H2S donors attenuate diabetic nephropathy in rats: Modulation of oxidant status and polyol pathway

被引:31
作者
Safar, Marwa M. [1 ]
Abdelsalam, Rania M. [1 ]
机构
[1] Cairo Univ, Fac Pharm, Dept Pharmacol & Toxicol, Cairo, Egypt
关键词
Diabetic nephropathy; Sulfurous mineral water; H2S; Insulin like growth factor-I (IGF-I); Polyol pathway; GLYCATION END-PRODUCTS; HYDROGEN-SULFIDE; OXIDATIVE STRESS; ALTERNATIVE THERAPY; SPA THERAPY; KIDNEY; INHIBITION; REDUCTASE; ACTIVATION; EXPRESSION;
D O I
10.1016/j.pharep.2014.08.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Sulfurous mineral water and its main active ingredient sodium hydrosulfide (NaHS) are major sources of H2S. The present study aimed to explore their protective effect on one of the serious long-term complications of diabetes; diabetic nephropathy. Methods: Sulfurous mineral water (as drinking water), NaHS (14 mu mol/kg/day; ip), and gliclazide (10 mg/kg; po) were administered daily for 6 weeks to streptozotocin (STZ)-diabetic rats. Results: STZ-induced diabetes was associated with body weight reduction, hyperglycemia, overproduction of glycated hemoglobin, as well as decline in serum insulin, C-peptide, and insulin like growth factor-I. Besides, diabetes impaired kidney functions and imposed oxidative and nitrosative stress as manifested by elevated contents of renal thiobarbituric acid reactive substances and nitric oxide, parallel to reduced glutathione content. These deleterious effects were antagonized by sulfurous water and to a better extent by NaHS. Activities of myeloperoxidase and sorbitol dehydrogenase were not altered by STZ or any of the treatments. However, STZ-induced diabetes was accompanied by an increment of aldose reductase which was only mitigated by gliclazide and NaHS. Histopathological examination of kidney sections corroborated the biochemical findings. Conclusion: This study suggests a novel therapeutic approach for diabetic nephropathy using H2S donors. (C) 2014 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier Urban & Partner Sp. z o.o. All rights reserved.
引用
收藏
页码:17 / 23
页数:7
相关论文
共 50 条
  • [31] Renal protection by acacetin in streptozotocin-induced diabetic nephropathy via TLR4/NF-κB pathway modulation in rats
    Yu, Hangying
    Guo, Min
    ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, 2025,
  • [32] The DR1-CSE/H2S system inhibits renal fibrosis by downregulating the ERK1/2 signaling pathway in diabetic mice
    Li, Hongzhu
    Sun, Fengqi
    Bai, Shuzhi
    Chang, Guiquan
    Wu, Ren
    Wei, Yaxin
    Wen, Xin
    Xi, Yuxin
    Hao, Jinghui
    Zaid, Altaany
    INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2022, 49 (01)
  • [33] The role of DJ-1/Nrf2 pathway in the pathogenesis of diabetic nephropathy in rats
    Sun, Qian
    Shen, Zi-ying
    Meng, Qing-tao
    Liu, Hui-zhang
    Duan, Wei-na
    Xia, Zhong-yuan
    RENAL FAILURE, 2016, 38 (02) : 294 - 304
  • [34] Modulation of inflammatory and vascular signalling by novel slow release and mitochondria-targeted H2S donors
    Whiteman, Matthew
    Perry, Alexis
    Le Trionnaire, Sophie
    Whatmore, Jacqueline L.
    Ahmed, Tahanver
    Fox, Bridget
    Kerr, Paul
    Haigh, Richard
    Winyard, Paul G.
    Wood, Mark E.
    NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2013, 31 : S13 - S13
  • [35] Administration of H2S improves erectile dysfunction by inhibiting phenotypic modulation of corpus cavernosum smooth muscle in bilateral cavernous nerve injury rats
    Qinyu-Zeng
    Shuhua-He
    Fengzhi-Chen
    Li-Wang
    Liren-Zhong
    Jialiang-Hui
    Wei-Ding
    Junhong-Fan
    Haibo-Zhang
    Anyang-Wei
    NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2021, 107 : 1 - 10
  • [36] SOCS2 overexpression alleviates diabetic nephropathy in rats by inhibiting the TLR4/NF-κB pathway
    Yang, Suxia
    Zhang, Junwei
    Wang, Shiying
    Zhao, Xinxin
    Shi, Jun
    ONCOTARGET, 2017, 8 (53) : 91185 - 91198
  • [37] Serotonin and Dopamine Protect from Hypothermia/Rewarming Damage through the CBS/H2S Pathway
    Talaei, Fatemeh
    Bouma, Hjalmar
    Van der Graaf, Adrianus
    Strijkstra, Arjen
    Schmidt, Martina
    Henning, Robert
    PLOS ONE, 2011, 6 (07):
  • [38] Radioprotective role of H2S/CSE pathway in Chang liver cells
    Pan, Yan
    Ye, Shuang
    Yuan, Dexiao
    Zhang, Jianghong
    Bai, Yang
    Shao, Chunlin
    MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2012, 738 : 12 - 18
  • [39] Polyol pathway and modulation of ischemia-reperfusion injury in Type 2 diabetic BBZ rat hearts
    Qing Li
    Yuying C Hwang
    Radha Ananthakrishnan
    Peter J Oates
    Dennis Guberski
    Ravichandran Ramasamy
    Cardiovascular Diabetology, 7
  • [40] Analysis of erectile responses to H2S donors in the anesthetized rat
    Jupiter, Ryan C.
    Yoo, Daniel
    Pankey, Edward A.
    Reddy, Vishwaradh V. G.
    Edward, Justin A.
    Polhemus, David J.
    Peak, Taylor C.
    Katakam, Prasad
    Kadowitz, Philip J.
    AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2015, 309 (05): : H835 - H843