Molecular hydrogen protects against ischemia-reperfusion injury in a mouse fatty liver model via regulating HO-1 and Sirt1 expression

Fatty liver has lower tolerance against ischemia-reperfusion (I/R) injury in liver operations, including liver transplantation. Seeking to ameliorate liver injury following I/R in fatty liver, we examined the protective effect of hydrogen (H2) saline on I/R liver injury in a methionine and choline-deficient plus high fat (MCDHF) diet-induced fatty liver mouse model. Saline containing 7 ppm H2 was administrated during the process of I/R. Livers were obtained and analyzed. Primary hepatocytes and Kupffer cells (KCs) were obtained from fatty liver and subjected to hypoxia/reoxygenation. Apoptosis-related proteins and components of the signaling pathway were analyzed after treatment with hydrogen gas. The MCDHF I/R group showed higher levels of AST and ALT in serum, TUNEL-positive apoptotic cells, F4/80 immunopositive cells, mRNA levels of inflammatory cytokines, constituents of the signaling pathway, pro-apoptotic molecules in liver, and KCs and/or primary hepatocytes, compared to the control group. In contrast, H2 treatment significantly suppressed the signs of I/R injury in fatty liver. Moreover, the expression of Bcl-2, HO-1, and Sirt1 in liver, KCs, and hepatocytes by hydrogen gas were increased, whereas caspase activation, Bax, and acetylation of p53 were suppressed by hydrogen gas. These results demonstrated that H2 treatment ameliorated I/R liver injury in a fatty liver model by reducing hepatocyte apoptosis, inhibiting macrophage activation and inflammatory cytokines, and inducing HO-1 and Sirt1 expression. Taken togather, treatment with H2 saline may have a protective effect and safe therapeutic activity during I/R events, such as in liver transplantation with fatty liver.

& ALT were elevated within 3 hr reperfusion following 15 min ischemia in steatotic liver, while the group with hydrogen saline administration effectively decreased the AST and ALT levels compared to the control group (Fig. 1B). Hydrogen saline could prevent histological alterations (necrosis). The histology of the steatotic livers showed that there were almost no inflammatory cells or necrotic areas in the MCDHF diet group, whereas inflammatory cell infiltration and necrotic areas were found after 3 hr reperfusion and 15 min ischemia (Fig. 1A). Necrotic areas of the steatotic liver were analyzed to determine the preventive effect of hydrogen saline treatment. Hydrogen saline pretreatment decreased the liver histological damage when subjected to I/R injury (Fig. 1A). The number of F4/80-positive cells, macrophages, was more widely distributed in the group with 3 hr reperfusion after 15 min ischemia than in control fatty liver. In contrast, pre-treatment with hydrogen saline significantly decreased the population of mouse EGF-like module-containing mucin-like hormone receptor-like 1 (EMR1 or F4/80) positive cells (Fig. 1B). After 3 hr reperfusion following 15 min ischemia, the amount of TUNEL-positive cells was significantly increased compared to fatty liver. Hydrogen saline administration dramatically suppressed the amount of TUNEL-positive cells (Fig. 1A). Moreover, the number of cells positive for 4-hydroxynonenal(4-HNE), product of lipid peroxide, was significantly decreased in the hydrogen saline treatment group, indicating that hydrogen saline protected hepatic parenchymal cells from I/R injury-induced peroxidation.

Hydrogen saline pretreatment induced HO-1 & Sirt1 expression in steatotic livers subjected to I/R injury.
In numerous studies, the high expression levels of HO-1 & Sirt1 can alleviate the ischemic injury.
