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复方芪麻胶囊对不同高血压模型大鼠血压及相关血管活性因子的影响

The effect of compound Qima capsule on blood pressure and related vasoactive factors in different hypertensive rat models

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收录情况: ◇ 统计源期刊 ◇ 北大核心 ◇ CSCD-C

机构: [1]广州中医药大学第五临床医学院 [2]广东省第二中医院广东省中医药工程技术研究院 [3]广东省中医药研究开发重点实验室
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关键词: Compound Qima capsule Hypertension Vasoactive factors

摘要:
Objective: This study aims to observe the hypotensive effect of compound Qima capsule on various experimental hypertensive rats and the regulation of related vasoactive factors. Methods: The effect of compound Qima capsule on dynamic changes of blood pressure and the levels of calcitonin gene-related peptide (CGRP), nitric oxide (NO) and neuropeptide Y (NPY) in spontaneously hypertensive rats (SHR), the blood pressure and NO concentration in hypertensive rats induced by L-nitroarginine, as well as the blood pressure and the levels of testosterone (T), angiotensin II (AngII) and aldosterone (Ald) in endogenous hypertensive rats induced by testosterone propionate were observed. The changes of blood pressure and the levels of CGRP, NO, NPY, T, AngII and Ald in rats after continuous intragastric administration of compound Qima capsule were detected. Results: Compound Qima capsule significantly reduced the systolic and diastolic blood pressures of SHR rats in conscious state. With the prolonging of medication time, its hypotensive effect gradually decreased and steadily stabilized. At the same time, it increased the contents of CGRP and NO (P<0.05), decreased the level of NPY (P<0.05); reduced the blood pressure of hypertensive rats induced by L-nitroarginine (P<0.01), increased NO content (P<0.01 or P<0.05); reduced blood pressure values in endogenous hypertensive rats induced by testosterone propionate (P<0.01), and decreased the contents of AngII and Ald (P<0.05 or P<0.01). Conclusion: Compound Qima capsule had significant hypotensive effect on various experimental hypertensive rat models. The mechanism was probably related to improvement of endothelial cell function, increasing the contents of CGRP and NO, decreasing NPY levels, inhibiting the secretions of AngII and Ald in blood vessels, and improving water and sodium retention in vivo. © 2020, Chinese Journal of New Drugs Co. Ltd. All right reserved.

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第一作者机构: [1]广州中医药大学第五临床医学院
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通讯机构: [2]广东省第二中医院广东省中医药工程技术研究院 [3]广东省中医药研究开发重点实验室
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