1. Introduction
Hyperbaric Oxygenation (HBO) defines therapeutic hyperoxygenation that has been used in clinical routine for more than six decades. HBO involves treatment in hyperbaric chambers where patients breathe 100% oxygen under elevated ambient pressure. In direct correlation with the pressure level, oxygen dissolves in the plasma resulting in an increase in arterial pO2. At pressures between 2.0 and 3.0 atmospheres, which are commonly used for therapy, paO2 between 1200 and 2000 (mm Hg) is achieved. This considerable dimension of plasma-mediated hyperoxygenation, which even obviates the presence of erythrocytes at three atmospheres, brings about pharmacological effects on the molecular level, that trigger functional and structural changes [1].
Indications for HBO comprise a wide range of diseases including intoxications, severe necrotizing infections, ischemia-reperfusion injury, crush-syndrome, central nervous injury, radiation-induced tissue damage, burn injury and chronic wounds. The common denominators of the therapeutic action of HBO are the modulation of tissue injury and tissue regeneration [2].
Though slightly different according to the various types of tissue, regeneration relies on complex mechanisms that are regulated by injury-responsive genes [3], and the mobilization of progenitor cells which irreversibly replace damaged cells in the scaffolding, differentiate into mature cells and proliferate accordingly [4]. These reactions are basically caused by the signaling of dying cells that triggers an immune response and inflammation [5] while cells surviving the injury respond to the resulting changes in the microenvironment [4].
2. Hyperbaric Oxygen and Regeneration
The effects of HBO on tissue regeneration have been studied extensively, both in experimental and clinical settings. By addressing the mechanisms involved in transcription, signaling, stress reaction, apoptosis and cell-death, cellular structure and cell-to-cell contacts, adhesion, migration as well as inflammation, HBO upregulates processes involved in repair while mechanisms perpetuating tissue damage are downregulated [1]. Though a large variety of HBO-induced changes on the molecular level have been described, there are still unresolved aspects in the mechanisms of HBO-induced tissue repair, some of them with specific impacts for well-determined types of tissues or injuries.
In a literature survey covering the last 10 years, we focused on original papers covering well-documented tissue repair mechanisms triggered by HBO. Use of the terms “hyperbaric, oxygen, tissue, repair” yielded 559 English publications in PUBMED, which were reduced to 522 after excluding papers that merely cited HBO as a treatment possibility without further addressing the topic. Adding the search term “mechanism” reduced the number of articles to 72. Thirty-four out of these publications were reviews, and therefore, excluded as were five articles dealing with the mere technical details of HBO (N = 2), retrospective case series without addressing mechanisms of HBO action and one unrelated experimental work. The remaining 33 articles were proven to be valid. By cross-referencing we identified four additional papers dating further back. Following an identical pathway, 26 out of 2195 articles in OVID were eligible. After the removal of 12 duplicates, a total of 39 papers were included.
The most prominent effector proteins and molecules involved in the HBO effects were outlined in detail. For an alphabetic list see Table 1. Table 2 lists the hyperbaric protocols, species and the type of study (experimental or clinical).
2.1. The Nuclear Factor Erythroid 2-Related Factor 2 (Nrf2)—Axis
Nuclear factor erythroid 2-related factor 2 (Nrf2), which is activated via the phosphatidylinositol-3-kinase (PI3K)/protein kinase B (AKT) pathway, is a redox-sensitive transcription factor involved in the protection from oxidant stress. Intracellular redox homeostasis is largely controlled by Nrf2, which induces the expression of cytoprotective genes, such as NAD(P)H:quinone dehydrogenase 1 (NQO1), superoxide dismutase 1 (SOD1, Cu/Zn-SOD), glutathione peroxidase (GSH-Px), glutathione reductase (GSH-R), glutathione S-transferase (GSH-T), heme oxygenase-1 (HO-1), glucose-6-phosphate dehydrogenase (G6PD), glutamate-cysteine ligase catalytic subunit (GCLc), glutamate-cysteine ligase modifier subunit (GCLM), sulfotransferases (SULFs), thioredoxin reductase (TR) or UDP-glucose dehydrogenase (UGDH) [6]. In addition, Nrf2 fosters the antioxidative potential of the cell [7]. It has been shown that the stimulation of the PI3K/AKT/Nrf2 signaling axis is a central issue in the improvement of the healing process of wounds [8].
HBO causes direct activation of Nrf-2 protein expression in the nucleus [9].
Wound Healing
Oxidative stress in wounded tissue induces the release of inflammatory mediators by macrophages and neutrophils resulting in hyperemia and increased permeability which causes edema. The activation of cytokine cascades by oxidative stress may interfere with healing, whilst apoptosis can be induced over various pathways. Nrf-2 can alleviate oxidative stress, thereby enabling wound healing [10].
In a study in patients with diabetic foot ulcers who significantly improved following HBO, Dhamodharan et al. found Nrf2 along with its downstream targets NAD(P) H:quinone oxidoreductase 1 (NQO-1), Heme-oxygenase-1 (HO-1) and Catalase (CAT) significantly increased when compared to controls. Tissue samples revealed higher levels of angiogenesis markers epidermal growth factor (EGF), vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF), fibroblast growth factor 2 (FGF-2) and CxC motiv chemokine 10 (interferon gamma induced protein; CXCL10) in the HBO group. Likewise, HBO enhanced endothelial nitric oxide (eNOS) and nitrite concentrations and the levels of neutrophil attractant interleukin-8 (CxC motif chemokine ligand 8; CXCL-8) which promotes the release of monocyte chemotactic protein 1 (CC chemokine ligand 2; CCL2), a mediator of neovascularization [11]. Godman et al. conducted a genome-wide microarray analysis of gene expression on human microvascular endothelial cells (HMEC-1) after HBO. Again, pronounced Nrf-2-mediated oxidative stress response was one of the primary effects of HBO, whereas normobaric 100% oxygen administration did not provoke a comparable effect. The increased expression of cytoprotective genes induced by HBO corresponded with enhanced cell proliferation and resistance to oxidative stress. Early transcription factors (FOS, FOSB, and JUNB) and metallothioneins as well as six molecular chaperones involved in protein damage control were upregulated immediately following HBOT [12].
2.2. Nitric Oxide
Besides causing vasodilation, nitric oxide (NO•) is able to modulate inflammation and eradicate bacterial infections [13] and shows anti- as well as proinflammatory properties, the exact underlying mechanisms of which are unknown [14,15]. Rising concentrations of interleukin one (IL-1) and tumor necrosis factor α (TNF-α) activate the inducible nitric oxide synthase (iNOS) resulting in the synthesis and release of NO• which serves as an immune regulator in the wound. Apart from killing pathogens, NO* can combine with free oxygen radicals to form highly toxic peroxynitrite and hydroxyl radicals [16]. The induction of VEGF and basic fibroblast growth factor (bFGF) NO• enhances wound healing, angiogenesis and muscle regeneration [17]. The anti-inflammatory effects of NO* are most likely caused by enhanced T cell apoptosis and by inhibition of cytokine expression. On the other hand, experiments with knockout mice have shown that NO* increases the levels of pro-inflammatory cytokines such as TNF-α, IL-2, IL-1ß or IFN-γ [14].
Via stimulation of nitric oxide synthase (NOS) HBO increases NO• levels in perivascular tissues [18]. In a study, using cell cultures Venetsanou et al. investigated the basic effects of HBO on NO•. The data showed a time-dependent dynamic change for NO• as well as the activation of oxidant-antioxidant mechanisms regardless of cell type. In general, the findings suggested a central role for NO• in HBO treatment effects [19].
2.2.1. Wound Healing
In a clinical study in patients with chronic wounds, Boykin et al. found a significant increase in local wound NO• levels after HBO suggesting that this mechanism may be involved in improving wound healing and wound closure [20]. Gajendrareddy et al. used a stress model in wounded mice to study the gene expression of wound iNOS. Expression of iNOS increased on days 1, 3 and 5 post-wounding by more than 200%, whereas HBO treatment of the stressed animals significantly reduced iNOS expression while improving healing to near-control levels [21]. Kendall et al. exposed endothelial cells to hypoxia in the presence of lipopolysaccharide and TNF-α, mimicking chronic wound conditions. Out of 20 genes involved in adhesion, angiogenesis, inflammation, and oxidative stress 19 were downregulated five hours after HBO. Only angiogenin gene expression promoting both angiogenesis and NO• production, reflected by increased eNOS expression, was upregulated. Accordingly, pro-inflammatory endothelial IL-8 mRNA and protein decreased. The effect subsided after one day, underlining the rationale for daily HBO applications as usually conducted in clinical routine [22]. In another study, using the same chronic wound model the very authors examined endothelial cells deriving from human umbilical veins and neutrophils. Treatment with HBO decreased hydrogen peroxide generation by neutrophils and induced NO-related protein modifications. In addition, it reversed neutrophil adhesion to endothelial cells whilst the expression of endothelial intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) were reduced [23]. As mentioned above, Dhamodharan et al. also documented a significant post-HBO increase in eNOS and nitrite concentrations in patients with diabetic foot ulcers [11]. Both the hypoxic gradient and NO in the bone marrow are central for the mobilization of endothelial progenitor cells (EPC) which promote wound healing. Goldstein et al. demonstrated that HBO increases bone marrow NO in vivo, subsequently enhancing the release of EPC. Pretreatment with a NOS inhibitor stalled the HBO effect [18].
2.2.2. Muscle Regeneration
Yamamoto et al. were able to show, that HBO promoted early blood vessel formation and muscle healing after experimental contusion in rats, promoting angiogenesis via the induction of NO• production. Accordingly, HBO significantly increased NO3−, VEGF, and bFGF levels and stabilized HIF1α within 1 day. The administration of a ROS inhibitor N-acetylcysteine (NAC) or the NOS-inhibitor (L-NAME) before HBO, suppressed angiogenesis and muscle regeneration even after HBO [17].