Analogously, our results showed that mRNA levels of HO-1 was dramatically upregulated in steatotic livers pretreated hydrogen saline and subjected to 15 min ischemia and 3 hr reperfusion compared with steatotic livers and steatotic livers subjected to I/R injury at the same time, as shown in Fig. 2. The expression of Sirt1 was also significantly increased in steatotic livers pretreated hydrogen saline and subjected to 15 min ischemia and 3 hr reperfusion compared with steatotic livers subjected to I/R injury, moreover, compared with the steatotic livers treated with sham operation. mRNA expression of inflammatory cytokines reduced by hydrogen saline in steatotic livers subjected to I/R. We evaluated the expression of inflammatory cytokines by detecting the following indicators: tumor necrosis factor α (TNF-α), interleukin-6 (IL-6), nuclear factor kappa B (NF-κB), toll-like receptor 4 (TLR-4) and NOD-like receptor 3 (Nlrp3). In contrast to fatty liver sham operation group, there was a marginally (TNF-α and IL-6) or significantly (TLR-4 and Nlrp3) higher level of expression of all of the above factors by evaluating mRNA in the steatotic livers following 3 hr reperfusion after 15 min ischemia (Fig. 2). In the hydrogen saline-treatment group the expressions of the above factors were reduced, moreover, monocyte chemoattractant protein-1 (MCP-1/CCL2) was down-regulated significantly. Hydrogen saline regulated inflammatory cytokines, HO-1, Sirt1, TLRs, and nuclear translocation of NF-κB mRNA expression in KCs isolated from steatotic livers subjected to I/R injury. In order to make further investigation into the role of hydrogen saline-treatment in protecting steatotic livers during I/R injury, we evaluated the inflammatory cytokine mRNA expression in KCs isolated from different groups of steatotic livers. KCs were isolated from steatotic livers subjected to 15 min ischemia and 3 hr reperfusion, pretreated or not with hydrogen saline. The KCs with hydrogen saline pretreatment showed decreased mRNA expression of inflammatory cytokines, such as IL-6 and TNF-α, more than KCs from steatotic livers subjected to I/R injury for the same time. Hydrogen saline suppressed Nlrp3. Meanwhile, the values of HO-1 and Sirt1 mRNA expression in KCs from steatotic livers were increased, especially Sirt1 was obviously up-regulated, after hydrogen saline pretreatment compared to saline treatment. In addition, we observed the mRNA expression of TLR-4 and NF-κB to further investigate the TLR-4/NF-κB signaling pathway on KCs, which were down-regulated after hydrogen saline treatment in KCs from steatotic livers after I/R injury (Fig. 3). HO-1 and Sirt1 were upregulated both in KCs and liver homogenate, confirmed by qRT-PCR analysis that indicated that hydrogen saline significantly reduced hepatic inflammation, which was induced by activation of high expression of HO-1 and Sirt1 in KCs.
Hydrogen gas alleviated apoptosis by up-regulation of HO-1 & Sirt1 expression, corrected Bax/Bcl-2 ratio, and depressed the acetylation of p53 in steatotic hepatocytes isolated from steatotic livers subjected to hypoxia/reoxygenation. As shown in Fig. 4, we investigated the HO-1/Sirt1 signaling pathway in steatotic primary hepatocytes after hypoxia/reoxygenation. We observed that the protein expressions of HO-1 and Sirt1 were up-regulated after hydrogen gas treatment in primary hepatocytes from steatotic livers. We observed higher expression of Sirt1 in primary hepatocytes from steatotic livers when exposed to hypoxia/reoxygenation. In addition, hypoxia/reoxygenation up-regulated the expression of Bax and slightly down-regulated or maintained almost the same level of Bcl-2 compared to the control group, whereas treatment with hydrogen gas dramatically aggravated the changes in Bax expression. The Bax/Bcl-2 ratio increased in steatotic primary hepatocytes subjected to hypoxia/reoxygenation, but significantly decreased after hydrogen gas treatment. Furthermore, there was almost 2-fold increase in the level of cleaved caspase-3 in steatotic primary hepatocytes subjected to hypoxia/reoxygenation, compared to the steatotic primary hepatocytes group. In contrast, the protein level of cleaved caspase-3 markedly decreased in the hydrogen gas treatment group.
The protein p53 can be activated through acetylation in response to apoptosis and extracellular stimulation. After hypoxia/reoxygenation, the oxidative stress reaction in steatotic hepatocytes isolated from steatotic livers is essential for apoptosis. In our study, the acetylation level of p53 was measured. The analysis results of the proportion of proteins reflected that the acetylation level of p53 in steatotic hepatocytes increased after hypoxia/ reoxygenation, which was consistent with apoptosis. After administration of hydrogen gas, a decline in acetyl-p53 expression in steatotic hepatocytes was observed. All the results indicated that hydrogen gas inhibited the acetylation of p53, a critical protein responsible for mitigating cell apoptosis (Fig. 4).

