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Properties of an opioid-mediated inhibition evoked by preganglionic axons in the superior cervical ganglion of the cat

Immunohistochemical studies have shown opioid peptides in sympathetic ganglia and preganglionic neurons. An inhibitory action of opioids has been demonstrated in some central and peripheral synapses. However, a physiological role of endogenous opioids in sympathetic ganglia has not been well characterized. The present study investigated endogenous opioid action in the SCG of the cat. The results obtained show that an endogenous opioid is released from preganglionic axon terminals, in a frequency range that matches the natural activity of sympathetic preganglionic neurons, and inhibits ganglionic transmission by acting on post-synaptic opiate receptors of the $ mu$ and $ delta$ subtypes coupled to PTX-sensitive G protein. The size of the store of the endogenous opioid in the preganglionic axon terminals is small and readily exhaustible. Protein synthesis and axonal transport are required for maintenance of the store. The opioid inhibition is under control of the PKC system. This study provides the first thorough characterization of the properties of an opioid-mediated inhibitory mechanism in a well-defined synapse.

Identiferoai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:QMM.41800
Date January 1994
CreatorsZhang, Chunyi
ContributorsPolosa, Canio (advisor)
PublisherMcGill University
Source SetsLibrary and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada
LanguageEnglish
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation
Formatapplication/pdf
CoverageDoctor of Philosophy (Department of Physiology.)
RightsAll items in eScholarship@McGill are protected by copyright with all rights reserved unless otherwise indicated.
Relationalephsysno: 001397792, proquestno: NN94729, Theses scanned by UMI/ProQuest.

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