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 Table of Contents  
RESEARCH ARTICLE
Year : 2022  |  Volume : 17  |  Issue : 2  |  Page : 409-417

Hydrogen-rich water ameliorates neuropathological impairments in a mouse model of Alzheimer’s disease through reducing neuroinflammation and modulating intestinal microbiota


1 College of Life Sciences and Oceanography, Guangdong Provincial Key Laboratory for Plant Epigenetics, Shenzhen University, Shenzhen, Guangdong Province, China
2 Guangdong Provincial Key Laboratory of Biomedical Measurements and Ultrasound Imaging, National-Regional Key Technology Engineering Laboratory for Medical Ultrasound, School of Biomedical Engineering, Health Science Center, Shenzhen University, Shenzhen, Guangdong Province, China
3 College of Life Sciences and Oceanography, Guangdong Provincial Key Laboratory for Plant Epigenetics, Shenzhen University; Shenzhen Bay Laboratory, Shenzhen, Guangdong Province, China

Date of Submission08-Oct-2020
Date of Decision19-Nov-2020
Date of Acceptance18-Mar-2021
Date of Web Publication08-Jul-2021

Correspondence Address:
Xiu-Bo Du
College of Life Sciences and Oceanography, Guangdong Provincial Key Laboratory for Plant Epigenetics, Shenzhen University; Shenzhen Bay Laboratory, Shenzhen, Guangdong Province
China
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Source of Support: This study was supported by the National Natural Science Foundation of China, No. 21771126 (to XBD); and the Shenzhen Bureau of Science, Technology and Information of China, No. JCYJ20180305124000597 (to XBD), Conflict of Interest: None


DOI: 10.4103/1673-5374.317992

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  Abstract 

Hydrogen exhibits the potential to treat Alzheimer’s disease. Stereotactic injection has been previously used as an invasive method of administering active hydrogen, but this method has limitations in clinical practice. In this study, triple transgenic (3×Tg) Alzheimer’s disease mice were treated with hydrogen-rich water for 7 months. The results showed that hydrogen-rich water prevented synaptic loss and neuronal death, inhibited senile plaques, and reduced hyperphosphorylated tau and neurofibrillary tangles in 3×Tg Alzheimer’s disease mice. In addition, hydrogen-rich water improved brain energy metabolism disorders and intestinal flora imbalances and reduced inflammatory reactions. These findings suggest that hydrogen-rich water is an effective hydrogen donor that can treat Alzheimer’s disease. This study was approved by the Animal Ethics and Welfare Committee of Shenzhen University, China (approval No. AEWC-20140615-002) on June 15, 2014.

Keywords: Alzheimer’s disease; amyloid-β; anti-inflammation; bioenergetics; gut microbiota; hydrogen therapy; neurodegenerative disease; neurofibrillary tangles


How to cite this article:
Lin YT, Shi QQ, Zhang L, Yue CP, He ZJ, Li XX, He QJ, Liu Q, Du XB. Hydrogen-rich water ameliorates neuropathological impairments in a mouse model of Alzheimer’s disease through reducing neuroinflammation and modulating intestinal microbiota. Neural Regen Res 2022;17:409-17

How to cite this URL:
Lin YT, Shi QQ, Zhang L, Yue CP, He ZJ, Li XX, He QJ, Liu Q, Du XB. Hydrogen-rich water ameliorates neuropathological impairments in a mouse model of Alzheimer’s disease through reducing neuroinflammation and modulating intestinal microbiota. Neural Regen Res [serial online] 2022 [cited 2021 Sep 17];17:409-17. Available from: http://www.nrronline.org/text.asp?2022/17/2/409/317992

Yi-Tong Lin, Qing-Qing Shi, Lei Zhang. These authors contributed equally to this work.
Chinese Library Classification No. R453; R741.05; R378.2





  Introduction Top


Although Alzheimer’s disease (AD) was identified more than 100 years ago, an effective treatment strategy currently remains lacking (Frere and Slutsky, 2018; Jack et al., 2018). The main pathological features of AD are senile plaques and neurofibrillary tangles (NFTs), which are formed by amyloid-β (Aβ) aggregates and hyperphosphorylated tau, respectively. In addition, oxidative stress, inflammatory responses, and autophagic abnormalities also contribute to the pathogenesis of AD (Markesbery, 1997; Mostafavi et al., 2018; Fang et al., 2019). Accumulating evidence suggests that neuroinflammation plays an active role in the development of AD (Park et al., 2018; Ozben and Ozben, 2019; Gray et al., 2020). Epidemiological data have revealed that non-steroidal anti-inflammatory drugs may decrease the incidence of AD (Daniels et al., 2016). However, other studies have demonstrated that non-steroidal anti-inflammatory drugs may aggravate conditions in AD or increase the risk of this disease (Sehajpal et al., 2018). It is therefore necessary to develop effective anti-inflammatory AD drugs with low toxicity.

