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依那普利对高血压和正常血压大鼠体内钠及氯化钠负荷处理的影响。

Effect of enalapril on body sodium and handling of a sodium chloride load in hypertensive and normotensive rats.

作者信息

Ledingham J M, Simpson F O

机构信息

Wellcome Medical Research Institute, University of Otago Medical School, Dunedin, New Zealand.

出版信息

Clin Exp Pharmacol Physiol. 1992 May;19(5):373-5. doi: 10.1111/j.1440-1681.1992.tb00475.x.

Abstract
  1. The effect of enalapril on handling of an Na load and on body Na during 96 h of zero Na intake was measured in hypertensive rats (GH and SHR) and their normotensive controls (N and WKY) by a whole body counting method. 2. Enalapril treatment led to a greater fall in body Na in the first 24 h after the Na load (as expected from the known effect of ACE inhibition on aldosterone production) and thus to a slightly faster excretion of an amount equivalent to the load. 3. Enalapril-treated rats were unable to maintain body Na on a zero Na intake. This was also expected from the known effect on aldosterone production, though other mechanisms are not excluded. The effect was more marked in the SHR and WKY than in GH and N but there was no significant difference in this effect between the hypertensives and their respective control strains.
摘要
  1. 通过全身计数法,在高血压大鼠(GH和SHR)及其正常血压对照大鼠(N和WKY)中测量了依那普利在96小时无钠摄入期间对钠负荷处理及体内钠的影响。2. 依那普利治疗导致钠负荷后最初24小时内体内钠下降幅度更大(正如血管紧张素转换酶抑制对醛固酮产生的已知作用所预期的那样),从而使相当于负荷量的钠排泄略快。3. 用依那普利治疗的大鼠在无钠摄入时无法维持体内钠水平。尽管不排除其他机制,但这同样是基于对醛固酮产生的已知作用所预期的。这种作用在SHR和WKY中比在GH和N中更明显,但高血压大鼠与其各自对照品系之间在这种作用上无显著差异。

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