeed, both green tea and grape seed avanols act as antidepressants in mice, enhancing performance in the forced-swim and tail suspension tests.2628 Similar observations were made in rats consuming a cocoa polyphenol (88.5% tannins,11.5% avanols) mixture.29 Studies of individual avanols corroborate these ndings; the green tea catechin ( )epigallocatechin gallate improved mouse performance in multiple assays of anxiety,9,10 whereas the avanol luteolin decreased immobility time in the forced-swim test in mice.30 In humans, consumption of a avanol-rich cocoa drink attenuated anxiety precipitated by a

demanding cognitive task.31 These polyphenols may inuence mood by modulating the monoaminergic systems, increasing neurotransmitter synthesis32 and decreasing enzymatic breakdown/removal.17,33 Furthermore, as decreased brain-derived neurotrophic factor (BDNF) levels are associated with adult depression,34,35 neurotrophin expression may also undergird avanol-driven mood improvements.

Dietary polyphenols, such as the Chinese herb Xiaobuxin-Tang (XBXT-2) and curcumin, increased adult dentate gyrus (DG) neurogenesis in models of chronic stress,32,3639 suggesting

another mechanism of action by which avanols may exert mood-modulating effects. Although in female mice ingestion of EC did not inuence new DG cell survival,24 effects on differentiation of adult-born neurons in male mice have not been evaluated. The DG, and in particular adult neurogenesis, is considered important for pattern separation.40,41 Indeed, in aging humans avanol consumption improved DG function and performance on a task requiring discrimination between highly similar visual stimuli.42 This ability to make ne distinctions may also be relevant to mood regulation, by preventing overgeneralization and thereby reducing anxiety.43 However, whether EC consumption provokes anxiolytic effects remains to be determined. Altogether, the aim of the present study is to evaluate effects of EC on pattern separation and anxiety, and to determine the underlying cellular mechanisms.

Neuroplasticity and Behavior Unit, Laboratory of Neurosciences, Intramural Research Program, National Institute on Aging, National Institutes of Health, Biomedical Research Center, Baltimore, MD, USA. Correspondence: Dr H van Praag, Neuroplasticity and Behavior Unit, Laboratory of Neurosciences, Intramural Research Program, National Institute on Aging, National Institutes of Health, Biomedical Research Center, Suite 100, 251 Bayview Boulevard, Baltimore, MD 21224, USA.

E-mail: mailto:[email protected]

Web End [email protected] Received 7 September 2014; revised 19 October 2014; accepted 17 November 2014

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MATERIALS AND METHODSSubjects and compound administration

Subjects. Male C57BL/6J mice (The Jackson Laboratory, Bar Harbor, ME, USA) were housed individually in standard cages at 6 weeks of age with a standard day/night cycle: lights were switched on at 0600 hours and off at 1800 hours. Animals were constrained to 90% of their free-feeding weight throughout the study. At 18 weeks of age, mice received for 5 days a daily intraperitoneal injection of bromodeoxyuridine (BrdU; dissolved in 0.9% saline, ltered sterile at 0.2 m, 50 mg kg1 body weight at 10 g ml1; Sigma Aldrich, St Louis, MO, USA) to label dividing cells. Following completion of behavioral testing, animals were deeply anesthetized at 28 weeks of age via inhalation of isourane and perfused transcardially with 0.9% saline (room temperature). The hippocampi and overlying cortices were dissected out of the left hemispheres and stored at 80 C for use in immunoblotting. The right hemispheres were stored in 4% paraformaldehyde at 4 C for subsequent immunohistochemical experiments. After 96 h in paraformaldehyde, tissue to be used for immunohistochemistry was equilibrated in 30% sucrose. Sequential coronal sections (40 m) were taken through the hippocampus and stored in phosphate-buffered glycerol at 20 C. Animals were maintained in accordance with the National Institutes of Health guidelines. All protocols for procedures were approved by the NIAs Institutional Animal Care and Use Committee.

