key: cord-0002703-tos0t3e8
authors: Wu, Dongdong; Luo, Ning; Wang, Lianqu; Zhao, Zhijun; Bu, Hongmin; Xu, Guoliang; Yan, Yongjun; Che, Xinping; Jiao, Zhiling; Zhao, Tengfu; Chen, Jingtao; Ji, Ailing; Li, Yanzhang; Lee, Garrick D.
title: Hydrogen sulfide ameliorates chronic renal failure in rats by inhibiting apoptosis and inflammation through ROS/MAPK and NF-κB signaling pathways
date: 2017-03-28
journal: Sci Rep
DOI: 10.1038/s41598-017-00557-2
sha: f9700deed61ea92d41891cf29eccddac0ee0ca15
doc_id: 2703
cord_uid: tos0t3e8

Chronic renal failure (CRF) is a major public health problem worldwide. Hydrogen sulfide (H(2)S) plays important roles in renal physiological and pathophysiological processes. However, whether H(2)S could protect against CRF in rats remains unclear. In this study, we found that H(2)S alleviated gentamicin-induced nephrotoxicity by reducing reactive oxygen species (ROS)-mediated apoptosis in normal rat kidney-52E cells. We demonstrated that H(2)S significantly improved the kidney structure and function of CRF rats. We found that H(2)S decreased the protein levels of Bax, Caspase-3, and Cleaved-caspase-3, but increased the expression of Bcl-2. Treatment with H(2)S reduced the levels of malondialdehyde and ROS and increased the activities of superoxide dismutase and glutathione peroxidase. H(2)S significantly abolished the phosphorylation of extracellular signal-regulated protein kinase 1/2, c-Jun N-terminal kinase, and p38 in the kidney of CRF rats. Furthermore, H(2)S decreased the expression levels of tumor necrosis factor-α, interleukin (IL)-6, IL-10, and monocyte chemoattractant protein-1, as well as the protein levels of p50, p65, and p-p65 in the kidney of CRF rats. In conclusion, H(2)S could ameliorate adenine-induced CRF in rats by inhibiting apoptosis and inflammation through ROS/mitogen-activated protein kinase and nuclear factor-kappa B signaling pathways.

Animals. Twenty-four male Wistar rats (7-9 weeks old), initially weighing 180-220 g, were purchased from the Nanjing Biomedical Research Institute of Nanjing University (Jiangsu, China). Rats were housed in individual ventilated cages under standard temperature (22 ± 2 °C), humidity (50-60%), and light conditions (12-hour light/dark cycle) with food and water ad libitum. Rats were allowed to acclimatize to new surroundings for 1 week before the experiment began. CRF was induced with 0.2% adenine mixed with powdered food for 4 weeks. A normal renal function control group was also allocated. The rats from control and CRF groups received an intraperitoneal (i.p.) injection of saline and the rats from the CRF+H 2 S group received an i.p. injection of NaHS (100 μmol/kg/day, dissolved in saline) 26 . Treatments with saline and NaHS were concomitant to adenine-induced CRF for 4 weeks. During the treatment periods, the rats were weighed weekly and the food intake, water intake, and urine volume were measured in 24 h. At the end of experiments, the rats were killed and the plasma was collected. Tissues were rapidly removed, weighed and thoroughly washed with ice-cold saline. Then the tissues were frozen in liquid nitrogen or immersed in 4% neutral buffered formalin or embedded in FSC 22 frozen section compound (Leica, Buffalo Grove, IL, USA). Plasma samples and frozen tissues were stored at −80 °C. Histological analysis. The renal tissues were fixed in formalin, embedded in paraffin, and cut into 5-μm-thick sections which were then stained with hematoxylin and eosin (HE) and Masson's trichrome (MT).

