Molecular hydrogen (H2) has emerged as a new therapeutic option in several diseases and is widely adopted by healthy people. However, molecular data to support therapeutic functions attributed to the biological activities of H2 remain elusive. Here, using transcriptomic and metabolomic approaches coupled with biochemistry and micro-CT technics, we evaluated the effect of long-term (6 months) and daily use of H2 on liver function. Rats exposed 2 h daily to H2 either by drinking HRW (H2 dissolved in H2O) or by breathing 4% H2 gas showed reduced lipogenesis and enhanced lipolysis in the liver, which was associated with apparent loss of visceral fat and brown adipose tissue together with a reduced level of serum lipids. Both transcripts and metabolites enriched in H2-treated rats revealed alteration of amino acid metabolism pathways and activation of purine nucleotides and carbohydrate biosynthesis pathways. Analysis of the interaction network of genes and metabolites and correlation tests revealed that NADP is the central regulator of H2 induced metabolic alterations in the liver, which was further confirmed by an increase in the level of components of metabolic pathways that require NADP as substrate. Evidence of immune response regulation activity was also observed in response to exposure to H2. This work is the first to provide metabolomic and transcriptomic data to uncover molecular targets for the effect of prolonged molecular hydrogen treatment on liver metabolism.
Molecular hydrogen (H2) is a tasteless and odorless gas and has demonstrated various biological and therapeutic effects on many diseases, from acute illnesses, including ischemia–reperfusion injury, to chronic diseases such as rheumatoid arthritis, neurodegenerative, and metabolic diseases1,2,3. H2 is non-toxic even when used at high concentrations and rapidly crosses different tissue barriers, including blood–brain barriers, and penetrates various organelles4,5,6. H2 is interferes with reactive oxygen species (ROS) in living systems, a characteristic that supports its well-established antioxidant functions that lead to its frequent use to treat diseases associated with oxidative stress3,7,8.
Molecular hydrogen is applied in therapeutics through various delivery routes, including hydrogen inhalation (HI), oral administration of hydrogen-rich water (HRW) or hydrogen tablets, and hydrogen-saturated saline injections. The concentration of H2 in tissues after exogenous supply depends on the type of organ4 and the H2 delivery route9. Liver is the organ that accumulates more exogenous H24,9, which appears to significantly affect its homeostasis10. H2 protected the liver against various acute and chronic injuries in animal models by suppressing excessive oxidative stress, inflammation, and cell death11,12. In addition to liver, preventive and therapeutic effects were obtained for H2 in various animal experiments of disease models2,3 and clinical trials in humans13,14,15. The preventive aspect of H2 in disease models, its antioxidant effects7,8, its function in aging13,16, among many others17,18,19, are paving the way for the use of H2 in healthy people to improve body performance or as a preventive therapeutic strategy.
In a recent clinical trial that was evaluated in a cohort of young and healthy people, the effects of inhaling 4% H2 20 min per day for 7 days on exercise performance revealed ergogenic properties such as improved running performance and torso strength20. Although Sim M. and colleagues had reported the beneficial effect of H2 inhalation on the increase of the antioxidant and anti-inflammatory response in healthy adults21, other groups found that H2 only reduced delayed-onset muscle soreness after running downhill22 or improved muscle function during exercise without any effect on blood oxidative markers23. These data suggest that still little is known about H2 performance under healthy conditions and therefore requires further research. As part of an effort to provide more data to help better understand the therapeutic functions attributed to the biological activities of H2 in health conditions, our laboratory has initiated a study that evaluated the effect of long-term (6 months) hydrogen intervention on the physiological function of healthy rats24. The study found that H2 induces a time-dependent alteration of different biochemical parameters, among which liver injury markers such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), and total bile acid (TBA) were significantly reduced in the serum of H2-treated rats24, suggesting that liver physiology and functions could be positively affected by prolonged exposure to H2. In the present study, we used transcriptomic and metabolomic approaches coupled with biochemistry and micro-CT techniques to access the global effects of long-term H2 treatment on the liver and its relationship with body conditions.
Materials and methods
Animals and experimental design
Three-week-old male Sprague-Dawley rats weighing 40–50 g were purchased from Vital River Laboratory Animal Technology Co., Ltd (Beijing, China). The animals were kept under standard conditions at 22 °C to 25 °C with a 12 h light–dark cycle and fed a normal diet. The animals were allowed to adapt to laboratory conditions one week before the experiment. Rats were randomly divided into three groups and treated with or without H2 for six months. Rats in the control group (n = 6) were kept under normal conditions; rats in the HRW group (n = 6) were given access to HRW for 1 h, twice a day; In the HI group (n = 6), rats were exposed to 4% hydrogen gas for 1 h and twice a day. All procedures were approved by the Institutional Animal Experiment Committee of the Chinese People's Liberation Army (PLA) General Hospital and were carried out in accordance with the Regulations for the Administration of Affairs Concerning Experimental Animals (China) and the ARRIVE guidelines.