( )EC administration. At 10 weeks of age, mice underwent shaping and conditioning to the touchscreen system for 4 weeks. At 14 weeks, mice were assigned to control (CON) or EC-treatment groups (n = 15 per group) that had been counterbalanced based on performance during touchscreen shaping. Animals were administered either standard water or a treatment liquid comprised of EC (Sigma, St Louis, MO, USA) dissolved in water at a concentration of 0.667 mg ml1. Fresh solution was made every other day. Using Nanodrop 2000 (Thermo Scientic, Waltham, MA, USA), absorbance of EC solution at 276 nm was measured after 24 and 48 h to conrm negligible variations (0.2% 0.3 and 1.4% 0.3 absorbance of fresh solution, respectively) due to EC oxidation. Treatment was available ad libitum and based on an average water consumption of 6 ml per day (that is, ~ 4 mg EC daily). Total duration of EC consumption was 14 weeks.

Spatial pattern separation in the touchscreenAnimals were shaped to the touchscreen chamber, which housed a six-window grid and a reward trough (Lafayette Instruments, Lafayette, IN, USA), at 10 weeks of age for 4 weeks. Shaping began by habituating the mice to the chamber for 2 days. Pavlovian training, a 1-h session, taught the animals to associate stimulus interaction (that is, nose poking an illuminated grid square) with the sounding of a tone and the dispensation of a liquid reward (strawberry milk, Nesquik, Vevey, Switzerland). The subsequent 3-day must touch phase required stimulus interaction to trigger reward presentation. Must initiate training taught the mice to initiate the next trial via a nose poke to the reward trough. During punish incorrect, the nal stage of shaping, an aversion toward interacting with non-stimulus grid squares was instilled through inversion of the house light and imposition of a short time-out period prior to trial resumption.

Shaping was followed by EC administration beginning at 14 weeks of age. The mice then participated in 5 days of task training. To reach criterion in this phase, the subjects were required to select the correct (that is, programmed to trigger liquid reward) choice from two identical but spatially discrete stimuli in seven out of eight consecutive trials. To progress to the next stage, subjects had to attain criterion at least once during three out of four consecutive days of training. During the sequent 16-day interval of probe trials, animals attempted to reach the prenominate criterion when presented with stimuli separated by larger and smaller distances than in task training. All touchscreen protocols were performed as described previously.44

Anxiety testsOpen eld. Mice were placed individually in an open-eld (OF) arena(27.3 27.3 cm, height 20.3 cm) housed within a sound-attenuating cubicle (Med Associates, St Albans, VT, USA) and permitted to move freely. Trials lasted for 30 min. Animal motion and cumulative path length were automatically tracked via three 16-beam infrared array and recorded by Activity Monitor software (Version 4.0, Med Associates).

Elevated plus maze. Animals were individually placed in the center of an elevated plus maze (EPM) (constructed on-site, made of white Plexiglas,

Total Plastics, Baltimore, MD, USA) on a 60-cm high stand, each arm 30 cm 5 cm, closed arms wall 16 cm high, 5 cm 5 cm center platform) and allowed to explore freely for 5 min. Time spent in the open and closed arms were recorded in semiautomatic fashion by video tracking software (ANY-maze, Stoelting, Wood Dale, IL, USA).

Adult neurogenesis histologyBrdU immunohistochemistry and cell counts. A one-in-six series of free-oating sections (40 m) was washed in tris-buffered saline (TBS) and pre-incubated with 0.6% H2O2 for 30 min to quench endogenous peroxidases.

After rinsing, the sections were incubated in 2 N HCl at 37 C for 30 min to denature DNA and then neutralized in 0.1 M borate buffer at room temperature. After thorough washing, the sections were blocked with TBS ++ (3% donkey serum, 0.05 M tris-buffered saline, 0.5% Triton-X 100) for 30 min at room temperature and incubated with rat anti-BrdU (1:200, Accurate Chemical, Westbury, NY, USA) overnight at 4 C. Thereafter, the sections were washed and immersed in biotin-SP-conjugated donkey anti-rat IgG (1:250, Jackson ImmunoResearch, West Grove, PA, USA) followed by 2 h in ABC reagent (Vectastain Elite; Vector Laboratories, Burlingame, CA, USA). The sections were then incubated with the substrate 3,3-diaminobenzidine (Sigma) for 5 min to visualize the cells that had incorporated BrdU. BrdU-positive cells were counted in a one-in-six series of sections (240 m apart) through a 20 objective (Olympus, BX51, Center Valley, PA, USA) throughout six sections per animal starting at the rostrocaudal granule cell layer as described previously.44

