Abstract

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.

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