Scientific RepoRts | 7: 455 | DOI: 10 .1038/s41598-017-00557-2

The histopathological score was obtained based on the loss of brush border, grading of tubular necrosis, tubular dilatation, and cast formation in six randomly chosen, non-overlapping fields as follows: 0 (none), 1 (≤10%), 2 (11-25%), 3 (26-45%), 4 (46-75%), and 5 (≥76%) 27 . The extent of renal interstitial fibrosis (RIF) was scored from 0 to 3 as follows: 0 = absent, 1 = less than 25% of the area, 2 = 25-50% of the area, and 3 = more than 50% of the area. The RIF index was obtained by the following formula: RIF index = (0 × n 0 + 1 × n 1 + 2 × n 2 + 3 × n 3)/(n 0 + n 1 + n 2 + n 3) × 100% 28 . All specimens were anonymized and evaluated in a blinded manner. The sections were observed with an Olympus BX51 microscope (Olympus, Tokyo, Japan) and analyzed by ImageJ software (National Institutes of Health, Bethesda, MD, USA). Biochemical analysis. Blood urea nitrogen (BUN), creatinine (Cre), and urinary protein (UP) were measured using Beckman Coulter AU5800 (Beckman Coulter Inc., Brea, CA, USA). The levels of white blood cell (WBC), red blood cell (RBC), hemoglobin (HGB), and hematocrit (HCT) were determined by Mindray BC-6900 (a) The cell proliferation was determined by EdU assay. The proliferative cell nuclei were stained by EdU assay with red, and all nuclei were stained by DAPI with blue (original magnification, ×100). (b) The cell proliferation rate was calculated. (c) The cell viability was detected by MTS assay. Values were presented as mean ± SEM (n = 6); *P < 0.05, **P < 0.01 compared with the control group; # P < 0.05, ## P < 0.01 compared with the GEN group.

Effects of H 2 S on the intracellular ROS production and apoptosis in GEN-treated NRK-52E cells. (a) The intracellular ROS production was detected using the fluorescent probe DCF-DA (shown in green; original magnification, ×100). (b) The cell apoptosis was determined by TUNEL assay. Apoptotic cell nuclei were stained by TUNEL assay with red, and all nuclei were stained by DAPI with blue (original magnification, ×100). (c) The intracellular ROS production was measured. (d) The apoptotic index was calculated. Values were presented as mean ± SEM (n = 6); *P < 0.05, **P < 0.01 compared with the control group; # P < 0.05, ## P < 0.01 compared with the GEN group. auto hematology analyzer (Mindray, Shenzhen, Guangdong, China). Monocyte chemoattractant protein (MCP)-1, tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-10 in kidney tissues were determined using commercial ELISA kits (Elabscience, Wuhan, Hubei, China) according to the manufacturer's protocols.

Western blot analysis. Renal tissues were homogenized in RIPA lysis buffer (Sigma, St. Louis, MO, USA). Protein concentrations of the homogenates were measured by the BCA protein assay kit (Beyotime Institute of Biotechnology, Shanghai, China). The extracted proteins (50 μg) were separated on SDS-PAGE gel and transferred to a PVDF-nitrocellulose membrane. After blocking, the membranes were incubated with primary antibodies to detect the target proteins. Anti-extracellular signal-regulated protein kinase 1/2 (ERK1/2), anti-phospho (p)-ERK1/2 (Thr202/Tyr204), anti-c-Jun N-terminal kinase (JNK), anti-p-JNK (Thr183/Tyr185), anti-p38, anti-p-p38 (Thr180/Tyr182), anti-p50, anti-p65, and anti-p-p65 (Ser536) antibodies were purchased from Cell Signaling Technology (Danvers, MA, USA). Anti-Bax, anti-Bcl-2, anti-Caspase-3, anti-Cleaved Caspase-3, and anti-β-actin antibodies were purchased from ProteinTech (Chicago, IL, USA). The horseradish peroxidase-conjugated secondary antibody was purchased from Cell Signaling Technology. The reaction was visualized using an enhanced chemiluminescence system (Thermo Fisher Scientific, Rockford, IL, USA). The bands were quantified by densitometry using ImageJ software.

