Hydrogen Sulfide, the Next Potent Preventive and Therapeutic Agent in Aging and Age-Associated Diseases
Hydrogen sulfide (H2S) is the third endogenous signaling gasotransmitter, following nitric oxide and carbon monoxide. It is physiologically generated by cystathionine-γ-lyase, cystathionine-β-synthase, and 3-mercaptopyruvate sulfurtransferase. H2S has been gaining increasing attention as an important endogenous signaling molecule because of its significant effects on the cardiovascular and nervous systems. Substantial evidence shows that H2S is involved in aging by inhibiting free-radical reactions, activating SIRT1, and probably interacting with the age-related gene Klotho. Moreover, H2S has been shown to have therapeutic potential in age-associated diseases. This article provides an overview of the physiological functions and effects of H2S in aging and age-associated diseases and proposes the potential health and therapeutic benefits of H2S.
Aging has been a topic of great interest to the scientific community for a long time. This biological process is characterized by a time-dependent progressive decline of physiological functions accompanied by an increased incidence of age-associated diseases. The basic cellular and biochemical features of aging are very complex to elucidate clearly. Although various theories have been proposed to explain the process of aging, there is none that has been generally accepted by gerontologists. Denham Harman proposed that aging and age-associated diseases are basically caused by the deleterious side attacks of free radicals on cell constituents and connective tissues (1). This proposal, which implies that limiting or inhibiting the formation of free radicals could reduce the rate of aging and prevent age-associated diseases, is receiving growing acceptance as a possible explanation of the aging theory. Studies showing that nutritional antioxidants (vitamin C, vitamin E, and resveratrol) and antioxidant enzymes (superoxide dismutase [SOD], catalase [CAT], and glutathione [GSH] peroxidase) can promote better health and longevity by suppressing free-radical reactions are still limited and equivocal (2). However, antioxidants are receiving considerable attention and their use is increasingly being adopted in Western countries. Hydrogen sulfide (H2S), which was previously regarded as a poisonous gas, is generated endogenously in mammals. With its antioxidant and other physiological functions, it has the potential to provide many health benefits. Several studies have shown that H2S prevents free radical-induced impairment and is beneficial in treating age-associated diseases. A recent study reported that the plasma H2S level in humans over 50 to 80 years of age declines with age (3). However, the precise relationship between H2S and physiological changes that constitute aging is largely unknown. This review aims to provide detailed information on the various physiological effects of H2S on aging and age-associated diseases known to date.
GENERATION OF ENDOGENOUS H2S
H2S is a colorless, flammable, water-soluble gas with the characteristic smell of rotten eggs. In the past several centuries, H2S had been known only for its toxicity and environmental hazards. However, as a member of a family of gasotransmitters that includes nitric oxide and carbon monoxide, it is produced endogenously in mammals, including humans, and has important physiological roles in the human body (4, 5). Previous studies reported that H2S is physiologically generated by cystathionine-γ-lyase (CSE) and cystathionine-β-synthase (CBS) (6, 7). These two pyridoxal-5′-phosphate-dependent enzymes, which are expressed in the liver, kidney, brain, thoracic aorta, ileum, pancreatic islets, uterus, and placenta, among other locations, are crucial in the synthesis of H2S (8–13). CBS is predominantly expressed in the brain and the nervous system (6, 14, 15). However, the expression of CSE proteins has been mainly observed in vascular smooth muscle cells and in the heart (16, 17). In addition, 3-mercaptopyruvate sulfurtransferase and cysteine aminotransferase localized to the endothelium of the thoracic aorta has also been reported to produce H2S from cysteine and alpha-ketoglutarate (18) (Fig. 1).