2.2.3. Abrogating Ischemia-Reperfusion Injury
In a rat model, Baynosa et al. investigated the impact of NOS release on the HBO-induced positive effect on ischemia-reperfusion injury. Early-phase NOS activity in pulmonary tissue was significantly increased after HBO compared with untreated controls. After 4 h of ischemia and 24 h of reperfusion eNOS mRNA and pulmonary protein in HBO-treated animals increased significantly. They concluded, that in ischemia-reperfusion injury the eNOS-dependent effects of HBO may result from a systemic early increase in eNOS enzymatic activity followed by a late-phase increase in eNOS protein expression [24].
2.3. Hypoxia Inducible Factor 1α ( HIF-1α)
Apart from disturbances in tissue homeostasis, hypoxic conditions at the wound site recruit macrophages and affect their function. Hypoxia-inducible factor (HIF-1α) is a transcription factor for inflammatory genes and plays a central role in macrophage activation. Biological regulation of monocytes/macrophages in response to circulating HIF-1α has essential roles in healing [25]. HIF-1α also regulates the expression of both α and ß integrins and is involved in the expression of heat-shock protein-90, vascular endothelial growth factor, the chemokine stromal cell-derived factor-1 and GLUT-1, a protein facilitating insulin-independent glucose uptake in tissues. Since all these substances are involved in wound healing, the pharmacological stabilization of HIF-1α enhances healing processes [26,27,28].
2.3.1. Wound Healing
In a diabetic mice wound model, Sunkari et al. documented a significant effect of HBO on HIF-1α at several levels, increasing both HIF-1α stability and activity, thereby inducing fibroblast proliferation [29]. In another study in patients with diabetic foot ulcers post-HBO, HIF-1α, nuclear factor Kappa-B (NFκB) and VEGF expression in wounds as well as circulating inflammatory cytokines were determined. All patients experienced relapse-free healing one month after HBO. HIF-1α, NFκB a protein complex involved in DNA transcription, cytokine production and cell survival, and VEGF expression increased alongside with an increase in fibrous tissue and angiogenesis, as did proinflammatory IL-6, while interferon-gamma decreased [30]. Similarly, Huang et al. exposed human skin fibroblast and human umbilical vein endothelial cells to high glucose and hyperbaric oxygen for studying patterns of gene expression and healing capacity in vitro. Alongside improved healing, HBO enhanced the expression of HIF-1α, NFκB, VEGF, CXC motif chemokine 12 (SDF-1), and CXC-motif chemokine receptor 4 (CXCR4) [31]. HBO promoted proliferation, migration, and the production of reactive oxygen species (ROS) [21].
Zhang et al. studied the effect of HBO on HIF-1-α expression by using ischemic skin flaps in a rat model of wound ischemia. Whilst HIF-1-α expression in wound extract increased and peaked on day 7 in the controls, both the increase and peak level were significantly reduced following HBO. The same was true for the expression of the cell cycle regulator p53. Though these findings on HIF-1-α contradict the abovementioned ones, HBO attenuated apoptosis as mirrored by increased expression of the anti-apoptotic key regulator B-cell lymphoma 2 (Bcl-2) while decreasing cleaved caspase-3, a pro-apoptotic mediator. The downregulation of inflammation went along with the reduction in VEGF, and the pro-inflammatory cyclooxygenase-2 (Cox2), and neutrophil infiltration in the ischemic wounds, which showed improved healing following HBO [32].
2.3.2. Regeneration following Stroke
Rats underwent HBO seven days after temporary middle cerebral artery occlusion. The treatment enhanced functional recovery and neurogenesis as mirrored by increased expression of neurogenin-1, synapsin-1 and doublecortin. The therapeutic action was most likely triggered by increasing ROS and HIF-1α since the inhibition of ROS and HIF-1α abrogated the effect of HBO [33]. Hadanny et al. hypothesized that the repeated hyperoxia resulting from the usual HBO treatment schedules induces the regeneration of neuronal tissue by increasing HIF in a similar way as hypoxia, yet without the deleterious effects of the latter [34].
2.3.3. Bone Regeneration
In cell culture and human peripheral blood monocytes, the effect of HBO on osteoclastic activity was studied. HBO significantly decreased the osteoclast formation and bone resorption induced by the Receptor activator of nuclear factor kappa-Β ligand (RANKL), a central regulator of bone metabolism. The suppressive action of HBO was at least in part mediated through inhibition of hypoxia-induced HIF-1α mRNA and protein expression and reduction in Nuclear factor of activated T-cells, cytoplasmic 1 (NFATc1) and dendritic cell-specific transmembrane protein (Dc-STAMP) expression, both of which are involved in osteoclast differentiation and development [35].
2.4. Matrix Metalloproteinases (MMP)
Matrix metalloproteinases 2 and 9 (MMP-2/-9), that are in part regulated by levels of IL-1β, are key tissue remodeling enzymes involved in the degradation of extracellular matrix components. They have multiple overlapping activities critical for wound healing, and regeneration of skeletal muscle or neural tissue [36,37,38]. While matrix metalloproteinases (MMPs) play important roles in the pathology of wounds, the active form of MMP-9 seems to be the main factor contributing to the non-healing of diabetic ulcers [39].
2.4.1. Wound Healing
Nguyen et al. found that due to a complex mechanism involving a decrease in ROS, HBO lowered the levels of active MMP-9 in diabetic mice, who accordingly showed accelerated wound healing [40].
2.4.2. Regeneration following Spinal Cord Injury and CO-Intoxication
The expression levels of MMP-2, MMP-9, IL-6, and VEGF as well as spinal cord water content were measured in rats with experimental spinal cord injury. In HBO-treated animals, IL-6, as well as MMP-2 und MMP-9 levels, were downregulated, positively correlating with the spinal cord water content, which was lower after HBO than in the controls, whereas VEGF was upregulated. HBO promoted the recovery of neuronal function [41]. Experimental carbon monoxide (CO) intoxication caused a dramatic increase in MMP-9 and caspase-3, whereas the ratio of anti-apoptotic Bcl-2 to pro-apoptotic Bcl-2-associated X protein (BAX) which determines the survival or death of cells following an apoptotic stimulus prominently decreased. HBO rapidly reduced MMP-9 and caspase-3 and restored the balance of Bcl-2 and BAX, thereby inhibiting apoptosis and cell death and facilitating neuronal recovery [42].
2.4.3. Cardiac Remodeling
HBO therapy mitigated adverse left ventricular remodeling caused by streptozotocin-induced diabetes in rats. Apart from preventing LV concentric remodeling, heterogeneous myocyte hypertrophy and fibrosis HBO increased MMP-2 gene expression. Moreover, it inhibited the induction of Transforming growth factor beta 1 (TGFB-1), a cytokine involved in cell growth, and apoptosis as well as MMP-9 mRNAs. HBO normalized TNF-α and VEGF protein expression and attenuated leucocyte infiltration [43].
2.5. Mechanistic/Mammalian Target of Rapamycin (mTOR)
Mammalian target of rapamycin (mTOR) is a key substance in regeneration mechanisms. In detail, mTOR signaling regulates cellular processes such as stem-cell maintenance, growth, proliferation, and differentiation, but also autophagy. Its signaling pathway interacts with Protein Kinase B (Akt) [44].
Regeneration following Spinal Cord Injury and Peripheral Nerve Injury
Following experimental spinal cord injury in rats Chen et al. described that HBO significantly promoted hind-limb locomotor recovery, whilst spinal cavitation or atrophy receded on MRI. Histological analysis showed that the changes in spinal cord neural structure in rats were markedly restored by HBO-PC treatment. Injury-induced increased levels of p-m-TOR, inflammatory cytokines and apoptosis in the spinal cord were attenuated. Intrathecal administration of an mTOR agonist reversed the abovementioned effects [45]. Liu et al. investigated a rat spinal nerve ligation model and reported that HBO attenuated neuropathic pain. On the molecular level, HBO inhibited autophagy impairment and blocked the activation of the mTOR pathway. The impact of HBO was enhanced after intrathecal administration of rapamycin, which decreases mTOR. Conversely, chloroquine which induces autophagy abrogated the HBO effect [46].
2.6. High-Mobility Group Protein B1/Toll-like Receptor 4/NFĸB Pathway
High-mobility group protein B1 (HMGB-1) is a transcription factor that enhances inflammatory processes and binds to the transmembrane proteins Toll-like receptors 4 and 2 (TLR-4, TLR-2), and activates NFκB. This pathway is essential in the acute inflammatory response and immune homeostasis. Hence, it is considered a possible target for therapeutic interventions. Further activation mechanisms of NFκB involve interleukin 1-beta (IL-1ß), or TNF-α [47].
Regeneration following Spinal Cord Injury
The inflammatory response to spinal cord injury causes secondary damage and is a crucial factor in regeneration. In a spinal trauma model in rats, Yang et al. applied HBO and found a significant improvement in locomotor activity compared with controls. Concomitantly, HBO downregulated the post-traumatically increased expression levels of NFĸB and HMGB-1 [48]. Sun et al. were able to demonstrate similar effects on signaling and neurological function recovery in patients with acute spinal cord injury; HBO therapy downregulated HMGB1 and NFĸB expression while motor/pain scores improved significantly when compared with controls [49]. The results were further corroborated by Kang et al. who inflicted spinal cord injury in rats which increased gene expressions of TLR-4, HMGB-1, NFκB and the TLR-4 protein expression. All substances significantly decreased after HBO correlating with significant improvement of the motility scores [50]. Tan et al. reported similar findings. They examined TLR-2 as a mediator of the host-response mechanism, NFκB, IL-1β and TNF-α levels following experimental spinal cord injury in rats. All parameters increased post-injury but were attenuated after HBO treatment. Neurological outcomes and histological findings improved accordingly [51].
2.7. Protein Kinase B (Akt), Extracellular-Signal Regulated Kinases (ERK), c-Jun-N-Terminal Kinases (JNK)
Activated by cytokines or pathogens, extracellular-signal regulated kinases (ERK) control cellular growth, proliferation, differentiation, and adhesion. The function of the Protein Kinase B (Akt) pathway is similar and additionally involves the regulation of apoptosis and cell survival. c-Jun-N-terminal Kinases are activated as a stress response and regulate intracellular signaling [52].