Hydrogen-rich water preparation
HRW (H2 concentration > 800 µM) was kindly provided by Shenzhen Kelieng Biomedical Co. Ltd. (Shenzhen, China) and stored under atmospheric pressure at 23 ± 2 °C in a stainless-steel bucket (KLE-8). The hydrogen concentration was monitored using a hydrogen electrode (Unisense A/S, Aarhus, Denmark), ensuring that the hydrogen concentration of HRW for rats was maintained above 800 µM.
Inhalation of hydrogen gas
In the HI experiments, the rats were placed in breathing boxes (72 × 53 × 45 cm, length × width × height), where a gas mixture of 4% H2 and 96% air containing 21% O2 were delivered by an Oxy-Hydrogen Machine (SG-3000; Gang’an Health Management [Beijing] Co., Ltd., Beijing, China). The mixture was administered twice a day for 1 h each and, its composition was monitored using the Thermal trace GC ultragas chromatography (Thermo Fisher, MA, USA).
Micro-computed tomography (micro-CT) analysis
After anesthesia, rats were scanned by Quantum GX microCT (PerkinElmer) with voltage at 74 kV, view imaging at 72 × 40 mm, and pixel size at 72 μm. Subcutaneous and visceral fat mass was analyzed by the software (Analyze 12.0, PerkinElmer).
Tissue and blood sampling
Blood was sampled by eyeball blood collection early in the morning from overnight fasting rats. Serum was prepared by 20 min centrifugation at 1000 × g. Rats were then sacrificed by cervical dislocation, and the livers were harvested, snap-frozen in liquid nitrogen, and stored at − 80 °C until subsequent analysis. Intraabdominal perirenal (pWAT), epididymal (eWAT), subcutaneous inguinal (sWAT) white adipose tissue, and brown adipose tissue (BAT) were dissected and weighted.
Serum total cholesterol, HDL-cholesterol (HDL-C), and LDL-cholesterol (LDL-C) were determined using commercially available kits (Nanjing Jiancheng Biochemistry, China) according to the manufacturer’s instructions. The hormone-sensitive lipase (HSL) activity and the level of epinephrine in serum were evaluated using ELISA kits from MEIMIAN Industrial Co., Ltd. (Jiangsu, China).
Total RNA was extracted from liver tissues with a standard Trizol RNA extraction procedure. RNA quality was assessed using the RNA Nano 6000 Assay Kit of the Bioanalyzer 2100 system (Agilent, USA). Sequencing libraries were generated using the NEBNextR Ultra RNA Library Prep Kit for Illumina® (#E7530L, NEB, USA). The size of the library insert was tested using the Agilent Bioanalyzer 2100 system (Agilent, USA). The Bio-RAD CFX 96 fluorescent quantitative PCR instrument and Bio-RAD KIT iQ SYBR GRN were used to perform Q-PCR for accurate quantification of the effective concentration of the library (effective concentration of the library > 10 nM). After cluster generation, the libraries were sequenced by the Illumina NovaSeq 6000 S4 platform with paired-end reads by Annoroad Gene Technology (Beijing, China). Differential gene expression (DEGs) analysis was performed using the DESeq2R package version 1.16.3. and the DEGs were selected with |LogFC|> 1 and FDR < 0.05.
Untargeted metabolomics analysis
The liver sample (50 mg) was homogenized in 500 µL prechilled methanol, vortexed, and sonicated for 20 min on ice, incubated at − 20 °C for 1 h, and centrifuged at 14,000 g for 20 min at 4 °C. The extracted metabolites were concentrated by complete drying using a speedvac (Labconco, USA), redissolved in 100 µL acetonitrile–water solution (1:1, v/v), and centrifuged at 14,000 g for 20 min at 4 °C. The supernatant was sent to the Metabolomics Facility at Tsinghua University Branch of the China National Center for Protein Sciences (Beijing, China) and used for HPLC–MS or MS analysis. Untargeted metabolomics was performed using an ultra-performance liquid chromatography Q-Exactive Orbitrap mass spectrometer (UPLC Q-Exactive Orbitrap MS). The metabolomics data analysis and interpretation were performed with the MetaboAnalyst 5.0 web-based interface25. Significant metabolites were selected with |FC|≥ 1.5 and p value < 0.05.
Annotation and network analysis
The WEB-based Gene Set Analysis Toolkit26 and annotation and network analysis modules in MetaboAnalyst 5.025 were used to get biological insights of genes and metabolites differentially expressed, respectively. GraphPad Prism version 9.0.0 (121) was used to plot data and perform statistical analysis. One-way ANOVA with Tukey’s post hoc test was used for error correction. Data were presented as the mean ± SEM, and a p value < 0.05 was considered significant.
