Robinson J L
Am J Physiol. 1986 Aug;251(2 Pt 2):H253-60. doi: 10.1152/ajpheart.1986.251.2.H253.
The effect of arginine vasopressin (AVP) and phenylephrine (PE) infusions on mean arterial pressure (MAP) and heart rate (HR) were compared in conscious dogs with all autonomic receptors intact (I), during muscarinic blockade (MB) and during ganglionic blockade (GB). After either MB or GB, the dose-MAP response curve for AVP and PE was shifted to the left of the I response curve; a greater shift was observed with AVP than with PE. The MAP threshold after GB for AVP and PE occurred at 10 and 50% of the threshold dose observed during the I response, respectively. Not only did the MAP threshold occur at a lower dose after MB and GB, but also the slope of the response curve was steeper than that of the I response. Comparing the amount of drug necessary to increase MAP 25 mmHg above control for PE and AVP before and after GB, the intact PE response required 4.3 +/- 1.0 (P less than 0.01) times more drug than during GB versus the intact AVP required 16.8 +/- 2.8 (P less than 0.01) times more drug than during GB. The baroreflex control of HR when all receptors were intact was 3.4 +/- 0.4 (P = 0.001) times more sensitive during AVP compared with PE; no differences were observed after MB. There were no significant changes in HR to AVP or PE after GB, thus indicating a lack of a direct effect of these agents on the HR. Our results show that MB and GB equally potentiate the pressor effects of AVP and PE, and the augmentation was much greater for AVP than for PE. The difference in the potentiation of these two vasoconstrictors is consistent with the finding that the baroreflex sensitivity during AVP was enhanced compared with PE. We have postulated that, in the resting conscious dog, AVP increases the sensitivity of the baroreflex primarily by producing a greater level of parasympathetic tone to the heart in response to a given pressure stimulus.
在自主神经受体完整的清醒犬(I组)、毒蕈碱阻断(MB)期间和神经节阻断(GB)期间,比较了输注精氨酸加压素(AVP)和去氧肾上腺素(PE)对平均动脉压(MAP)和心率(HR)的影响。在MB或GB后,AVP和PE的剂量 - MAP反应曲线均向左移至I组反应曲线的左侧;AVP的移位幅度大于PE。GB后AVP和PE的MAP阈值分别出现在I组反应中观察到的阈值剂量的10%和50%。不仅MB和GB后的MAP阈值出现在较低剂量时,而且反应曲线的斜率也比I组反应的斜率更陡。比较GB前后使MAP比对照升高25 mmHg所需的PE和AVP的药物量,完整状态下的PE反应所需药物量比GB期间多4.3±1.0倍(P<0.01),而完整状态下的AVP所需药物量比GB期间多16.8±2.8倍(P<0.01)。当所有受体完整时,AVP期间HR的压力反射控制比PE期间敏感3.4±0.4倍(P = 0.001);MB后未观察到差异。GB后对AVP或PE的HR无显著变化,因此表明这些药物对HR缺乏直接作用。我们的结果表明,MB和GB均同等程度地增强了AVP和PE的升压作用,且AVP的增强幅度远大于PE。这两种血管收缩剂增强作用的差异与AVP期间压力反射敏感性高于PE的发现一致。我们推测,在静息清醒犬中,AVP主要通过对给定压力刺激产生更高水平的迷走神经张力来增加压力反射的敏感性。