Hydrogen molecules are a special kind of antioxidant. As a gas molecule, hydrogen possesses the advantages of easy diffusion, fast action, and no obvious adverse reactions (Ohta, 2015; Iida et al., 2016). Furthermore, it is regarded as a promising potential therapy for many inflammation-related diseases, including neurodegenerative diseases, cancer, stroke, and ischemic injury (Iida et al., 2016; Yang et al., 2018; Zhang et al., 2019). Hydrogen has therefore been suggested as another important biologically active gas molecule, after nitric oxide, hydrogen sulfide, and carbon monoxide (Zhang and Bian, 2014; Olas, 2017; Kumar and Sandhir, 2018; Corpas et al., 2019). Recently, we developed palladium hydride nanoparticles and delivered them to the brains of AD model mice using stereotactic injection. This treatment showed promising potential as an AD therapy by eliminating oxidative stress and alleviating mitochondrial dysfunction (Zhang et al., 2019). However, stereotactic brain injection is invasive. In the present study, we therefore investigated the effects of hydrogen-rich water (HRW) treatment, which is a safer and more convenient administration route for hydrogen, on AD pathology. We used HRW in a mouse model of AD and observed its therapeutic effects.


  Materials and Methods Top


Ethics statement

All animal handling and experiments were performed in strict accordance with the institutional guidelines of Shenzhen University regarding experimental animal use, and were approved on June 15, 2014, by the Animal Ethics and Welfare Committee of Shenzhen University (approval No. AEWC-20140615-002). All procedures were conducted in accordance with the ethical standards of the National Institutes of Health Guide for the Care and Use of Laboratory Animals.

Animals and intervention

The HRW was gifted from Beijing Vitality Hydrogen Source Beverage Ltd. (Beijing, China), and the hydrogen concentration was greater than 1.6 parts per million. The triple transgenic (3×Tg)-AD model mice expressed the mutant human genes TauP301L and APPswe, and the mutant mouse gene PS1M146V. According to previous research on this mouse model (Oddo et al., 2003; Billings et al., 2005), Aβ begins to accumulate in the neurons at 4 months old, and gradually spreads outside the neurons. The accumulation of Aβ may cause neuronal dysfunction, which can lead to cognitive deficits. The 3×Tg-AD mice (n = 30, 25–30 g) and B6:129SF2/J (wild-type, WT) mice (n = 15, 25–30 g) were purchased from the Jackson Laboratory (Bar Harbor, ME, USA). To avoid the influences of sex and estrogen, three-month-old male mice only were used in the study. The 3×Tg-AD mice were randomly divided into 3×Tg-AD (AD; n = 15) and HRW-treated 3×Tg-AD (AD + HRW; n = 15) groups, and the B6:129SF2/J mice were used as controls (n = 15). After being trained with a time-limited water supply (water was only provided from 10:00 a.m. to 2:00 p.m. every day) for 30 days, the 3-month-old 3×Tg-AD mice in the AD + HRW group were given HRW for 7 months, while the mice in the AD group were treated with normal drinking water for 7 months.

Behavioral tests

The Morris water maze experiment was used to test the spatial learning and memory abilities of 10-month-old mice, as previously described (Xie et al., 2018). The entire experiment lasted for 8 days, and consisted of two parts: training (days 1 to 5) and testing (days 6 and 8). Each mouse was gently placed in the water in the first quadrant and was allowed 60 seconds to find the platform. If the mouse failed to find the platform within 60 seconds, it was gently guided to the platform and allowed to remain there for 10 seconds. The escape latency was recorded by a camera system. The probe tests, with the platform removed, were performed 24 and 72 hours after the final training trial to assess short- and long-term memory consolidation. During the tests, mice were released into the water from an identical point in the first quadrant and allowed to swim freely for up to 120 seconds. Time spent in the target quadrant (quadrant III) and the number of target crossings (i.e., the former platform site) were recorded. All tests were analyzed using an automatic water maze program (Water Maze MT-200, Taimeng Technology Co., Ltd., Chengdu, China).

The open-field test was performed according to previous protocols (Hammer et al., 2014; Shoji et al., 2016) with a few modifications. A polyvinyl chloride box (100 cm × 100 cm × 40 cm) (Zhishu Duobao Biotechnology Co., Ltd., Beijing, China) with the bottom equally divided into 25 squares was used as the open field. During the test, each mouse was released into the center of the box and then allowed to explore for 3 minutes. Three parameters were collected: number of grids crossed (grids were only counted if all limbs of the mouse entered the grid), rearing frequency, and defecation frequency.

Sample collection

After the behavioral tests, mice were anaesthetized using isoflurane (Reward Life Technology Co., Ltd., Shenzhen, China). The mouse brains were then collected and soaked in phosphate-buffered saline (PBS) for 30 minutes before being divided into the left and right hemispheres. The hippocampus and cortex were dissected from the right hemisphere and stored at –80°C for the subsequent biochemical and western blot analyses. The other hemisphere was fixed in 4% phosphate-buffered paraformaldehyde for immunofluorescence, silver staining, and Nissl staining. In addition, the cecal contents (150–200 mg) were collected and frozen for the gut microbiota analysis.

Western blot analysis

Western blot analysis was performed to determine protein levels in the mouse hippocampus, as previously described (Xie et al., 2018). The blots were incubated with primary antibody overnight at 4°C, and were then incubated with horseradish peroxidase-conjugated secondary antibody for 2 hours at room temperature. All primary and secondary antibodies used in this study are summarized in Additional Table 1. Protein bands were visualized using the Image Station (Tanon-5200, Tanon Science & Technology Co., Ltd., Shanghai, China) using an enhanced chemiluminescence detection reagent. The band intensities of immunoblots were quantified using ImageJ software (National Institutes of Health, Bethesda, MD, USA).