H2 influences liver metabolism of lipids, carbohydrates, amino acids, and nucleic acids
We recently found that H2-treated rats (HRW and HI) had reduced serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), and total bile acid (TBA)24, suggesting that prolonged exposure to H2 could influence liver physiology and functions. To study the global effects of long-term H2 treatment on the liver, we performed an RNA sequencing (RNA seq) analysis of liver tissues collected from untreated rats (Control group), rats given hydrogen-rich water (HRW) or inhaled 4% H2 (HI) 2 h daily for 6 months (Fig. 1A, B). We identified from the liver transcriptome, 828 differentially expressed genes (DEGs): 321 in HRW versus CTRL, 435 in HI versus C, and 72 in HI versus HRW, of which there were 625 unique DEGs (Supplementary file 1). Profiling the expression of these 625 DEGs in all experimental groups showed three distinct expression clusters (Fig. 1B). The genes in cluster 1, down-regulated in the HRW and HI groups, are mainly involved in biological functions related to lipid metabolism and hormone synthesis; the genes in cluster 2, up-regulated by HRW and HI, play functions in cellular amino acid catabolic and carboxylic acid biosynthesis process; The cluster 3 regrouped genes enriched in immune system-related functions, and their expression appeared to be more specific to HI (Fig. 1B, Supplementary file 1). These data suggest that H2 could also induce changes in liver immune functions in addition to its metabolic regulatory activities.
To further our understanding of the impact of H2 on liver metabolism, we considered a comparative metabolomics approach that generates a profile of over 500 metabolites from various chemical classes. We observed a significant alteration in more than 100 metabolites, including organic acids, carbohydrates, nucleic acids, fatty acyls, and sterol lipids in the liver of H2-treated rats compared to untreated rats (Fig. 1C–E, Supplementary file 2). A closer inspection of the organic acid groups affected by H2 treatment revealed a reduced level of amino acids such as L-serine, L-threonine, and Guanidineacetic acid, components of the glycine, serine and threonine metabolic pathways, and 4-Guanidinobutanoate and 4-Acetamidobutanoate, members of the arginine and proline metabolic pathways (Fig. 1F, G; Supplementary file 2).
The level of nucleoside diphosphate sugars, uridine 5'-diphosphogalactose and uridine 5'-diphosphoglucuronic acid, the two most common nucleotide sugar donors in animal cells27 for the biosynthesis of polysaccharides, glycoproteins, and glycolipids28,29, was reduced, consistent with the increased level of carbohydrates observed in H2 treated rats (Fig. 1I, P; Supplementary file 2). Rats treated with H2 also showed an altered liver level of metabolites enriched in purine metabolism pathways. These rats had reduced levels of adenine (Fig. 1I), an increased level of deoxyadenosine and deoxyinosine (Fig. 1J, K), which, together with the unchanged liver content in uric acid and its reduced serum level (Supplementary Figure1A, B), suggests that long-term exposure to H2 may activate purine biosynthetic pathways.
Although long-term H2 treatment induced a reduced level of fatty acyls and sterol lipids enriched in the biosynthesis pathways of lipids, bile acids, and steroid hormones (Fig. 1L, O; Supplementary file 2), it increases the level of acylcarnitines (Fig. 1M, N), fundamental players in the transport of organic acids and fatty acids from the cytoplasm to mitochondria30 for oxidation to produce energy (Supplementary file 2). Furthermore, we note that H2 treatment induced an increased level of acetoacetate (Fig. 1M), a ketone body produced from fatty acid oxidation30,31 and previously reported to increase lipolysis and decrease lipid synthesis32, supporting the role of H2 in promoting liver fatty acid oxidation.
Taken together, our data support the function of long-term use of H2 in inducing lipolysis, amino acid catabolism to eventually support the pathways of biosynthesis of carbohydrates and purine nucleotides.