Double-immunouorescence staining and new cell phenotype analysis. After denaturation, neutralization, washing and blocking steps described above, free-oating sections (1:12 series, 480 m apart) were co-incubated with primary antibodies, anti-rat BrdU (1:100, Accurate Chemical) and the neuronal marker anti-mouse NeuN (1:100, Millipore, Billerica, MA, USA) for 72 h at 4 C. Therafter, sections were co-incubated with donkey anti-rat Alexa Fluor 488 (1:250, Thermo Fisher, Waltham, MA, USA) and donkey anti-mouse Cy3 (1:250, Jackson ImmunoResearch) for 2 h at room temperature. Thirty BrdU+ cells in the DG per animal were randomly selected and imaged for phenotype analysis (Olympus FV1000). The percentage of BrdU+/NeuN+ cells was calculated.

Western blottingImmunoblotting was employed in samples derived from in vivo administration of the compound to determine its effects on relative expression of neurotrophins, their receptors, kinases, transcription factors and neuro-transmitters. Cortices and hippocampi derived from the left hemispheres of mice that had ingested the compound for 14 weeks were homogenized and quantied via the Bradford assay (lysis buffer: RIPA lysis buffer (Millipore) with Complete ULTRA tablets (Roche, Basel, Switzerland)). Thirty micrograms of protein from homogenized tissue were denatured via boiling and separated on a polyacrylamide gel. Proteins were then transferred to Immobilon-FL membranes (Millipore), which were treated with rabbit anti--tubulin (1:2500, Li-Cor Biosciences, Lincoln, NE, USA), rabbit anti-Akt, rabbit anti-phospho-Akt (1:1000, Cell Signaling Technologies, Danvers, MA, USA), rabbit anti-phospho-ERK 1/2, mouse anti-ERK 1/2, mouse anti-CREB, rabbit anti-phospho-CREB (1:1000, Santa Cruz Bio-technologies, Santa Cruz, CA, USA), rabbit anti-MAO-B (1:3000, Sigma Aldrich), goat anti-MAO-A (1:1000, Santa Cruz Biotechnologies), mouse anti-pro-BDNF (1:7500, GeneCopoeia, Rockville, MD, USA), rabbit anti-BDNF (1:500, Santa Cruz Biotechnologies), rabbit anti-tyrosine hydroxylase (1:200, Abcam, Cambridge, MA, USA), and rabbit anti-glyceraldehyde-3-phosphate dehydrogenase (GADPH, 1:1000, Sigma Aldrich). Membranes were then tagged with 800 CW uorescent goat anti-mouse or anti-rabbit IRDye (1:15 000), read in an OdysseyR infrared imager (Li-Cor Biosciences, Lincoln, NE, USA), and evaluated using Odyssey 2.0 software (Li-Cor Biosciences). Precision Plus Protein Ladder (Bio-Rad, Hercules, CA, USA) was used as a marker.

Statistical analysisStudents t-test was used for behavioral, immunohistological and immunoblotting experiments with a P-value cutoff of 0.05. All statistical analyses were carried out using Statview (Abacus Corporation, Baltimore, MD, USA).

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RESULTS( )EC has no effect on spatial pattern separationMice were trained in a pattern-separation task in the touchscreen.44 After 1 month of shaping protocols in the touchscreen, mice (n = 15 per group) were given standard drinking water or water supplemented with EC for the duration of the experiments (Figure 1a). Animal weights were taken at monthly intervals and did not differ between cohorts at the onset of avanol treatment (CON: 19.66 0.29 g; EC: 19.43 0.26 g) or end (CON: 27.0 0.36 g; EC: 26.71 0.39 g) of the study (P40.34).

