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肾素-血管紧张素系统阻断后肾脏反应的性别差异。

Gender differences in the renal response to renin-angiotensin system blockade.

作者信息

Miller Judith A, Cherney David Z, Duncan John A, Lai Vesta, Burns Kevin D, Kennedy Christopher R J, Zimpelmann Joseph, Gao Wei, Cattran Daniel C, Scholey James W

机构信息

Toronto General Hospital, 8N-846, 585 University Avenue, Toronto, Ontario, M5G 2N2.

出版信息

J Am Soc Nephrol. 2006 Sep;17(9):2554-60. doi: 10.1681/ASN.2005101095. Epub 2006 Aug 16.

DOI:10.1681/ASN.2005101095
PMID:16914541
Abstract

Evidence suggests that gender differences exist in renin-angiotensin system (RAS) function. It was hypothesized that women may differ also in their response to RAS blockade. The renal and peripheral hemodynamic responses to incremental dosages of an angiotensin receptor blocker and the degree of angiotensin II (AngII) insensitivity achieved during 8 wk were examined in men and women. Participants were 30 young healthy men (n = 15; mean age 27 +/- 2) and women (n = 15; mean age 28 +/- 2) who were on a controlled sodium and protein diet for 1 wk before each study. The humoral, renal, and systemic response to incremental dosages of irbesartan (75 mg for 4 wk, then 150 mg for 4 wk) was assessed, as was the pressor response to AngII (3 ng/kg per min), at 2-wk intervals. AngII type 1 receptor expression in skin biopsies was assessed at baseline and after 8 wk by a real-time PCR protocol. Men and women both exhibited significant declines in BP. Women achieved significantly reduced AngII sensitivity compared with men at lower dosages, showing no pressor response at 4 wk of 75 mg/d irbesartan, whereas men continued to exhibit a pressor response at 4 wk of 150 mg/d. Receptor expression at baseline did not differ between men and women but by 8 wk was significantly decreased in women and unchanged in men. Our findings indicate that men may require larger dosages of angiotensin receptor blocker than do women and that the BP response cannot be used as a surrogate marker for adequate RAS blockade of the renal microvasculature.

摘要

有证据表明,肾素 - 血管紧张素系统(RAS)功能存在性别差异。据推测,女性对RAS阻断的反应可能也有所不同。研究了男性和女性对血管紧张素受体阻滞剂递增剂量的肾脏和外周血流动力学反应,以及在8周内达到的血管紧张素II(AngII)不敏感程度。参与者为30名年轻健康男性(n = 15;平均年龄27±2岁)和女性(n = 15;平均年龄28±2岁),在每项研究前均进行为期1周的钠和蛋白质控制饮食。在2周的间隔内,评估了对厄贝沙坦递增剂量(4周75毫克,然后4周150毫克)的体液、肾脏和全身反应,以及对AngII(3纳克/千克每分钟)的升压反应。通过实时PCR方案在基线和8周后评估皮肤活检中1型AngII受体的表达。男性和女性的血压均显著下降。与男性相比,女性在较低剂量时AngII敏感性显著降低,在75毫克/天厄贝沙坦治疗4周时无升压反应,而男性在150毫克/天治疗4周时仍有升压反应。基线时男性和女性的受体表达无差异,但到8周时,女性显著下降,男性则无变化。我们的研究结果表明,男性可能比女性需要更大剂量的血管紧张素受体阻滞剂,并且血压反应不能用作肾脏微血管充分RAS阻断的替代标志物。

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