2.7.1. Regeneration following Brain Injury
Yang et al. used rats for a traumatic brain injury model including neural stem cell transplantation. HBO accelerated neural stem cell proliferation and their migration into the lesion area and increased the levels of ERK, VEGF, VEGR2, rapidly accelerated fibrosarcoma protein kinase (Raf-1) and MEK 1/2 protein kinase which are part of the ERK signaling pathway. Neurological function in HBO-treated rats improved significantly more than in controls [53].
In a mouse model of traumatic brain injury, He et al. documented an increase in apoptotic neurons and mRNA expression, as well as activated caspase 3 protein. In addition, brain injury caused the lowering of pAkt/Akt, and its downstream products phosphorylated/unphosphorylated glycogen synthase kinase 3β (pGSK3β/GSK3β), and β-catenin, both of which instigate neuronal apoptosis. By upregulating of pAkt/Akt, pGSK3β/GSK3β, and the structural protein beta-catenin, HBO attenuated the apoptotic process [54].
Recently, Xia et al. investigated whether HBO therapy exerts neuroprotective effects in a rat model of traumatic brain injury, which provoked an increase in apoptosis in the injured cortex. They found that phosphorylated extracellular signal-regulated kinase (p-ERK), phospho-c-Jun N-terminal kinase (p-JNK) and p-NFκB, as well as CXCL1 and chemokine (C-X-C motif) receptor (CXCR2), increased after experimental trauma. Inhibitors of ERK, JNK and NFκB attenuated the expression of CXCL1 and CXCR2. The same was true for HBO therapy which down-regulated both the expression of ERK and the formation of p-ERK, p-JNK, p-NFκB, CXCL1, and CXCR2, and reduced nerve cell apoptosis, improved the neurological function of rats following traumatic brain injury, and ultimately alleviated the secondary injury [55].
2.7.2. Bone Regeneration
HBO promoted the proliferation of growth-arrested osteoblasts in vitro after 3 days of treatment. It caused significantly increased mRNA expression of fibroblast growth factor (FGF)-2 as well as enhanced protein expression levels of Akt, p-ERK, NFκB, protein kinase Cα (PKCα), and p-JNK [56].
The effect of HBO on the stress-induced JNK signaling pathway was investigated in rats. The administration of IL-1β induced an inflammatory response in chondrocytes, resulting in enhanced expression of JNK and c-Jun. The administration of a selective JNK inhibitor or HBO treatment likewise lowered the expression of JNK and c-Jun, proving that hyperbaric oxygen can inhibit IL-1β induced inflammatory response in chondrocytes by blocking JNK/c-Jun signaling [57].
2.8. Rho-Associated Protein Kinase
Rho-associated protein kinase (ROCK) is the effector of Rho-proteins. They interact with the cytoskeleton, regulating smooth muscle tone, and regulating shape, migration and cell-to-cell adhesion. In particular, Rho-proteins influence the actin cytoskeleton, and thereby, smooth muscle tone regulation and seem to be important for modulating tight-junction protein function [58,59].
Restoring Intestinal Barrier Function
The disturbance in the intestinal barrier function, which is often associated with spinal cord injury, was studied in an experimental setting. Following spinal cord injury intestinal mucosal injury score, intestinal permeability, and levels of Rho and ROCK1 were higher, whereas tight junction proteins were significantly lower than in controls. HBO downregulated the expression of Rho and ROCK1, whilst the expression of the junctional proteins Occludin and ZO-1 was elevated yielding decreased intestinal permeability while intestinal mucosal injury declined significantly [59].
2.9. Wnt/ß-Catenin Signaling
Wnt glycoproteins initiate a signaling pathway important in embryogenesis. In consequence, some hereditary conditions are associated with mutations in Wnt pathway components. They are also involved in stem-cell homeostasis and cellular repair mechanisms. Mutations in Wnt genes are also found in some malignant—predominantly intestinal—tumors [60].
The Wnt signaling pathway plays a central role in bone metabolism, where Wnt regulates the osteogenic differentiation of stem cells and activates osteoblasts [60,61].
Bone Regeneration
In an animal model of bone healing using rabbits, HBO caused upregulation of mRNA and levels of Wnt3a, Wnt protein, β-catenin and Runx 2, a transcription factor that is essential for osteoblast differentiation and chondrocyte maturation. Accordingly, HBO treatment resulted in osteogenic differentiation of mesenchymal stem cells as documented by specific staining methods. On the other hand, glycogen synthase kinase-3 (GSK-3β), the over-expression of which causes loss of bone mass, was downregulated showing a complex effect of hyperbaric oxygen on Wnt secretion, processing and signaling. In addition, HBO increased alkaline phosphatase activity and calcium deposition [62].
2.10. Micro-RNA (Non-Coding RNA)
Micro-RNA or non-coding RNA are highly specific regulators of genes at the post-transcriptional level. They effectuate a sort of “fine-tuning” of gene expression by reducing the latter or by silencing genes, either inhibiting translation or causing the degradation of RNA [63].
2.10.1. Neuronal Regeneration (Stroke Model)
Pyroptosis is a type of lytic cell death and is usually found as a reaction to intracellular infection. It is triggered by inflammasomes that contain a set of caspases that eventually cause the eradication of the initial stimulus. Recently it has been shown that oxygen-glucose deprivation following a stroke can provoke pyroptosis of neural stem cells. In a culture of murine neural stem cells, oxygen-glucose deprivation-induced nucleotide-binding oligomerization domain-like receptors (NOD)-like receptor protein 3 (NLRP-3) inflammasome expression caused the pyroptosis of neuronal stem cells. HBO protected neural stem cells against pyroptosis by modulating the complex inflammasome axis (lncRNA-H19/miR-423-5p/NLRP3 axis) resulting in the upregulation of miR-423-5p which inhibited NLRP3 expression. Thereby neurogenesis was enhanced [64].
2.10.2. Regeneration of Cartilage
In degenerated discs, the expression of both high-mobility group box 1 (HMGB1) and receptor for advanced glycation end-products (RAGE) are upregulated as part of the inflammatory reaction. The micro-RNA (miR107) which modulates HMGB1 by a matching sequence is downregulated during hypoxia. HBO markedly induced miR-107, which caused simultaneous suppression of HMGB1 and thereby attenuated the inflammatory reaction. In addition, HBO downregulated the cytokine-induced extracellular signal-regulated protein kinase (ERK), and c-Jun N- terminal kinase (JNK) as well as the secretion of MMP-3, MMP-9, and MMP-13 [65].
Like degenerated discs, osteoarthritic cartilage shows the downregulation of micro-RNA 107 expression, whereas the proinflammatory HMGB-1, Toll-like receptors (TLRs), and RAGE are upregulated. In rabbit cartilage, HBO induced miR-107 expression which caused marked simultaneous suppression of HMGB-1 by downregulation of the mRNA and protein expression of HMGB-1 and the secretion of HMGB-1. Moreover, RAGE, TLR2, TLR-4, and iNOS, NFκB, and the secretion of MMPs were markedly reduced. Accordingly, immunohistochemistry showed enhanced cartilage repair following HBO. The HBO effect could be reversed by the knockdown of miR107 [66].
In a more recent study in intervertebral disc degeneration in human nucleus pulposus cells, Lin et al. investigated the effect of HBO on microRNA 573 (miR-573) which was found downregulated in the degenerative cells, whereas the pro-apoptotic Bcl-2-associated X protein (BAX) levels, the mRNA of which contained a matching sequence for miR-573 were increased. HBO induced MiR-573 resulting in the suppression of BAX in the cartilage cells. Accordingly, the overexpression of miR-573 following HBO inhibited apoptosis and enhanced proliferation. As in the preceding study, transfection with an antagonist of miR-573 partly suppressed the effects of HBO [67].
2.10.3. Angiogenesis
Metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) is a proangiogenic long noncoding RNA. Shyu et al. investigated the effect of HBO-induced MALAT1 exosomes from cardiac myocytes on myocardial infarction in rats. They found that HBO upregulated MALAT1 thereby increasing cell proliferation and capillary-like network formation. MALAT1 small interfering RNA (siRNA) also reduced miR-92a expression which exerts an inhibitory effect on the vasoprotective Krüppel-like factor 2 (KLF2). Consequently, KLF2 expression increased following HBO boosting neoangiogenesis. HBO and HBO-induced exosomes significantly increased cell proliferation and capillary-like network formation [68].
2.11. Integrins
Integrins are transmembrane receptors responsible for adhesion to both the extracellular matrix and cell-to-cell. They facilitate rapid responses in hemostasis or immunological challenges and are important for wound healing. Their function in signal transduction contributes to proliferation and cellular homeostasis [69].
Wound Healing
In a study using neutrophils from patients with chronic, nonhealing wounds HBO dramatically reduced β2 integrin expression on neutrophils one month beyond the end of actual treatment. Cell adhesion function of both neutrophilic integrins, α4β1 and β2 was reduced by 70% and 67%, respectively, corresponding to both a decrease in neutrophil adhesion to the endothelium and recruitment into the perilesional area. Of note, α4β1 integrin remained sensitive to antagonist inhibition in the presence of fibronectin—a fact that may indicate the possibility of combining HBO with integrin antagonists [70].
3. Conclusions
Throughout six decades HBO has been applied in a large variety of acute diseases but also with the purpose of tissue regeneration in chronic disease [71]. Especially in wound healing and in regeneration following acute spinal cord or brain injury, single cases and case-controlled trials have shown remarkable results. However, due to logistic problems in creating viable setups for high-quality randomized clinical studies, undisputable data are still scarce. On the other hand, extensive experimental work within the last 20 years is shedding light on the molecular mechanisms of HBO various aspects of which have been summarized in a number of recent reviews [72,73,74,75,76,77].
The present compilation as depicted in Figure 1 puts the focus on conditions where the use of HBO in clinical practice has shown positive effects on regeneration. In particular, these indications involve wound healing, regeneration following brain or spinal cord injury, regeneration of bone and cartilage, cardiovascular issues and muscle regeneration, apart from a multitude of further applications. The list of mechanisms presented herein is far from depicting the complete state of the results.