Immunofluorescence, glycine silver staining, and Nissl staining

Brain tissue was fixed in 4% paraformaldehyde for 24 hours, cryopreserved overnight in graded sucrose solutions at 4°C, and embedded in optimal cutting temperature compound. Subsequently, the embedded tissue blocks were cut into 8 μm sections, which were mounted onto adhesive glass slides.

For immunofluorescence experiments, sections were rinsed with PBS, permeabilized with 2% Triton X-100, and blocked with 1% bovine serum albumin in PBS with Tween-20. Next, sections were incubated overnight at 4°C with primary antibodies, followed by incubation with Dylight 488/594-conjugated secondary antibodies for 1.5 hours at room temperature (Additional Table 1). After being washed with PBS with Triton X-100, the sections were stained with 4′,6-diamidino-2-phenylindole for 5 minutes and then sealed with anti-fluorescence quenching sealant (Beyotime, Shanghai, China). Finally, the images were captured using a confocal microscope (FV1000, Olympus Corporation, Tokyo, Japan). The Aβ, ionized calcium-binding adapter molecule 1 (Iba-1), and DAPI signals were evaluated using Image Pro Plus software (Media Cybernetics, Inc., Rockville, MD, USA), and the results were expressed as Aβ/DAPI or Iba-1/DAPI.

For the glycine sliver staining, sections were de-stained and sequentially treated with xylene, anhydrous ethanol, 75% ethanol, and water. The sections were subsequently stained in an acidic formaldehyde solution for 5 minutes and washed three times with distilled water. Thereafter, the sections were stained for 3–5 minutes with glycine silver solution that had been preheated to 37°C, and were then treated with reducing solution and washed with distilled water. Finally, the sections were observed using a confocal microscope (FV1000, Olympus Corporation). The NFT-positive areas were evaluated using Image Pro Plus software, and the results were expressed as the percentage of NFT-occupied area.

For Nissl staining, the sections were washed twice with PBS, dehydrated through an ethanol gradient, and immersed in xylene. After being stained with cresyl violet (0.5%) for 10 minutes, the sections were observed using a fluorescence microscope (BX51, Olympus Corporation). The Nissl-positive areas were assessed using Image Pro Plus software, and the results were expressed as the percentage of Nissl-positive area.

Adenosine triphosphate measurement

Adenosine triphosphate (ATP) levels in fresh hippocampal tissue were measured using an ATP assay kit (Beyotime). Each sample (20 mg) was homogenized in lysis buffer (150 μL; Beyotime) and centrifuged at 12,000 r/min for 5 minutes at 4°C. The collected supernatants were seeded into the wells of a 96-well plate containing ATP assay medium (100 μL). Subsequently, the relative light unit was determined using a luminometer (SpectraMAX 190 Microplate Reader, Molecular Devices, San Jose, CA, USA) and normalized against protein concentrations that were quantified using the bicinchoninic acid assay (Smith et al., 1985).

Gut microbiota analysis

The 16S ribosomal RNA gene was sequenced from cecal contents. The MetaVx Library Preparation kit (GENEWIZ, Inc., South Plainfield, NJ, USA) was used to prepare amplicon libraries. The DNA library was then evaluated using Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA), and quantified with Qubit 2.0 Fluorometer (Thermo Fisher Scientific, Waltham, MA, USA). The 16S ribosomal RNA data analysis was performed using QIIME data analysis software (http://www.wernerlab.org/software/macqiime/citations). Quality filtering was executed to remove any low-quality sequences. Next, sequences with 97% similarity were quantified into operational taxonomic unit thresholds using the clustering program VSEARCH 1.9.6 (https://zenodo.org/record/44512). The taxonomy of the sequences was further determined using the Ribosomal Database Project Classifier (http://rdp.cme.msu.edu/classifier/classifier.jsp) at a minimum threshold of 0.8. With the analysis of operational taxonomic units, the α diversity indices Chao1 and Shannon were calculated using a random sampling method of sample sequence, and rarefaction curves were drawn. Unbiased UniFrac analysis (Lozupone and Knight, 2005) was used to determine whether there were significant differences in microbial communities between samples.

Statistical analysis

All data are expressed as the mean ± standard error of the mean (SEM). The significance level was established as P < 0.05. Statistical analyses were performed using one-way analysis of variance followed by Tukey’s post hoc test with GraphPad Prism 8.0 (GraphPad Software Inc., San Diego, CA, USA).


