Abstract

Recent evidence suggests the presence of multiple tachykinins, i.e. substance P (SP), neurokinin A (NKA), neuropeptide K (NPK) and an eledoisin-like peptide (ELE) in capsaicin-sensitive primary afferent neurons [1]. Some of these neurons also contain calcitonin gene-related peptide (CGRP) [2]. Release of SP from collateral branches of primary afferents terminating in prevertebral ganglia [3] appears to be responsible for the generation of a non-cholinergic slow excitatory postsynaptic potential (EPSP) [4,5,6]. Here we present biochemical and electrophysiological studies on guinea-pig sympathetic ganglia.

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