Most controlled studies have verified that the clinical efficacy of HBO derives from the modulation of signaling and transduction cascades, leading to the synthesis of structural proteins or growth factors and promoting healing and ameliorating post-ischemic and post-inflammatory injuries [78]. Yet, the various substances and pathways that HBO modifies must not be considered separately since many of these very molecular mechanisms are intricately interdependent.
One line of action of HBO is the modulation of ERK and of the PKB/Akt pathway. Both are activated by cytokines or pathogens and control cellular growth, proliferation, differentiation, and adhesion, whereas Akt also involves the regulation of apoptosis and cell survival [52]. One of the targets of Akt is Nrf2, a central component in healing processes. Its upregulation by HBO enhances tissue regeneration in chronic wounds [7,8,11]. Another target of PKB/AKT is mTOR, a pivotal substance regulating regeneration processes. It is involved in stem-cell maintenance, proliferation, and differentiation, growth, cell survival but also autophagy [44]. The downregulation of mTOR by HBO has been connected to the promotion of recovery following experimental spinal-cord injury [79] and alleviation of neuropathic pain [46]. Since Rapamycin potentiates this effect, its combination with HBO is worthwhile to investigate.
Another target of HBO is NO•, the smallest signaling molecule. NO• is a potent vasodilator, enhances synaptic plasticity, modulates inflammatory processes and enhances the release of endothelial progenitor cells. It is produced by three isoforms (iNOS, eeNOS and neuronal nNOS) of synthases [13,80]. Apart from being activated by inflammation mediators such as TNF-α, they respond to HBO as a trigger [11,18,66] which instigates healing processes. What is more, eNOS modulation by HBO seems to be an important issue in abrogating the deleterious effects of ischemia-reperfusion [24]. A seemingly contradictory finding of HBO increasing local NO*-levels in chronic wounds [20] and reducing iNOS expression in wounds under stress conditions [21] might reflect the potential of HBO in restoring homeostasis. Since HBO improved healing in both instances, it may be hypothesized that initial NO- levels had been too low in chronic and too high in stressed wounds, in both cases impeding the healing process. As shown in Table 1 similar, apparently contradictory effects of HBO have been published for other substances.
Chemokines play key roles at each stage of the wound healing process to help coordinate the interaction of cells within the wound. Whilst chemokines act beneficially in early post-wounding, a prolonged inflammatory response exacerbated by chemokines can lead to the formation of chronic non-healing wounds. Therefore, approaches to chemokine inhibition should most likely be adapted to the respective phase the wound is in [81]. HBO seems to fulfill these requirements, as shown by its action on Hypoxia inducible factor and Matrix metalloproteinases. Due to its central role in macrophage activation, Hypoxia inducible factor (HIF-1α) has considerable influence on healing. Macrophages initiate inflammatory immune response following changes in the tissue microenvironment [26,27,28]. In addition, HIF-1α modulates the expression of further substances involved in the healing process such as integrins, heat-shock protein-90, vascular endothelial growth factor, the chemokine stromal cell derived factor-1 and GLUT-1, a protein facilitating insulin-independent glucose uptake in tissues. However, as also found in NO*, the effect of HBO on HIF-1α is not unidirectional. Whereas downregulation was found during the healing of chronic diabetic ulcers [29,31] and a model of bone regeneration [34], HBO instigated upregulation of previously decreased HIF-1α in a model of acute wound ischemia, thereby also improving healing [32]. A similar observation was made in experimental stroke [33]. Thus, as in ERK and Akt, the effect of HBO seems to be a modulating one, ensuring enhanced expression in case of HIF-1α deficiency, whilst downregulating the substance in the presence of chronic inflammation.
The pro-inflammatory IL-1ß which is grossly downregulated by HBO is involved in the regulation of the tissue remodeling enzymes MMP-2 and MMP-9. Metalloproteinases influence not only wound healing but also the regeneration of neural or muscular tissue [34,35,36,37,38]. The multiple and complex functions of MMPs are barely understood, yet the active form of MMP-9 seems to be the main factor contributing to the non-healing of diabetic ulcers [39]. HBO lowered MMP levels in chronic wounds, acute spinal and cerebral injury, and cardiac muscle degradation with beneficial effects [40,41,43]. This is remarkable since MMP inhibitors have not yet yielded convincing therapeutic results [82]. Again, HBO seems to restore physiological balance rather than merely counteracting a substance.
The transcription factor High-mobility group protein B1 (HMGB1) also acts as a cytokine mediator of inflammation. In an essential inflammatory pathway, it binds to the transmembrane proteins TLR-4 and TLR-2, thereby activating NFκB. Alternatively, Interleukin 1-beta (IL-1β) or TNF-α activate NFĸB [46]. Both in clinical and experimental spinal cord injury HBO downregulated HMGB1 and NFĸB as well as TLR, IL-1β and TNF-α levels and yielded morphological and clinical improvement [48,49,50,51].
HBO also influences structural proteins involved in tissue regeneration such as Rho-associated protein kinase (ROCK) which interacts with the cytoskeleton regulating, shape, migration, and cell-to-cell adhesion. In this context HBO downregulated ROCK in spinal cord injury, thereby reducing pathologically increased intestinal permeability [58]. Similarly, the transmembrane receptor family of Integrins regulates intercellular and cellular-extracellular adhesion, thereby also influencing cellular migration as necessary for rapid cellular immune response or hemostasis [69]. HBO-induced downregulation of integrins in neutrophils reduces their adhesion ability, alleviating the inflammatory reaction in chronic wounds [70].
The complex Wnt glycoprotein/β-catenin signaling pathway is involved in embryogenesis and carcinogenesis. In addition, Wnt plays a role in the regeneration of bone, where it regulates the osteogenic differentiation of stem cells. HBO-induced upregulation of Wnt enhanced osteogenic differentiation [60,61,62].
Micro-RNA or non-coding RNA are highly specific regulators of genes at the post-transcriptional level. They effectuate the silencing of genes by either inhibition of translation or by RNA-degradation [63].
In conclusion, though the impact of HBO on various substances seems straightforward, the understanding of its complex effects on transcription, signaling, cell-to-cell interaction and structure is merely scratching the surface. The in-part contradictory action on single effector proteins or molecules which often involves both up-or downregulation, respectively, probably mirrors a generally stabilizing potential of HBO that tends to restore the physiological balance rather than enhancing or counteracting single mechanisms.
Table 1Tissue regeneration. Mechanisms involved in effectiveness of HBO; The arrows indicate the effect of HBO on the level of the effector molecule initially found during respective study (in alphabetical order).
| Effector Protein/Molecule | Abbreviation | Field of Action | Change |
|---|---|---|---|
| A-4 integrin [70] | IA4 (CD49D) | Adhesion | ↔ |
| A-4beta-1 integrin (very late activation antigen 4) [70] | VLA-4 |
Adhesion | ↓ |
| Angiogenin (Ribonuclease 5) [22] | ANG (RNASE5) | Transcription | ↑ |
| Anti-apoptotic B-cell lymphoma 2 [32,42] | Bcl-2 | anti-apoptotic | ↑ |
| Bcl-2-associated X protein [42,67] | Bax | pro-apoptotic | ↓ |
| Beta catenin-1 [54,62] | CTNNB1 | Adhesion; tissue homeostasis | ↑ |
| Beta-2 integrin [70] | CD18 | Adhesion | ↓ |
| C-Jun-N terminal kinases [12,55,56,57,65] | JNK | Stress induced kinases; pro-apoptotic | ↑↓ |
| Cleaved caspase 3 [64] | CASP-3 | Apoptosis | ↓ |
| Cryopyrin [64] | NLRP3 (NACHT) | interacts with components of damaged cells; forms NLRP-inflammasome | ↓ |
