Dual mechanism for catecholamine secretion in the dogfish shark Squalus acanthias

• Published in: The American journal of physiology Vol. 244; no. 5; p. R641
• Main Authors: Opdyke, D F, Bullock, J, Keller, N E, Holmes, K
• Format: Journal Article
• Language: English
• Published: United States 01.05.1983
• Subjects: Animals; Antihypertensive Agents - pharmacology; Blood Pressure - drug effects; Catecholamines - secretion; Dimethylphenylpiperazinium Iodide - pharmacology; Dogfish - physiology; Heart Rate - drug effects; Hexamethonium; Hexamethonium Compounds - pharmacology; Potassium - pharmacology; Respiration - drug effects; Sharks - physiology
• ISSN: 0002-9513
• DOI: 10.1152/ajpregu.1983.244.5.r641

Both 1,1-dimethyl-4-phenylpiperazinium iodide, a ganglionic stimulating drug (DMPP), and potassium ion (K+) cause a pressor response when injected into Squalus acanthias, an elasmobranch. The pressor responses are due to increased secretion of epinephrine and norepinephrine. The pressor response to DMPP can be blocked by prior infusion of hexamethonium, a ganglionic blocking drug. However, ganglionic blockade does not inhibit the pressor response to K+. Plasma catecholamine concentrations do not increase significantly in response to challenge with DMPP after hexamethonium infusion, but exceedingly high levels of plasma catecholamines quickly appear after K+ injection following hexamethonium infusion. It is concluded that there are at least two mechanisms controlling catecholamine secretion in the dogfish, one of which involves the ganglion cells that are intimately associated with chromaffin cells in the chromophil bodies that are so characteristic of this species and elasmobranchs in general.