PHYSIOLOGICAL EFFECTS OF ENDOGENOUS H2S
H2S has various physiological effects on the human body. First, H2S is a major endothelium-derived hyperpolarizing factor (EDHF) that causes hyperpolarization and vasorelaxation of vascular endothelium and smooth muscle cells by activating ATP-sensitive, intermediate-conductance and small-conductance potassium channels through cysteine S-sulfhydration (19, 20). Second, H2S can prevent cytokine- or oxidant-induced oxidative damage through its antioxidative effects (21–23). Additionally, H2S can inhibit the expression of proinflammatory factors by downregulating NF-κB activation or by upregulating heme oxygenase 1 expression (24–28). Moreover, H2S may help regulate various functions of the human body with its cytoprotective, antifibrotic, antiapoptotic, and angiogenic properties (29–32). Taken together, these known functions of H2S imply an important role in aging and age-associated diseases (Table 1).
ROLE OF H2S IN REGULATION OF AGING
H2S inhibits free-radical reactions and oxidative stress.
Continuous accumulation of deleterious free-radical reactions in cells and tissues is a major contributor to aging. Hence, the aging process may be caused by free-radical reactions. Free radicals and oxidative stress are believed to be important risk factors in aging and various age-associated diseases. A judicious selection of diet and antioxidant supplements is expected to promote longevity (34, 35). Consistent with this idea, many healthy volunteers with improved body redox status benefit from sulfurous water consumption, which can reduce biomolecule oxidation and provide valid protection against oxidative damage commonly associated with aging and age-related degenerative diseases. However, endogenously produced H2S can be hydrolyzed to hydrosulfide and sulfide ions. Interestingly, it has been reported that levels of both lipid and protein oxidation products, namely, malondialdehyde (the lipid peroxidation product), advanced oxidation protein products, and carbonyls decrease significantly in plasma samples of healthy volunteers subjected to a cycle of hydroponic therapy with H2S-rich water (500 ml day−1 for 2 weeks) (36). Although the underlying mechanisms of this effect are not completely understood, it implies that H2S can protect against oxidative stress. Oxidative damage to biological macromolecules is caused by increased levels of free radicals, reactive oxygen species (ROS), and reactive nitrogen species (RNS) which can disrupt the cellular reduction-oxidation (redox) balance. The primary ROS/RNS species generated in a cell are superoxide (O2−), hydrogen peroxide (H2O2), and nitric oxide (NO) (37). H2S can protect mouse brain endothelial cells (bEnd3) from methionine (Met)-induced oxidative stress and cytotoxicity. Pretreatment of bEnd3 cells with NaHS (0.05 mM) can decrease H2O2, peroxynitrite (ONOO−), and O2− generation induced by Met. In the ROS scavenging pathway, SOD converts O2− to H2O2, which is subsequently reduced to H2O and O2 by CAT. However, low concentrations of H2S can synergistically increase inhibitory effects of apocynin, N-acetyl-l-cysteine (NAC), reduced GSH, CAT, SOD, and Nω-nitro-l-arginine methyl ester (L-NAME) on ROS production and redox enzyme levels induced by Met (38). ONOO−, a powerful oxidant and cytotoxic species that can induce nitration of tyrosine and tyrosine residues in proteins, is formed from rapid interaction of NO and O2− (39). H2S has also been considered a potent scavenger of ONOO−. H2S at low concentrations (30 μM) can significantly inhibit tyrosine nitration mediated by ONOO− to an extent similar to that seen with reduced GSH, a major antioxidant in the cellular defense against oxidative stress. Additionally, H2S can also significantly inhibit cytotoxicity mediated by ONOO− in human neuroblastoma SH-SY5Y cells at physiological levels (40). In addition, Whiteman et al. have shown that H2S can similarly quench NO to form a novel nitrosothiol compound in vitro. This suggests that H2S has direct chemical interactions with NO free radicals to suppress oxidative stress (41). Moreover, Kimura et al. demonstrated that H2S can protect mouse brain neuroblastoma Neuro2a cells from oxidative stress caused by H2O2 and recover GSH levels suppressed by H2O2 in those cells (42). Furthermore, modulation of oxidative stress by calorie restriction (CR) is recommended as one mechanism to slow the aging process and decline of body functions in animals (43). Thus, H2S may also slow the aging process by inhibiting free-radical reactions and oxidative stress.
