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茯苓素:一种潜在的醛固酮拮抗剂
PQRIATIN: A POTENTIAL ALDOSTERONE ANTAGONIST
【摘要】 茯苓素体外可结合到大鼠肾胞浆膜醛固酮受体上,体内可拮抗醛固酮活性,提高尿中Na~+/K~+比值,具有剂量依赖关系。它不影响大鼠血浆醛固酮和血管紧张素Ⅱ的水平。实验表明它可能是一种醛固酮受体拮杭剂。
【Abstract】 Poriatin can bind to renal cytopiasmic aldosterone receptors in vitro and have an anti-aldosterone activity and enhances urinary Na+/K+ ratio with dose-dependence in rats. It did not affect the aldosteroae and angiotensinⅡ concentrations in rat plasma. These suggest that poriatin is an aldosterone antagonist.
【关键词】 茯苓素;
醛固酮;
醛固酮拮抗剂;
醛固酮受体;
Na~+/K~+比值;
【Key words】 Poriatin: Aldosterone; Aldosterone antagonist; Aldosterone receptor; Na+/K+ ratio;
【Key words】 Poriatin: Aldosterone; Aldosterone antagonist; Aldosterone receptor; Na+/K+ ratio;
- 【文献出处】 中国抗生素杂志 ,Chinese Journal of Antibiotics , 编辑部邮箱 ,1992年01期
- 【被引频次】233
- 【下载频次】694