H2-induced alteration of liver metabolism is accompanied by lipolysis
Liver plays a central role in the regulation of metabolism and represents a communication bridge between organ systems33, suggesting that H2-induced alteration of liver metabolism could affect the whole-body metabolism and, therefore, body condition. To assess the effect of long-term use of H2 on body composition, we measured the change in body weight (Fig. 2A) and fat mass (Fig. 2B–F) and change in serum metabolites (Fig. 2G–J). Long-term H2 intervention reduced the body weight of rats in the HI group (455.20 ± 31.57 g), while no significant changes were observed in the HRW group (498.80 ± 18.50 g) compared to controls (525.00 ± 17.78 g) (Fig. 2A)24. Visceral fat volume (HRW: 7760 ± 429 mm3; HI: 6260 ± 1624 mm3; CTRL: 13,960 ± 4138 mm3) (Fig. 2B, C) and brown adipose tissue mass (BAT) (HRW: 0.54 ± 0.27 g; HI: 0.33 ± 0.10 g; CTRL: 0.63 ± 0.20) (Fig. 2F) were reduced in rats exposed to H2; white adipose tissue mass (WAT) (Fig. 2E) and subcutaneous fat (Fig. 2B, D) were unchanged. Although the total triglyceride level in serum was unchanged (Fig. 2J)24, we found the lipolytic stimulator epinephrine34,35 (HI: 525.4 ± 42.40 pg/ml, HRW: 403.8 ± 62.48 pg/ml, CTRL: 335.4 ± 45.52 pg/ml,) (Fig. 2L) and the hormone sensitive lipase HSL (HI: 279.90 ± 53.76 U/L vs. CTRL: 218.50 ± 22.28 U/L, p = 0.022) (Fig. 2K), high in serum and liver respectively of H2 treated rats compared to control groups. These data, together with our previous report24 on the decreased level of serum lipids, such as total cholesterol, high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C), induced by long-term treatment with H2 (Fig. 2G–I), showed that long-term exposure to H2 could modulate body mass by affecting body fat composition.
H2 induces metabolic alteration in liver by modulating NADP/NADPH redox pathways
To gain further insight into the mechanism associated with the reprogramming of liver metabolism by long-term H2 intervention, we performed an interaction network analysis for genes and metabolites with a significant change in response to H2 exposure. The analysis identified six subnets of genes encoding metabolic enzymes and the corresponding metabolites (Fig. 3A, Supplementary file 3). NADP has the highest degree of node and connected metabolic enzyme-coding genes enriched in biological functions related to the metabolic process of lipids, amino acids, and carboxylic acids (Fig. 3B, C), the main alteration that we observed (Figs. 1, 2) during the H2 intervention. Long-term H2 intervention decreased the liver level of NADP (Fig. 3B, Supplementary Fig. 2) that was positively correlated with a reduced expression of genes coding for lipid and hormone metabolizing enzymes, while a negative correlation was observed for enzyme-coding genes involved in the metabolism of amino acids and carboxylic acids biosynthetic process (Fig. 3B). Knowing that the reduced form of NADP, NADPH provides high energy electrons for antioxidant defense and is necessary for nucleotide, amino acid, and lipid biosynthesis36,37, we hypothesized that the H2-induced decrease in the level of NADP would affect metabolic pathways that required NADP as the final acceptor of electrons. NADP and its reduced form NADPH are produced or consumed in the cell cytosol during reactions of cellular energy metabolism that involve glycolysis and the pentose phosphate pathway (PPP) and in the mitochondria during the tricarboxylic acid cycle (TCA)36,37,38,39,40. The NADP/NADPH pool can also be affected by metabolism reactions involving CYP450s that utilize NADPH as an electron donor41. Analysis of the effect of H2 on the level of components of these metabolic pathways showed that H2 treatment increased the level of metabolites such as G6P and 6PG (PPP) and malic acid (TCA cycle and cytosol) involved in reactions that reduced NADP to NADPH (Fig. 3D). However, the expression level of genes that encode cytochrome P450 oxidoreductases such as Cyp26b1, Cyp26a1, which lead to the accumulation of NADP, was found to be down-regulated after H2 treatment (Fig. 3B). Together, these data suggest that H2 induces reprogramming of liver metabolism through modulation of biological pathways that required NADP as an electron acceptor (reduction of NADP to NADPH).
The therapeutic potential of H2 has been widely evaluated in various diseases1,2,5 since 2007, when the first report showed the cytoprotective function of H2 as an effective antioxidant that eliminated cytotoxic oxygen radicals7,42. Thousands of studies in different disease models ranging from acute to chronic diseases, including cancer, support the hypothesis that H2 has a wide spectrum of activity. Unlike conventional drugs, a specific primary target has not yet been identified for H2, which would explain its broad efficacy in different diseases. H2 showed great success in controlling various diseases1,2,5 and is being evaluated for clinical applications in healthy people to improve performance and body condition13,20,23. However, it remains unknown how H2 performs under healthy conditions. Therefore, this study aimed to fill this gap by providing molecular data to help further our understanding of the biological activities of H2.
As we previously reported, long-term H2 intervention significantly affects physiological and biochemical parameters of healthy rats, with a significant alteration noted for liver biomarkers24. Moreover, no significant changes were observed for indicators of oxidative stress such as superoxide dismutase (SOD), catalase (CAT), and malondialdehyde (MDA) (Supplementary Figure 1C-E). Given that liver is the central and metabolic hub that connects most organs33 and has the highest H2 accumulation rate4,9, we have focused our study for this time on the molecular alteration in liver that can result from H2 intervention. Furthermore, we have not observed any significant change for the global liver transcriptomes or metabolites between HRW and HI; therefore, the data in the present manuscripts are presented and discussed without any discrimination between the two H2 groups.