The free-radical theory was revised when mitochondria were found to be responsible for the initiation of most free-radical reactions occurring in cells. The life span is also postulated to be determined by the rate of free-radical damage to mitochondria. In fact, owing to continuous generation of free radicals throughout the life of a cell, mitochondria, especially mitochondrial DNA, are the key targets of free-radical attack (44). Kimura and coworkers showed that H2S reduces cystine to cysteine in the extracellular space and increases intracellular concentrations of cysteine to increase the production of intracellular GSH and enhances the redistribution of GSH into mitochondria in Neuro2a cells. It enables H2S to suppress oxidative stress in the mitochondria (42). In rat models of ischemia and reperfusion (I/R) injury, it has been observed that preconditioning with H2S can prevent mitochondrial dysfunction in rat intestinal mucosa by a calcium-activated, large-conductance potassium channel-dependent mechanism (45). Under I/R conditions, production of ROS increases, which has a pivotal role in the pathogenesis of myocardial I/R injury. Inhibition of oxidative stress has been reported to underlie the cardioprotective effects of H2S under I/R conditions. Sun et al. showed that treating cardiomyocytes with 50 μM NaHS, which is close to the level found in rat plasma, decreases the levels of ROS by inhibiting mitochondrial complex IV3 and increasing SOD activities in cardiomyocytes under I/R conditions. H2S has also been found to inhibit electron transport to reduce harmful ROS generation under cardiac I/R conditions (46). Thus, protection against oxidative stress-induced mitochondrial damage may be a novel mechanism through which H2S could furnish valid protection and possibly increase life span.
H2S activates SIRT1 to resist aging.
The silent information regulator 2 gene (SIR2) family, which is conserved from prokaryotes to eukaryotes (Staphylococcus aureus, fission yeast, Arabidopsis, Caenorhabditis elegans, mouse, rat, human), has functions in silencing, cell cycle progression, and chromosome stability (47). SIR2 is a determinant of life span in yeast mother cells. It can promote longevity in Saccharomyces cerevisiae by suppressing the generation and accumulation of extrachromosomal ribosomal DNA (rDNA) circles, which are considered a cause of aging in yeast (48). Similarly, it has been demonstrated that SIR2, which encodes a histone deacetylase, extends the life span of Caenorhabditis elegans through signaling pathways involving DAF-2/insulin receptor and DAF-16/FOXO (49, 50). Mammals have seven Sir2 homologues (SIRT1 to -7), of which SIRT1 is most closely related to Sir2. These proteins have a highly conserved NAD-dependent sirtuin core domain, first identified in the yeast Sir2 protein, making them good candidates for life span regulators (51). Interestingly, it has been reported that exogenous H2S has a protective effect on maintaining the circadian rhythm of clock genes in isolated hepatocytes by changing the NAD+/NADH ratio and enhancing the activity of SIRT1 protein (52). SIRT1 has thus emerged as a major life span regulator, and H2S has been hypothesized to delay aging, in part by activating SIRT1.