  Results Top


HRW improves cognitive impairment in 3×Tg-AD mice

To investigate the role of HRW in the learning and memory abilities of 3×Tg-AD mice, the Morris water maze test was performed after 7 months of HRW treatment. The 3×Tg-AD mice had difficulties in searching for the hidden platform compared with WT mice, and had chaotic and irregular swimming traces, suggesting that these mice have defective learning and memory abilities. In contrast, after HRW treatment, the 3×Tg-AD mice exhibited improvements in cognitive impairment. Escape latency was gradually shortened during the 5 days of spatial training in all of these mice [Figure 1]A and [Figure 1]B.
Figure 1: HRW improves the cognitive impairment in 3×Tg-AD mice.
(A) Typical swimming traces in the probe test. The red circle indicates the hidden platform. The black line indicates the swimming trace. (B) Escape latency to find the hidden platform in the training task. (C) Number of crossings of the platform in the probe test. (D) Time spent in the target quadrant in the probe test. (E) Numbers of times the mice crossed the grids, defecated, and reared in the open-field test. Data are expressed as the mean ± SEM (n = 15 mice/group). *P < 0.05, **P < 0.01, ***P < 0.001 (one-way analysis of variance followed by Tukey’s post hoc test). AD: Alzheimer’s disease; HRW: hydrogen-rich water; WT: wild type.


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At 24 or 72 hours later, short- or long-term memory retention, respectively, was assessed using the probe trials. As shown in [Figure 1]C and [Figure 1]D, the number of platform crossings and the amount of time mice spent in the target quadrant were much lower in the AD group than in the WT group (P < 0.001), indicating memory impairments in the 3×Tg-AD mice. Surprisingly, HRW-treated 3×Tg-AD mice demonstrated noticeable increases in the number of platform crossings and the amount of time spent in the target quadrant (P < 0.05 or P < 0.01, vs. AD group). In particular, the long-term memory dysfunction of 3×Tg-AD mice was significantly improved by HRW.

In addition, to evaluate the anti-depression and anti-anxiety effects of HRW, the anxiety behaviors of mice were evaluated using the open-field test. Compared with WT mice, the number of grids crossed and the amount of rearing by the 3×Tg-AD mice were significantly lower, while defecation frequency was increased (P < 0.001). These findings demonstrate the typical depression- and anxiety-like symptoms of 3×Tg-AD mice. In contrast, HRW treatment improved these emotional disorders in 3×Tg-AD mice, with an increased frequency of grid crossings and rearing and a decreased frequency of defecation (P < 0.05; [Figure 1]E). The results of these behavioral tests indicate that HRW treatment ameliorates the spatial learning and cognitive impairments of 3×Tg-AD mice.

HRW prevents synaptic loss and neuronal damage in 3×Tg-AD mice

The effects of HRW on the hippocampal levels of typical synaptic markers (postsynaptic density protein 95 and synaptophysin) were evaluated. As shown in [Figure 2]A and [Figure 2]B, the levels of these two synaptic proteins in 3×Tg-AD mice with HRW treatment reached or even exceeded those in the WT mice (P < 0.05), suggesting that HRW promotes the recovery of synaptic function in AD model mice.
Figure 2: HRW prevents synaptic loss and neuronal death in 3×Tg-AD mice.
(A) Effects of HRW on the hippocampal levels of PSD95 and Syna by western blot assay. (B) Quantification of PSD95 and Syna expression, normalized against β-actin. (C) Effects of HRW on the density and activity of neurons (arrows) in the CA1, CA3, DG, and cortex by Nissl staining. 3×Tg-AD mice exhibited decreased density and number of Nissl bodies; these were significantly recovered after HRW treatment. Scale bars: 50 μm. (D) Quantification of Nissl-positive neurons in the CA1, CA3, DG, and cortex. Data are expressed as the mean ± SEM (n = 3 mice/group). *P < 0.05, **P < 0.01 (one-way analysis of variance followed by Tukey’s post hoc test). AD: Alzheimer’s disease; DG: dentate gyrus; HRW: hydrogen-rich water; PSD95: postsynaptic density protein 95; Syna: synaptophysin; WT: wild type.


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Neuronal death leads to the collapse of neural networks and further contributes to memory and cognitive impairments in neurodegenerative diseases, including AD (Vilalta and Brown, 2018). Here, neuronal injury in the CA1, CA3, dentate gyrus, and cortex (Paxinos and Franklin, 2013) was analyzed by Nissl staining. As shown in [Figure 2]C and [Figure 2]D, HRW treatment significantly increased the density and number of Nissl bodies in 3×Tg-AD mice (P < 0.05 or P < 0.01). Thus, our findings indicate that HRW protects synaptic proteins and reverses neuronal damage in 3×Tg-AD mice.

HRW suppresses Aβ production and deposition in the hippocampus of 3×Tg-AD mice

To investigate the effects of HRW on Aβ pathology, the hippocampal levels of APP, secreted soluble APP α (sAPPα), and β-site APP-cleaving enzyme 1 (BACE1/β-secretase) were measured [Figure 3]. In the western blot analysis, the levels of APP were higher in 3×Tg-AD mice than in WT mice (P < 0.05), and were significantly reduced after HRW treatment (P < 0.001; [Figure 3]A and [Figure 3]B). The BACE1 levels were also significantly reduced after HRW treatment (P < 0.001).
Figure 3: HRW suppresses Aβ production and deposition in the hippocampus of 3×Tg-AD mice.
(A) Effects of HRW on hippocampal APP, sAPP-α, and BACE1 by western blot assay. (B) Quantification of APP, sAPP-α, and BACE1, normalized against β-actin. (C) Immunofluorescence images showing more Aβ (6E10) deposition (arrows) in the 3×Tg-AD mouse hippocampus compared with WT mice; this deposition was markedly reduced after HRW administration. Scale bar: 20 μm. (D) Quantification of Aβ deposition in the CA3 region of the hippocampus. Data are expressed as the mean ± SEM (n = 3 mice/group). *P < 0.05, **P < 0.01, ***P < 0.001 (one-way analysis of variance followed by Tukey’s post hoc test). AD: Alzheimer’s disease; APP: amyloid precursor protein; BACE1: beta-site APP cleaving enzyme 1; DAPI: 4′,6-diamidino-2-phenylindole; HRW: hydrogen-rich water; sAPP-α: soluble amyloid precursor protein α; WT: wild type.