Measurement of oxidative stress products. The kidney tissues were placed in cold physiological saline, homogenized with a homogenizer machine (Scientz Biotechnology Co., Ltd., Ningbo, Zhejiang, China), and then centrifuged at 1000 g for 10 min to produce the supernatant fluid. The levels of malondialdehvde (MDA) and ROS, as well as the activities of glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD) were measured using commercial kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, Jiangsu, China) according to the manufacturer's instructions. Statistical analysis. All results were presented as the mean ± standard error of the mean (SEM). Statistical differences were analyzed by one-way analysis of variance (ANOVA) using SPSS 17.0 software, followed by LSD post hoc test. A P value of less than 0.05 was considered to be statistically significant.

As revealed by the EdU assay, the incubation of NRK-52E cells with GEN (3 mM) led to a significant reduction in cell proliferation (Fig. 1a,b) . By contrast, administration of H 2 S induced a significant increase in cell viability, compared with the GEN group. Furthermore, as shown in Fig. 1c , GEN decreased the cell viability, while H 2 S treatment significantly increased the cell viability. Collectively, these data demonstrate that H 2 S could effectively relieve GEN-induced cytotoxicity in NRK-52E cells.

tosis is a key nephrotoxic mechanism in GEN-treated NRK-52E cells 22 . ROS have been considered important mediators of GEN-induced apoptosis. ROS generation is often involved in the mitochondrion-mediated signaling The extent of the renal lesions was represented by the RIF index. Values were presented as mean ± SEM (n = 6); **P < 0.01 compared with the control group; # P < 0.05, ## P < 0.01 compared with the CRF group.

pathway of apoptosis 29 . Compared with the control group, ROS generation increased 5.8-fold in GEN group, and H 2 S significantly reduced ROS generation by 3.8-fold compared with the GEN group (Fig. 2a,c) . In addition, apoptotic index increased 21.8% in GEN group compared with the control group and decreased 13.4% in the GEN+H 2 S group compared with the GEN group (Fig. 2b,d) . These results indicate that H 2 S could alleviate GEN-induced nephrotoxicity by reducing ROS production and apoptosis in NRK-52E cells. were detected by Western blot. β-actin was used as an internal control. Bar graphs showed the quantification of Bax (b), Bcl-2 (c), Caspase-3 (d), and Cleaved Caspase-3 (e). Values were presented as mean ± SEM (n = 3); *P < 0.05, **P < 0.01 compared with the control group; # P < 0.05, ## P < 0.01 compared with the CRF group.

Scientific RepoRts | 7: 455 | DOI:10.1038/s41598-017-00557-2 H 2 S improves general status of CRF rats. As shown in Fig. 3a ,b, in comparison with the control group, CRF rats exhibited decreased food intake and increased water intake, H 2 S treatment significantly reversed these changes. A trend in the decrease of body weight in CRF rats, which was altered by H 2 S, has been observed (Fig. 3c ). In addition, CRF rats showed increased relative kidney weight, urine volume, and urinary protein when compared with the control group, which were dramatically reversed by H 2 S treatment ( Fig. 3d-f ). In sum, these results show that H 2 S could significantly improve the general status of the rats with adenine-induced renal damage.