Calorie restriction is the only established antiaging experimental paradigm in a variety of species, including mammals, flies, nematodes, and yeast, that has been accepted by many researchers. It has been reported that CR can extend life span by increasing Sir2 activity and activating Sir2 deacetylase in yeast and Drosophila. Additionally, the expression of mammalian Sir2 (SIRT1) is induced in calorie-restricted rats and also in human cells cultured in the presence of serum from such rats. SIRT1 can deacetylate the DNA repair factor Ku70, causing it to sequester the proapoptotic factor Bax away from the mitochondria, thereby inhibiting stress-induced apoptotic cell death. A major cause of aging is perceived to arise from the cumulative effects of cell loss over time. Moreover, it has also been reported that CR can inhibit the insulin/insulin-like growth factor 1 (IGF-1) pathway to increase SIRT1 expression. Thus, CR can promote longevity by inducing SIRT1 expression and promoting long-term survival of irreplaceable cells (33). Correspondingly, when exposed to H2S, nematodes are apparently healthy and do not exhibit phenotypes consistent with metabolic inhibition. Instead, animals exposed to H2S are long-lived, and this phenotype requires Sir2 activity, which may translate environmental changes into physiological alterations to improve survival (53). CR also has potential benefits for CSE and CBS in both the aorta and liver by reducing oxidative stress and ameliorating the negative effect of age on H2S concentration. Consistent with this, Predmore et al. inferred from their study that CR may help maintain the H2S signaling system during aging (54). CR and H2S apparently have a synergistic antiaging effect by regulating SIRT1 activity. Our laboratory recently demonstrated that H2S has protective effects against human umbilical vein endothelial cell senescence, which may involve the regulation of SIRT1 activity. Similar to resveratrol, H2S is likely a CR mimetic with potential antiaging functions mediated via SIRT1 activation. It has been reported that SIRT1 could deacetylase the FOXO transcription factors in vitro and within mammalian cells to increase cellular stress resistance, which is correlated with extended organismal longevity (55). However, the hypothesis that the antiaging effects of H2S are mediated via the SIRT1/FOXO pathway needs to be validated with further investigations.
Resveratrol, a polyphenol found in red wine, is a CR mimetic with potential antiaging and antidiabetogenic properties. Resveratrol ameliorates age-related metabolic phenotypes by inhibiting cyclic AMP (cAMP) phosphodiesterases (PDE). Inhibiting PDE4 with rolipram reproduces all the metabolic benefits of resveratrol, including prevention of diet-induced obesity and promotion of mitochondrial function, physical stamina, and glucose tolerance in mice. Therefore, PDE4 inhibitors may also prevent and ameliorate the symptoms of age-related metabolic diseases (56). H2S also acts as an endogenous inhibitor of phosphodiesterase activity (57). However, whether H2S uses the same mechanism for inhibiting phosphodiesterases to prevent age-related diseases and for exerting antiaging effects via SIRT1 activation remains unknown. Figure 2 gives an overview of the pathways that underlie the antiaging effects of H2S.
Effect of H2S on the age-related gene Klotho.
The age-related gene Klotho suppresses the expression of multiple age-associated phenotypes to extend life span. Klotho increases resistance to oxidative stress by activating the FOXO forkhead transcription factors that induce expression of manganese SOD (58). Klotho also represses DAF-2 (insulin/IGF-like) receptors under physiological conditions, thereby inducing derepression of DAF-16 (FOXO) and subsequent overexpression of factors such as antioxidant enzymes that improve longevity and stress resistance (59).
Klotho is predominantly expressed in the kidney. Downregulation of Klotho in the kidneys aggravates the development of renal damage induced by angiotensin II via increased oxidative stress, whereas induction of Klotho expression has therapeutic effects against angiotensin II-induced end organ damage (60). Yoon et al. confirmed that angiotensin II plays a pivotal role in regulating expression of Klotho in cyclosporine (CsA)-induced renal injury and that an angiotensin II type 1 (AT1) receptor blocker inhibits aging by decreasing CsA-induced oxidative stress (61). Interestingly, H2S has a direct inhibitory effect on angiotensin-converting enzyme (ACE) activity, which catalyzes the conversion of angiotensin I into angiotensin II (62). Moreover, H2S can decrease angiotensin II-induced mitogen-activated protein kinase (MAPK) activation, AT1 receptor binding, and the binding affinity of AT1 receptor in a dose-dependent manner (63). In addition, Lu et al. demonstrated that H2S inhibits renin activity, which participates in the renin-angiotensin system (64). Thus, H2S may enhance Klotho expression via negative regulation of angiotensin II activity. Given these findings, H2S may be a potent preventive and therapeutic agent in aging and age-associated diseases. Figure 3 summarizes the indirect effects of H2S on Klotho expression to show that H2S may be involved in regulation of aging through the Klotho pathway.