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We used an anti-Aβ (6E10) antibody to perform immunofluorescence staining of hippocampal sections (CA3 region) to study Aβ deposition [Figure 3]C. The immunofluorescence-positive area of Aβ deposition in the 3×Tg-AD mouse hippocampus was markedly larger than that of WT mice (P < 0.01), and was significantly reduced after HRW administration (P < 0.05; [Figure 3]C and [Figure 3]D). In addition, the decreased sAPPα levels in 3×Tg-AD mice were partially recovered by HRW treatment, suggesting a neuroprotective effect of hydrogen (P < 0.05; [Figure 3]A and [Figure 3]B). Together, these results indicate that HRW treatment has an intervention effect on the proteolysis of APP and on Aβ formation and deposition.

HRW suppresses tau hyperphosphorylation and NFT formation in 3×Tg-AD mice

As shown in [Figure 4]A and [Figure 4]B, HRW treatment significantly inhibited tau phosphorylation at Ser422 and Ser404 in 3×Tg-AD mice (P < 0.05). In addition, glycine silver-positive NFTs were significantly decreased in the CA3 region in the HRW-treated group compared with 3×Tg-AD mice (P < 0.05; [Figure 4]C and [Figure 4]D). These results indicate that HRW treatment can reduce tau pathology, which may prevent synaptic and neuronal damage and memory deficits in AD mice.
Figure 4: HRW suppresses tau pathology in 3×Tg-AD mice.
(A) Effects of HRW on the hippocampal levels of pS422-, pS262-, and pS404-tau by western blot assay. (B) Quantification of pS422-, pS262-, and pS404-tau, normalized against GAPDH. (C) Glycine silver staining for NFTs in the mouse hippocampus, showing that the higher levels of NFTs (red arrows) in 3×Tg-AD mice were significantly reduced by HRW. Scale bar: 50 μm. (D) Quantification of NFTs in the hippocampal CA3 region. Data are expressed as the mean ± SEM (n = 3 mice/group). *P < 0.05 (one-way analysis of variance followed by Tukey’s post hoc test). AD: Alzheimer’s disease; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; HRW: hydrogen-rich water; NFTs: neurofibrillary tangles; WT: wild type.


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HRW inhibits inflammation and transforms microglia in an anti-inflammatory direction in 3×Tg-AD mice

After the continuous administration of HRW for 7 months, levels of the pro-inflammatory factors interleukin-6 and interleukin-1β were decreased (P < 0.05 or P < 0.01) compared with the AD group, while levels of the anti-inflammatory factor chitinase 3-like protein 3 (Ym-1) were increased (P < 0.01; [Figure 5]A and [Figure 5]B). Iba-1 and glial fibrillary acidic protein are the classic indicators of microglia and astrocyte activation, respectively. Further western blot and immunofluorescence experiments demonstrated that hydrogen had a regulatory effect on glial cells, including microglia and astrocytes [Figure 5]A and [Figure 5]C, [Figure 5]D, [Figure 5]E, [Figure 5]F, [Figure 5]G. By western blot analysis, the levels of microglia and astrocytes were increased in 3×Tg-AD mice compared with WT mice (P < 0.01 or P < 0.05), while HRW treatment significantly reduced the levels of these two glial cell types (P < 0.01 or P < 0.05; [Figure 5]A and [Figure 5]C). In addition, the immunofluorescence-positive area of Iba-1 in the 3×Tg-AD mouse cortex was larger than that of WT mice (P < 0.001), and was significantly reduced after HRW treatment in both the cortex and DG (P < 0.001 or P < 0.05; [Figure 5]D, [Figure 5]E, [Figure 5]F, [Figure 5]G). These findings indicate that HRW can reduce pro-inflammatory cytokine production and enhance the secretion of anti-inflammatory factors, thereby exerting anti-inflammatory effects.
Figure 5: Effects of HRW treatment on inflammation in the 3×Tg-AD mice.
(A) Effects of HRW on the hippocampal levels of Ym-1, IL-6, TNF-α, IL-1β, Iba-1, and GFAP in mice. (B, C) Quantification of Ym-1, IL-6, TNF-α, IL-1β, Iba-1, and GFAP, normalized against GAPDH. (D, F) The deposition of Iba-1 in the cortex (D) and hippocampal DG (F) was detected by immunofluorescence, and the overactivation of microglia in AD mice was clearly inhibited by HRW. Arrows indicate active Iba-1 (microglia). Scale bars: 50 μm. (E, G) Quantification of Iba-1 deposition in the cortex and hippocampal DG (G). Data are expressed as the mean ± SEM (n = 3 mice/group). *P < 0.05, **P < 0.01, ***P < 0.001 (one-way analysis of variance followed by Tukey’s post hoc test). AD: Alzheimer’s disease; DAPI: 4′,6-diamidino-2-phenylindole; DG: dentate gyrus; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GFAP: glial fibrillary acidic protein; HRW: hydrogen-rich water; Iba-1: ionized calcium-binding adapter molecule 1; IL-1β: interleukin-1β; IL-6: interleukin-6; TNF-α: tumor necrosis factor-α; WT: wild type; Ym-1: chitinase 3-like protein 3.