Analysis of liver gene expression of healthy rats collected at the end of 6 months of H2 intervention revealed a significant alteration of lipid metabolism pathways, confirming the observation of previous reports, which had shown the ability of H2 to modulate lipid profile and functions43,44,45. Like in short-term studies of H2 interventions, we have found long-term exposure to H2 to reduce the serum level of total cholesterol24. This effect appears to be likely extended to other sterol lipids, as we observed a decrease in the level of several other sterol lipids, including glycocholic acid, ursodeoxycholic acid, turochenodeoxycholic acid, and corticosterone from the metabolomic study. The level of low-density lipoprotein cholesterol (LDL-C) was reduced, and no significant changes were observed for high-density lipoprotein cholesterol (HDL-C) in HRW-treated rats, consistent with previous observations24,43,44,45. Meanwhile, we found that HDL-C is significantly reduced by inhalation of H2. The biological relevance of this alteration would require further investigation, as HDL-C can sometimes become bad cholesterol and increase the risk of atherogenesis46,47,48. Our data, like others, confirmed that H2 possesses lipid metabolic regulatory activities. Moreover, the absence of accumulation of lipids in the liver (Supplementary Fig. 3), as a consequence of the low serum cholesterol level, makes H2 a relevant therapeutic option for people with disorders of lipid metabolism.
It is still unclear how H2 fulfills the regulatory function of lipid metabolism. In the present study, we found that in addition to decreasing the level of serum and liver sterol lipids, long-term H2 treatment reduced the level of liver fatty acyls by probably inducing their transport to mitochondria for oxidation, as evidenced by the increase in the level of mitochondrial fatty acid transporters, acylcarnitines. These results, together with the increase in the level of acetoacetate, a marker of ketogenesis in the liver30,31, suggest that H2 induces oxidation of fatty acids and ketogenesis. Circulating epinephrine regulates the activity of hormone-sensitive lipase that controls the rate of ketogenesis31,34,35. Hormone-sensitive lipase is responsible for mobilizing free fatty acids from adipose tissues to serve as substrate for ketogenesis31,49,50. Considering the substantial loss of adipose tissue and the increased level of hormone-sensitive lipase and epinephrine in H2-treated rats, H2 appears to promote lipolysis in adipose tissue, resulting in the release of free fatty acids which are transported and converted to ketone bodies in the hepatic mitochondria.
The transcriptional profile of rats treated with H2 showed a significant up-regulation of genes enriched in the amino acid catabolic process, consistent with the reduced level of amino acids involved in the glycine, serine, and threonine metabolic pathways and the arginine and proline metabolic pathways. We also found that H2 treated rats have purine nucleotides and carbohydrates biosynthesize pathways activated. Knowing that the main use of amino acid breakdown is to provide building blocks for the synthesis of nitrogen-based compounds, protein synthesis, and as metabolic fuels51, it is possible that H2 triggered the catabolism of these amino acids to support ketogenesis, nucleotide, and carbohydrates biosynthesis reactions.
Although a specific target has not yet been identified to support the therapeutic effects of H2, there is a consensus on its antioxidant properties. Cells respond to oxidative stress by modulating the redox system, which depends on the availability of reducing agents, including NADPH. NADP is essential for generating NADPH to provide the reduction power that maintains redox homeostasis and regulates cell metabolism36,37. In this study, we found that H2 significantly decreases the level of NADP, which was accompanied by the activation of NADPH production pathways such as PPP. The level of NAD, which can also be generated by NADP dephosphorylation52,53, remained unchanged (Supplementary Figure 2), suggesting that H2 induces NADP reduction into NADPH. Type 2 cytochrome P450s located in the endoplasmic reticulum use cytochrome P450 oxidoreductase (POR) as their redox partner. POR transfers electrons from NADPH to CYP450s in reactions that result in the generation of NADP41. In the present study, NADP levels decreased after H2 treatment. Furthermore, the genes that encode differentially expressed POR enzymes and enzymes such as Hmgcs1, Hmgcr, Dhcr24 upstream of the Cyp51-dependent cholesterol synthesis pathway were negatively regulated, except for Cyp8b1, Cyp7b1, which are involved in cholesterol metabolism into bile acids54. The enzymatic activity of Hmgcr and CYP7A1 measured in liver homogenates from experimental rats, showed no significant differences (Supplementary Figure 4). Furthermore, analysis of the network of interaction of genes and metabolites connects NADP to metabolic pathways significantly affected by the long-term H2 intervention. These findings indicate that H2 must modulate biological pathways that involve the reduction of NADP to NADPH, and suggested that investigating biological pathways that require NADP as electron acceptors, such as PPP, could help identify the mechanisms to support the metabolic alteration observed in the liver during prolonged use of H2.