H2S: A NOVEL THERAPEUTIC AGENT IN AGE-ASSOCIATED DISEASES?
H2S has been generally recognized as an important signaling molecule in cardiovascular and nervous systems. Enhancement of the physiological effects of H2S has been confirmed by understanding the therapeutic implications of H2S in age-associated diseases, such as cardiovascular system diseases, central nervous system degenerative diseases, diabetes, and cancer, among others (Table 2).
|Age-associated disease||Exptl model||H2S level||The cellular response elicited by H2S or its donors||Reference(s)|
|Hypertension||Spontaneously hypertensive rats||↓||Relaxing vascular muscle cell by involving different ion channels||65|
|Atherosclerotic disease||Human monocyte-derived macrophages||↓||Inhibiting foam cell formation by downregulating CD36, SR-A, and ACAT1 expression via the KATP-ERK1/2 pathway||66, 67|
|PD||6-OHDA-induced PD rat||↓||Inhibiting NADPH oxidase activation and oxygen consumption; inhibiting accumulation proinflammatory factors via NF-κB pathway; inhibiting neuronal apoptosis by improving Bcl-2/Bax||68, 69|
|AD||Amyloid β-induced cell toxicity in murine BV-2 microglial cells||↓||Inhibition of inflammation; promotion of cell growth and preservation of mitochondrial function in a p38- and JNK-MAPK-dependent manner||70, 71, 72|
|Diabetes||Streptozotocin-induced diabetes in mice||In pancreas, ↑||Stimulating β-cell apoptosis and inducing KATP channel activity||73, 74, 75, 76|
|In plasma, ↓||Protecting diabetic vascular endothelial cells||77|
|Prostate cancer||PC-3 cells (a human prostate cancer cell line)||?||Inhibiting PC-3 cells viability by activating p38 MAPK and JNK||78|
|ER(−) breast cancer||Mice with human ER(−) breast cancer xenografts||?||Suppressing the growth of cancer cells by induction of G0/G1 arrest and apoptosis; downregulation of NF-κB; reduction of thioredoxin reductase activity; increased levels of reactive oxygen species||79|
|Colon cancer||HT-29 human colon cancer cells||?||Inhibiting cell proliferation by reducing PCNA expression; inducing G0/G1 cell cycle arrest and apoptosis||80|
Cardiovascular system diseases.
Aging is considered a principal risk factor in the progression of hypertension (81). The plasma concentration of H2S in spontaneously hypertensive rats is substantially lower than that in normotensive control animals (65). Similarly, the plasma H2S level and H2S production are greatly reduced and transcription and activity of CSE in vascular tissues are also obviously inhibited in rats with hypertension induced by NG-nitro-l-arginine methyl ester (l-NAME). However, H2S can prevent the development of hypertension induced by l-NAME. This suggests that the H2S synthase/H2S pathway participates in the pathogenesis of hypertension (82). The fundamental hemodynamic abnormality in hypertension is increased peripheral vascular resistance (83). It has been reported that H2S can relax rat aortic tissues in vitro in an ATP-sensitive K+ (KATP) channel-dependent manner and that H2S at physiologically relevant concentrations induces vasorelaxation via activation of KATP channels in isolated mesenteric artery smooth muscle cells (17, 84). KATP channels are activated by binding of its Kir subunits to phosphatidylinositol-4,5-bisphosphate (PIP2) along with a reduction in binding to the inhibitor ATP (85). H2S causes vascular endothelial and smooth muscle cell hyperpolarization and vasorelaxation by activating KATP channels through cysteine S-sulfhydration, which can enhance Kir6.1-PIP2 binding and reduce Kir6.1-ATP binding (19). Additionally, considering that human hypertensive pulmonary vascular disease represents a disease of excessive smooth muscle cell proliferation (86), H2S could also suppress the proliferation of cultured aortic vascular smooth muscle cells of rats in vitro through the MAPK pathway (87). Because H2S is a major EDHF and a primary determinant of vasorelaxation in numerous vascular beds (20), drugs that alter CSE activity or H2S-mediated channel sulfhydration may be effective therapeutic agents for treating hypertension.