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HRW improves bioenergetics in the brains of 3×Tg-AD mice

We determined the levels of several proteins that are related to mitochondrial energetics (pyruvate dehydrogenase component α subunit [PDHE1α], cytochrome c oxidase [COX] IV, and NADH dehydrogenase subunit 1 [ND1]) to assess the effects of HRW on mitochondrial energy metabolism. By western blot, the levels of these proteins were markedly lower in 3×Tg-AD mice compared with WT mice (P < 0.05, P < 0.01, or P < 0.001; [Figure 6]A and [Figure 6]B), indicating the typical impaired mitochondrial function and bioenergetic deficiency of AD. HRW treatment significantly increased the PDHE1α levels (P < 0.05). Similarly, ATP concentrations in the 3×Tg-AD mouse hippocampus were also increased by HRW treatment (P < 0.05; [Figure 6]C). In this study, HRW was shown to be effective in reducing metabolic dysfunction and neuroinflammation in AD by manipulating the bioenergetic pathway.
Figure 6: Effects of HRW on bioenergetics in the hippocampus of 3×Tg-AD mice.
(A) Effects of HRW on the hippocampal levels of PDHE1α, COX IV, and ND1 by western blot assay. (B) Quantification of PDHE1α, COX IV, and ND1, normalized against the levels of VDAC1. (C) Quantitative analysis of the related ATP levels. Data are expressed as the mean ± SEM (n = 3 mice/group). *P < 0.05, **P < 0.01, ***P < 0.001 (one-way analysis of variance followed by Tukey’s post hoc test). AD: Alzheimer’s disease; COX IV: cytochrome C oxidase subunit IV; HRW: hydrogen-rich water; ND1: NADH-ubiquinone oxidoreductase chain 1; PDHE1α: α-subunit of pyruvate dehydrogenase; VDAC1: voltage-dependent anion channel 1; WT: wild type.


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HRW regulates the gut microbiota of 3×Tg-AD mice

The bacterial 16S ribosomal RNA genes were extracted from intestinal samples of 10-month-old mice and sequenced. In terms of bacterial communities, the Chao1 index was significantly smaller in 3×Tg-AD mice than in WT mice (P < 0.01), while HRW treatment increased the Chao1 index [Figure 7]A. The diversification reflected in the Shannon index was similar to that in the Chao1 index [Figure 7]B. The α diversity analysis (Chao1 and Shannon indices) revealed that the richness of bacterial species and diversity were lower in the intestines of 3×Tg-AD mice than in WT mice; HRW administration increased the richness and diversity of intestinal microflorae in 3×Tg-AD mice. The rarefaction curve also illustrated that HRW treatment recovered the richness and diversity of intestinal microbiota in the 3×Tg-AD mice [Figure 7]C.
Figure 7: Effects of HRW on gut microbiota in 3×Tg-AD mice.
(A–D) 16s ribosomal RNA gene sequencing showed changes to microbial diversity in mice, including in the box diagrams of Chao1 (A), Shannon diversity (B), the rarefaction curve (C), and the relative abundances of the main species at genus level (D). (E) The relative abundance of Lachnospiraceas_NK4A136_group, Ruminococcaceae_UCG-014, and Helicobacter in the three groups. Data are expressed as the mean ± SEM (n = 6 mice/group). *P < 0.05, **P < 0.01 (one-way analysis of variance followed by Tukey’s post hoc test). AD: Alzheimer’s disease; HRW: hydrogen-rich water, WT: wild type.


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The Lachnospiraceae-NK4A136-group was the dominant bacterial type in all three groups of mice [Figure 7]D, except for unclassified bacteria. Other genera with a relative abundance higher than 3% in each group are also depicted in [Figure 7]D, including Helicobacter in all three groups, Ruminococcaceae-UCG-014 in the WT and HRW-treated groups, and Alloprevotella in the 3×Tg-AD and HRW-treated groups. Compared with the WT mice, the relative abundances of Lachnospiraceae-NK4A136-group (7%) and Ruminococcaceae-NK4A136-group (< 4%, classified into “others”) were lower in the 3×Tg-AD mice (P < 0.05; [Figure 7]D and [Figure 7]E). Interestingly, the relative abundances of Lachnospiraceae-NK4A136-group and Ruminococcaceae-UCG-014 were enhanced after HRW treatment [Figure 7]D and [Figure 7]E, which may be one reason underlying the protective effects of HRW against the development of AD pathology. In addition, the abundance of Helicobacter in 3×Tg-AD mice was decreased from 6% to 4% by HRW treatment [Figure 7]E. Together, our findings indicate a correlation between microbiota and the anti-AD effects of HRW administration. HRW treatment increased the abundance and diversity of intestinal microbiota in AD mice and regulated the relative abundance of specific flora, which may affect the pathological process of AD.


