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肾素抑制剂ES-1005对钠缺乏狨猴肾脏肾素基因表达的影响。

The effect of the renin inhibitor ES-1005 on the expression of the kidney renin gene in sodium-depleted marmosets.

作者信息

Kitami Y, Hiwada K, Murakami E, Muneta S, Kokubu T

机构信息

2nd Department of Internal Medicine, Ehime University School of Medicine, Japan.

出版信息

J Hypertens. 1990 Dec;8(12):1143-6. doi: 10.1097/00004872-199012000-00011.

Abstract

The effect of the renin inhibitor ES-1005 or captopril on the expression of the kidney renin gene was investigated in sodium-depleted marmosets. We measured the level of kidney renin messenger RNA (mRNA) after continuous administration of ES-1005 (48 mg/kg per day) or captopril (2 mg/kg per day) intraperitoneally, via an osmotic mini-pump, for one week. The level of kidney renin mRNA was measured by densitometric Northern blot analysis using an alpha-32P-labelled human renin cDNA fragment as the hybridization probe. Captopril treatment markedly increased plasma renin activity and the level of kidney renin mRNA by 4.7-fold and 6.3-fold, respectively. ES-1005 treatment completely inhibited plasma renin activity and significantly decreased the level of kidney renin mRNA (46% of the normal control P less than 0.01). However, plasma immunoreactive renin concentration was significantly increased by the treatment with ES-1005 (P less than 0.05). These results suggest that the treatment with the renin inhibitor ES-1005 for one week has a paradoxical effect on kidney renin gene expression and renin release from the kidney in sodium-depleted marmosets.

摘要

在钠缺乏的狨猴中研究了肾素抑制剂ES - 1005或卡托普利对肾脏肾素基因表达的影响。通过渗透微型泵连续一周腹腔内给予ES - 1005(每天48mg/kg)或卡托普利(每天2mg/kg)后,我们测量了肾脏肾素信使核糖核酸(mRNA)的水平。使用α - 32P标记的人肾素cDNA片段作为杂交探针,通过密度计Northern印迹分析测量肾脏肾素mRNA的水平。卡托普利治疗使血浆肾素活性和肾脏肾素mRNA水平分别显著增加4.7倍和6.3倍。ES - 1005治疗完全抑制了血浆肾素活性,并显著降低了肾脏肾素mRNA水平(为正常对照的46%,P<0.01)。然而,ES - 1005治疗使血浆免疫反应性肾素浓度显著增加(P<0.05)。这些结果表明,在钠缺乏的狨猴中,用肾素抑制剂ES - 1005治疗一周对肾脏肾素基因表达和肾脏肾素释放具有矛盾的影响。

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