| Cyclooxygenase 2 (Prostaglandin synthase 2) [32] | COX-2 (PGHS-2) | Pro-inflammatory signaling | ↓ |
| CxC motic chemokine Ligand 1 [55] | CXCL1 | Inflammatory chemoattractant | ↓ |
| CxC motiv chemokine 10 [11] |
CXCL10 | Inflammation, Signaling | ↑ |
| CxC motiv chemokine 12 [31] | SDF-1 | Inflammation, Signaling | ↑ |
| CxC motiv chemokine ligand 8 [11] |
CXCL8 |
Transcription, inflammation | ↑↓ |
| CXC-Motiv-Chemokinreceptor 2 (IL-8 Receptor beta) [55] | CXCR2 | Signaling; pro inflammatory | ↓ |
| CXC-motiv-chemokinreceptor 4 [31] | CXCR4 | Inflammation, Signaling | ↑ |
| Dendritic cell-specific transmembrane protein [35] | Dc-STAMP | co-regulator in osteoclast development | ↓ |
| Endothelial nitric oxide gene expression [11,22,24] | eNOS | Signaling (vascular) | ↑ |
| Epidermal growth factor [11] | EGF | Induction of mitosis in epithelial cells | ↑ |
| Extracellular signal-regulated protein kinase [53,55,56,65] | ERK | Regulates growth and differentiation | ↑↓ |
| Fibroblast growth factor 2 (basic fibroblast growth factor 2) [11,17,56] | FGF-2 | Transcription | ↑ |
| FOS protein [12] | FOS (AP-1; c-fos) | Transcription | ↑ |
| FOSB protein [12] | FOSB (G0/G1 switch regula-tory protein 3; G0S3) | Transcription | ↑ |
| Glycogen synthase kinase-3 [54,62] | GSK3 |
proliferation, differentiation, energy metabolism, neuronal development | ↑↓ |
| High mobility group box 1 protein [48,65,66] | HMGB1 | Cytokine mediator of inflammation | ↓ |
| Hypoxia inducible factor 1 α subunit [29,30,31,32,33,35] | HIF-1α (HIF1A) | Regulator of cellular response to oxygen levels | ↑↓ |
| Inducible nitric oxide synthase [21,66] | i-NOS (NOS-2) | Signaling | ↓↑ |
| Interferon gamma [11,30] | IFG | Cytokine | ↓ |
| Interleukin 1beta [51,57] | IL-1 ß (IL-1; IL1B) | Pro-inflammatory cytokine | ↓ |
| Interleukin-6 [30,46] |
IL-6 |
apoptosis and proliferation of leucocytes | ↑↓ |
| Intracellular adhesion molecule- 1 [23] | ICAM-1 (CD54) | Adhesion | ↓ |
| Krüppel-like factor 2 [68] | KLF-2 | Vasoprotective; Inhibited by miR-92a | ↑ |
| Matrix Metalloproteinase-9 [40,41,42,43,65,66] | MMP-9 (GELB) | Signaling (vascular), migration | ↓ |
| Matrix Metalloproteinase-2 [41,43,65,66] | MMP-2 (CLG4A) | tissue remodeling, angiogenesis and cell migration | ↓ |
| Matrix Metalloproteinase-13 [65,66] | MMP-13 (CLG3) | Cleaves Type II collagen | ↓ |
| Mechanistic target of rapamycin [46,79] | m-TOR (FRAP-1) | Proliferation, differentiation, autophagy | ↓ |
| Metastasis associated lung adenocarcinoma transcript 1 [68] | MALAT 1 | Transcription | ↑ |
| Micro-RNA 92a [68] | miR-92a | Downregulates KLF-2 | ↓ |
| Monocyte chemotactic protein 1 (CC chemokine ligand 2) [11] | MCP1 |
Chemokine secreted by inflammatory cells. Binds to epithelia, attracting and fixating mainly monocytes | ↑↓ |
| Nitric oxide (endothelium derived relaxing factor) [17,18,19,20,21,22,23,24,66] | NO |
Free radical, causes vasodilation | ↑ |
| Nuclear factor erythroid 2-related factor 2 [11,12] | Nrf2 | Transcription of cytoprotective genes | ↑ |
| Nuclear factor kappa-B [29,31,48,49,50,51,55,56] | NF-ĸB | Transcription, Inflammation | ↓↑ |
| Nuclear factor of activated T-cells, cytoplasmic 1 [35] | NFATc1 | factor in gene transcription during immune response; involved in regulation of bone-mass | ↓ |
| Occludin [59] | OCLN | Tight junctions; preserves barrier function of epithelia | ↑ |
| p53 [32] | p53 | Transcription | ↓ |
| phosphorylated/unphosphorylated glycogen synthase kinase 3 [54,62] | pGSK3beta/GSK3beta | Neuronal Apoptosis | ↓ |
| Platelet derived growth factor [11] | PDGF | Transcription | ↑ |
| Protein kinase B [54] |
p-Akt | Transcription; regulates proliferation and cell death | ↑↓ |
| Protein kinase C A [56] | Pkc α | Adhesion, tight junctions | ↑ |
| Receptor for advanced glycation end products [65,66] | RAGE | Induces cell survival, differentiation or apoptosis according to activity | ↓ |
| Rho-associtaed protein kinase [59] | ROCK | Regulates cell shape and migration | ↓ |
| Runt-related transcription factor 2 [62] | Runx 2 | Master regulator of bone development | ↑ |
| Toll-like receptor 4 [50,66] | TLR4 | pro-inflammatory cytokine signaling | ↓ |
| Toll-like receptor 2 [51,66] | TLR2 | Pathogen recognition signaling | ↓ |
| Transforming growth factor beta 1 [43] | TGFB1 | Proliferation, differentiation | ↓ |
| Transcription factor JUNB [12] | JUNB | Transcription | ↑ |
| Tumor necrosis factor α [22,43,51] | TNF-α | Transcription; pro inflammatory | ↓ |
| Reactive oxygen species [31,33,40] | ROS | Signaling; dose dependent effect | ↑↓ |
| Vascular cell adhesion molecule-1 [23] | VCAM-1 (CD106) | Adhesion | ↓ |
| Vascular endothelial growth factor [11,17,30,31,43,53] | VEGF | Transcription, vascular signaling | ↓↑ |
| Wnt family member 3a [62] | Wnt-3a | skeletal differentiation and development; maintenance of bone-mass | ↑ |
| Zonula occludens-1 [59] | ZO-1 | cross-links and anchors tight junction proteins | ↑ |
Hyperbaric protocols, type of study.
| Ref. No | N HBO |
N |
Pressure |
Duration |
Species | Tissue/Indication/Experiment |
|---|---|---|---|---|---|---|
| [11] | 25 | 1 | 2.2 | 60 | Human (patients) | Diabetic foot ulcer |
| [12] | 1 | 1 | 2.4 | 60 | Human | Cells (endothelial, microvascular) |
| [17] | 5 | 1 | 2.5 | 120 | Rat | Contused muscle |
| [18] | 5–8 | 1 | 2.4 | 90 | Mouse | Limb ischemia |
| [19] | 5 | 1 | 2.8 | 60 | Human | Cells (fibroblasts, epithelia) |
| [20] | 20 | 1 | 2.0 | 90 | Human (patients) | Chronic wound |
| [21] | 5 | 1 | 2.5 | 120 | Mouse | Wound model |
| [22] | 1 | 1 | 2.4 | 90 | Human | Cells (chronic wound condition) |
| [23] | 1 | 2 | 2.4 | 90 | Human | Umbilical cord. neutrophils |
| [24] | 1 | 1 | 2.5 | 90 | Rat | Muscle (Reperfusion injury) |
| [29] | 1 | 1 | 2.5 | 60 | Human | Cells (monocytes, fibroblasts) |
| 1 | 1 | 2.0 | 90 | Mouse | Diabetic wound model | |
| [30] | 20 | 1 | 2.4 | 70 | Human (patients) | Diabetic foot ulcer |
| [31] | 30 | 1 | 2.0 | 90 | Mouse | Diabetic wound model |
| [32] | 3–14 | 1 | 2.4 | 90 | Rat | Ischemic wound model |
| [33] | 7 | 1 | 2.5 | 90 | Rat | Stroke model |
| [35] | 4 | 1 | 2.4 | 90 | Human | Cells (RAW 264.7, macrophages) |
| [40] | 10 | 1 | 2.0 | 90 | Mouse | Wound model |
| [41] | 2–10 | 2 | 2.5 | 60 | Rat | Spinal cord injury |
| [42] | 1–21 | 1 | 2.5 | 90 | Rat | CO-poisoning |
| [43] | 35 | 1 | 2.5 | 60 | Rat | Diabetic heart model |
| [46] | 5 | 1 | 2.0 | 60 | Rat | Nerve ligation |
| [48] | 2–20 | 1–2 | 2.5 | 70 | Rat | Spinal cord injury |
| [49] | 30 | 1 | 2.0 | 115 | Human (patients) | Spinal cord injury |
| [50] | 1–14 | 1 | 2.0 | 70 | Rat | Spinal cord injury |
| [51] | 1 | 1 | 2.4 | 60 | Rat | Spinal cord injury |
| [53] | 7 | 1 | 2.0 | 110 | Rat | Traumatic brain injury |
| [54] | 1 | 1 | 2.8 | 90 | Mouse | Traumatic brain injury |
| [55] | 3 | 1 | 2.0 | 60 | Rat | Traumatic brain injury |
| [56] | 4 | 1 | 2.5 | 80 | Mouse | Cells (osteoblast-like) |
| [57] | 1 | every 2nd day | 0.5 | 90 | Rat | Chondrocytes |
| [59] | 1–14 | 1 | 2.0 | 60 | Rat | Spinal cord injury |
| [62] | 1–7 | every 3rd day | 2.5 | 90 | Mouse | Traumatic brain inury |
| [64] | 1 | 1 | 2.0 | 70 | Mouse | Cells (Neurons hippocampus) |
| [65] | 3 | every 2nd day | 2.5 | 120 | Human | Cells (nucleus pulposus cells) |
| [66] | 3 | every 2nd day | 2.5 | 90 | Human | Cells (Chondrocytes) |
| [67] | 3 | every 2nd day | 2.5 | 120 | Human | Cells (degenerated disc cells) |
| [68] | 1–14 | 1 | 2.5 | 60 | Rat | Myocardial infarction model |
| [70] | 15 | 1 | 2.45 | 90 | Human (patients) | Chronic wound |
| [79] | 10 | 1 | 2.0 | 100 | Rat | Spinal cord injury |
Conceptualization, F.-M.S.-J. and L.K.; methodology, J.L. and W.G.; writing—original draft preparation, J.L.; writing—review and editing, F.-M.S.-J. and J.S.; supervision, W.G. All authors have read and agreed to the published version of the manuscript.
Ethical review and approval were waived for this study because it is a pure literature review.
Not applicable.
The data used in this review are published in the cited references.
The authors declare no conflict of interest.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Enlarge this image.Figure 1. Main points of action of HBO in tissue regeneration.
