Hypertension Unit, Univ. of Ottawa Heart Institute, H3228, 40 Ruskin St., Ottawa, ON, Canada K1Y 4W7.
Am J Physiol Heart Circ Physiol. 2010 Aug;299(2):H422-30. doi: 10.1152/ajpheart.00256.2010. Epub 2010 May 28.
An increase in plasma ANG II causes neuronal activation in hypothalamic nuclei and a slow pressor response, presumably by increasing sympathetic drive. We evaluated whether the activation of a neuromodulatory pathway, involving aldosterone and "ouabain," is involved in these responses. In Wistar rats, the subcutaneous infusion of ANG II at 150 and 500 ng x kg(-1) x min(-1) gradually increased blood pressure up to 60 mmHg at the highest dose. ANG II at 500 ng x kg(-1) x min(-1) increased plasma ANG II by 4-fold, plasma aldosterone by 25-fold, and hypothalamic aldosterone by 3-fold. The intracerebroventricular infusion of an aldosterone synthase (AS) inhibitor prevented the ANG II-induced increase in hypothalamic aldosterone without affecting the increase in plasma aldosterone. Neuronal activity, as assessed by Fra-like immunoreactivity, increased transiently in the subfornical organ (SFO) but progressively in the paraventricular nucleus (PVN) and supraoptic nucleus (SON). The central infusion of the AS inhibitor or a mineralocorticoid receptor blocker markedly attenuated the ANG II-induced neuronal activation in the PVN but not in the SON. Pressor responses to ANG II at 150 ng x kg(-1) x min(-1) were abolished by an intracerebroventricular infusion of the AS inhibitor. Pressor responses to ANG II at 500 ng x kg(-1) x min(-1) were attenuated by the central infusion of the AS inhibitor or the mineralocorticoid receptor blocker by 70-80% and by Digibind (to bind "ouabain") by 50%. These results suggest a novel central nervous system mechanism for the ANG II-induced slow pressor response, i.e., circulating ANG II activates the SFO, leading to the direct activation of the PVN and SON, and, in addition, via aldosterone-dependent amplifying mechanisms, causes sustained activation of the PVN and thereby hypertension.
血管紧张素 II(ANG II)水平升高会引起下丘脑核神经元激活和升压反应缓慢,这可能是通过增加交感神经驱动实现的。我们评估了涉及醛固酮和“哇巴因”的神经调节途径的激活是否参与了这些反应。在 Wistar 大鼠中,150 和 500ng·kg(-1)·min(-1)的 ANG II 皮下输注逐渐将血压升高至最高剂量时的 60mmHg。500ng·kg(-1)·min(-1)的 ANG II 使血浆 ANG II 增加 4 倍,血浆醛固酮增加 25 倍,下丘脑醛固酮增加 3 倍。脑室内输注醛固酮合酶(AS)抑制剂可防止 ANG II 诱导的下丘脑醛固酮增加,而不影响血浆醛固酮的增加。Fra 样免疫反应性评估的神经元活性在脑室外侧核(SFO)短暂增加,但在室旁核(PVN)和视上核(SON)中逐渐增加。AS 抑制剂或盐皮质激素受体阻滞剂的中枢输注显著减弱了 ANG II 诱导的 PVN 神经元激活,但对 SON 没有影响。脑室内输注 AS 抑制剂可消除 150ng·kg(-1)·min(-1) ANG II 的升压反应。AS 抑制剂或盐皮质激素受体阻滞剂的中枢输注将 500ng·kg(-1)·min(-1) ANG II 的升压反应分别减弱 70-80%,Digibind(结合“哇巴因”)减弱 50%。这些结果表明,ANG II 诱导的缓慢升压反应存在一种新的中枢神经系统机制,即循环 ANG II 激活 SFO,导致 PVN 和 SON 的直接激活,并且通过醛固酮依赖性放大机制,导致 PVN 的持续激活,从而导致高血压。