Discussion
I/R has been considered as a major, unmodifiable risk factor for fatty liver transplantation. In a a previous study 16 , we established that the MCD diet induced a hepatic steatosis model. MCD has been widely used to induce steatosis in experimental models of fatty liver. There are some kinds of diet that can induce a fatty liver mouse model, such as a high-fat diet and MCD diet. If we use a high-fat diet, steatosis and inflammation will be observed at 12-16 weeks 17 . However, in the MCD diet mouse model, fatty liver and inflammation were induced by the administration of a MCD diet in just 3 weeks. From the viewpoint of time and effect, we chose the MCD diet to establish the fatty liver mouse model. The purpose of our study was to test the protective effect of molecular hydrogen (including hydrogen-rich saline and hydrogen gas) preconditioning on I/R injury of fatty liver in vivo and hypoxia/reoxygenation-induced injury on primarily cultured fatty hepatocytes in vitro.
Molecular hydrogen acts as a novel medical application. In addition to hydrogen, nitric oxide (NO) and carbon monoxide (CO), which offer cytoprotection against cellular stress, have drawn attention 18 . The molecular hydrogen exerts cytoprotective effects in the nervous, cardiovascular, and digestive systems [19][20][21] . In the present study, hepatic protection by molecular hydrogen was investigated in a fatty liver mouse I/R model in vivo and hypoxia/ reoxygenation-induced injury in a fatty hepatocyte in vitro model. Notably, hydrogen saline exerted marked hepatic protection by preventing hepatocyte death and inhibiting macrophage recruitment compared with mice treated with saline alone (Fig. 1). Furthermore, its application impeded hypoxia/reoxygenation-induced damage in fatty hepatocytes (Fig. 4). During ischemia/hypoxia and subsequent reperfusion/reoxygenation, a large number of harmful substances are produced from the activated KCs, such as pro-inflammatory cytokines, and induce hepatocyte apoptosis.
KCs are considered to make an important contribution to the whole process of hepatic I/R injury. The initial stages of reperfusion produce dramatic morphological changes on activated KCs and impel them to extend into the sinusoids 22 . Activated KCs are major contributors to not only release of large amounts of cytokines, but also intracellular oxidative species (ROS) 23 . Evidence suggests that there is liver parenchymal cell injury in the hypoxic phase of the I/R injury process. The pharmacological preconditioning with the hepatic protection from pharmaceutical preparations against hepatic I/R injury by inactivation of KCs has been reported. For instance, Mosher et al. 24 reported that gadolinium chloride relieves liver cell damage caused by hepatic I/R by inhibiting KC activity. In the present study, treatment with molecular hydrogen resulted in significantly increased HO-1 expression both in liver homogenate and KCs isolated from fatty liver that underwent I/R injury (Figs 2 and 3). Moreover, the proinflammatory cytokines TNF-α and IL-6 expression levels were much lower, not only in the groups with I/R injury to the liver and treated with hydrogen saline, but also in the KCs isolated from fatty liver, than those in the no-treatment groups. These data indicated that molecular hydrogen alleviated hepatic I/R injury by attenuating KC activation and possibly the expression of co-stimulatory molecules. This further confirmed the key role of KCs in the process of liver I/R injury. Moreover, this finding clearly shows that the molecular hydrogen attenuates liver I/R injury by reducing the activation of KCs, although other types of non-parenchymal cells in the liver that undergo I/R injury were not examined here.
There is growing evidence suggesting that the protective effect of molecular hydrogen is not only interrelated with simple elimination of oxygen free radicals, but also associated with various intercellular signals 25,26 . Kawamura et al. 27 reported that molecular hydrogen gas ameliorated lung injury by promoting expression of Nrf2 and contributing to HO-1 expression. Cai et al. 28 revealed that molecular hydrogen therapy relieved TNF-α induced rat osteoblast inflammatory injury via downregulation of the NF-κB pathway. Furthermore, there is also evidence indicating that molecular hydrogen reduced lung injury induced by transplantation by inducing elevated expression of HO-1 27 . In the present study, hydrogen saline exposure was found to markedly increase the expression of HO-1 in vivo. The mechanism of HO-1 in hypoxia/reoxygenation-induced hepatic insult (e.g., apoptosis) was further elucidated using in vitro study.