References
1. Lindenmann, J.; Smolle, C.; Kamolz, L.P.; Smolle-Juettner, F.M.; Graier, W.F. Survey of Molecular Mechanisms of Hyperbaric Oxygen in Tissue Repair. Int. J. Mol. Sci.; 2021; 22, 11754. [DOI: https://dx.doi.org/10.3390/ijms222111754]
2. Mathieu, D.; Marroni, A.; Kot, J. Tenth European Consensus Conference on Hyperbaric Medicine: Recommendations for accepted and non-accepted clinical indications and practic of hyperbaric oxygten treatment. Diving Hyperb. Med.; 2017; 47, pp. 24-32. [DOI: https://dx.doi.org/10.28920/dhm47.2.131-132] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28641327]
3. Lee, J.; Cho, Y. Comparative gene expression profiling reveals the mechanisms of axon regeneration. FEBS J.; 2021; 288, pp. 4786-4797. [DOI: https://dx.doi.org/10.1111/febs.15646]
4. Das, D.; Fletcher, R.B.; Ngai, J. Cellular mechanisms of epithelial stem cell self-renewal and differentiation during homeostasis and repair. Wiley Interdiscip. Rev. Dev. Biol.; 2020; 9, e361. [DOI: https://dx.doi.org/10.1002/wdev.361]
5. Julier, Z.; Park, A.J.; Briquez, P.S.; Martino, M.M. Promoting tissue regeneration by modulating the immune system. Acta Biomater.; 2017; 53, pp. 13-28. [DOI: https://dx.doi.org/10.1016/j.actbio.2017.01.056] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28119112]
6. Fão, L.; Mota, S.I.; Rego, A.C. Shaping the Nrf2-ARE-related pathways in Alzheimer’s and Parkinson’s diseases. Ageing Res Rev.; 2019; 54, 100942. [DOI: https://dx.doi.org/10.1016/j.arr.2019.100942] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/31415806]
7. Victor, P.; Sarada, D.; Ramkumar, K.M. Pharmacological activation of Nrf2 promotes wound healing. Eur. J. Pharmacol.; 2020; 886, 173395. [DOI: https://dx.doi.org/10.1016/j.ejphar.2020.173395] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32710954]
8. Chen, D.; Wu, Z.; Wu, L.N.; Jiang, J.; Hu, G.N. Theaflavin Attenuates TBHP-Induced Endothelial Cells Oxidative Stress by Activating PI3K/AKT/Nrf2 and Accelerates Wound Healing in Rats. Front. Bioeng. Biotechnol.; 2022; 10, 830574. [DOI: https://dx.doi.org/10.3389/fbioe.2022.830574]
9. Meng, X.E.; Zhang, Y.; Li, N.; Fan, D.F.; Yang, C.; Li, H.; Guo, D.Z.; Pan, S.Y. Effects of hyperbaric oxygen on the Nrf2 signaling pathway in secondary injury following traumatic brain injury. Genet. Mol. Res.; 2016; 15, pp. 1-7. [DOI: https://dx.doi.org/10.4238/gmr.15016933]
10. Li, Y.; Shen, C.; Zhou, X.; Zhang, J.; Lai, X.; Zhang, Y. Local Treatment of Hydrogen-Rich Saline Promotes Wound Healing In Vivo by Inhibiting Oxidative Stress via Nrf-2/HO-1 Pathway. Oxid. Med. Cell. Longev.; 2022; 2022, 2949824. [DOI: https://dx.doi.org/10.1155/2022/2949824]
11. Dhamodharan, U.; Karan, A.; Sireesh, D.; Vaishnavi, A.; Somasundar, A.; Rajesh, K.; Ramkumar, K.M. Tissue-specific role of Nrf2 in the treatment of diabetic foot ulcers during hyperbaric oxygen therapy. Free Radic. Biol. Med.; 2019; 138, pp. 53-62. [DOI: https://dx.doi.org/10.1016/j.freeradbiomed.2019.04.031] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/31035003]
12. Godman, C.A.; Chheda, K.P.; Hightower, L.E.; Perdrizet, G.; Shin, D.-G.; Giardina, C. Hyperbaric oxygen induces a cytoprotective and angiogenic response in human microvascular endothelial cells. Cell Stress Chaperones; 2010; 15, pp. 431-442. [DOI: https://dx.doi.org/10.1007/s12192-009-0159-0] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/19949909]
13. Malone-Povolny, M.J.; Maloney, S.E.; Schoenfisch, M.H. Nitric Oxide Therapy for Diabetic Wound Healing. Adv. Health Mater.; 2019; 8, e1801210. [DOI: https://dx.doi.org/10.1002/adhm.201801210] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/30645055]
14. Man, M.Q.; Wakefield, J.S.; Mauro, T.M.; Elias, P.M. Regulatory Role of Nitric Oxide in Cutaneous Inflammation. Inflammation; 2022; 45, pp. 949-964. [DOI: https://dx.doi.org/10.1007/s10753-021-01615-8] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35094214]
15. Van der Vliet, A.; Eiserich, J.P.; Cross, C.E. Nitric oxide: A pro-inflammatory mediator in lung disease?. Respir. Res.; 2000; 1, pp. 67-72. [DOI: https://dx.doi.org/10.1186/rr14] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/11667967]
16. Broughton, G., 2nd; Janis, J.E.; Attinger, C.E. The basic science of wound healing. Plast. Reconstr. Surg.; 2006; 117, (Suppl. S7), pp. 12S-34S. [DOI: https://dx.doi.org/10.1097/01.prs.0000225430.42531.c2]
17. Yamamoto, N.; Oyaizu, T.; Enomoto, M.; Horie, M.; Yuasa, M.; Okawa, A.; Yagishita, K. VEGF and bFGF induction by nitric oxide is associated with hyperbaric oxygen-induced angiogenesis and muscle regeneration. Sci. Rep.; 2020; 10, 2744. [DOI: https://dx.doi.org/10.1038/s41598-020-59615-x]
18. Goldstein, L.J.; Gallagher, K.A.; Bauer, S.M.; Bauer, R.J.; Baireddy, V.; Liu, Z.J.; Buerk, D.G.; Thom, S.R.; Velazquez, O.C. Endothelial progenitor cell release into circulation is triggered by hyperoxia-induced increases in bone marrow nitric oxide. Stem Cells; 2006; 24, pp. 2309-2318. [DOI: https://dx.doi.org/10.1634/stemcells.2006-0010]
19. Venetsanou, K.; Fildissis, G.; Tokta, R.; Brinias, C.; Baltopoulos, G. The role of nitric oxide in cellular response to hyperbaric conditions. Eur. J. Appl. Physiol.; 2012; 112, pp. 677-687. [DOI: https://dx.doi.org/10.1007/s00421-011-2027-8]
20. Boykin, J.V., Jr.; Baylis, C. Hyperbaric oxygen therapy mediates increased nitric oxide production associated with wound healing: A preliminary study. Adv. Skin Wound Care; 2007; 20, pp. 382-388. [DOI: https://dx.doi.org/10.1097/01.ASW.0000280198.81130.d5]
21. Gajendrareddy, P.K.; Sen, C.K.; Horan, M.P.; Marucha, P.T. Hyperbaric oxygen therapy ameliorates stress-impaired dermal wound healing. Brain Behav. Immun.; 2005; 19, pp. 217-222. [DOI: https://dx.doi.org/10.1016/j.bbi.2004.09.003] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/15797310]
22. Kendall, A.C.; Whatmore, J.L.; Harries, L.W.; Winyard, P.G.; Smerdon, G.R.; Eggleton, P. Changes in inflammatory gene expression induced by hyperbaric oxygen treatment in human endothelial cells under chronic wound conditions. Exp. Cell Res.; 2012; 318, pp. 207-216. [DOI: https://dx.doi.org/10.1016/j.yexcr.2011.10.014] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/22063471]
23. Kendall, A.C.; Whatmore, J.L.; Winyard, P.G.; Smerdon, G.R.; Eggleton, P. Hyperbaric oxygen treatment reduces neutrophil-endothelial adhesion in chronic wound conditions through S-nitrosation. Wound Repair Regen.; 2013; 21, pp. 860-868. [DOI: https://dx.doi.org/10.1111/wrr.12108] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24134224]
24. Baynosa, R.C.; Naig, A.L.; Murphy, P.S.; Fang, X.H.; Stephenson, L.L.; Khiabani, K.T.; Wang, W.Z.; Zamboni, W.A. The effect of hyperbaric oxygen on nitric oxide synthase activity and expression in ischemia-reperfusion injury. J. Surg. Res.; 2013; 183, pp. 355-361. [DOI: https://dx.doi.org/10.1016/j.jss.2013.01.004]
25. Hutami, I.R.; Izawa, T.; Khurel-Ochir, T.; Sakamaki, T.; Iwasa, A.; Tanaka, E. Macrophage Motility in Wound Healing Is Regulated by HIF-1α via S1P Signaling. Int. J. Mol. Sci.; 2021; 22, 8992. [DOI: https://dx.doi.org/10.3390/ijms22168992]
26. Li, G.; Ko, C.N.; Li, D.; Yang, C.; Wang, W.; Yang, G.J.; Di Primo, C.; Wong, V.K.W.; Xiang, Y.; Lin, L. et al. A small molecule HIF-1α stabilizer that accelerates diabetic wound healing. Nat. Commun.; 2021; 12, 3363. [DOI: https://dx.doi.org/10.1038/s41467-021-23448-7]
