Background
Nonenzymatic glycation of proteins and the Maillard reaction result in the formation of advanced glycation end products (AGEs), which are associated with the pathogenesis of type 2 diabetes [
1]. During the formation of AGEs, α,β-dicarbonyl compounds such as glyoxal, methylglyoxal, and 3-deoxyglucosone are produced as reactive intermediates [
2]. Patients with type 2 diabetes have increased plasma levels of these compounds [
3]. Moreover, AGEs [
4,
5], and α,β-dicarbonyl compounds [
6] produce reactive oxygen species (ROS). Oxidative stress is of particular interest in the pathogenesis of diabetic nephropathy [
7], the latter being the leading cause of end-stage renal disease.
Molecular hydrogen (H
2), a potent free radical scavenger, selectively reduces the levels of the hydroxyl radical and peroxynitrite, which is the most cytotoxic ROS [
8]. Consumption of water saturated with H
2 [H
2-rich water (HRW)] increases the blood H
2 level and reduces renal oxidative stress in mice with cisplatin-induced nephrotoxicity [
9], rats with chronic kidney disease [
10], and rats with chronic allograft nephropathy [
11].
We previously demonstrated that HRW confers considerable benefits against renal abnormalities in SHR.Cg-
Lepr
cp
/NDmcr (SHRcp) rats, which are metabolic syndrome models, at least by preventing glomerulosclerosis and ameliorating creatinine clearance [
12]. Furthermore, a sufficient supply of HRW may prevent or delay the development and progression of type 2 diabetes [
13] and metabolic syndrome [
14] by protecting against oxidative stress. However, the exact mechanisms of the beneficial effects of HRW on diabetic nephropathy remain unknown.
Given the potent free radical-scavenging activity of H2, we hypothesized that HRW may attenuate the production of α,β-dicarbonyl compounds as well as the production of ROS from AGEs and α,β-dicarbonyl compounds. In this study, we investigated whether HRW could inhibit glucose- and α,β-dicarbonyl compound-induced ROS production in vitro and in vivo.
Discussion
The present study revealed that HRW prevented glucose- and α,β-dicarbonyl compound-induced ROS production in vitro (Figure
2) and in vivo (Figure
3). In the in vivo study, HRW decreased the levels of α,β-dicarbonyl compounds in the plasma and kidney (Figure
4).
α,β-Dicarbonyl compounds reportedly form from degradation of glucose in 200 mM PBS (pH, 7.4) [
17]. These compounds can produce free radicals [
7,
18] such as the hydroxyl radical [
19], peroxynitrate [
20], and the acetyl radical [
21]. H
2 selectively decreases the levels of the hydroxyl radical and peroxynitrite [
8]. Data from the present study showed that HRW inhibited ROS production induced by the Fenton reaction and α,β-dicarbonyl compounds. Taken together, these results suggest that HRW decreases hydroxyl radical and peroxynitrate production induced by α,β-dicarbonyl compounds.
α,β-Dicarbonyl compound- and glucose-induced oxidative stress is considered to be a cause of renal dysfunction in vivo. Methylglyoxal and glucose induce renal oxidative damage and podocyte apoptosis in Zucker diabetic fatty rats [
22] and
db/dB mice [
23]. Patients with type 2 diabetes have increased plasma levels of these compounds [
3]. In the present study, we investigated whether HRW could inhibit α,β-dicarbonyl compound-induced oxidative stress in vivo. SHRcp rats were chosen for the present study because they exhibit several metabolic disorders, such as hypertension, hyperglycemia, hyperinsulinemia, and hyperlipidemia [
24]. Histologically, islet area expansion, fatty liver, and glomerulosis can be observed in these rats. Therefore, they are considered to be a suitable animal model for renal dysfunction with the metabolic syndrome. Renal ROS levels were significantly decreased in the HRW-treated SHRcp rats compared with the control group (Figure
3). Furthermore, glyoxal and methylglyoxal levels in plasma and glyoxal, methylglyoxal, and 3-deoxyglucosone levels in the kidney were significantly decreased in HRW-treated animals compared with the control group (Figure
4). These results indicate that HRW inhibits ROS production by inhibiting α,β-dicarbonyl compound production.
Renoprotection does not necessarily depend on blood pressure or glycemic control [
25]. Caloric restriction [
26] and treatment with angiotensin II receptor blocker [
27], pioglitazone [
28], or cobalt [
29] protect against renal dysfunction without blood pressure or glycemic control in SHRcp rats. These reports indicate that renoprotection is associated with decreased AGE formation and oxidative stress, thus suggesting that they are potential therapeutic strategies for renal dysfunction in patients with type 2 diabetes and metabolic syndrome. We previously reported that HRW does not affect blood pressure or blood glucose levels but prevents glomerulosclerosis in SHRcp rats [
12]. In the present study, we noted that HRW inhibited the production of α,β-dicarbonyl compounds and ROS in these rats, suggesting that HRW has a potential therapeutic application for patient with renal dysfunction.
There are other possible molecular mechanisms to prevent oxidative stress cause by HRW. Kawamura et al. [
30] have reported that in lung allograft in rats, H
2 induces heme oxygenase-1 expression, decreases proinflammatory cytokines and the proapoptotic protein Bax, and increases expression of antiapoptotic protein Bcl-2. H
2 reduces the binding of several transcription factors such as AP1 and NFκB to the iNOS promoter via inhibition of signal transduction in macrophages [
31]. These reports suggest that the molecular target for HRW not only inhibits ROS generation but also induces gene expression of antioxidative enzymes at the transcriptional level. Further studies are necessary to explore these effects.
It has been reported that consumption of HRW for 8 weeks increases superoxide dismutase levels by 39% and decreases thiobarbituric acid reactive substance levels by 43% in the urine of subjects with potential metabolic syndrome [
14]. Consumption of HRW is also associated with a significant decrease in the urinary levels of 8-isoprostanes, which are endogenous lipid peroxidation products [
13]. These results indicate that HRW may have antioxidant activity in humans. Further studies are necessary to confirm the effects of HRW on renal dysfunction associated with type 2 diabetes and metabolic syndrome in humans.
Aminoguanidine, a prototype AGE formation inhibitor, acts by scavenging α,β-dicarbonyl compounds. Aminoguanidine has been shown to inhibit the formation of AGEs and slow the progression of diabetic nephropathy in animal models [
32,
33]. It also significantly decreases proteinuria in treated subjects [
34]. However, aminoguanidine is a nonspecific AGE inhibitor that also inhibits nitric oxide synthase [
35] and causes DNA damage [
36]. Aminoguanidine cannot be used for the treatment of diabetic nephropathy because of safety concerns, and additional clinical studies are required to address the safety and efficacy of other types of AGE inhibitors [
37]. On the other hand, consumption of HRW had no adverse effects on hematological parameters and biometric parameters during an 8-week study period in humans [
14], suggesting that HRW is safe.
Competing interests
The author(s) declare that they have no competing interests
Authors’ contributions
MK participated in the design of the study and carried out the incubation studies, LC/MS analysis, and drafted the manuscript. YT performed the statistical analysis. OS participated in the sequence alignment. MH conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.