H 2 S enhances the kidney function of CRF rats. Plasma BUN and Cre are the most commonly used markers of kidney function in clinical practice 30, 31 . The concentrations of BUN and Cre and WBC count were significantly increased whereas HGB, HCT, and RBC count were dramatically decreased in CRF group compared to the control group (Fig. 4) . These results indicate that the rat model exhibited typical pathologic features associated with CRF. Compared with the CRF group, the CRF+H 2 S group showed remarkably lower Cre and BUN levels and WBC count and significantly higher HGB, HCT, and RBC count (Fig. 4) . These results demonstrate that the kidney function of CRF rats could be effectively enhanced by administration of H 2 S. H 2 S ameliorates renal injury in CRF rats. Figure 5 showed representative photomicrographs of the HE and MT stainings of the kidney tissues from the control, CRF, and CRF+H 2 S groups. There were no signs of damage in the control group. The kidney tissues of CRF rats showed severe renal injury marked by severe interstitial inflammatory cell infiltration, tubular dilation and atrophy, as well as fibrosis. These results indicate that the rat model exhibited the typical pathological features associated with CRF, which were consistent with previous studies 32, 33 . The severity of renal injury in rats with CRF was significantly ameliorated by treatment with H 2 S. H 2 S reduces apoptosis level in the kidney of CRF rats. Cell apoptosis can be widely detected in CRF patients and inhibition of apoptosis could delay the progress of CRF and reduce the occurrence of related complications 7 . Compared to the control group, the protein expression levels of Bax, Caspase-3, and Cleaved-caspase-3 were dramatically increased in the kidney of CRF rats (Fig. 6a,b,d,e) . In contrast, the protein expression of Bcl-2 in CRF group was significantly lower than that in the control group (Fig. 6a,c) . The protein expressions of Bax, Caspase-3, and Cleaved-caspase-3 were remarkably reduced in CRF+H 2 S group, in comparison with CRF group (Fig. 6a,b,d,e) . In addition, the protein expression of Bcl-2 increased significantly in CRF+H 2 S group (Fig. 6a,c) . These findings suggest that the apoptosis level is increased in the kidney of CRF rats, which could be reversed by administration of H 2 S. H 2 S abates oxidative stress in the kidney of CRF rats. A recent study showed that adenine treatment significantly depressed total antioxidant capacity in the kidney of rats 33 . To observe the effect of H 2 S on oxidative stress induced by adenine, the activities of antioxidant enzymes, MDA generation, and ROS accumulation were determined. As shown in Fig. 7 , the levels of MDA and ROS were markedly increased, and the activities of SOD and GSH-Px were significantly decreased compared with the control group, which were all reversed by treatment with H 2 S. These results indicate that H 2 S could abate adenine-induced oxidative stress in the kidney of CRF rats.

MAPK signaling pathway mediates a number of cellular activities in response to extracellular stimuli such as heat and stress 34 . ERK1/2, JNK, and p38 are three major components of MAPK which play important roles in cell migration and apoptosis 35, 36 . As shown in Fig. 8 , CRF triggered the phosphorylation of p38, JNK, ERK with distinct patterns. However, administration of H 2 S significantly abolished the increase of MAPKs phosphorylation induced by CRF, suggesting that H 2 S could reduce the apoptosis level in the kidney of CRF rats through MAPK signaling pathway.

H 2 S alleviates renal inflammation in CRF rats. Adenine treatment could induce a highly significant increase in plasma concentrations of some inflammatory cytokines, such as TNF-α and interleukin-1 beta (IL-1β) 33 . Whether H 2 S could reduce renal inflammation in CRF rats remains unknown. In this study, the inflammatory cytokine levels in the kidney were determined using ELISA techniques. Compared with the control group, the expression levels of TNF-α, IL-6, IL-10, and MCP-1 were significantly increased. Treatment with H 2 S remarkably decreased the levels of TNF-α, IL-6, IL-10, and MCP-1 (Fig. 9) , suggesting that H 2 S could effectively alleviate renal inflammation in CRF rats. Figure 9 . Effects of H 2 S on the cytokine levels in the kidney of CRF rats were assayed using ELISA techniques. The expression levels of TNF-α (a), IL-6 (b), MCP-1 (c), and IL-10 (d) were measured. Values were presented as mean ± SEM (n = 8); *P < 0.05, **P < 0.01 compared with the control group; ## P < 0.01 compared with the CRF group.