27. Goggins, B.J.; Minahan, K.; Sherwin, S.; Soh, W.S.; Pryor, J.; Bruce, J.; Liu, G.; Mathe, A.; Knight, D.; Horvat, J.C. et al. Pharmacological HIF-1 stabilization promotes intestinal epithelial healing through regulation of α-integrin expression and function. Am. J. Physiol. Gastrointest. Liver Physiol.; 2021; 320, pp. G420-G438. [DOI: https://dx.doi.org/10.1152/ajpgi.00192.2020]
28. Zhu, Y.; Wang, Y.; Jia, Y.; Xu, J.; Chai, Y. Roxadustat promotes angiogenesis through HIF-1α/VEGF/VEGFR2 signaling and accelerates cutaneous wound healing in diabetic rats. Wound Repair Regen.; 2019; 27, pp. 324-334. [DOI: https://dx.doi.org/10.1111/wrr.12708]
29. Sunkari, V.G.; Lind, F.; Botusan, I.R.; Kashif, A.; Liu, Z.-J.; Yla-Herttuala, S.; Brismar, K.; Velazquez, O.; Catrina, S.B. Hyperbaric oxygen therapy activates hypoxia-inducible factor 1 (HIF-1), which contributes to improved wound healing in diabetic mice. Wound Repair Regen.; 2015; 23, pp. 98-103. [DOI: https://dx.doi.org/10.1111/wrr.12253]
30. Anguiano-Hernandez, Y.M.; Contreras-Mendez, L.; de Los Angeles Hernandez-Cueto, M.; Muand Oz-Medina, J.E.; Santillan-Verde, M.A.; Barbosa-Cabrera, R.E.; Delgado-Quintana, C.A.; Trejo-Rosas, S.; Santacruz-Tinoco, C.E.; Gonzalez-Ibarra, J. et al. Modification of HIF-1α, NF-aκB, IGFBP-3, VEGF and adiponectin in diabetic foot ulcers treated with hyperbaric oxygen. Undersea Hyperb. Med.; 2019; 46, pp. 35-44. [DOI: https://dx.doi.org/10.22462/01.03.2019.4]
31. Huang, X.; Liang, P.; Jiang, B.; Zhang, P.; Yu, W.; Duan, M.; Guo, L.; Cui, X.; Huang, M.; Huang, X. Hyperbaric oxygen potentiates diabetic wound healing by promoting fibroblast cell proliferation and endothelial cell angiogenesis. Life Sci.; 2020; 259, 118246. [DOI: https://dx.doi.org/10.1016/j.lfs.2020.118246] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32791151]
32. Zhang, Q.; Chang, Q.; Cox, R.A.; Gong, X.; Gould, L.J. Hyperbaric oxygen attenuates apoptosis and decreases inflammation in an ischemic wound model. J. Investig. Dermatol.; 2008; 128, pp. 2102-2112. [DOI: https://dx.doi.org/10.1038/jid.2008.53] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/18337831]
33. Hu, Q.; Liang, X.; Chen, D.; Chen, Y.; Doycheva, D.; Tang, J.; Tang, J.; Zhang, J.H. Delayed hyperbaric oxygen therapy promotes neurogenesis through reactive oxygen species/hypoxia-inducible factor-1α/β-catenin pathway in middle cerebral artery occlusion rats. Stroke; 2014; 45, pp. 1807-1814. [DOI: https://dx.doi.org/10.1161/STROKEAHA.114.005116] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24757104]
34. Hadanny, A.; Efrati, S. The Hyperoxic-Hypoxic Paradox. Biomolecules; 2020; 10, 958. [DOI: https://dx.doi.org/10.3390/biom10060958] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/32630465]
35. Al Hadi, H.; Smerdon, G.R.; Fox, S.W. Hyperbaric oxygen therapy suppresses osteoclast formation and bone resorption. J. Orthop. Res.; 2013; 31, pp. 1839-1844. [DOI: https://dx.doi.org/10.1002/jor.22443]
36. Dai, J.; Shen, J.; Chai, Y.; Chen, H. IL-1β Impaired Diabetic Wound Healing by Regulating MMP-2 and MMP-9 through the p38 Pathway. Mediat. Inflamm.; 2021; 2021, 6645766. [DOI: https://dx.doi.org/10.1155/2021/6645766]
37. Hingorani, D.V.; Lippert, C.N.; Crisp, J.L.; Savariar, E.N.; Hasselmann, J.P.C.; Kuo, C.; Nguyen, Q.T.; Tsien, R.Y.; Whitney, M.A.; Ellies, L.G. Impact of MMP-2 and MMP-9 enzyme activity on wound healing, tumor growth and RACPP cleavage. PLoS ONE; 2018; 13, e0198464. [DOI: https://dx.doi.org/10.1371/journal.pone.0198464]
38. Bobadilla, M.; Sáinz, N.; Rodriguez, J.A.; Abizanda, G.; Orbe, J.; de Martino, A.; García Verdugo, J.M.; Páramo, J.A.; Prósper, F.; Pérez-Ruiz, A. MMP-10 is required for efficient muscle regeneration in mouse models of injury and muscular dystrophy. Stem Cells; 2014; 32, pp. 447-461. [DOI: https://dx.doi.org/10.1002/stem.1553]
39. Jones, J.I.; Nguyen, T.T.; Peng, Z.; Chang, M. Targeting MMP-9 in Diabetic Foot Ulcers. Pharmaceuticals; 2019; 12, 79. [DOI: https://dx.doi.org/10.3390/ph12020079]
40. Nguyen, T.T.; Jones, J.I.; Wolter, W.R.; Perez, R.L.; Schroeder, V.A.; Champion, M.M.; Hesek, D.; Lee, M.; Suckow, M.A.; Mobashery, S. et al. Hyperbaric oxygen therapy accelerates wound healing in diabetic mice by decreasing active matrix metalloproteinase-9. Wound Repair Regen.; 2020; 28, pp. 194-201. [DOI: https://dx.doi.org/10.1111/wrr.12782]
41. Yang, J.; Wang, G.; Gao, C.; Shao, G.; Kang, N. Effects of hyperbaric oxygen on MMP-2 and MMP-9 expression and spinal cord edema after spinal cord injury. Life Sci.; 2013; 93, pp. 1033-1038. [DOI: https://dx.doi.org/10.1016/j.lfs.2013.10.015] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24436993]
42. Xue, L.; Wang, W.L.; Li, Y.; Gong, X.; Bao, J.X.; Zhang, H.J.; Xie, X.P.; Chang, Y.M.; Li, J.S. Effects of hyperbaric oxygen on hippocampal neuronal apoptosis in rats with acute carbon monoxide poisoning. Undersea Hyperb. Med.; 2017; 44, pp. 121-131. [DOI: https://dx.doi.org/10.22462/3.4.2017.5] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28777902]
43. Silva, F.S.; de Souza, K.S.C.; Galdino, O.A.; de Moraes, M.V.; Ishikawa, U.; Medeiros, M.A.; Lima, J.P.M.S.; de Paula Medeiros, K.C.; da Silva Farias, N.B.; de Araújo Júnior, R.F. et al. Hyperbaric oxygen therapy mitigates left ventricular remodeling, upregulates MMP-2 and VEGF, and inhibits the induction of MMP-9, TGF-β1, and TNF-α in streptozotocin-induced diabetic rat heart. Life Sci.; 2022; 295, 120393. [DOI: https://dx.doi.org/10.1016/j.lfs.2022.120393] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35167880]
44. Lund-Ricard, Y.; Cormier, P.; Morales, J.; Boutet, A. mTOR Signaling at the Crossroad between Metazoan Regeneration and Human Diseases. Int. J. Mol. Sci.; 2020; 21, 2718. [DOI: https://dx.doi.org/10.3390/ijms21082718]
45. Chen, C.; Chen, W.; Nong, Z.; Nie, Y.; Chen, X.; Pan, X.; Guo, Y.; Yao, M.; Deng, W. Hyperbaric oxygen alleviated cognitive impairments in mice induced by repeated cerebral ischemia-reperfusion injury via inhibition of autophagy. Life Sci.; 2020; 241, 117170. [DOI: https://dx.doi.org/10.1016/j.lfs.2019.117170]
46. Liu, Y.D.; Wang, Z.B.; Han, G.; Zhao, P. Hyperbaric oxygen treatment attenuates neuropathic pain by elevating autophagy flux via inhibiting mTOR pathway. Am. J. Transl. Res.; 2017; 9, pp. 2629-2638.
47. Yu, H.; Lin, L.; Zhang, Z.; Zhang, H.; Hu, H. Targeting NF-κB pathway for the therapy of diseases: Mechanism and clinical study. Signal Transduct. Target. Ther.; 2020; 5, 209. [DOI: https://dx.doi.org/10.1038/s41392-020-00312-6]
48. Yang, J.; Liu, X.; Zhou, Y.; Wang, G.; Gao, C.; Su, Q. Hyperbaric oxygen alleviates experimental (spinal cord) injury by downregulating HMGB1/NF-kappaB expression. Spine; 2013; 38, pp. E1641-E1648. [DOI: https://dx.doi.org/10.1097/BRS.0000000000000005]
49. Sun, L.; Zhao, L.; Li, P.; Liu, X.; Liang, F.; Jiang, Y.; Kang, N.; Gao, C.; Yang, J. Effect of hyperbaric oxygen therapy on HMGB1/NF-kappaB expression and prognosis of acute spinal cord injury: A randomized clinical trial. Neurosci. Lett.; 2019; 692, pp. 47-52. [DOI: https://dx.doi.org/10.1016/j.neulet.2018.10.059]
50. Kang, N.; Hai, Y.; Yang, J.; Liang, F.; Gao, C.J. Hyperbaric oxygen intervention reduces secondary spinal cord injury in rats via regulation of HMGB1/TLR4/NF-κB signaling pathway. Int. J. Clin. Exp. Pathol.; 2015; 8, pp. 1141-1153.