Atherosclerosis, characterized by lesions in large and medium arteries, is the primary cause of coronary artery disease. Not only is this condition a chronic inflammatory disease that can lead to an acute clinical event by plaque rupture and thrombosis, but it is also an inevitable degenerative consequence of aging (88). Atherosclerosis is characterized by multiple key events, including endothelial dysfunction, infiltration of monocytes and their differentiation into macrophages, conversion of lesion-resident macrophages into foam cells, and smooth muscle cell proliferation. Fortunately, atherosclerosis can be interrupted by H2S. Increasing evidence has proven that H2S plays a significant role in all these biological processes and that disruption of H2S homeostasis may contribute to the pathogenesis of atherosclerosis (89). For instance, H2S plays an antiatherogenic role by suppressing the formation of human macrophage foam cells. H2S inhibits the formation of macrophage-derived foam cells, which is a crucial event in the development of atherosclerosis, by downregulating CD36, SR-A, and ACAT-1 expression and inhibiting oxidized low-density lipoprotein (oxLDL) binding and uptake of macrophages (66, 67). In addition to its important role in preventing atherosclerosis, H2S has also direct benefits for coronary heart disease (CHD) patients. Plasma H2S levels in patients with CHD show a significant inverse correlation with the severity of CHD and changes in the coronary artery (90). Moreover, providing H2S balneotherapy to CHD patients has been shown to result in significant prolongation of stress bicycle exercise. In the hot climate of arid zones, use of moderate H2S baths raises the tolerance of CHD patients to exercise, attenuates clinical manifestations of CHD, and consequently reduces daily nitrate need (91). Additionally, stem cell transplantation has become a promising therapeutic approach for treatment of myocardial infarction (MI). However, poor survival of the donor cells after transplantation has restricted its therapeutic efficacy. H2S has been applied to inhibit cell apoptosis and promote cell survival in such cases. It has been demonstrated that H2S preconditioning effectively promotes stem cell survival under conditions of ischemic injury and helps cardiac repair after MI (92).
Degenerative diseases of the central nervous system.
Parkinson's disease (PD) is a neurodegenerative disease characterized by progressive loss of dopaminergic neurons in the substantia nigra (SN). In a 6-hydroxydopamine (6-OHDA)-induced PD rat model, the endogenous H2S level has been found to be markedly reduced in the SN. However, H2S treatment can specifically inhibit 6-OHDA-evoked NADPH oxidase activation, oxygen consumption, and microglial activation in the SN, and accumulation of proinflammatory factors in the striatum (68). PD is one of the most common neurodegenerative diseases with various manifestations, among which cognitive deficiency, namely, dementia, has a prominent role. Dementia is usually ascribed to changes in the nucleus basalis of Meynert and the cerebral cortex (93). H2S has also been suggested to attenuate vascular dementia injury via inhibition of apoptosis by markedly improving the ratio of Bcl-2 to Bax, upregulating Bcl-2 expression, and downregulating Bax expression (69).
Alzheimer's disease (AD) is the most common form of dementia. AD initially targets memory and progressively destroys the mind (94). This disease is pathologically characterized by the accumulation of senile plaques containing activated microglia and amyloid beta peptides (Abeta) (95). As mentioned previously, endogenous H2S is predominantly produced in the brain from cysteine by CBS (5, 96). Endogenous levels of H2S of between 50 and 160 μM are detected in the brains of humans (40). In the brains of AD patients, lower levels of H2S as well as accumulation of homocysteine (Hcy), a strong risk factor for the development of Alzheimer's disease (AD), are observed (71, 72). Neurotoxicity of elevated Hcy is associated with inhibition of endogenous H2S generation and downregulation of expression and activity of CBS in PC12 cells, which is mediated by extracellular signal-regulated kinase 1 and 2 (ERK1/2) activation. It has been suggested that H2S could reduce neurotoxicity induced by Hcy and that enhancement of H2S synthesis may be a useful therapeutic strategy against Hcy-induced AD (97). Accordingly, Liu and Bian have demonstrated that H2S demonstrates protective effects against Abeta-induced cell injury by inhibiting inflammation, promoting cell growth, and preserving mitochondrial function in a p38- and Jun N-terminal protein kinase (JNK)–mitogen-activated protein kinase (MAPK)-dependent manner (70). Moreover, H2S can protect neurons from oxidative stress, which is responsible for neuronal damage and degeneration in AD. H2S protects neurons against glutamate-mediated oxidative stress by enhancing the activities of γ-GCS and cystine transport, which results in incremental changes of glutathione levels (98). These findings suggest that H2S is a promising therapeutic target for treating neurodegenerative diseases.