  Discussion Top


The synapse is the basic unit for building neural networks in the brain (Vilalta and Brown, 2018). Aβ oligomers, phosphorylated tau, and oxidative stress all contribute to synaptic deficits, which are regarded as an early event of AD (Hong et al., 2016; Forner et al., 2017; Batista et al., 2018; Rice et al., 2019). In the present study, HRW treatment repaired the loss of synapses and neuronal damage in an AD mouse model. As reported previously, damage by reactive oxygen species contributes to the important neuropathological hallmarks of AD, including synaptic deficits and neuronal death (Rai et al., 2014; Deas et al., 2016; Angelova and Abramov, 2018). Thus, we hypothesize that hydrogen reduces the overproduction of reactive oxygen species, exerts further protection to synapses and neurons, and thus restores cognitive functions in AD.

Aβ is generated by the sequential proteolysis of APP by β- and γ-secretases (Allsop et al., 1988; Billings et al., 2005). Aβ1–40 is the most abundant form of Aβ species (about 80–90% of all Aβ), whereas Aβ1–42 (about 5–10% of all Aβ) is the main form that results in synaptic damage and neuronal death in the AD brain (Bozso et al., 2010). APP is cleaved by α- and γ-secretases to produce sAPPα through the non-amyloidogenic pathway. sAPPα is reported to have a variety of neuroprotective effects (Kojro et al., 2001; Selkoe and Schenk, 2003). In the current study, HRW treatment significantly decreased the levels of APP and Aβ in 3×Tg-AD mice, but increased sAPPα levels, suggesting that HRW has an intervention effect on the proteolysis of APP and on Aβ formation and deposition.

Tau is a microtubule-associated protein (Roberson et al., 2011; Guo et al., 2017). However, under pathological conditions, hyperphosphorylated tau disassociates from microtubules and assembles into NFTs (Congdon and Sigurdsson, 2018; Lowe et al., 2018), which are a critical pathological marker of AD (Spires-Jones et al., 2017; Villemagne et al., 2018). Tau and phosphorylated tau (pTau) have attracted considerable attention in recent years in terms of mechanism studies and drug discovery for AD. We revealed that HRW treatment reduced tau pathology, which may prevent synaptic and neuronal damage and memory deficits in AD mice.

Increasing evidence indicates that neuroinflammation is characteristic of AD. Inflammation is not only the main pathophysiological mechanism of Aβ production and senile plaque formation, but it is also a main factor in tau hyperphosphorylation, NFT formation, neuronal degeneration, and acetylcholine decline (Billings et al., 2005; Iketani and Ohsawa, 2017; Yang et al., 2018; Du et al., 2021). Inflammation disrupts synaptic plasticity as a direct driver of cognitive impairment in AD (Hong et al., 2016). Microglia and astrocytes are the main cell types involved in inflammatory responses of the central nervous system, which are extensively activated in AD brains (Heneka et al., 2015). At present, most treatments of large-scale anti-inflammatory drugs for AD deliver no significant improvement. Although some non-steroidal anti-inflammatory drugs have provided some improvement in AD symptoms in clinical trials, the overall significance is not great (Daniels et al., 2016; Sehajpal et al., 2018). Recently, molecular hydrogen has been reported to exhibit anti-inflammatory effects in many studies (Kura et al., 2019). In the current study, we observed that an anti-inflammatory role of hydrogen also existed in 3×Tg-AD mice. The inflammatory and anti-inflammatory factors that we detected, which are mainly produced and released by activated microglia, are thought to play important roles in AD pathogenesis, and lead to neuronal damage, apoptosis, and immune modulation. Activated microglia include classical inflammatory (M1) phenotypes and alternatively activated (M2) phenotypes (Kabba et al., 2018). M1 microglia produce and release destructive pro-inflammatory cytokines (Kumar et al., 2016); in contrast, M2 microglia express anti-inflammatory factors (Jha et al., 2016). Our results indicate that hydrogen may inhibit the excessive activation of microglia, transforming them in an anti-inflammatory direction (i.e., to M2 phenotypes).

Bioenergetic deficits have been regarded as a major contributor to cognitive decline and memory deficits (Su et al., 2014; Zhou et al., 2018; Filippov et al., 2021). The bioenergy hypothesis proposes events ranging from metabolic defects to aging and neurodegeneration. Loss of mitochondrial bioenergetics in AD leads to the decreased activity of relevant enzymes, which causes a reduction in the electron transport chain as well as energy (i.e., ATP) depletion (Ohno et al., 2012; Sheng and Cai, 2012; Su et al., 2014; Park et al., 2018; Zhou et al., 2018; Kempuraj et al., 2020). Pyruvate dehydrogenase complex is a key enzyme in aerobic carbohydrate metabolism (Zhong et al., 2015) whose deficiency is known to cause severe metabolic and neurodegenerative diseases (Zhou et al., 2018). Mitochondrial COX, a multimeric complex that is the last enzyme of the respiratory chain, is essential for aerobic energy generation in the form of ATP (Su et al., 2014; Kocha et al., 2015). NADH is a part of mitochondrial complex 1, which is the initial enzyme of the mitochondrial respiratory chain. Some previous research has suggested that inflammatory signals result in the enhanced phosphorylation of mitochondrial targets, including COX, leading to the inhibition of mitochondrial function, reduction of mitochondrial membrane potential, and energy failure (Zhong et al., 2016; Nishida and Otsu, 2017; Tilg et al., 2017; Biczo et al., 2018; Li et al., 2018). Moreover, mitochondrial dysfunction can also cause neuroinflammation (Zhou et al., 2018). In the present study, hydrogen was effective in reducing metabolic dysfunction and neuroinflammation in AD by manipulating the bioenergetic pathway.