Apoptosis and necrosis are common reactions in liver when sustaining injuries induced by ischemia, radiation, and poisonous substances [29][30][31] . The liver and especially the hepatic parenchymal cells are sensitive to the damage caused by I/R injury 32,33 . In I/R injury, the oxidative damage to the enzyme complexes, and anti-apoptotic proteins, decrease apoptosis 34 . Inhibition of the caspase family notably attenuated liver injury caused by I/R, indicating that apoptosis plays an important role in I/R injury 35 . The hepatocyte apoptosis leads to elevated AST and ALT levels and further reduction of liver function 36 . Our investigations in vitro and in vivo support this, as seen with I/R-induced hepatocellular apoptosis by TUNEL staining (Fig. 1). The apoptotic hepatocytes were significantly increased after I/R injury, which is consistent with the results of other studies of hepatic damage after I/R 37 . The pretreatment with hydrogen saline could improve this situation. The depressed serum levels of the liver-associated transaminases ALT and AST in the group of I/R injury treated with hydrogen saline (Fig. 1) revealed that molecular hydrogen is a critical attenuator of I/R-induced hepatocyte apoptosis. A variety of molecules are involved in the regulation of apoptosis, including pro-apoptotic factor Bax and anti-apoptotic factor Bcl-2 38 . In steatosis hepatocytes sustaining hypoxia/reoxygenation injury, Bax expression was significantly increased and the expression of Bcl-2 was decreased dramatically. The hydrogen gas effectively suppressed the expression of Bax and was associated with activation of cleaved caspase-3. Meanwhile, it also promoted the expression of Bcl-2 (Fig. 4). In summary, the protective effect of molecular hydrogen against I/R was achieved by inhibiting the factors stimulating apoptosis.
HO-1, an important rate-limiting enzyme, contributes to heme degradation and produces biliverdin and CO. CO has anti-apoptotic and anti-inflammatory properties as well as cytoprotective effects 16 . Sirt1 is one kind of NAD-dependent protein deacetylase. It helps to regulate cytosolic metabolism and ameliorate ROS-caused apoptosis 39 . In the liver, it has been reported that Sirt1 has a hepatoprotective effect by reducing fibrosis 40 . However, the protective effect of molecular hydrogen by inducing the HO-1/Sirt1 expression in hepatocytes has not been detected until now. HO-1 is known to induce the Sirt1 expression by activating PGC-1α/ERRα 41 . Therefore, we conjectured that the anti-apoptosis effects of molecular hydrogen might be regulated by elevating HO-1-mediated induction of high expression of Sirt1. Consistent with our in vitro data that hydrogen gas could up-regulate the expression of Sirt1 in fatty hepatocytes, we presented the data that treatment with hydrogen saline induced the expression of Sirt1 in fatty liver. Animal studies showed that, after hydrogen saline treatment, a marked increase of HO-1 expression in the liver occurred. Furthermore, in the in vitro study, fatty hepatocytes exposed to hypoxia/ reoxygenation exhibited an increase in the signs of apoptosis compared with normoxia; this situation was inhibited by hydrogen gas preconditioning. In addition, p53 (one of the substrates of Sirt1) is capable of binding to Sirt1 to cause deacetylation of the lysine residue in the C-terminal domain, resulting in lowering the ability of p53 to activate downstream genes, and ultimately reduces apoptosis 42 . HO-1 induces Sirt1 expression, and meanwhile, Sirt1 up-regulates tumor suppressor protein alternative reading frame (Arf) inhibited activity of p53 in macrophage-regulated hepatic sterile inflammation 43 . Our results showed that the acetylation of p53 was significantly increased in the I/R injury group, after molecular hydrogen treatment p53 acetylation was decreased, at the same time the anti-apoptotic protein Bcl-2 expression was increased, and pro-apoptotic protein Bax expression was decreased. As the data have shown, we demonstrated that the major modulator of the deacetyation of p53 is the activation of Sirt1, which in turn affects the inflammatory response and apoptosis of the affected tissue. We found that preconditioning with hydrogen gas could enhance HO-1/Sirt1 expression and reduce the expression of Bax, acetylation of p53, and cleaved caspase-3, and subsequently affect the hepatocyte apoptosis. In summary, from our data we showed a mechanism of molecular hydrogen protection against I/R-induced liver injury or hypoxia/reoxygenation-induced apoptosis of hepatocytes (Fig. 5). The protective effect of molecular hydrogen among HO-1, Sirt1, and activation of the p53 axis is by the following model. HO-1 positively regulates expression of Sirt1, while HO-1 and Sirt1 attenuates KC activation. Sirt1 inhibits activity of the p53 pathway by directly inducing apoptosis regulator Bcl-2 and by inhibiting transcription of Bax and activation of cleaved caspase-3.
