Villarreal D, Reams G, Freeman R H
Departments of Internal Medicine and Physiology, University of Missouri, and Harry S. Truman Memorial Veterans' Hospital, Columbia, Missouri, USA.
Kidney Int. 2000 Sep;58(3):989-94. doi: 10.1046/j.1523-1755.2000.00256.x.
Previous studies from this laboratory have reported a marked attenuation of the renal responses to pharmacologic doses of synthetic murine leptin infused in the spontaneously hypertensive rat (SHR) model compared with normotensive Sprague-Dawley and lean Zucker rat models.
In the present study, the hemodynamic and renal excretory effects of an intravenous bolus administration of pharmacologic doses of synthetic murine leptin were examined in groups of anesthetized SHR with unilateral nephrectomy and renal denervation or sham-denervation of the remaining kidney.
In the SHR with acute renal denervation (N = 8), an intravenous bolus of 1600 microg/kg of leptin produced a significant twofold to fourfold elevation in sodium excretion but did not increase natriuresis in the sham-denervated group (N = 6). Chronic renal denervation of one-week duration (N = 8) was associated with qualitatively and quantitatively similar increases of sodium excretion in response to leptin administration. Mean arterial pressure remained unchanged in all groups after the administration of leptin.
Collectively, these results are interpreted to suggest that the blunted natriuretic and diuretic responses to leptin observed in the SHR with intact renal nerves may be partially explained by the antinatriuretic effect of an enhanced baseline efferent renal sympathetic activity and/or leptin's stimulation of the sympathetic nervous system.
本实验室先前的研究报告称,与正常血压的斯普拉格-道利大鼠和瘦型 Zucker 大鼠模型相比,在自发性高血压大鼠(SHR)模型中,给予药理剂量的合成小鼠瘦素后,肾脏反应明显减弱。
在本研究中,对单侧肾切除并对剩余肾脏进行去神经支配或假去神经支配的麻醉 SHR 组,静脉推注药理剂量的合成小鼠瘦素,检测其血流动力学和肾脏排泄效应。
在急性肾去神经支配的 SHR(N = 8)中,静脉推注 1600 μg/kg 的瘦素使钠排泄量显著升高两倍至四倍,但在假去神经支配组(N = 6)中并未增加钠利尿。持续一周的慢性肾去神经支配(N = 8)与给予瘦素后钠排泄量在质量和数量上的类似增加有关。给予瘦素后,所有组的平均动脉压均保持不变。
总体而言,这些结果被解释为提示,在肾神经完整的 SHR 中观察到的对瘦素的利钠和利尿反应减弱,可能部分归因于增强的基线肾传出交感神经活动的抗利钠作用和/或瘦素对交感神经系统的刺激。