Diabetes is a chronic metabolic disease with an influence on the metabolism of carbohydrates and other nutrients. The pathogenesis of diabetes is associated with decreased functional beta-cell mass and increased activities of KATP channels in pancreatic beta cells (99, 100). It has been reported that in streptozotocin-induced diabetes in mice, pancreatic H2S production, and CSE activity are significantly upregulated (73, 76). Similarly, it has also been found that pancreatic CSE expression and H2S production are higher in Zucker diabetic fatty (ZDF) rats than in Zucker fatty and Zucker lean rats (101). Enhanced endogenous production of H2S in diabetes can induce apoptosis of insulin-secreting beta cells by enhancing endoplasmic reticulum (ER) stress via p38 MAPK activation and also stimulate KATP channels in insulin-secreting cells (73–75). These results imply that H2S at high concentrations contributes to the pathogenesis of diabetes mellitus.
Diabetes mellitus is also characterized by the resistance of peripheral tissues to insulin (102, 103). l-Cysteine which is synthesized from methionine is a main precursor of H2S. However, adipose tissue is an important organ of methionine metabolism (104) and is also an insulin-sensitive organ that mediates glucose uptake and metabolism. With age, the endogenous CSE/H2S system is upregulated in adipose tissues. Increased H2S in adipose tissues inhibits basal or insulin-stimulated glucose metabolism and regulates insulin sensitivity. This suggests that H2S may be a novel insulin resistance regulator (105). Additionally, Kaneko et al. suggested that elevation of the H2S levels as a result of l-cysteine metabolism may inhibit insulin release from isolated mouse islets and the mouse β-cell line MIN6 under diabetic conditions (11). In ZDF rats, the abnormally high pancreatic production of H2S has been reported to suppress insulin release (101). These findings indicate that high concentrations of H2S in the pancreas could have deleterious effects on the development of diabetes and that new therapeutic measures for diabetes may involve inhibiting endogenous H2S production from the pancreas.
In contrast, Jain et al. have reported that blood H2S levels are significantly lower in type 2 diabetes patients than in age-matched healthy subjects and in streptozotocin-treated diabetic rats than in control Sprague-Dawley rats. Low blood H2S levels may contribute to the vascular inflammation observed in diabetes because supplementation with H2S can prevent inflammatory factor interleukin-8 (IL-8) and monocyte chemoattractant protein 1 (MCP-1) secretion by monocytes cultured in a high-glucose medium (77). It has also been observed that H2S levels in plasma and aortic tissue are progressively reduced in nonobese diabetic (NOD) mice. This suggests that reduced endogenous H2S production is associated with diabetes-related endothelial dysfunction in NOD mice (106). Endothelial dysfunction plays a pathogenic role in the development of diabetic vascular complications. However, the protective effects of H2S on the endothelial cells under high-glucose conditions have also been observed. Pretreatment with NaHS (50 μmol/liter) protects against high-glucose-induced apoptosis in endothelial cells by increasing SOD activity, decreasing ROS generation and malondialdehyde levels, and downregulating the Bax/Bcl-2 ratio (107). These findings are consistent with those of Suzuki et al. showing that in vitro hyperglycemia is associated with increased H2S degradation caused by mitochondrial ROS overproduction and that H2S replacement has cytoprotective effects on endothelial cells in hyperglycemia in vitro. H2S protects against the development of hyperglycemia-induced endothelial dysfunction by attenuating the hyperglycemia-induced enhancement of ROS formation, attenuating nuclear DNA injury, reducing the activation of the nuclear enzyme poly(ADP-ribose) polymerase, and improving cellular viability (108).