Taken together, our results provide the therapeutic strategies to inhibit I/R-induced liver injury and hypoxia/ reoxygenation-induced hepatocyte apoptosis via HO-1/Sirt1 activation using molecular hydrogen. Unfortunatoly this study has limination, because we use warm ischemia/reperfusion model without transplantation instead of cold ischemia/reperfusion model with transplantation. Therefore, the further examination using animal liver transplantation model should be needed to ensure the result of this study. In conclusion, molecular hydrogen may act as a potential therapeutic agent to ameliorate ischemia reperfusion injury caused by hepatic surgery or liver transplantation with steatosis.

Materials and Methods
Animals. Eight-week-old male C57BL/6 (B6) mice, purchased from Shizuoka Laboratory Animal Center (Shizuoka, Japan), were raised in a feeding room with automatically controlled light and temperature. Mice were cared for in agreement with the guidelines of the Institutional Animal Care and Use Committee and in agreement with National Research Institute for Child Health and Development guidelines on laboratory animal welfare.

Grouping of animals and experimental protocol.
In order to establish the steatotic liver model, mice were fed with the methionine, choline-deficient plus high fat (MCDHF) diet for 21 days. To be specific, MCDHF contains 25% oil, 20% sugar, and 55% MCD. We chose 15 min ischemia followed by 3 hr reperfusion when performing animal experiments, as described previously 44 . The mice were randomly divided into 3 groups (n = 10, each group), as follows: (1) MCDHF group:fatty liver mice with sham operation; (2) MCDHF I/R group: fatty liver mice pre-treated with saline before I/R, then sacrificed after 3 hr reperfusion; 1 ml saline spreaded on the liver after clipping hepatic portal vein with a microvascular clamp for ischemia; (3) MCDHF I/R + HS group: fatty liver mice treated with hydrogen saline before I/R, then sacrificed after 3 hr reperfusion. 1 ml 7 ppm hydrogen saline spreaded on the liver after clipping hepatic portal vein with a microvascular clamp for ischemia.

Preparation of hydrogen saline.
A solution of high-concentration, hydrogen-rich saline (7 ppm) was prepared as described previously 45 . In brief, using a hydrogen-generating agent (MiZ Co. Ltd. Kanagawa, Japan) including metallic aluminium grains and calcium hydroxide, 0.5 g of the mixture was enclosed within a nonwoven fabric and heat-sealed. Hydrogen-generating agent was inserted into a small bottle, 1 mL of pure water was added, and a cap with a check valve was placed and then tightly closed. The one-way valve bottle was inserted into a 500 mL bottle filled with 5% physiological saline. We obtained 7 ppm hydrogen saline after rocking vigorously for 5 min and storing at 4 °C for 24 hr.
Establishment of model of hepatic ischemia reperfusion in steatotic liver. The model of hepatic I/R in steatotic liver was established according to previous works 16, 44 . In particular, the steatotic liver mice ischemia was subjected by occluding the hepatic portal vein with a microvascular clamp for 15 mins followed by Histopathological examination. Liver tissue was harvested for histopathological examination. In detail, the specimens of liver tissue were fixed in 10% formalin, routinely processed, and sliced into sections 4 μm thick. The severity of necrosis in steatotic liver (percentage of necrotic area) was checked by hemotoxylin-eosin (HE) staining and quantified by WinRoof V.6.1 software (Mitani Corporation, Tokyo, Japan).