A mounting number of studies have reported that microbiota, which live in symbiosis with animals, are a very important factor influencing the health of the host (Kabba et al., 2018; Yao and Zu, 2020). The gut microbiota integrate into the microbiota-gut-brain axis to regulate brain function and behavior (Valles-Colomer et al., 2019), and a correlation analysis has revealed that gut microbial metabolites are associated with AD (MahmoudianDehkordi et al., 2019; Tran et al., 2019). A variety of factors, including diet, can cause changes in gut microbiota and gut physiology. Here, we further investigated whether HRW may interfere with the gut microbiota of AD mice.

Previous studies have shown that Lachnospiraceae-NK4A136-group and Ruminococcaceae-UCG-014 are beneficial bacteria. Lachnospiraceae-NK4A136-group belongs to the family of Lachnospiraceae, which is thought to be relevant for the metabolism of carbohydrates into short-chain fatty acids that can be used by the host for energy (Manuel et al., 2019; Wang et al., 2019). Helicobacter pillory is related to gastritis and is a causative agent of gastric and duodenal ulcers (Albaret et al., 2020). The relative abundance of the Lachnospiraceae-NK4A136-group may be associated with increased intestinal mucosal permeability in patients with depression (Cheng et al., 2018). Ruminococcaceae-UCG-014, which belongs to the family of Ruminococcaceae, is regarded as a special functional microflora that can modulate the metabolism of host amino acids. It has great regulatory potential for persistent mental illnesses, such as mental state wilting and drowsiness (Gopalakrishnan et al., 2018). Thus, the decreased relative abundance of these two beneficial bacteria in the intestines of 3×Tg-AD mice may be associated with declined metabolic capacity, altered mental state, depression-like behavior, and wilting in 3×Tg-AD mice.

Some limitations of the study should be noted. First, young mice were subjected to long-term treatment of single-dose HRW. This study therefore suggests more of a preventative effect rather than a therapeutic effect of HRW on AD. Furthermore, we were unable to identify whether the effect was dose-dependent. Second, the current study did not provide any information about the specific receptors/enzymes or cellular pathways on which HRW might act during neuroprotection. This should be considered in a future study.

In conclusion, a strong relationship between inflammation and the pathogenesis of AD has been demonstrated in numerous studies. As a novel and innovative therapeutic treatment, hydrogen may be developed as a potential therapy to treat diverse inflammatory diseases, including AD. In the current study, 3×Tg-AD mice were treated with HRW, which reversed cognitive impairment, prevented synaptic loss and neuronal death, inhibited Aβ generation and deposition, and reduced tau hyperphosphorylation and NFTs. We further demonstrated that HRW treatment exerted anti-inflammatory effects that were accompanied by improved bioenergetics and gut microbiota regulation in AD model mice. These findings demonstrate the encouraging potential of hydrogen as a therapeutic and prophylactic agent for neurodegenerative diseases, and suggest a new direction for AD treatment in the future.

Acknowledgments: We thank Beijing Vitality Hydrogen Source Beverage Ltd. for providing the hydrogen-rich water.

Author contributions: Study conception and design: YTL, QQS, LZ, QJH, QL, XBD; experiment implementation: YTL, QQS, LZ, CPY, ZJH, XXL; data analysis: QQS, LZ; manuscript draft: YTL, QQS, LZ. All authors read and approved the final manuscript.

Conflicts of interest: The authors declare no conflicts of interest.

Financial support: This study was supported by the National Natural Science Foundation of China, No. 21771126 (to XBD); and the Shenzhen Bureau of Science, Technology and Information of China, No. JCYJ20180305124000597 (to XBD). The funding sources had no role in study conception and design, data analysis or interpretation, paper writing or deciding to submit this paper for publication.

Institutional review board statement: This study was approved by the Animal Ethics and Welfare Committee of Shenzhen University (approval No. AEWC-20140615-002) on June 15, 2014.

Copyright license agreement: The Copyright License Agreement has been signed by all authors before publication.

Data sharing statement: Datasets analyzed during the current study are available from the corresponding author on reasonable request.

Plagiarism check: Checked twice by iThenticate.

Peer review: Externally peer reviewed.

Open peer reviewer: Ahmed Abdel-Zaher, Assiut University, Egypt.

Additional files:

Additional Table 1: Antibody information[Additional file 1].

Additional file 1: Original data of the experiment[Additional file 2].

Funding: This study was supported by the National Natural Science Foundation of China, No. 21771126 (to XBD); and the Shenzhen Bureau of Science, Technology and Information of China, No. JCYJ20180305124000597 (to XBD).

 
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P-Reviewer: Abdel-Zaher A; C-Editor: Zhao M; S-Editors: Yu J, Li CH; L-Editors: Gardner B, Yu J, Song LP; T-Editor: Jia Y


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