Furthermore, inhibiting ACE, a Zn-dependent enzyme, has been recommended to prevent diabetic nephropathy (109). The H2S level and CSE expression in the renal cortex of diabetic rats have been shown to be significantly decreased (110). As indicated earlier, H2S at a physiological concentration exhibits direct inhibitory action on ACE activity in human umbilical vein endothelial cells by interfering with the Zn2+ in the active center of the enzyme (62). Thus, it appears that H2S could also protect against diabetes nephropathy by functioning as an ACE inhibitor. These findings imply that H2S at normal physiological concentrations may have beneficial effects on the control of diabetes owing to its anti-inflammatory and antioxidative roles. Therefore, inhibiting pancreatic H2S biosynthesis may be a potential approach to protect β cells from death during the induction phase of diabetes, whereas supplementation with H2S could be considered a potential approach to maintain diabetic blood vessel potency (111).
The slow-releasing H2S donor GYY4137 can kill seven different human cancer cell lines (HeLa, HCT-116, Hep G2, HL-60, MCF-7, MV4-11, and U2OS) in a concentration-dependent manner. This indicates that H2S could be a potential anticancer agent (112). Moreover, H2S-releasing nonsteroidal anti-inflammatory drugs (HS-NSAID) composed of a traditional NSAID to which an H2S-releasing moiety is covalently attached have significant anti-inflammatory properties. It has been shown that HS-NSAID can inhibit the growth of all cancer cells, such as human colon, breast, pancreatic, prostate, lung, and leukemia cancer cells, by inhibiting cell proliferation, inducing apoptosis, and causing G0/G1 cell cycle block. These data indicate that H2S may have potential antigrowth activity against various human cancer cells (113).
Sulforaphane, a sulfur-containing compound with properties against prostate cancer, can release a large amount of H2S. Pei et al. showed that H2S can decrease the viability of PC-3 cells (a human prostate cancer cell line) in a dose-dependent manner (78). Importantly, both CSE and CBS are expressed in the prostate. Thus, H2S-releasing diets or drugs may be beneficial in the treatment of prostate cancer. Similarly, H2S-releasing aspirin, a novel and safer derivative of aspirin, has shown promise as an anticancer agent against hormone-independent estrogen receptor-negative breast cancers by inhibiting cell proliferation, inducing apoptosis, and decreasing NF-κB levels (79). Moreover, NOSH-aspirin, a NO- and H2S-releasing agent, has been found to inhibit colon cancer growth by inhibiting cell proliferation, inducing apoptosis, and causing G0/G1 cell cycle block (80). Overall, these results indirectly demonstrate that H2S has strong anticancer potential that merits further evaluation.
The findings discussed in this review strongly argue in favor of a role for H2S in aging and age-associated diseases. However, the mechanisms of action of this role of H2S have not yet been sufficiently characterized and await elucidation by further studies. A better understanding of the roles of H2S in aging can provide insights into potential therapeutic interventions against aging and reduce age-associated diseases. More specifically, data available so far strongly suggest that H2S may become the next potent preventive and therapeutic agent for preventing and ameliorating the symptoms of aging and age-associated diseases, and this should be addressed in future studies.
This work was supported by grants from the National Natural Science Foundation of China (81170277 to Z.-S.J.), by the Special Research Fund for the Doctoral Program of Higher Education of China Project (20124324110003 to Z.-S.J.), and by the Aid Program for Science and Technology Innovative Research Team in Higher Educational Institutions of Hunan Province.
Published ahead of print 7 January 2013