Immunohistochemical examination of tissue sections. Immunohistochemistry was performed on paraffin sections by using monoclonal antibody against F4/80 and polyclonal antibody against 4-HNE (Abcam, Cambridge, MA). After immunohistochemical staining, specimens were photographed under a microscope (Olympus, Tokyo, Japan).

TUNEL assay.
To measure hepatocyte apoptosis, the TUNEL assay was performed on liver paraffin sections to label the 3′-end of fragmented DNA by an apoptosis detection kit according to the manufacturer's instructions (Chemicon International, Inc. Billerica, MA).
Serum AST and ALT enzyme activity. Whole blood samples were harvested by routine processing after 15 min ischemia and 3 hr reperfusion. Serum was collected from blood samples after standing for 40 min at 25 °C and then centrifuged at 1800 × g for 20 min at 4 °C. The serum was then evaluated for AST and ALT (values expressed as U/L). AST and ALT measurements were performed by using commercially available kits (Fujifilm, Tokyo, Japan) and an automatic biochemical analyzer (DRI-CHEM 3500i, Fujifilm) according to the manufacturer's instructions.

RNA preparation and qRT-PCR analysis. RNA was extracted from frozen tissues using the RNeasy Mini
Kit (Qiagen, Valencia, CA). Each 0.8 μg aliquot of RNA was reverse transcribed to cDNA using the Prime Script RT reagent Kit (RR037A, Takara, Japan). Quantitative RT-PCR was performed using the primer/probe sets system (the sequences are listed in Table 1) on the Applied Biosystem PRISM7900 (ABI Japan, Co. Ltd. Tokyo, Japan). The conditions of PCR cycles were 50 °C for 2 min, 95 °C for 15 min, 40 cycles of 95 °C for 30 s, 60 °C for 1 min, and 25 °C for 2 min. The ΔΔCt method was used for the relative expression, and the results were normalized by subtracting the 18 S expression.
Fatty primary hepatocyte culture and establishment of the hypoxia/reoxygenation, hydrogen gas, and hypoxia/reoxygenation plus hydrogen gas conditions. Primary hepatocytes were isolated from the mouse fatty liver. Hepatocytes containing fat droplets were incubated in a 5% CO 2 atmosphere and cultured in Dulbecco's Modified Eagle's Medium (DMEM, GIBCO, UK) with 10% fetal bovine serum (FBS, GIBCO). The cells were cultured at 37 °C under hypoxic conditions (1% O 2 , 5% CO 2 , and N 2 as the base gas) in a modulator incubator chamber. Reoxygenation was obtained by replacing the cells in normal culture conditions. The hydrogen gas condition consisted of 21% O 2 , 5% CO 2 , 3.8% H 2 , and N 2 as the base gas in a modulator incubator chamber (Billups-Rothenberg Inc. Del Mar, CA). The hypoxia/reoxygenation plus hydrogen gas condition consisted of 1% O 2 , 5% CO 2 , 3.8% H 2 , and N 2 as the base gas for the hypoxia plus hydrogen gas phase and 21% O 2 , 5% CO 2 , 3.8% H 2 , and N 2 as the base gas for the reoxygenation plus hydrogen gas phase; all were contained in a modulator incubator chamber. After adjusting the concentration of gas, the modulator incubator chamber was placed in a 37 °C incubator.
In vitro experimental design. The primary hepatocytes bearing fat droplets isolated from steatotic liver were randomly divided into four groups as follows: Group 1: Control group, fatty primary hepatocytes; Group 2: Hydrogen gas group, fatty primary hepatocytes treated 10 hr with hydrogen gas; Group 3: Hypoxia/reoxygenation group, fatty primary hepatocytes subjected to 4 hr of hypoxia and 6 hr of reoxygenation; Group 4: Hypoxia/reoxygenation + hydrogen gas group, fatty primary hepatocytes treated with hydrogen gas plus hypoxia/reoxygenation.
