内科学
内分泌学
胱硫醚β合酶
内生
肾
胱硫醚γ裂解酶
化学
医学
酶
生物化学
半胱氨酸
作者
Pan Huang,Siyao Chen,Yuan Wang,Jia Liu,Qiuyu Yao,Yaqian Huang,Hongxia Li,Mingzhu Zhu,Suxia Wang,Lin Li,Chaoshu Tang,Yong Tao,Guosheng Yang,Junbao Du,Hongfang Jin
出处
期刊:Nitric Oxide
[Elsevier]
日期:2015-04-01
卷期号:46: 192-203
被引量:72
标识
DOI:10.1016/j.niox.2015.01.004
摘要
The study was designed to explore the significance of endogenous H2S in the development of high-salt-induced hypertension in rats.High-salt-induced hypertension rat model was made by feeding Dahl rat high-salt diet containing 8% NaCl for 8 weeks with SD rats as control. SBP and aorta structure in rats were observed. Endogenous H2S content and expression of cystathionine β-lyase (CBS), cystathionine γ-lyase and mercaptopyruvate sulfurtransferase in renal tissues were detected. Mechanisms for the impact of high-salt on CBS/H2S in renal tissues were studied, targeting HIF-1α pathway. The effect of H2S on RAS in serum and renal tissue of rats were tested.High-salt reduced endogenous H2S content and inhibited the expression of CBS in renal tissue in salt-sensitive Dahl rats. H2S donor, however, inhibited salt-sensitive hypertension, reversed aortic structural remodeling and inhibited activation of the RAS system in renal tissues in Dahl rats. Expression of HIF-1α was decreased but expression of PHD2 was increased in renal tissue of Dahl rats with high-salt diet, whereas they did not alter in renal tissue of SD rats with high-salt diet. Ex vivo experiment showed that inhibitor of HIF-1α degradation could rescue down-regulated CBS/H2S pathway in renal tissue of Dahl rats with high-salt. In contrast, inhibitor of HIF-1α activity decreased the CBS/H2S pathway in the renal tissue of SD rats treated with high-salt.Down-regulated CBS/H2S pathway in renal tissues under high-salt insult might be an important pathogenesis of salt-sensitive hypertension.
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