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Effects of sex and estrogen levels on ACE1-ang II-ATR axis in renovascular hypertension rats / 中国药理学通报
Chinese Pharmacological Bulletin ; (12): 859-863, 2019.
Artículo en Chino | WPRIM | ID: wpr-857240
ABSTRACT

Aim:

To investigate the effects of gender differences and estrogen levels on ACE, -Ang II -ATR axis in the aorta tissue of renovascular hypertension (RVH) rats.

Methods:

Forty-five rats were made two-kidney one-clip (2K1C) model of renovascular hypertension and divided into three groups female two kidney one clip group (2K1C-F), male two kidney one clip group (2K1C-M), and ovariectomized group (2K1C-0VX). After 32 weeks of routine feeding, the blood pressure was measured, blood was taken and-serum and plasma were prepared. Serum estrogen and plasma Ang II were measured and mRNA and protein expression levels of ACE, AT, R, AT2R in aorta tissue were detected.

Results:

Systolic blood pressure of 2K1C-F group was significantly higher than that of 2K1C-M group and 2K1C-0VX group (P < 0.05). The content of Ang II in 2K1C-F group was significantly lower than that in 2K1C-M and 2K1C-0VX group(P <0. 01). Compared with 2K1C-F group, the mRNA and protein expressions of ACE!, AT, R, AT2R in 2K1C-M group were up-regulated significantly (P < 0. 05), while the mRNA expression of ATlb R, ACE, was up-regulated, and the mRNA expression of AT2R was down-regulated in 2K1C-OVX group (P < 0. 05); compared with 2K1C-M group, the mRNA expression of ACE, ATlb R, AT2R and protein expression of ACE, AT2R were down-regulated significantly in 2K1C-OVX group(P < 0. 05).

Conclusions:

The mRNA and protein expressions of ACE, Ang II, AT1aR and AT1bR in aorta tissue show gender and estrogen differences, and estrogen can reduce the activity of ACE, -Ang II -AT, R axis.

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Idioma: Chino Revista: Chinese Pharmacological Bulletin Año: 2019 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Idioma: Chino Revista: Chinese Pharmacological Bulletin Año: 2019 Tipo del documento: Artículo