Katholi R E
Am J Physiol. 1983 Jul;245(1):F1-14. doi: 10.1152/ajprenal.1983.245.1.F1.
Efferent renal innervation is composed of postganglionic sympathetic fibers to the renal arterioles, juxtaglomerular apparatus, and renal tubules. Increased efferent renal sympathetic nerve activity results in increased renal vascular resistance, renin release, and sodium retention. These responses from enhanced renal sympathetic activity contribute to normal cardiovascular homeostasis but could also facilitate the development of hypertension by shifting the arterial pressure-renal sodium excretion curve to the right. Accordingly, interruption of the renal nerves should prevent the development of hypertension in animal models in which increased sympathetic nervous system activity has been implicated. Renal denervation delays the development of hypertension and results in greater sodium excretion in the Okamoto and New Zealand spontaneously hypertensive rat and in the DOCA-salt-treated rat, suggesting that these responses are due, at least in part, to loss of efferent renal nerve activity. Similar sympathetically mediated renal vasoconstriction has been implicated in the pathogenesis of early essential hypertension in man. Recent studies indicate that the kidney is a sensory organ with mechano-receptive and chemoreceptive afferent renal nerves involved in renorenal and cardiovascular regulation. Renal denervation in established one-kidney one-clip and two-kidney one-clip Goldblatt hypertension in the rat and chronic coarctation in the dog results in an attenuation of the hypertension. The depressor effect of renal denervation in these models is not due to change in renin activity or sodium excretion but is associated with decreased activity of the sympathetic nervous system. These findings suggest that the afferent renal nerves contribute to the pathogenesis of renovascular hypertension by enhancing the activity of the sympathetic nervous system. The role of the afferent renal nerves in renovascular hypertension in humans warrants further study.
肾传出神经支配由至肾小动脉、肾小球旁器和肾小管的节后交感神经纤维组成。肾传出交感神经活动增强会导致肾血管阻力增加、肾素释放及钠潴留。肾交感神经活动增强所引发的这些反应有助于维持正常的心血管稳态,但也可能通过使动脉压 - 肾钠排泄曲线右移而促进高血压的发展。因此,在交感神经系统活动增强被认为与之相关的动物模型中,切断肾神经应可预防高血压的发生。在冈本和新西兰自发性高血压大鼠以及去氧皮质酮 - 盐处理的大鼠中,肾去神经支配可延缓高血压的发展并导致钠排泄增加,这表明这些反应至少部分归因于肾传出神经活动的丧失。类似的交感神经介导的肾血管收缩也被认为与人原发性高血压早期的发病机制有关。最近的研究表明,肾脏是一个感觉器官,其机械感受性和化学感受性肾传入神经参与肾肾及心血管调节。在大鼠已建立的单肾单夹和双肾单夹戈德布拉特高血压模型以及犬慢性缩窄模型中,肾去神经支配可使高血压减轻。在这些模型中,肾去神经支配的降压作用并非由于肾素活性或钠排泄的改变,而是与交感神经系统活性降低有关。这些发现提示,肾传入神经通过增强交感神经系统的活性而参与肾血管性高血压的发病机制。肾传入神经在人类肾血管性高血压中的作用值得进一步研究。