Blair M L
Am J Physiol. 1981 Jun;240(6):E682-8. doi: 10.1152/ajpendo.1981.240.6.E682.
This study was designed to determine whether renal alpha-adrenoceptors can mediate tonic neural stimulation of renin secretion. The effect of alpha-adrenoceptor blockade by phenoxybenzamine (POB) or prazosin on renin secretion rate (RSR) was studied in pentobarbital-anesthetized dogs in which renal perfusion pressure was held constant with an adjustable aortic clamp. POB alone (100 micrograms.kg-1.min-1 iv) did not change arterial plasma renin activity (PRA). However, when beta-adrenoceptors were blocked by intravenous propranolol, intravenous POB infusion (100 micrograms.kg-1.min-1) decreased PRA and RSR to 48 +/- 8 and 21 +/- 9% of previous levels within 30 min. This effect was abolished by acute bilateral renal denervation. Direct intrarenal POB infusion (10 or 3.3 micrograms.kg-1.min-1) decreased RSR, whereas intravenous POB (3.3 micrograms.kg-1.min-1) had no effect on either RSR or PRA in propranolol-pretreated dogs. Prazosin (1 microgram.kg-1.min-1 iv) also significantly decreased PRA. These data indicate that when beta-adrenoceptors are blocked by propranolol, tonic neural stimulation of renin secretion is mediated by renal alpha-adrenoceptors.
本研究旨在确定肾α-肾上腺素能受体是否能介导肾素分泌的紧张性神经刺激。在戊巴比妥麻醉的犬中,使用可调节的主动脉夹使肾灌注压保持恒定,研究了苯氧苄胺(POB)或哌唑嗪对肾素分泌率(RSR)的α-肾上腺素能受体阻断作用。单独使用POB(100微克·千克⁻¹·分钟⁻¹静脉注射)并未改变动脉血浆肾素活性(PRA)。然而,当静脉注射普萘洛尔阻断β-肾上腺素能受体时,静脉注射POB(100微克·千克⁻¹·分钟⁻¹)在30分钟内将PRA和RSR分别降至先前水平的48±8%和21±9%。急性双侧肾去神经支配消除了这种作用。在普萘洛尔预处理的犬中,直接肾内注射POB(10或3.3微克·千克⁻¹·分钟⁻¹)降低了RSR,而静脉注射POB(3.3微克·千克⁻¹·分钟⁻¹)对RSR或PRA均无影响。哌唑嗪(1微克·千克⁻¹·分钟⁻¹静脉注射)也显著降低了PRA。这些数据表明,当普萘洛尔阻断β-肾上腺素能受体时,肾素分泌的紧张性神经刺激由肾α-肾上腺素能受体介导。