51. Tan, J.; Zhang, F.; Liang, F.; Wang, Y.; Li, Z.; Yang, J.; Liu, X. Protective effects of hyperbaric oxygen treatment against spinal cord injury in rats via toll-like receptor 2/nuclear factor-kappaB signaling. Int. J. Clin. Exp. Pathol.; 2014; 7, pp. 1911-1919. [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24966901]
52. Gao, Q. Oxidative Stress and Autophagy. Adv. Exp. Med. Biol.; 2019; 1206, pp. 179-198. [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/31776986]
53. Yang, Y.; Wei, H.; Zhou, X.; Zhang, F.; Wang, C. Hyperbaric oxygen promotes neural stem cell proliferation by activating vascular endothelial growth factor/extracellular signal-regulated kinase signaling after traumatic brain injury. Neuroreport; 2017; 28, pp. 1232-1238. [DOI: https://dx.doi.org/10.1097/WNR.0000000000000901]
54. He, H.; Li, X.; He, Y. Hyperbaric oxygen therapy attenuates neuronal apoptosis induced by traumatic brain injury via Akt/GSK3beta/beta-catenin pathway. Neuropsychiatr. Dis. Treat.; 2019; 15, pp. 369-374. [DOI: https://dx.doi.org/10.2147/NDT.S183632] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/30774348]
55. Xia, A.; Huang, H.; You, W.; Liu, Y.; Wu, H.; Liu, S. The neuroprotection of hyperbaric oxygen therapy against traumatic brain injury via NF-κB/MAPKs-CXCL1 signaling pathways. Exp. Brain Res.; 2022; 240, pp. 207-220. [DOI: https://dx.doi.org/10.1007/s00221-021-06249-8]
56. Hsieh, C.P.; Chiou, Y.L.; Lin, C.Y. Hyperbaric oxygen-stimulated proliferation and growth of osteoblasts may be mediated through the FGF-2/MEK/ERK 1/2/NF-κB and PKC/JNK pathways. Connect. Tissue Res.; 2010; 51, pp. 497-509. [DOI: https://dx.doi.org/10.3109/03008201003746679]
57. Sun, Q.; Wu, G.; Chen, H.; Chen, L.; Chen, H.; Zhu, G.; Zhao, H. Hyperbaric oxygen protects type II collagen in interleukin-1β-induced mandibular condylar chondrocyte via inhibiting the JNK/c-Jun signaling pathway. Oncotarget; 2017; 8, pp. 60312-60323. [DOI: https://dx.doi.org/10.18632/oncotarget.19294]
58. Nunes, K.P.; Webb, R.C. New insights into RhoA/Rho-kinase signaling: A key regulator of vascular contraction. Small GTPases; 2021; 12, pp. 458-469. [DOI: https://dx.doi.org/10.1080/21541248.2020.1822721]
59. Liu, X.; Liang, F.; Zhang, J.; Li, Z.; Yang, J.; Kang, N. Hyperbaric Oxygen Treatment Improves Intestinal Barrier Function After Spinal Cord Injury in Rats. Front. Neurol.; 2020; 11, 563281. [DOI: https://dx.doi.org/10.3389/fneur.2020.563281]
60. Clevers, H.; Nusse, R. Wnt/β-catenin signaling and disease. Cell; 2012; 149, pp. 1192-1205. [DOI: https://dx.doi.org/10.1016/j.cell.2012.05.012]
61. Liu, J.; Xiao, Q.; Xiao, J.; Niu, C.; Li, Y.; Zhang, X.; Zhou, Z.; Shu, G.; Yin, G. Wnt/β-catenin signalling: Function, biological mechanisms, and therapeutic opportunities. Signal Transduct. Target. Ther.; 2022; 7, 3. [DOI: https://dx.doi.org/10.1038/s41392-021-00762-6] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34980884]
62. Lin, S.S.; Ueng, S.W.; Niu, C.C.; Yuan, L.J.; Yang, C.Y.; Chen, W.J.; Lee, M.S.; Chen, J.K. Effects of hyperbaric oxygen on the osteogenic differentiation of mesenchymal stem cells. BMC Musculoskelet. Disord.; 2014; 15, 56. [DOI: https://dx.doi.org/10.1186/1471-2474-15-56] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/24568330]
63. Mohr, A.M.; Mott, J.L. Overview of microRNA biology. Semin. Liver Dis.; 2015; 35, pp. 3-11. [DOI: https://dx.doi.org/10.1055/s-0034-1397344] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/25632930]
64. Ye, Y.; Feng, Z.; Tian, S.; Yang, Y.; Jia, Y.; Wang, G.; Wang, J.; Bai, W.; Li, J.; He, X. HBO Alleviates Neural Stem Cell Pyroptosis via lncRNA-H19/miR-423-5p/NLRP3 Axis and Improves Neurogenesis after Oxygen Glucose Deprivation. Oxid. Med. Cell. Longev.; 2022; 2022, 9030771. [DOI: https://dx.doi.org/10.1155/2022/9030771]
65. Niu, C.C.; Lin, S.S.; Yuan, L.J.; Lu, M.L.; Ueng, S.W.N.; Yang, C.Y.; Tsai, T.T.; Lai, P.L. Upregulation of miR-107 expression following hyperbaric oxygen treatment suppresses HMGB1/RAGE signaling in degenerated human nucleus pulposus cells. Arthritis Res. Ther.; 2019; 21, 42. [DOI: https://dx.doi.org/10.1186/s13075-019-1830-1]
66. Lin, S.S.; Yuan, L.J.; Niu, C.C.; Tu, Y.K.; Yang, C.Y.; Ueng, S.W.N. Hyperbaric oxygen inhibits the HMGB1/RAGE signaling pathway by upregulating Mir-107 expression in human osteoarthritic chondrocytes. Osteoarthr. Cartil.; 2019; 27, pp. 1372-1381. [DOI: https://dx.doi.org/10.1016/j.joca.2019.05.011]
67. Lin, S.S.; Niu, C.C.; Yuan, L.J.; Tsai, T.T.; Lai, P.L.; Chong, K.Y.; Wei, K.C.; Huang, C.Y.; Lu, M.L.; Yang, C.Y. et al. Mir-573 regulates cell proliferation and apoptosis by targeting Bax in human degenerative disc cells following hyperbaric oxygen treatment. J. Orthop. Surg. Res.; 2021; 16, 16. [DOI: https://dx.doi.org/10.1186/s13018-020-02114-6]
68. Shyu, K.G.; Wang, B.W.; Fang, W.J.; Pan, C.M.; Lin, C.M. Hyperbaric oxygen-induced long non-coding RNA MALAT1 exosomes suppress MicroRNA-92a expression in a rat model of acute myocardial infarction. J. Cell. Mol. Med.; 2020; 24, pp. 12945-12954. [DOI: https://dx.doi.org/10.1111/jcmm.15889]
69. Ginsberg, M.H. Integrin activation. BMB Rep.; 2014; 47, pp. 655-659. [DOI: https://dx.doi.org/10.5483/BMBRep.2014.47.12.241]
70. Baiula, M.; Greco, R.; Ferrazzano, L.; Caligiana, A.; Hoxha, K.; Bandini, D.; Longobardi, P.; Spampinato, S.; Tolomelli, A. Integrin-mediated adhesive properties of neutrophils are reduced by hyperbaric oxygen therapy in patients with chronic non-healing wound. PLoS ONE; 2020; 15, e0237746. [DOI: https://dx.doi.org/10.1371/journal.pone.0237746]
71. Bennett, M.H.; Mitchell, S.J. Emerging indications for hyperbaric oxygen. Curr. Opin. Anaesthesiol.; 2019; 32, pp. 792-798. [DOI: https://dx.doi.org/10.1097/ACO.0000000000000773] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/31343466]
72. Ahmadi, F.; Khalatbary, A.R. A review on the neuroprotective effects of hyperbaric oxygen therapy. Med. Gas Res.; 2021; 11, pp. 72-82. [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/33818447]
73. De Wolde, S.D.; Hulskes, R.H.; Weenink, R.P.; Hollmann, M.W.; van Hulst, R.A. The Effects of Hyperbaric Oxygenation on Oxidative Stress, Inflammation and Angiogenesis. Biomolecules; 2021; 11, 1210. [DOI: https://dx.doi.org/10.3390/biom11081210] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34439876]
74. Gottfried, I.; Schottlender, N.; Ashery, U. Hyperbaric Oxygen Treatment-From Mechanisms to Cognitive Improvement. Biomolecules; 2021; 11, 1520. [DOI: https://dx.doi.org/10.3390/biom11101520] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34680155]
75. Oropallo, A.R.; Serena, T.E.; Armstrong, D.G.; Niederauer, M.Q. Molecular Biomarkers of Oxygen Therapy in Patients with Diabetic Foot Ulcers. Biomolecules; 2021; 11, 925. [DOI: https://dx.doi.org/10.3390/biom11070925] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/34206433]
76. Ortega, M.A.; Fraile-Martinez, O.; García-Montero, C.; Callejón-Peláez, E.; Sáez, M.A.; Álvarez-Mon, M.A.; García-Honduvilla, N.; Monserrat, J.; Álvarez-Mon, M.; Bujan, J. et al. A General Overview on the Hyperbaric Oxygen Therapy: Applications, Mechanisms and Translational Opportunities. Medicina; 2021; 57, 864. [DOI: https://dx.doi.org/10.3390/medicina57090864]
77. Smolle, C.; Lindenmann, J.; Kamolz, L.; Smolle-Juettner, F.M. The History and Development of Hyperbaric Oxygenation (HBO) in Thermal Burn Injury. Medicina; 2021; 57, 49. [DOI: https://dx.doi.org/10.3390/medicina57010049]
78. Camporesi, E.M.B.G. Mechanisms of action of hyperbaric oxygen therapy. Undersea Hyperb. Med.; 2018; 41, pp. 247-252.
79. Chen, H.; Xu, G.; Wu, Y.; Wang, X.; Wang, F.; Zhang, Y. HBO-PC Promotes Locomotor Recovery by Reducing Apoptosis and Inflammation in SCI Rats: The Role of the mTOR Signaling Pathway. Cell. Mol. Neurobiol.; 2020; 41, pp. 1537-1547. [DOI: https://dx.doi.org/10.1007/s10571-020-00921-3]
80. Förstermann, U.; Sessa, W.C. Nitric oxide synthases: Regulation and function. Eur. Heart J.; 2012; 33, pp. 829-837. [DOI: https://dx.doi.org/10.1093/eurheartj/ehr304]
81. Ridiandries, A.; Tan, J.T.M.; Bursill, C.A. The Role of Chemokines in Wound Healing. Int. J. Mol. Sci.; 2018; 19, 3217. [DOI: https://dx.doi.org/10.3390/ijms19103217] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/30340330]
82. De Almeida, L.G.N.; Thode, H.; Eslambolchi, Y.; Chopra, S.; Young, D.; Gill, S.; Devel, L.; Dufour, A. Matrix Metalloproteinases: From Molecular Mechanisms to Physiology, Pathophysiology, and Pharmacology. Pharmacol. Rev.; 2022; 74, pp. 712-768. [DOI: https://dx.doi.org/10.1124/pharmrev.121.000349] [PubMed: https://www.ncbi.nlm.nih.gov/pubmed/35738680]
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Details
; Kamolz, L 2
; Graier, W 3
; Smolle, J 4
; F-M Smolle-Juettner 1
1 Division of Thoracic and Hyperbaric Surgery, Medical University of Graz, A-8036 Graz, Austria
2 Division of Plastic, Aesthetic and Reconstructive Surgery, Medical University of Graz, A-8036 Graz, Austria
3 Gottfried Schatz Research Center for Cell Signaling, Metabolism and Aging, Molecular Biology and Biochemistry, A-8036 Graz, Austria
4 Institute of Informatics, Statistics and Documentation, Medical University of Graz, A-8036 Graz, Austria