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用单克隆抗体阻断内源性下丘脑前部心房利钠肽可降低自发性高血压大鼠的血压。

Blockade of endogenous anterior hypothalamic atrial natriuretic peptide with monoclonal antibody lowers blood pressure in spontaneously hypertensive rats.

作者信息

Yang R H, Jin H K, Chen Y F, Wyss J M, Oparil S

机构信息

Department of Medicine, University of Alabama, Birmingham 35294.

出版信息

J Clin Invest. 1990 Dec;86(6):1985-90. doi: 10.1172/JCI114933.

Abstract

We have previously shown that the atrial natriuretic peptide (ANP) content of the anterior hypothalamic region of NaCl-sensitive spontaneously hypertensive rats (SHR-S) is higher than that of Wistar-Kyoto (WKY) rats. ANP has been shown to inhibit neuronal norepinephrine release and to reduce the excitability of hypothalamic neurons. This study tested the hypothesis that blockade of endogenous ANP in the anterior hypothalamus by local microinjection of a monoclonal antibody to ANP (MAb KY-ANP-II) lowers blood pressure in SHR-S. Purified MAb KY-ANP-II (0.055 and 0.55 micrograms) or control mouse IgG in 200 nl saline was microinjected into the anterior hypothalamic area (AHA) of conscious SHR-S and control WKY rats. As a further control, Mab KY-ANP-II (0.55 microgram) was microinjected into the posterior hypothalamic area (PHA) of SHR-S. Anterior hypothalamic microinjection of MAb KY-ANP-II caused significant dose-related decreases in mean arterial pressure (MAP) and heart rate (HR) in SHR-S but not in WKY rats. Control injections of equal volumes of IgG had no effect on MAP or HR. Microinjection of Mab KY-ANP-II into PHA produced no significant alteration in MAP or HR in SHR-S. These data provide the first demonstration that endogenous ANP in a region of brain known to influence cardiovascular function mediates BP and HR control in the rat. These findings suggest that the increased endogenous ANP in the anterior hypothalamus of SHR-S may be involved in the central regulation of BP in the model.

摘要

我们之前已经表明,盐敏感型自发性高血压大鼠(SHR-S)下丘脑前部区域的心房利钠肽(ANP)含量高于Wistar-Kyoto(WKY)大鼠。研究表明,ANP可抑制神经元去甲肾上腺素释放,并降低下丘脑神经元的兴奋性。本研究检验了以下假设:通过局部微量注射抗ANP单克隆抗体(MAb KY-ANP-II)阻断下丘脑前部的内源性ANP可降低SHR-S的血压。将纯化的MAb KY-ANP-II(0.055和0.55微克)或对照小鼠IgG溶于200 nl盐水中,微量注射到清醒的SHR-S和对照WKY大鼠的下丘脑前部区域(AHA)。作为进一步的对照,将Mab KY-ANP-II(0.55微克)微量注射到SHR-S的下丘脑后部区域(PHA)。下丘脑前部微量注射MAb KY-ANP-II可使SHR-S的平均动脉压(MAP)和心率(HR)出现与剂量相关的显著降低,但对WKY大鼠无此作用。等量IgG的对照注射对MAP或HR无影响。将Mab KY-ANP-II微量注射到PHA对SHR-S的MAP或HR无显著改变。这些数据首次证明,已知影响心血管功能的脑区中的内源性ANP介导大鼠的血压和心率控制。这些发现表明,SHR-S下丘脑前部内源性ANP的增加可能参与了该模型中血压的中枢调节。

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