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向最后区微量注射内皮素所诱导的心血管反应。

Cardiovascular responses induced by endothelin microinjection into area postrema.

作者信息

Ferguson A V, Smith P

机构信息

Department of Physiology, Queen's University, Kingston, ON, Canada.

出版信息

Regul Pept. 1990 Jan;27(1):75-85. doi: 10.1016/0167-0115(90)90206-c.

Abstract

The recently described endothelium derived constricting factor endothelin (ET) is a 21 amino acid peptide which is the most potent endogenous vasoconstrictor yet described. Binding sites for this peptide have been demonstrated within the circumventricular structures of the brain. One of these structures, the area postrema (AP), has been implicated in central cardiovascular control mechanisms. We have therefore examined the effects of AP microinjection of ET on blood pressure in urethane-anaesthetised rats. Such treatment resulted in dose-dependent biphasic changes in arterial blood pressure (increases followed by decreases). Low doses of ET (0.2-1.0 pmol) induced significant increases (P less than 0.01), and high doses (5.0 pmol) significant decreases (P less than 0.01), while at intermediate concentrations (2.0 pmol) ET caused significant increases (P less than 0.05) followed by significant decreases (P less than 0.01) in mean blood pressure. Other vasoconstrictors were found to be without effect following AP administration, suggesting these changes to be the result of specific action of ET. In contrast, both ET and methoxamine had similar cardiovascular actions when microinjected into regions anatomically adjacent to the AP such as the NTS, indicating that vasoconstriction in these areas induces changes in femoral arterial blood pressure. These data suggest a specific role for ET as a chemical messenger involved in central nervous system control of the cardiovascular system within AP.

摘要

最近描述的内皮衍生收缩因子内皮素(ET)是一种由21个氨基酸组成的肽,是迄今所描述的最有效的内源性血管收缩剂。已在脑的室周结构中证实了该肽的结合位点。这些结构之一,即最后区(AP),已被认为参与中枢心血管控制机制。因此,我们研究了向AP微量注射ET对乌拉坦麻醉大鼠血压的影响。这种处理导致动脉血压出现剂量依赖性双相变化(先升高后降低)。低剂量的ET(0.2 - 1.0皮摩尔)引起显著升高(P < 0.01),高剂量(5.0皮摩尔)引起显著降低(P < 0.01),而在中间浓度(2.0皮摩尔)时,ET导致平均血压先显著升高(P < 0.05),随后显著降低(P < 0.01)。发现其他血管收缩剂在给予AP后无作用,提示这些变化是ET特异性作用的结果。相比之下,当向与AP在解剖学上相邻的区域如孤束核(NTS)微量注射ET和甲氧明时,二者具有相似的心血管作用,表明这些区域的血管收缩会引起股动脉血压变化。这些数据表明ET作为一种化学信使在AP内参与中枢神经系统对心血管系统的控制中具有特定作用。

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