Koyama S, Hosomi H
Am J Physiol. 1986 Jun;250(6 Pt 2):R973-9. doi: 10.1152/ajpregu.1986.250.6.R973.
The present study was designed to evaluate renal opiate receptor mediation of the renin secretion response to electrical stimulation of the renal nerves in the pentobarbital sodium-anesthetized dog by use of the opiate agonist leucine-enkephalin (Leu-enk) and the opiate antagonist naloxone. In all animals studied, left kidneys were pump perfused at a constant renal blood flow. Renal perfusion pressure (RPP) and glomerular filtration rate (GFR) were unaltered at a stimulation frequency of 1.0 Hz; however, renin secretion rate (RSR) increased significantly in the nontreated group. High-frequency renal nerve stimulation (10 Hz) increased RPP and decreased GFR. RSR at the high-frequency stimulation was significantly augmented in the nontreated group. Renal arterial infusion of either Leu-enk (25 micrograms X kg-1 X min-1) or naloxone (7 micrograms X kg-1 X min-1) did not alter base-line levels of renal hemodynamics and RSR and did not produce significant changes in these variables even when renal nerves were stimulated at the low frequency; however, Leu-enk inhibited RPP and RSR responses to the high-frequency stimulation, and naloxone augmented these responses. Phentolamine (13 micrograms X kg-1 X min-1) prevented renal hemodynamic responses to the renal nerve stimulation, whereas RSR responses to the stimulation were unaffected. Propranolol (8 micrograms X kg-1 X min-1) resulted in decreases in RSR at the renal nerve stimulation despite the presence of changes in renal hemodynamics similar to the other groups. The results indicate that intrarenal opiate receptors may participate in inhibiting renal secretion of renin mediated by the renal nerves when renal vasoconstriction and reduction of GFR occurred at the high-frequency stimulation.
本研究旨在通过使用阿片类激动剂亮氨酸脑啡肽(Leu-enk)和阿片类拮抗剂纳洛酮,评估戊巴比妥钠麻醉犬肾阿片受体对肾神经电刺激所致肾素分泌反应的介导作用。在所有研究的动物中,左肾以恒定肾血流量进行泵灌注。在刺激频率为1.0 Hz时,肾灌注压(RPP)和肾小球滤过率(GFR)未改变;然而,未处理组的肾素分泌率(RSR)显著增加。高频肾神经刺激(10 Hz)使RPP升高,GFR降低。未处理组在高频刺激时的RSR显著增加。肾动脉输注Leu-enk(25微克·千克⁻¹·分钟⁻¹)或纳洛酮(7微克·千克⁻¹·分钟⁻¹)均未改变肾血流动力学和RSR的基线水平,即使在低频刺激肾神经时,这些变量也未产生显著变化;然而,Leu-enk抑制了对高频刺激的RPP和RSR反应,而纳洛酮增强了这些反应。酚妥拉明(13微克·千克⁻¹·分钟⁻¹)可防止对肾神经刺激的肾血流动力学反应,而对刺激的RSR反应未受影响。普萘洛尔(8微克·千克⁻¹·分钟⁻¹)尽管肾血流动力学变化与其他组相似,但在肾神经刺激时导致RSR降低。结果表明,当高频刺激导致肾血管收缩和GFR降低时,肾内阿片受体可能参与抑制肾神经介导的肾素分泌。