Effects of hydrogen saline on inflammation and cytotoxicity in KCs isolated from steatotic liver after I/R injury. Perfusion solution was delivered to the portal vein of the anesthetized steatotic mouse liver, then the inferior vena cava was cut immediately to establish the perfusion circulatory pathway, and the speed was set at 3 mL/min. Collagenase solution replaced the liver perfusion solution after 5 min perfusion, and the collagenase solution perfusion continued for 8 min at the same speed. After collagenase continued the digestion, the liver was removed to a sterilized 100 mm culture dish, and then was ground to form a homogenate. The liver homogenate was re-suspended in culture medium, and passed through a 70 μm filter for removing undigested clots. Cell suspensions were centrifuged at 720 × g (Beckman Coulter Allegra X-12R, Indianapolis, IN) for 7 min at 4 °C. The top aqueous phase was discarded and the cell sediments were reserved. Cell sediments were re-suspended in 30 mL DMEM and centrifuged at 720 × g for 7 min at 4 °C, the aqueous phase was discarded, and the cell sediments were reserved. Cell sediments were re-suspended in 10 mL GBSS-B and mixed with 14 mL GBSS-A containing Nycodenz, and then centrifuged (1900 × g, 20 min, 4 °C). Harvested cells of the white layer were re-suspended in 30 mL GBSS-B and centrifuged (50 × g, 7 min, 4 °C). The top aqueous phase was transferred into a 50 mL tube and centrifuged (720 × g, 7 min, 4 °C). The cell sediments were seeded into a 6-well plate at the density of 1 × 10 7 /well in DMEM medium with 10% FBS and 100 U/mL penicillin/streptomycin and incubated in a 5% CO 2 incubator at 37 °C. Four hours later, non-adherent cells were removed by washing twice with PBS; the adherent cells were KCs.
The total RNA was extracted from KCs, reverse transcribed to cDNA, and detected by qRT-PCR.
Effects of hydrogen gas on anti-apoptosis in fatty hepatocytes isolated from steatotic liver subjected to hypoxia/reoxygenation. The method of liver perfusion and digestion was the same as for the KCs. The liver homogenate was re-suspended in culture medium, and passed through a 100 μm filter for removing undigested clots. Cell suspensions were centrifuged at 80 × g (Beckman Coulter Allegra X-12R) for 1 min at 4 °C. The top aqueous phase was discarded and the cell sediments were reserved. Cell sediments were re-suspended in 30% Percoll and centrifuged at 80 × g for 5 mins at 4 °C, the aqueous phase was discarded, and the cell sediments were reserved. Cell sediments were re-suspended with 45% Percoll and centrifuged at 80 × g for 2 mins at 4 °C. The top aqueous phase was mixed with 2 folds of DMEM and transferred to a 50 mL tube and centrifuged (80 × g, 1 min, 4 °C). The cell sediments were seeded into a 6-well plate at the density of 1 × 10 6 /well in DMEM medium with 10% FBS and 100 U/mL of penicillin/streptomycin and incubated in a 5% CO 2 incubator at 37 °C. Twenty-four hours later non-adherent cells were removed by washing twice with PBS; the adherent cells were fatty hepatocytes. Then the total RNA was extracted from fatty hepatocytes, reverse transcribed to cDNA and detected by qRT-PCR. The protein of fatty hepatocytes was disintegrated by radioimmunoprecipitation assay (RIPA) lysis buffer and stored in liquid nitrogen for western blot analysis.
Western blot analysis. Proteins from fatty hepatocytes were homogenized with RIPA lysis buffer (Wako, Osaka, Japan) containing phosphatase inhibitor cocktail and protease inhibitor cocktail. Proteins were blotted onto PVDF membranes (Bio-Rad, Hercules, CA). The membranes were incubated with appropriate primary antibodies overnight at 4 °C after being blocked with skim milk for 1 hr at room temperature. Afterwards, the membranes were washed three times with TBST and incubated with secondary antibodies for 1 hr at room temperature. The blots were visualized by enhanced chemiluminescence. The primary antibodies were as follows: Statistical analysis. Data were presented as means ± SEM (means with standard errors) and analyzed statistically by a one-way ANOVA followed by Student's t-test. A value of p < 0.05 was considered to be statistically significant.