Down-regulated CBS/H2S pathway is involved in high-salt-induced hypertension in Dahl rats

被引:72
作者
Huang, Pan [1 ]
Chen, Siyao [1 ]
Wang, Yuan [1 ]
Liu, Jia [1 ]
Yao, Qiuyu [1 ]
Huang, Yaqian [1 ]
Li, Hongxia [1 ]
Zhu, Mingzhu [1 ]
Wang, Suxia [2 ]
Li, Lin [3 ]
Tang, Chaoshu [4 ,5 ]
Tao, Yinghong [6 ]
Yang, Guosheng [6 ]
Du, Junbao [1 ,4 ]
Jin, Hongfang [1 ]
机构
[1] Peking Univ, Hosp 1, Dept Pediat, Xi An Men Str 1, Beijing 100034, Peoples R China
[2] Peking Univ, Hosp 1, Lab Elect Microscopy, Beijing 100034, Peoples R China
[3] Peking Univ, Hosp 1, Cent Lab, Beijing 100034, Peoples R China
[4] Minist Educ, Key Lab Mol Cardiol, Beijing 100191, Peoples R China
[5] Peking Univ, Hlth Sci Ctr, Dept Physiol & Pathophysiol, Beijing 100191, Peoples R China
[6] Peking Univ, Hosp 1, Anim Ctr, Beijing 100034, Peoples R China
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2015年 / 46卷
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Hydrogen sulfide; Salt; Hypertension; Kidney; HYDROGEN-SULFIDE; ANGIOTENSIN-II; SENSITIVE HYPERTENSION; BLOOD-PRESSURE; DIETARY-SODIUM; PATHOGENESIS; GENERATION; INHIBITION; KIDNEY; CELLS;
D O I
10.1016/j.niox.2015.01.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: The study was designed to explore the significance of endogenous H2S in the development of high-salt-induced hypertension in rats. Methods: 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 beta-lyase (CBS), cystathionine gamma-Iyase 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-1 alpha pathway. The effect of H2S on RAS in serum and renal tissue of rats were tested. Results: 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-1 alpha 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-1 alpha degradation could rescue down-regulated CBS/H2S pathway in renal tissue of Dahl rats with high-salt. In contrast, inhibitor of HIF-1 alpha activity decreased the CBS/H2S pathway in the renal tissue of SD rats treated with high-salt. Conclusions: Down-regulated CBS/H2S pathway in renal tissues under high-salt insult might be an important pathogenesis of salt-sensitive hypertension. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:192 / 203
页数:12
相关论文
共 53 条
[1]   Pathophysiology of salt sensitivity hypertension [J].
Ando, Katsuyuki ;
Fujita, Toshiro .
ANNALS OF MEDICINE, 2012, 44 :S119-S126
[2]   Tight Control of Hypoxia-inducible Factor-α Transient Dynamics Is Essential for Cell Survival in Hypoxia [J].
Bagnall, James ;
Leedale, Joseph ;
Taylor, Sarah E. ;
Spiller, David G. ;
White, Michael R. H. ;
Sharkey, Kieran J. ;
Bearon, Rachel N. ;
See, Violaine .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (09) :5549-5564
[3]   A mechanism for salt-sensitive hypertension: abnormal dietary sodium-mediated vascular response to angiotensin-II [J].
Chamarthi, Bindu ;
Williams, Jonathan S. ;
Williams, Gordon H. .
JOURNAL OF HYPERTENSION, 2010, 28 (05) :1020-1026
[4]   KALLIKREIN EXCRETION IN DAHL SALT-SENSITIVE AND SALT-RESISTANT RATS WITH NATIVE AND TRANSPLANTED KIDNEYS [J].
CHURCHILL, PC ;
CHURCHILL, MC ;
BIDANI, AK ;
RABITO, SF .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1995, 269 (05) :F710-F717
[5]   HISTAMINE-RELEASE BY EXOCYTOSIS FROM RAT MAST-CELLS ON REDUCTION OF EXTRACELLULAR SODIUM - SECRETORY RESPONSE INHIBITED BY CALCIUM, STRONTIUM, BARIUM, OR MAGNESIUM [J].
COCHRANE, DE ;
DOUGLAS, WW .
JOURNAL OF PHYSIOLOGY-LONDON, 1976, 257 (02) :433-+
[6]   Hydrogen sulfide is endogenously generated in rat skeletal muscle and exerts a protective effect against oxidative stress [J].
Du Jian-tong ;
Li Wei ;
Yang Jin-yan ;
Tang Chao-shu ;
Li Qi ;
Jin Hong-fang .
CHINESE MEDICAL JOURNAL, 2013, 126 (05) :930-936
[7]   A Newly Found Gasotransmitter, Hydrogen Sulfide, in the Pathogenesis of Hypertension and Other Cardiovascular Diseases [J].
Du, Junbao ;
Zhang, Chunyu ;
Yan, Hui ;
Tang, Chaoshu .
CURRENT HYPERTENSION REVIEWS, 2006, 2 (02) :123-126
[8]   Hydrogen Sulfide Suppresses Oxidized Low-density Lipoprotein (Ox-LDL)-stimulated Monocyte Chemoattractant Protein 1 generation from Macrophages via the Nuclear Factor kB ( NF- kB) Pathway* [J].
Du, Junbao ;
Huang, Yaqian ;
Yan, Hui ;
Zhang, Qiaoli ;
Zhao, Manman ;
Zhu, Mingzhu ;
Liu, Jia ;
Chen, Stella X. ;
Bu, Dingfang ;
Tang, Chaoshu ;
Jin, Hongfang .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (14) :9741-9753
[9]   Inducible hydrogen sulfide synthesis in chondrocytes and mesenchymal progenitor cells: is H2S a novel cytoprotective mediator in the inflamed joint? [J].
Fox, Bridget ;
Schantz, Jan-Thorsten ;
Haigh, Richard ;
Wood, Mark E. ;
Moore, Phillip K. ;
Viner, Nick ;
Spencer, Jeremy P. E. ;
Winyard, Paul G. ;
Whiteman, Matthew .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2012, 16 (04) :896-910
[10]   Hydrogen sulfide attenuates angiotensin II-induced hypertension, proteinuria and renal damage [J].
Frenay, Anne-Roos S. ;
Snijder, Pauline M. ;
Koning, Anne M. ;
Bachtler, Matthias ;
Pasch, Andreas ;
Kwakernaak, Arjan J. ;
van den Berg, Else ;
Bos, Eelke M. ;
Hillebrands, Jan-Luuk ;
Navis, Gerjan ;
Leuvenink, Henri G. D. ;
van Goor, Harry .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2014, 39 :S23-S24