Following the shaping period, subjects underwent 6 days of task training in which they discriminated between visually identical, spatially discrete stimuli with an intermediate separation to gain a liquid reward. No difference was found in the average number of days each group required to complete task training

(CON, 3.6 0.16 days; EC, 3.6 0.19 days; P = 1.00). During probe trials, which alternated between testing big and small separations, the EC and CON cohorts evinced no difference in performance [small separation: CON, 49.04 3.72; EC, 51.29 4.02 trials to criterion (t(28) = 1.17, P40.70); big separation: CON, 29.92 2.30;

EC, 26.11 1.73 trials to criterion (t(28) = 0.38, P40.25)], (Figure 1b).

Overall, these data suggest that there is not a selective effect of EC on the DG-related pattern-separation function.

( )EC does not affect adult neurogenesisTo determine whether ( )EC administration has a role in hippocampal newborn cell survival, mice were injected with BrdU daily for 5 days at 18 weeks of age. Post mortem, immunohisto-chemical staining and quantication of BrdU-labeled cells in the

Figure 1. Pattern separation and adult hippocampal neurogenesis. (a) Timeline of the experiments (TS, touchscreen; TT, task training; PT, probe trials; B, BrdU injections; OF, open eld; EPM, elevated plus maze; w, weeks of age). (b) The touchscreen paradigm acquisition of big and small separation between two identical stimuli was tested in control (CON) and ( )epicatechin (EC)-treated mice, which were trained to reach a criterion where seven of eight trials were performed correctly. Pattern separation did not differ between the CON and EC groups when the separation between the stimuli was either large or small. (c) Bromodeoxyuridine (BrdU)-positive cell number did not differ between the groups. (d) The percentage of new DG neurons showed no differences between CON and EC-treated mice. Photomicrographs of new cells surviving 9 weeks after the last BrdU injection, in tissue derived from (e) CON and (f) EC-treated subjects. Neuronal phenotype was determined by double-labeling for BrdU (green) and NeuN (red) in (g) CON and (h) EC-treated mice. Error bars denote s.e.m.

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right DG was undertaken (CON, 409 42 cells, n = 9; EC, 397 32 cells, n = 10; Figures 1c, e and f). No difference in the number of surviving newborn DG cells was observed (t(17) = 0.23, P40.82). In

addition, co-expression analysis of BrdU and NeuN (CON, n = 6; EC, n = 6) for neuronal phenotype was performed. There was no difference between the groups in percentage of BrdU/NeuN-positive cells (t(10) = 0.65, P40.53; Figures 1d, g and h). The absence of a neurogenic effect is consistent with the observed lack of change by ( )EC consumption in spatial pattern separation.

Effects of ( )EC administration on OF and EPM behaviorTo determine whether EC exerts anxiolytic effects similar to those reported for green-tea avanols9 and cocoa avonoids,29 mice were tested in the OF paradigm for 30 min. No signicant difference was found between the total distance travelled by each cohort [CON, 102.8 m 5.1 m; EC, 100.4 m 5.5 m; (t(28) = 0.29,

P40.77)]. However, the ratio of time spent in the central region of the eld compared with time in the periphery was signicantly higher in the EC-treatment animals compared with the CON group [CON, 0.203 0.009; EC, 0.249 0.01 (t(28) = 3.59, Po0.002)], as well

as the ratio of the distance travelled in the central region compared with the distance in the periphery [CON, 0.097 0.006; EC, 0.119 0.008 (t(28) = 2.31, Po0.03)], (Figures 2a and b). The OF data suggest that EC consumption mitigates anxiety.

These results were supported by the outcome of subject evaluation in the EPM trials, an assay to evaluate anxiety-like behavior.45 The mice were monitored in the EPM over a 5-min period. The CON animals spent a signicantly higher amount of time in the closed arms of the maze than in the open arms [open arms, 90.2 6.1 s; closed arms, 126.8 6.5 s (t(28) = 4.11,

Po0.0003)]. The EC-treatment mice, on the other hand, spent equal amounts of time in the open and closed arms [open arms, 103.2 6.8 s; closed arms, 112.3 6.1 s; (t(28) = 1.005, P40.32)],

(Figure 2c). Altogether, ( )EC appears to function as an anxiolytic that promotes exploratory behavior.

