Elijovich F, Barry C R, Krakoff L R, Kirchberger M
Am J Physiol. 1984 Dec;247(6 Pt 2):H973-7. doi: 10.1152/ajpheart.1984.247.6.H973.
The effect of vasopressin infusion on the pressor dose responses to angiotensin II and norepinephrine was studied in pentobarbital-anesthetized and unanesthetized nephrectomized rats. Pressor vasopressin (2-15 ng X kg-1 X min-1) given to anesthetized rats decreased sensitivity to angiotensin II in a dose-dependent manner (r = 0.88), an effect completely reversible by dPMeTyrAVP, a vasopressin vascular antagonist. Subpressor vasopressin (0.5-1 ng X kg-1 X min-1) given to unanesthetized rats diminished sensitivity to angiotensin II in the presence or absence of pentolinium (10 mg/kg). Shifts in dose-response curves to angiotensin II were always parallel. In contrast, dose responses to norepinephrine were not modified by vasopressin in pentolinium-treated rats and showed a small nonparallel rightward shift in animals without pentolinium. In animals without pentolinium, the baroreflex-mediated reduction in heart rate elicited by angiotensin II was not altered by vasopressin infusion. Our data suggest that vasopressin reduces angiotensin II pressor action by diminishing pressor sensitivity to the peptide. They indicate that the effect may be specific, mediated through the vascular receptor for vasopressin and independent of actions of this hormone on the autonomic nervous system.
在戊巴比妥麻醉和未麻醉的肾切除大鼠中,研究了输注血管加压素对血管紧张素II和去甲肾上腺素升压剂量反应的影响。给麻醉大鼠输注升压剂量的血管加压素(2 - 15 ng·kg⁻¹·min⁻¹)以剂量依赖方式降低了对血管紧张素II的敏感性(r = 0.88),血管加压素血管拮抗剂dPMeTyrAVP可完全逆转这种作用。给未麻醉大鼠输注低于升压剂量的血管加压素(0.5 - 1 ng·kg⁻¹·min⁻¹),无论是否存在潘托铵(10 mg/kg),均降低了对血管紧张素II的敏感性。血管紧张素II剂量反应曲线的移位始终是平行的。相比之下,在潘托铵处理的大鼠中,血管加压素不改变对去甲肾上腺素的剂量反应,而在未用潘托铵的动物中,对去甲肾上腺素的剂量反应显示出小的非平行右移。在未用潘托铵的动物中,血管加压素输注不改变血管紧张素II引起的压力感受器介导的心率降低。我们的数据表明,血管加压素通过降低对该肽的升压敏感性来降低血管紧张素II的升压作用。它们表明这种作用可能是特异性的,通过血管加压素的血管受体介导,且独立于该激素对自主神经系统的作用。