In conclusion, long-term use of H2 appears to trigger lipid and amino acid catabolism in the liver to provide energy and building blocks for purine nucleotides and carbohydrates biosynthesize reactions by modulating pathways involving the redox couple NADP / NADPH. This study is the first to provide molecular data to help better understand the biological effect of H2 on liver metabolism under healthy conditions. Furthermore, the significant impact of H2 on lipid metabolism observed in this study provides a context to recommend its use in lipid metabolism disorders.
Total bile acid
Brown adipose tissue
White adipose tissue mass
Yang, M. et al. Hydrogen: A novel option in human disease treatment. Oxid. Med. Cell. Longev. 2020, 8384742. https://doi.org/10.1155/2020/8384742 (2020).
Ohta, S. Molecular hydrogen as a preventive and therapeutic medical gas: Initiation, development and potential of hydrogen medicine. Pharmacol. Ther. 144, 1–11. https://doi.org/10.1016/j.pharmthera.2014.04.006 (2014).
Ohta, S. In Methods in Enzymology, (eds. Cadenas, E. & Packer, L.) vol. 555, 289–317 (Academic Press, 2015).
Yamamoto, R., Homma, K., Suzuki, S., Sano, M. & Sasaki, J. Hydrogen gas distribution in organs after inhalation: Real-time monitoring of tissue hydrogen concentration in rat. Sci. Rep. 9, 1255. https://doi.org/10.1038/s41598-018-38180-4 (2019).
Huang, L. Molecular hydrogen: A therapeutic antioxidant and beyond. Med. Gas Res. 6, 219–222. https://doi.org/10.4103/2045-9912.196904 (2016).
Ohta, S. Recent progress toward hydrogen medicine: Potential of molecular hydrogen for preventive and therapeutic applications. Curr. Pharm. Des. 17, 2241–2252. https://doi.org/10.2174/138161211797052664 (2011).
Ohsawa, I. et al. Hydrogen acts as a therapeutic antioxidant by selectively reducing cytotoxic oxygen radicals. Nat. Med. 13, 688–694. https://doi.org/10.1038/nm1577 (2007).
Fukuda, K. et al. Inhalation of hydrogen gas suppresses hepatic injury caused by ischemia/reperfusion through reducing oxidative stress. Biochem. Biophys. Res. Commun. 361, 670–674. https://doi.org/10.1016/j.bbrc.2007.07.088 (2007).
Liu, C. et al. Estimation of the hydrogen concentration in rat tissue using an airtight tube following the administration of hydrogen via various routes. Sci. Rep. 4, 5485. https://doi.org/10.1038/srep05485 (2014).
Zhang, Y., Xu, J. & Yang, H. Hydrogen: An endogenous regulator of liver homeostasis. Front. Pharmacol. https://doi.org/10.3389/fphar.2020.00877 (2020).
Yan, M. et al. Hydrogen gas inhalation attenuates sepsis-induced liver injury in a FUNDC1-dependent manner. Int. Immunopharmacol. 71, 61–67. https://doi.org/10.1016/j.intimp.2019.03.021 (2019).
Matsuno, N. et al. Beneficial effects of hydrogen gas on porcine liver reperfusion injury with use of total vascular exclusion and active venous bypass. Transpl. Proc. 46, 1104–1106. https://doi.org/10.1016/j.transproceed.2013.11.134 (2014).
Zanini, D. et al. The effects of 6-month hydrogen-rich water intake on molecular and phenotypic biomarkers of aging in older adults aged 70 years and over: A randomized controlled pilot trial. Exp. Gerontol. 155, 111574. https://doi.org/10.1016/j.exger.2021.111574 (2021).
Korovljev, D., Stajer, V., Ostojic, J., LeBaron, T. W. & Ostojic, S. M. Hydrogen-rich water reduces liver fat accumulation and improves liver enzyme profiles in patients with non-alcoholic fatty liver disease: A randomized controlled pilot trial. Clin. Res. Hepatol. Gastroenterol. 43, 688–693. https://doi.org/10.1016/j.clinre.2019.03.008 (2019).
LeBaron, T. W. et al. The effects of 24-week, high-concentration hydrogen-rich water on body composition, blood lipid profiles and inflammation biomarkers in men and women with metabolic syndrome: A randomized controlled trial. Diabetes Metab. Syndr. Obes. 13, 889–896. https://doi.org/10.2147/DMSO.S240122 (2020).
Liu, B. et al. Protective effect of molecular hydrogen following different routes of administration on d-galactose-induced aging mice. J. Inflamm. Res. 14, 5541–5550. https://doi.org/10.2147/jir.S332286 (2021).
Fransson, A. E., Videhult Pierre, P., Risling, M. & Laurell, G. F. E. Inhalation of molecular hydrogen, a rescue treatment for noise-induced hearing loss. Front. Cell. Neurosci. 15, 658662. https://doi.org/10.3389/fncel.2021.658662 (2021).