Scientific RepoRts | 7: 455 | DOI:10.1038/s41598-017-00557-2 H 2 S decreases the expression of NF-κB in the kidney of CRF rats. NF-κB is a transcription factor that plays an important role in regulating the expression of cytokine genes involved in several inflammatory diseases, including diabetes, atherosclerosis, and metabolic syndrome 37 . The most abundant form of NF-κB is the heterodimer composed of p50 and p65 38, 39 . In the present study, the protein expressions of p50, p65, and p-p65 in the kidney of rats were measured to investigate the underlying mechanism of H 2 S on the cytokine regulation. Compared with the control group, the protein expressions of p50, p65, and p-p65 and the p-p65/p65 ratio were significantly increased (Fig. 10) . Treatment with H 2 S remarkably decreased the expression levels of p50, p65, and p-p65, as well as the ratio of p-p65/p65 in the kidney of CRF rats (Fig. 10) , indicating that H 2 S could reduce kidney inflammation induced by CRF through the down-regulation of NF-κB expression. Figure 10 . Effects of H 2 S on the NF-κB pathway in the kidney of CRF rats. (a) The expression levels of p50, p65, and p-p65 were detected by Western blot. β-actin was used as an internal control. Bar graphs showed the quantification of p50 (b), p65 (c), p-p65 (d), and p-p65/p65 (e). Values were presented as mean ± SEM (n = 3); *P < 0.05, **P < 0.01 compared with the control group; # P < 0.05, ## P < 0.01 compared with the CRF group.

H 2 S has recently been recognized as an endogenous gaseous signaling molecule, along with nitric oxide and carbon monoxide 8-10, 15, 28 . A growing body of evidence indicates that H 2 S plays important and complex roles in renal physiological and pathophysiological processes 11, 13, 14 . The NRK-52E cell line has been widely used in in vitro models for studying GEN-induced nephrotoxicity [20] [21] [22] . Our results showed that H 2 S treatment significantly increased the viability and proliferation of the GEN-treated NRK-52E cells. Inducing apoptosis is an important nephrotoxic mechanism of GEN in NRK-52E cells 22 . The results indicated that H 2 S dramatically decreased the apoptotic index in GEN-treated NRK-52E cells. An increasing number of evidence indicates that ROS are important mediators of GEN-induced apoptosis 20 . H 2 S treatment significantly reduced ROS generation in GEN-treated NRK-52E cells. These results together suggest that H 2 S could alleviate GEN-induced nephrotoxicity by reducing ROS-mediated apoptosis in NRK-52E cells.

Currently, there are two experimental animal models for CRF, namely the chemical model (using adenine in the food) and the surgical model (5/6 remnant kidney model, or renal mass reduction model) 23 . Adenine-induced CRF avoids the potential complications of alternative techniques that require surgery to induce chronic kidney disease 40 . In addition, this method produces more pronounced reductions in glomerular filtration rate compared with the model of 5/6 nephrectomy 41 . Thus, adenine-induced CRF in rats was adopted as a disease model for the evaluation of the effect of H 2 S on CRF. The results showed that the rats fed on the adenine diet for 4 weeks showed increased water intake, urine production, urinary protein, and relative kidney weight, which were similar to the signs and symptoms in rats with adenine-induced CRF 41, 42 . In addition, a previous study has reported a reduction in body weight in adenine-fed rats which could be attributed to the reduced food consumption 43 . Our results were in good accordance with the findings. Administration of H 2 S effectively ameliorated all the above adenine-induced changes.

BUN and Cre are the most commonly used markers for detecting nephrotoxicity in traditional clinical pathology 44 . Treatment with H 2 S significantly decreased the levels of BUN and Cre, suggesting that H 2 S could reduce nephrotoxicity in CRF rats. Another common complication of CRF is anemia which often contributes to poor functional status and quality of life for CRF patients 40 . The RBC, HGB and HCT values of CRF rats were significantly lower than those of the control group, confirming that anemia had developed in our animal model of CRF. Our results showed that H 2 S was able to reduce the extent of anemia observed in rats with CRF, which was in line with a recent study 45 .

