Wolzt M, Gerschlager W, Zweytick B, Jilma B, Riemer H, Sertl K, Eichler H G
Department of Clinical Pharmacology, Vienna University Hospital, Allgemeines Krankenhaus, Austria.
Naunyn Schmiedebergs Arch Pharmacol. 1994 Aug;350(2):194-200. doi: 10.1007/BF00241096.
The direct and noradrenaline-modulating effects of neuropeptide Y (NPY) and vasoactive intestinal peptide (VIP) on venous smooth muscle were studied in healthy volunteers employing the dorsal hand vein compliance technique. Local infusions of NPY had no measurable effect on venous tone, but coinfusion of a constant high dose of NPY (242 pmol/min) with noradrenaline caused a 2.9-fold increase in the mean ED50 for noradrenaline. The dilating effect of VIP on preconstricted hand veins was weak, maximal venodilation could not be achieved, because systemic side effects occurred at submaximally venodilating doses. Coinfusion of noradrenaline with a weakly venodilating, constant dose of VIP (93.2 pmol/min) caused a 0.5-fold decrease in the sensitivity for noradrenaline. Although functional interactions between NPY or VIP and noradrenaline could be demonstrated, the dosages of the peptides required were high. Thus our results indicate that neither NPY nor VIP exert a major direct or noradrenaline-modulating effect on human veins.
采用手背静脉顺应性技术,在健康志愿者中研究了神经肽Y(NPY)和血管活性肠肽(VIP)对静脉平滑肌的直接作用以及对去甲肾上腺素的调节作用。局部输注NPY对静脉张力没有可测量的影响,但将恒定高剂量的NPY(242 pmol/分钟)与去甲肾上腺素共同输注会导致去甲肾上腺素的平均半数有效剂量(ED50)增加2.9倍。VIP对预收缩的手部静脉的舒张作用较弱,无法实现最大程度的静脉舒张,因为在亚最大静脉舒张剂量时就出现了全身副作用。将去甲肾上腺素与弱静脉舒张的恒定剂量VIP(93.2 pmol/分钟)共同输注会导致对去甲肾上腺素的敏感性降低0.5倍。虽然可以证明NPY或VIP与去甲肾上腺素之间存在功能相互作用,但所需的肽剂量很高。因此,我们的结果表明,NPY和VIP对人体静脉均未发挥主要的直接作用或对去甲肾上腺素的调节作用。