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Arteriolar vasodilatation in frog skeletal muscle in vivo: modification of second messenger systems
Author(s) -
Fuglsang A
Publication year - 1991
Publication title -
experimental physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.925
H-Index - 101
eISSN - 1469-445X
pISSN - 0958-0670
DOI - 10.1113/expphysiol.1991.sp003545
Subject(s) - ibmx , forskolin , cyclic nucleotide , vasodilation , medicine , sodium nitroprusside , endocrinology , second messenger system , phosphodiesterase inhibitor , phosphodiesterase , adenosine , cyclase , chemistry , vascular smooth muscle , cyclic nucleotide phosphodiesterase , cyclic guanosine monophosphate , bucladesine , intracellular , biology , nucleotide , biochemistry , nitric oxide , enzyme , stimulation , smooth muscle , gene
This study was concerned with the role of cyclic nucleotides in the post‐junctional vasodilatation mechanism. Interventions with second messenger systems involving cyclic adenosine monophosphate (cyclic AMP) and cyclic guanosine monophosphate (cyclic GMP), allowed the role of these nucleotides in vascular smooth muscle to be evaluated in the autoperfused, transparent frog muscle, m. cutaneous pectoris. The microcirculation was observed by intravital microscopy, and arteriolar diameters were continuously recorded. Pre‐ and post‐junctional effects were distinguished by comparing results in control frogs with those obtained in frogs that had been chemically sympathectomized with either 6‐hydroxydopamine or tetrodotoxin. Arterioles that were pre‐contracted with adrenaline dilated in response to topical application of forskolin or sodium nitroprusside, which are direct activators of intracellular adenylate cyclase and guanylate cyclase, respectively. Arterioles were also dilated by 3‐isobutyl‐1‐methylxanthine (IBMX), which is a non‐selective inhibitor of cyclic AMP‐ and cyclic GMP‐phosphodiesterase, and by rolipram, which is a selective inhibitor of the calcium‐independent cyclic AMP‐phosphodiesterase. Dibutyryl‐cyclic AMP and dibutyryl‐cyclic GMP also caused vasodilatation. These results indicate that in vascular smooth muscle, intracellular mechanisms involving cyclic nucleotides (cyclic AMP and cyclic GMP) are important in vasodilatation. They may act in conjunction with pre‐junctional inhibitory mechanisms on sympathetic nerves.