Fransson, A. E. et al. Hydrogen inhalation protects against ototoxicity induced by intravenous cisplatin in the Guinea pig. Front. Cell. Neurosci. 11, 280. https://doi.org/10.3389/fncel.2017.00280 (2017).
Kurioka, T., Matsunobu, T., Satoh, Y., Niwa, K. & Shiotani, A. Inhaled hydrogen gas therapy for prevention of noise-induced hearing loss through reducing reactive oxygen species. Neurosci. Res. 89, 69–74. https://doi.org/10.1016/j.neures.2014.08.009 (2014).
Javorac, D., Stajer, V., Ratgeber, L., Betlehem, J. & Ostojic, S. Short-term H2 inhalation improves running performance and torso strength in healthy adults. Biol. Sport 36, 333–339. https://doi.org/10.5114/biolsport.2019.88756 (2019).
Sim, M. et al. Hydrogen-rich water reduces inflammatory responses and prevents apoptosis of peripheral blood cells in healthy adults: A randomized, double-blind, controlled trial. Sci. Rep. 10, 12130. https://doi.org/10.1038/s41598-020-68930-2 (2020).
Kawamura, T. et al. Effects of hydrogen bathing on exercise-induced oxidative stress and delayed-onset muscle soreness. Jpn. J. Phys. Fitness Sports Med. 65, 297–305. https://doi.org/10.7600/jspfsm.65.297 (2016).
Aoki, K., Nakao, A., Adachi, T., Matsui, Y. & Miyakawa, S. Pilot study: Effects of drinking hydrogen-rich water on muscle fatigue caused by acute exercise in elite athletes. Med. Gas Res. 2, 12. https://doi.org/10.1186/2045-9912-2-12 (2012).
Xun, Z.-M. et al. Effects of long-term hydrogen intervention on the physiological function of rats. Sci. Rep. 10, 18509. https://doi.org/10.1038/s41598-020-75492-w (2020).
Pang, Z. et al. MetaboAnalyst 5.0: Narrowing the gap between raw spectra and functional insights. Nucl. Acids Res. 49, W388–W396. https://doi.org/10.1093/nar/gkab382 (2021).
Liao, Y., Wang, J., Jaehnig, E. J., Shi, Z. & Zhang, B. WebGestalt 2019: Gene set analysis toolkit with revamped UIs and APIs. Nucl. Acids Res. 47, W199–W205. https://doi.org/10.1093/nar/gkz401 (2019).
Freeze, H., Hart, G. & Schnaar, R. In Essentials of Glycobiology [internet] (eds. Varki, A., Cummings, R. D. & Esko, J. D.) (Cold Spring Harbor Laboratory Press, 2017).
Mohammad, M. A., Hadsell, D. L. & Haymond, M. W. Gene regulation of UDP-galactose synthesis and transport: Potential rate-limiting processes in initiation of milk production in humans. Am. J. Physiol. Endocrinol. Metab. 303, E365–E376. https://doi.org/10.1152/ajpendo.00175.2012 (2012).
Mikkola, S. Nucleotide sugars in chemistry and biology. Molecules (Basel, Switzerland) 25, 5755. https://doi.org/10.3390/molecules25235755 (2020).
Bhagavan, N. V. In Medical Biochemistry, 4th edn. (ed. Bhagavan, N. V.) 365–399 (Academic Press, 2002).
Laffel, L. Ketone bodies: A review of physiology, pathophysiology and application of monitoring to diabetes. Diabetes Metab. Res. Rev. 15, 412–426. https://doi.org/10.1002/(SICI)1520-7560(199911/12)15:6%3c412::AID-DMRR72%3e3.0.CO;2-8 (1999).
Li, L. et al. Acetic acid influences BRL-3A cell lipid metabolism via the AMPK signalling pathway. Cell. Physiol. Biochem. 45, 2021–2030. https://doi.org/10.1159/000487980 (2018).
Priest, C. & Tontonoz, P. Inter-organ cross-talk in metabolic syndrome. Nat. Metab. 1, 1177–1188. https://doi.org/10.1038/s42255-019-0145-5 (2019).
Qvisth, V. et al. Human skeletal muscle lipolysis is more responsive to epinephrine than to norepinephrine stimulation in vivo. J. Clin. Endocrinol. Metab. 91, 665–670. https://doi.org/10.1210/jc.2005-0859 (2006).
Mora-Rodriguez, R. & Coyle, E. F. Effects of plasma epinephrine on fat metabolism during exercise: Interactions with exercise intensity. Am. J. Physiol. Endocrinol. Metab. 278, E669–E676. https://doi.org/10.1152/ajpendo.2000.278.4.E669 (2000).