EC consumption modulates expression of mood-related proteins Treatments of mood disorders generally aim to increase the availability of monoamines (norepinephrine, serotonin and dopamine) in the brain. To determine whether the effects of EC are mediated through monoaminergic mechanisms, we performed immunoblotting experiments with homogenized hippo-campal and cortical tissue (CON, n = 57; EC, n = 57). EC consumption increased tyrosine hydroxylase (TH) levels in both hippocampus (1.51-fold EC/CON; t(12) = 2.63, Po0.03) and cortex

(1.79-fold EC/CON; t(12) = 3.22, Po0.01), (Figures 2d and e). A decrease in expression of monoamine oxidase-A (MAO-A), which metabolizes serotonin, norepinephrine and dopamine, was observed in cortex (0.69-fold, t(11) = 2.22, Po0.05) of EC-

consuming animals compared with the CON groups, but not in hippocampi (0.92-fold EC/CON; t(12) = 1.08, P40.30), whereas

MAO-B, which metabolizes dopamine, remained unchanged in both hippocampus (t(11) = 1.31, P40.21) and cortex (t(11) = 0.48,

P40.64), (Figures 2d and e). Together these data suggest that EC ingestion modulates mood by increasing monoaminergic neuro-transmitter synthesis and by concurrently inhibiting their enzymatic degradation.

EC elevates hippocampal pro-BDNF and mature BDNF protein levels

To determine whether the precursor of BDNF (pro-BDNF) and mature BDNF may instantiate the observed anxiolytic effects, we performed immunoblotting experiments with homogenized hippocampal and cortical tissue (CON, n = 57; EC, n = 57). Hippocampal tissue from animals treated with EC was found to

contain signicantly higher levels of pro-BDNF (1.74-fold; t(11) = 2.58, Po0.03) and mature BDNF (1.34-fold; t(12) = 2.19,

Po0.05) compared with the CON group (Figure 3a). However, neurotrophin proteins were not changed in cortex (Figure 3b), suggesting that the modulation of BDNF is specic to the hippocampus. To further investigate the effects of EC upon the BDNF signaling pathway, we evaluated the levels of protein kinase B (Akt), extracellular-signal-regulated kinase 2 (ERK2) and cAMP response element-binding protein (CREB) phosphorylation. EC intake induced signicant increase of the levels of pAkt in the hippocampus (1.47-fold; t(12) = 2.20, Po0.05; Figure 3c) and in the cortex (2.33 fold; t(11) = 2.79, Po0.02; Figure 3d). Neither pERK2

[hippocampus (t(12) = 0.58, P40.57); cortex (t(11) = 0.14, P40.89)] nor pCREB [hippocampus (t(12) = 0.37, P40.72); cortex (t(12) = 1.32, P40.21)] were modied by the intake of EC (Figures 3e and f).

DISCUSSIONIn this study, we show that EC consumption alleviated anxiety in the OF and EPM. These behavioral changes may be attributed to alterations in relevant signaling pathways. Specically, EC intake concurrently increased hippocampal and cortical TH levels and diminished production of cortical MAO-A, but not MAO-B. Increased monoamine levels may lead to the observed elevation in pro-BDNF and BDNF protein levels in the hippocampi of EC-supplemented animals. In addition, increased levels of pAKT, but not pCREB or pERK, were found in both hippocampus and cortex. Adult hippocampal neurogenesis and spatial pattern separation remained unchanged, suggesting a non-neurogenic mechanism of action of this avanol. Altogether, our data provide support for EC as an anxiolytic compound that concurrently affects multiple complementary cell signaling pathways.

Pattern separation, which is the distinct encoding of very similar events or stimuli,46 is deemed closely linked to adult neurogenesis44 and BDNF protein levels,47 and considered relevant to both memory and mood regulation.43 Our results indicate that EC had no effect on adult neurogenesis, consistent with an absence of improvement in the touchscreen pattern-separation tasks. The lack of a neurogenic effect is consistent with our previous study24 and recent research by others.48 Other dietary polyphenols, such as the Chinese herb Xiaobuxin-Tang (XBXT-2) and curcumin, have been demonstrated to boost cell proliferation.32,3639 However, these studies used rodent models of chronic stress32,36,38 with likely a lower baseline rate of

neurogenesis. It may be that avonoids enhance neurogenesis in models of stress and pathology via their antioxidant and anti-inammatory properties, mitigating oxidative damage to promote cell survival and differentiation.49 However, in young healthy animals no change in neurogenesis was evident after 3 months of compound consumption, suggesting that other components of polyphenol-enriched diets may mediate potential neurogenic effects.

