Machová J
Neuropharmacology. 1987 Feb-Mar;26(2-3):125-9. doi: 10.1016/0028-3908(87)90199-7.
Effects of vasoactive intestinal polypeptide (VIP) in the superior cervical ganglion (SCG) of the cat were investigated in situ. Vasoactive intestinal polypeptide (0.075-1.5 nmol) induced a dose-dependent depolarization of the superior cervical ganglion, characterized by a long-latency, slow onset, small amplitude and long duration. Initial short-lasting hyperpolarization of the superior cervical ganglion was observed in 5 out of 8 experiments after administration of VIP in a dose of 0.75 nmol. Vasoactive intestinal polypeptide (0.075-1.5 nmol) unmasked the muscarinic slow negative potential, following the compound action potential and unmasked or enhanced the stimulus-bound decremental oscillatory potentials induced by the muscarinic agonist McN-A-343 in the superior cervical ganglion. Vasoactive intestinal peptide induced a slight, but significant increase in the amplitude of the postganglionic action potentials evoked by preganglionic stimulation. The data mentioned above suggest that VIP may act as a neuromodulator of cholinergic transmission at the ganglionic synapse.
研究了血管活性肠肽(VIP)在猫颈上神经节(SCG)中的原位效应。血管活性肠肽(0.075 - 1.5 nmol)可诱导颈上神经节产生剂量依赖性去极化,其特点为潜伏期长、起始缓慢、幅度小且持续时间长。在8次实验中的5次里,给予0.75 nmol剂量的VIP后,观察到颈上神经节最初出现短暂的超极化。血管活性肠肽(0.075 - 1.5 nmol)在复合动作电位之后揭示了毒蕈碱慢负电位,并揭示或增强了由毒蕈碱激动剂McN - A - 343在颈上神经节中诱导的与刺激相关的递减振荡电位。血管活性肠肽使节前刺激诱发的节后动作电位幅度略有但显著增加。上述数据表明,VIP可能作为神经节突触处胆碱能传递的神经调节剂发挥作用。