Lunt, S. Y. & Van der Heiden, M. G. Aerobic glycolysis: Meeting the metabolic requirements of cell proliferation. Annu. Rev. Cell Dev. Biol. 27, 441–464. https://doi.org/10.1146/annurev-cellbio-092910-154237 (2011).
Van der Heiden, M. G., Cantley, L. C. & Thompson, C. B. Understanding the Warburg effect: The metabolic requirements of cell proliferation. Science 324, 1029–1033. https://doi.org/10.1126/science.1160809 (2009).
Lewis, C. A. et al. Tracing compartmentalized NADPH metabolism in the cytosol and mitochondria of mammalian cells. Mol. Cell 55, 253–263. https://doi.org/10.1016/j.molcel.2014.05.008 (2014).
Chen, L. et al. NADPH production by the oxidative pentose-phosphate pathway supports folate metabolism. Nat. Metab. 1, 404–415. https://doi.org/10.1038/s42255-019-0043-x (2019).
Jiang, P. et al. p53 regulates biosynthesis through direct inactivation of glucose-6-phosphate dehydrogenase. Nat. Cell Biol. 13, 310–316. https://doi.org/10.1038/ncb2172 (2011).
Guengerich, F. P. Mechanisms of cytochrome P450-catalyzed oxidations. ACS Catal. 8, 10964–10976. https://doi.org/10.1021/acscatal.8b03401 (2018).
Wood, K. C. & Gladwin, M. T. The hydrogen highway to reperfusion therapy. Nat. Med. 13, 673–674. https://doi.org/10.1038/nm0607-673 (2007).
Zong, C. et al. Administration of hydrogen-saturated saline decreases plasma low-density lipoprotein cholesterol levels and improves high-density lipoprotein function in high-fat diet-fed hamsters. Metab. Clin. Exp. 61, 794–800. https://doi.org/10.1016/j.metabol.2011.10.014 (2012).
Song, G. et al. Hydrogen-rich water decreases serum LDL-cholesterol levels and improves HDL function in patients with potential metabolic syndrome. J. Lipid Res. 54, 1884–1893. https://doi.org/10.1194/jlr.M036640 (2013).
Song, G. et al. Hydrogen activates ATP-binding cassette transporter A1-dependent efflux ex vivo and improves high-density lipoprotein function in patients with hypercholesterolemia: A double-blinded, randomized, and placebo-controlled trial. J. Clin. Endocrinol. Metab. 100, 2724–2733. https://doi.org/10.1210/jc.2015-1321 (2015).
Koizumi, J. et al. Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia. Atherosclerosis 58, 175–186. https://doi.org/10.1016/0021-9150(85)90064-4 (1985).
Barter, P. & Genest, J. HDL cholesterol and ASCVD risk stratification: A debate. Atherosclerosis 283, 7–12. https://doi.org/10.1016/j.atherosclerosis.2019.01.001 (2019).
Rosenson, R. S. et al. Dysfunctional HDL and atherosclerotic cardiovascular disease. Nat. Rev. Cardiol. 13, 48–60. https://doi.org/10.1038/nrcardio.2015.124 (2016).
Kraemer, F. B. & Shen, W.-J. Hormone-sensitive lipase knockouts. Nutr. Metab. 3, 12. https://doi.org/10.1186/1743-7075-3-12 (2006).
Alves-Bezerra, M. & Cohen, D. E. Triglyceride metabolism in the liver. Compr. Physiol. 8, 1–8. https://doi.org/10.1002/cphy.c170012 (2017).
Newsholme, P., Stenson, L., Sulvucci, M., Sumayao, R. & Krause, M. In Comprehensive Biotechnology, 2nd edn. (ed. Moo-Young, M.) 3–14 (Academic Press, 2011).
Kawai, S. & Murata, K. Structure and function of NAD kinase and NADP phosphatase: Key enzymes that regulate the intracellular balance of NAD(H) and NADP(H). Biosci. Biotechnol. Biochem. 72, 919–930. https://doi.org/10.1271/bbb.70738 (2008).
Agledal, L., Niere, M. & Ziegler, M. The phosphate makes a difference: Cellular functions of NADP. Redox Rep. 15, 2–10. https://doi.org/10.1179/174329210X12650506623122 (2010).
Debose-Boyd, R. A. A helping hand for cytochrome p450 enzymes. Cell Metab. 5, 81–83. https://doi.org/10.1016/j.cmet.2007.01.007 (2007).
This work was supported by Military Logistics Key Open Research Projects (BHJ17L018).
The authors declare no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Adzavon, Y.M., Xie, F., Yi, Y. et al. Long-term and daily use of molecular hydrogen induces reprogramming of liver metabolism in rats by modulating NADP/NADPH redox pathways. Sci Rep 12, 3904 (2022). https://doi.org/10.1038/s41598-022-07710-6
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.