Rapid accumulation of inositol phosphates in isolated rat superior cervical sympathetic ganglia exposed to V1-vasopressin and muscarinic cholinergic stimuli

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Authors

Colleges, School and Institutes

External organisations

  • University of Birmingham

Abstract

1. An accumulation of 3H-labelled inositol phosphates is observed when prelabelled rat superior cervical sympathetic ganglia are exposed to [8-arginine]vasopressin or to muscarinic cholinergic stimuli. The response to vasopression is much greater than the response to cholinergic stimuli. 2. The response to vasopressin is blocked by a V1-vasopressin antagonist, and oxytocin is a much less potent agonist than vasopression. Vasopressin causes no increase in the cyclic AMP content of ganglia. These ganglia therefore appear to have functional V1-vasopressin receptors that are capable of activating inositol lipid breakdown, but no V2-receptors coupled to adenylate cyclase. 3. The first [3H]inositol-labelled products to accumulate in stimulated ganglia are inositol trisphosphate and inositol bisphosphate, suggesting that the initiating reaction in stimulated inositol lipid metabolism is a phosphodiesterase-catalysed hydrolysis of phosphatidylinositol 4,5-bisphosphate (and possibly also phosphatidylinositol 4-phosphate) 4. This response to exogenous vasopressin occurs in ganglia incubated in media of reduced Ca2+ concentration. 5. The physiological functions of the V1-vasopressin receptors of these ganglia remain unknown.

Details

Original languageEnglish
Pages (from-to)803-811
Number of pages9
JournalBiochemical Journal
Volume221
Issue number3
Publication statusPublished - 1 Jan 1984