The anxiolytic and antidepressant effects of dietary polyphenols have been reported in a growing number of studies, both in humans50 and in animal models.29,36,51 The EPM has been used to

show a decrease in anxiety-induced behavior in polyphenol-fed animals; for instance, OF1 mice supplemented with green tea leaves improved their performance in the EPM test.9 Our results from the OF and EPM led us to posit that EC affected dopaminergic or serotonergic systems, common targets of anxiolytic drugs.52 Immunoblotting data showed that TH, an enzyme critical to monoamine synthesis, was produced in far greater amounts in the cortices and hippocampi of EC-supplemented mice than in CON. This nding is consistent with previous studies, showing polyphenol-induced TH overexpression both in vitro, for instance by rosmarinic acid of Rosmarinus ofcinalis,53 and in vivo in C57 mice by teaavin of black tea.54 Further, MAO-A, an enzyme that deaminates and catalyzes

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Figure 2. Behavioral and cellular assays relevant to mood. (ac) Anxiety was assayed in the open eld (OF) and the elevated plus maze (EPM). (a) Animals were placed inside the OF chamber for 30 min following 7 weeks of ( )epicatechin (EC) consumption. The ratio of time spent and of distance (DIST) travelled by EC subjects in the center of the chamber, relative to the periphery, was signicantly higher than that of controls (CON). (b) Total distance travelled in the OF did not differ between the groups. (c) In the EPM, subjects consuming EC displayed no preference between the open or closed arms, whereas CON animals spent a signicantly greater amount of time in the closed arms than in the open arms. (d and e) Hippocampi and cortices were assayed for tyrosine hydroxylase (TH), monoamine oxidase (MAO)-A and MAO-B. (d) EC-consuming animals evinced signicantly greater hippocampal expression of TH. (e) Increased expression of TH and a reduction in MAO-A was observed in the cortices of EC-supplemented animals (*Po0.05). GADPH, glyceraldehyde-3-phosphate dehydrogenase. Error bars denote s.e.m.

synaptic serotonin and dopamine,55 was found to be expressed in signicantly lower levels in the cortices of EC-treated mice. Indeed, berry anthocyanins56 and Uncaria rhynchophylla,57 extracts rich in avanols, inhibit MAOs in vitro. These results suggest that EC consumption leads to increased production of dopamine coupled with greater availability of synaptic dopamine and serotonin and so may help alleviate anxiety. Our data are consistent with in vitro assays, demonstrating that avanols can enhance serotonergic function.27,33 ( )Epigallocatechin gallate, curcumin and transresveratrol have been found to inhibit the activity of MAOs, thereby boosting performance in assays of rat depression.26,50,58 It

should be noted that ( )EC increases hippocampal angiogenesis,24 possibly by regulation of nitric oxide synthase.59,60 Interestingly, nitric oxide has been linked to anxiety and serotonin receptor signaling61 and may be another mechanism, in addition to the concurrent MAO-A inhibition and TH upregulation observed in this study, which mediates anxiolytic effects of ( )EC in vivo.

Elevated monoamine levels may result in increased neurotrophin levels.62 The neurotrophin hypothesis of depression

postulates that antidepressant and anxiolytic therapeutic drugs might exert their effects through BDNF upregulation in the hippocampus (for a review, see Martinovich et al. ). Hippocampal BDNF messenger RNA levels increase by administration of chemical antidepressants,64 and BDNF administration in rodents reverses depression-related behaviors in rodents.65,66 The reason

for ECs enhancement of hippocampal rather than cortical neurotrophin levels remains unclear at present. In aged rats, administration of a diet containing a mixture of EC and (+)catechin similarly provoked a predominant increase in BDNF messenger RNA levels the hippocampus.13 In addition, a avanol-containing diet elevated hippocampal BDNF levels in rats that were not behaviorally tested.67 Interestingly, our data show that levels of pro-BDNF also increased notably in mouse hippocampus after EC administration. The role of pro-BDNF overall,68 and in depression in particular, has not been well understood,69 however, our data suggest that EC may result in processing of the precursor to increase mature BDNF levels by an as yet undened mechanism.

