Rands Vicky F, Seth Dale M, Kobori Hiroyuki, Prieto Minolfa C
Department of Physiology, School of Medicine, Tulane University, 1430 Tulane Avenue, New Orleans, LA 70112, USA.
Gend Med. 2012 Aug;9(4):207-18. doi: 10.1016/j.genm.2012.06.001. Epub 2012 Jul 12.
The intrarenal renin-angiotensin system contributes to hypertension by regulating sodium and water reabsorption throughout the nephron. Sex differences in the intrarenal components of the renin-angiotensin system have been involved in the greater incidence of high blood pressure and progression to kidney damage in males than females.
This study investigated whether there is a sex difference in the intrarenal gene expression and urinary excretion of angiotensinogen (AGT) during angiotensin II (Ang II)-dependent hypertension and high-salt (HS) diet.
Male and female Sprague-Dawley rats were divided into 5 groups for each sex: Normal-salt control, HS diet (8% NaCl), Ang II-infused (80 ng/min), Ang II-infused plus HS diet, and Ang II-infused plus HS diet and treatment with the Ang II receptor blocker, candesartan (25 mg/L in the drinking water). Rats were evaluated for systolic blood pressure (SBP), kidney AGT mRNA expression, urinary AGT excretion, and proteinuria at different time points during a 14-day protocol.
Both male and female rats exhibited similar increases in urinary AGT, with increases in SBP during chronic Ang II infusion. HS diet greatly exacerbated the urinary AGT excretion in Ang II-infused rats; males had a 9-fold increase over Ang II alone and females had a 2.5-fold increase. Male rats displayed salt-sensitive SBP increases during Ang II infusion and HS diet, and female rats did not. In the kidney cortex, males displayed greater AGT gene expression than females during all treatments. During Ang II infusion, both sexes exhibited increases in AGT gene message compared with same-sex controls. In addition, HS diet combined with Ang II infusion exacerbated the proteinuria in both sexes. Concomitant Ang II receptor blocker treatment during Ang II infusion and HS diet decreased SBP and urinary AGT similarly in both sexes; however, the decrease in proteinuria was greater in the females.
During Ang II-dependent hypertension and HS diet, higher intrarenal renin-angiotensin system activation in males, as reflected by higher AGT gene expression and urinary excretion, indicates a mechanism for greater progression of high blood pressure and might explain the sex disparity in development of salt-sensitive hypertension.
肾内肾素 - 血管紧张素系统通过调节整个肾单位的钠和水重吸收来导致高血压。肾内肾素 - 血管紧张素系统各组分的性别差异与男性高血压发病率更高以及比女性更易进展为肾损伤有关。
本研究调查了在血管紧张素 II(Ang II)依赖性高血压和高盐(HS)饮食期间,肾内血管紧张素原(AGT)的基因表达和尿排泄是否存在性别差异。
将雄性和雌性斯普拉格 - 道利大鼠按性别各分为5组:正常盐对照组、HS饮食组(8%氯化钠)、输注Ang II组(80 ng/分钟)、输注Ang II加HS饮食组,以及输注Ang II加HS饮食并使用血管紧张素II受体阻滞剂坎地沙坦治疗组(饮水中含25 mg/L)。在为期14天的实验方案中的不同时间点,对大鼠的收缩压(SBP)、肾AGT mRNA表达、尿AGT排泄和蛋白尿进行评估。
在慢性输注Ang II期间,雄性和雌性大鼠的尿AGT均有类似增加,同时SBP也升高。HS饮食极大地加剧了输注Ang II大鼠的尿AGT排泄;雄性大鼠比仅输注Ang II时增加了9倍,雌性大鼠增加了2.5倍。在输注Ang II和HS饮食期间,雄性大鼠表现出盐敏感性SBP升高,而雌性大鼠没有。在肾皮质中,在所有处理过程中雄性大鼠的AGT基因表达均高于雌性大鼠。在输注Ang II期间,与同性对照组相比,两性的AGT基因信息均增加。此外,HS饮食与输注Ang II相结合加剧了两性的蛋白尿。在输注Ang II和HS饮食期间,同时使用血管紧张素II受体阻滞剂治疗使两性的SBP和尿AGT同样降低;然而,雌性大鼠蛋白尿的降低幅度更大。
在Ang II依赖性高血压和HS饮食期间,男性肾内肾素 - 血管紧张素系统激活程度更高,表现为AGT基因表达和尿排泄增加,这表明高血压进展更严重的一种机制,可能解释了盐敏感性高血压发生中的性别差异。