Blockade of Endogenous Angiotensin-(1–7) in Hypothalamic Paraventricular Nucleus Attenuates High Salt-Induced Sympathoexcitation and Hypertension
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  • 英文篇名:Blockade of Endogenous Angiotensin-(1–7) in Hypothalamic Paraventricular Nucleus Attenuates High Salt-Induced Sympathoexcitation and Hypertension
  • 作者:Xiao-Jing ; Yu ; Yu-Wang ; Miao ; Hong-Bao ; Li ; Qing ; Su ; Kai-Li ; Liu ; Li-Yan ; Fu ; Yi-Kang ; Hou ; Xiao-Lian ; Shi ; Ying ; Li ; Jian-Jun ; Mu ; Wen-Sheng ; Chen ; Wei ; Cui ; Guo-Qing ; Zhu ; Philip ; J.Ebenezer ; Joseph ; Francis ; Yu-Ming ; Kang
  • 英文作者:Xiao-Jing Yu;Yu-Wang Miao;Hong-Bao Li;Qing Su;Kai-Li Liu;Li-Yan Fu;Yi-Kang Hou;Xiao-Lian Shi;Ying Li;Jian-Jun Mu;Wen-Sheng Chen;Wei Cui;Guo-Qing Zhu;Philip J.Ebenezer;Joseph Francis;Yu-Ming Kang;Department of Physiology and Pathophysiology, Xi'an Jiaotong University School of Basic Medical Sciences, Key Laboratory of Environment and Genes Related to Diseases,Ministry of Education;Genetic Engineering Laboratory, College of Biotechnology,Xi'an University;Department of Plastic and Cosmetic Surgery, Gansu Provincial Hospital;Department of Pharmacology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center;Department of Cardiovascular Medicine, First Affiliated Hospital of the Medical College of Xi'an Jiaotong University;Department of Cardiovascular Surgery, Xijing Hospital,Fourth Military Medical University;Department of Endocrinology and Metabolism, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an Jiaotong University Health Science Center;Key Laboratory of Cardiovascular Disease and Molecular Intervention, Department of Physiology, Nanjing Medical University;Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University;
  • 英文关键词:High-salt diet;;Hypertension;;Angiotensin(1–7);;Paraventricular nucleus;;Pro-inflammatory cytokines
  • 中文刊名:ZSJK
  • 英文刊名:神经科学通报(英文版)
  • 机构:Department of Physiology and Pathophysiology, Xi'an Jiaotong University School of Basic Medical Sciences, Key Laboratory of Environment and Genes Related to Diseases,Ministry of Education;Genetic Engineering Laboratory, College of Biotechnology,Xi'an University;Department of Plastic and Cosmetic Surgery, Gansu Provincial Hospital;Department of Pharmacology, School of Basic Medical Sciences, Xi'an Jiaotong University Health Science Center;Department of Cardiovascular Medicine, First Affiliated Hospital of the Medical College of Xi'an Jiaotong University;Department of Cardiovascular Surgery, Xijing Hospital,Fourth Military Medical University;Department of Endocrinology and Metabolism, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an Jiaotong University Health Science Center;Key Laboratory of Cardiovascular Disease and Molecular Intervention, Department of Physiology, Nanjing Medical University;Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University;
  • 出版日期:2019-02-01
  • 出版单位:Neuroscience Bulletin
  • 年:2019
  • 期:v.35
  • 基金:supported by the National Natural Science Foundation of China(81600333,81770426,91439120,and 91639105);; the China Postdoctoral Science Foundation(2016M602835 and 2016M592802);; the Shaanxi Postdoctoral Science Foundation(2016BSHEDZZ91)
  • 语种:英文;
  • 页:ZSJK201901006
  • 页数:10
  • CN:01
  • ISSN:31-1975/R
  • 分类号:53-62
摘要
Angiotensin(Ang)-(1–7) is an important biologically-active peptide of the renin-angiotensin system. This study was designed to determine whether inhibition of Ang-(1–7) in the hypothalamic paraventricular nucleus(PVN) attenuates sympathetic activity and elevates blood pressure by modulating pro-inflammatory cytokines(PICs)and oxidative stress in the PVN in salt-induced hypertension. Rats were fed either a high-salt(8% NaCl) or a normal salt diet(0.3% NaCl) for 10 weeks, followed by bilateral microinjections of the Ang-(1–7) antagonist A-779 or vehicle into the PVN. We found that the mean arterial pressure(MAP), renal sympathetic nerve activity(RSNA), and plasma norepinephrine(NE) were significantly increased in salt-induced hypertensive rats. The high-salt diet also resulted in higher levels of the PICs interleukin-6, interleukin-1 beta, tumor necrosis factor alpha, and monocyte chemotactic protein-1, as well as higher gp91 phoxexpression and superoxide production in the PVN. Microinjection of A-779(3 nmol/50 nL) into the bilateral PVN of hypertensive rats not only attenuated MAP, RSNA, and NE, but also decreased the PICs and oxidative stress in the PVN. These results suggest that the increased MAP and sympathetic activity in salt-induced hypertension can be suppressed by blockade of endogenous Ang-(1–7) in the PVN, through modulation of PICs and oxidative stress.
        Angiotensin(Ang)-(1–7) is an important biologically-active peptide of the renin-angiotensin system. This study was designed to determine whether inhibition of Ang-(1–7) in the hypothalamic paraventricular nucleus(PVN) attenuates sympathetic activity and elevates blood pressure by modulating pro-inflammatory cytokines(PICs)and oxidative stress in the PVN in salt-induced hypertension. Rats were fed either a high-salt(8% NaCl) or a normal salt diet(0.3% NaCl) for 10 weeks, followed by bilateral microinjections of the Ang-(1–7) antagonist A-779 or vehicle into the PVN. We found that the mean arterial pressure(MAP), renal sympathetic nerve activity(RSNA), and plasma norepinephrine(NE) were significantly increased in salt-induced hypertensive rats. The high-salt diet also resulted in higher levels of the PICs interleukin-6, interleukin-1 beta, tumor necrosis factor alpha, and monocyte chemotactic protein-1, as well as higher gp91 phoxexpression and superoxide production in the PVN. Microinjection of A-779(3 nmol/50 nL) into the bilateral PVN of hypertensive rats not only attenuated MAP, RSNA, and NE, but also decreased the PICs and oxidative stress in the PVN. These results suggest that the increased MAP and sympathetic activity in salt-induced hypertension can be suppressed by blockade of endogenous Ang-(1–7) in the PVN, through modulation of PICs and oxidative stress.
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