The combined increment in pro-BDNF and BDNF by EC in the hippocampus may reduce anxiety. It would be of interest to test

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Figure 3. Neurotrophin brain-derived neurotrophic factor (BDNF) and related signaling pathway proteins. (a and b) Immunoblotting of hippocampal and cortical tissue derived from the behaviorally tested animals. (a) ( )Epicatechin (EC)-consuming animals evinced signicantly greater expression of pro-BDNF and BDNF proteins in the hippocampus. (b) Growth factor levels did not change in the cortex. (c and d) EC increased the expression of pAkt in the hippocampus and cortex with respect to the control group. (e and f) Neither pERK2 nor pCREB levels were modied by the intake of EC in the hippocampus and cortex. (*Po0.05). Error bars denote s.e.m.

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EC in the context of the Val66Met polymorphism, a single-nucleotide mutation that hampers the secretion and trafcking of BDNF.70 Men homozygous for the met allele are more susceptible to adult depression and suffer from more acute symptoms than non-carriers; the mutation is associated with a higher risk of childhood and geriatric depression generally.35,7173 In both mice

and humans, this polymorphism causes decrements in episodic memory70 and extinction learning,74 whereas mouse models prove refractory to rescue of plasticity by antidepressants.75 The

effects wrought by the Val66Met mutation seem to lie at antipodes to those of chronic EC administration. Although these studies do not necessarily suggest that increased expression of BDNF would obtund anxiety or improve memory, it is not unreasonable to hypothesize that hippocampal BDNF may be the point of articulation that links EC consumption to cognition and mood. Indeed, improvement of memory function associated with phytochemical consumption13,24,76 may be mediated in part

by reduced anxiety resulting from BDNF modulation.

BDNF can trigger phosphatidylinositide-3 kinase-dependent signaling,77 relevant to antidepressant effects.78 A major component of this signaling pathway is protein kinase B (also known as Akt, a factor considered important for synaptic plasticity68), which

targets and inhibits glycogen synthase kinase 3 (GSK3). In mouse models, Akt-induced inhibition of GSK3 decreased anxiety and reduced tendency to develop depression.79 Our immunoblotting results showed increased activated Akt in both hippocampi and cortices in EC-supplemented mice. These data, together with an increase of BDNF and pro-BDNF and the lack of change in other BDNF-dependent pathways components such as ERK and CREB, support the hypothesis that EC exerts anxiolytic effects via BDNF activation of the Akt pathway in the hippocampus. Indeed, a closer study of the components and the targets of the PIK3-Akt signaling pathway would be of interest to determine whether different isoforms80 may be upregulated in hippocampus and cortex. For example, Akt1 is involved in bipolar disorder81 and

growth.82 Akt3 is crucial for brain development,83 whereas Akt2 has been identied as the main isoform for anxiety and depression behavior in mice.84 It would be interesting to study whether there is divergent regulation of Akt isoforms by EC consumption in different brain areas. Indeed, the mechanism underlying Akt induction in cortex is unclear. It is possible that a specic avanol receptor, such as has been described in arterial endothelial cells85 might be expressed in the brain8 and activate the Akt signaling pathway, having a role in anxiety regulation.

Overall, our ndings indicate that chronic ( )EC administration evokes mood-related benets through the modulation of monoaminergic and neurotrophic systems. It is our hope that this work will serve as a rachis for future attempts to uncover the workings of this avanol, as well as open options for a more natural way to improve human mood disorders.

CONFLICT OF INTEREST

The authors declare no conict of interest.

ACKNOWLEDGMENTS

This work was supported by the Intramural Research Program of the National Institute on Aging. We thank Sarah Collica for technical assistance and Linda Kitabayashi for preparation of the photomicrograph.

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