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依普利酮对甲状腺功能减退症大鼠肾素-血管紧张素-醛固酮系统的影响。

The effect of eplerenone on the renin-angiotensin-aldosterone system of rats with thyroid dysfunction.

机构信息

College of Medicine, Hawler Medical University, Erbil, Iraq.

Department of Pharmacy, Medical Technical Institute, Erbil Polytechnic University, Erbil, Iraq.

出版信息

J Pharm Pharmacol. 2019 Dec;71(12):1800-1808. doi: 10.1111/jphp.13168. Epub 2019 Oct 3.

Abstract

OBJECTIVES

This study was conducted to evaluate the effect of eplerenone on the RAAS and kidney function in rats with thyroid hormone disorders.

METHODS

This study involved 30 male Wistar albino rats, divided into three groups. The first group (N = 6) served as a control. The second group involved 12 rats with experimentally induced hypothyroidism through receiving propylthiouracil (0.05% w/v) in drinking water for one month, which was divided into two subgroups of six rats each. The first subgroup served as a positive hypothyroid control, and the second subgroup received oral daily dose of eplerenone (100 mg/kg) for 14 days. The third group included 12 rats with induced hyperthyroidism with L-thyroxin (0.0012% w/v) in drinking water, and rats in this group were also divided into two subgroups. The first subgroup served as a positive hyperthyroid control, and the second subgroup received oral eplerenone 100 mg/kg.

RESULTS

Eplerenone indicated a significant increase in renin and angiotensin I from 184.09 pg/ml and 178.66 pg/ml to 603.31 pg/ml and 250.88 pg/ml, respectively, meanwhile, aldosterone indicated no significant changes after inducing hypothyroidism and eplerenone administration. The induction of hyperthyroidism led to a significant increase in angiotensin I from 248.84 pg/ml to 292.22 pg/ml. Oral administration of eplerenone for 14 days caused a significant increase aldosterone from 364.23 pg/ml to 497.02 pg/ml.

CONCLUSION

Eplerenone significantly increased the serum renin and angiotensin I in hypothyroid and aldosterone and angiotensin I in hyperthyroid rats. Aldosterone in hypothyroid rats was not changed by eplerenone.

摘要

目的

本研究旨在评估依普利酮对甲状腺激素紊乱大鼠肾素-血管紧张素系统(RAAS)和肾功能的影响。

方法

本研究纳入 30 只雄性 Wistar 白化大鼠,分为三组。第一组(n=6)作为对照组。第二组共 12 只大鼠,通过饮用含丙硫氧嘧啶(0.05% w/v)的水一个月来诱导实验性甲状腺功能减退症,该组再分为两组,每组 6 只。第一组作为阳性甲状腺功能减退对照组,第二组给予依普利酮(100mg/kg)口服,每天一次,共 14 天。第三组共 12 只大鼠通过饮用含 L-甲状腺素(0.0012% w/v)的水来诱导甲状腺功能亢进症,该组也分为两组。第一组作为阳性甲状腺功能亢进对照组,第二组给予依普利酮 100mg/kg 口服。

结果

依普利酮使大鼠的肾素和血管紧张素 I 分别从 184.09pg/ml 和 178.66pg/ml 显著增加至 603.31pg/ml 和 250.88pg/ml,而甲状腺功能减退症诱导和依普利酮给药后醛固酮没有显著变化。甲状腺功能亢进症的诱导使血管紧张素 I 从 248.84pg/ml 显著增加至 292.22pg/ml。依普利酮连续口服 14 天导致大鼠的醛固酮从 364.23pg/ml 显著增加至 497.02pg/ml。

结论

依普利酮显著增加了甲状腺功能减退症大鼠的血清肾素和血管紧张素 I,以及甲状腺功能亢进症大鼠的醛固酮和血管紧张素 I。甲状腺功能减退症大鼠的醛固酮未受依普利酮影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65bb/6900172/6d2e5f1dfa44/JPHP-71-1800-g001.jpg

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