Apoptosis is an intrinsic cell-suicide program that is critical for the normal development and maintenance of tissue homeostasis in multicellular organisms 46 . There are two main apoptotic signaling pathways: the death receptor-mediated extrinsic pathway and the mitochondria-mediated intrinsic pathway 47 . The proteins of the Bcl-2 family are key regulators of the mitochondrial pathway, including pro-apoptotic members (such as Bax) and anti-apoptotic members (such as Bcl-2), which can regulate the activation of caspases that cleave a number of cellular proteins, such as caspase-3 47, 48 . Recent studies found that CRF rats had increased apoptosis levels, up-regulated Bax expression, and down-regulated Bcl-2 expression in renal tissues 48, 49 . In line with the above findings, our results showed that the expression levels of Bax, Caspase-3, and Cleaved Caspase-3 were significantly increased and the expression level of Bcl-2 was dramatically decreased in CRF rats. Treatment with H 2 S remarkably decreased the levels of Bax, Caspase-3, and Cleaved Caspase-3, whereas it increased kidney Bcl-2 expression in CRF rats, suggesting that H 2 S could effectively reduce the apoptotic levels induced by CRF in rats.

It is widely accepted that relatively high level of ROS causes redox imbalance, induces cell apoptosis or necrosis during a wide variety of physiological and pathological conditions 47, 50, 51 . Our results indicated that the levels of ROS and MDA were markedly increased, and the activities of anti-oxidative enzymes, SOD and GSH-Px, were significantly decreased compared with the control group, suggesting that ROS could induce apoptosis in the kidney of CRF rats. All these changes were reversed by administration of H 2 S. Recent studies have proven that ROS can activate MAPKs and apoptotic cell death induced by ROS is mediated by MAPK pathway [52] [53] [54] . The present study identified that CRF increased the phosphorylation of p38, JNK, and ERK, whereas H 2 S treatment significantly reversed the CRF-induced increase in MAPKs phosphorylation. These results demonstrated that H 2 S was able to reduce the apoptotic levels induced by CRF through ROS-mediated MAPK pathway.

Inflammatory cytokines play important roles in the development and progression of CRF 55, 56 . It is well documented that the levels of several inflammatory cytokines were higher in CRF patients compared with control subjects, such as TNF-α, IL-6, IL-10, and MCP-1 [55] [56] [57] . Similarly, our data indicated that the levels of these cytokines were significantly increased compared with the control group. High levels of TNF-α, IL-6, and MCP-1 indicated activation and increased production of cytokines, which can lead to an inflammatory state in the kidney of CRF rats. High levels of IL-10 in the kidney could be suggestive of an aberration in the pro anti-inflammatory adjustment. Administration of H 2 S effectively alleviated renal inflammation in CRF rats. The NF-κB network is involved in a wide range of inflammatory, autoimmune, and malignant disorders 37, 58, 59 . The p50/p65 heterodimer is considered the most important transcription factor of the NF-κB pathway and is specifically referred to as NF-κB 59, 60 . A recent study indicated that the expression of NF-κB was upregulated in the kidney of CRF rats 61 . Our results showed that CRF increased kidney p50, p65, and p-p65 protein expressions as well as the p-p65/p65 ratio, suggesting that CRF induced an inflammatory state in the kidney of rats. However, treatment with H 2 S significantly reversed the changes induced by CRF, suggesting that H 2 S could reduce kidney inflammation through the downregulation of NF-κB expression.

In conclusion, our results demonstrate that H 2 S is able to ameliorate CRF in rats by inhibiting apoptosis and inflammation through the ROS/MAPK and NF-κB signaling pathways (Fig. 11) . Therefore, H 2 S or its releasing compounds may serve as a potential therapeutic molecule for CRF.

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This study was supported by grants from the National Natural Science 

G.L., Y.L. and D.W. conceived and coordinated the project. D.W., N.L., L.W., Z.Z., H.B., G.X., Y.Y., X.C., Z.J., T.Z., J.C. and A.J. designed experiments, performed statistical analyses and prepared figures. D.W., G.L. and Y.L. wrote the manuscript. All authors approved the final version prior to submission.

Supplementary information accompanies this paper at doi:10.1038/s41598-017-00557-2Competing Interests: The authors declare that they have no competing interests.Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/