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Neurogenic vasodilatation in isolated bovine and canine penile arteries.
Author(s) -
Bowman A,
Gillespie J S
Publication year - 1983
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.1983.sp014827
Subject(s) - vasodilation , guanethidine , tetrodotoxin , endocrinology , inhibitory postsynaptic potential , vasoactive intestinal peptide , medicine , adrenergic , penis , stimulation , atropine , erectile tissue , acetylcholine , phenylephrine , anatomy , chemistry , biology , receptor , neuropeptide , blood pressure
Field stimulation of isolated, perfused bovine or canine penile arteries produced dilatation, after the adrenergic motor component of the response had been blocked with guanethidine and the vessels had developed a background tone. The vasodilatation was blocked by tetrodotoxin but not by atropine. The vasodilator responses to field stimulation were compared with those produced by ATP, by vasoactive intestinal peptide (VIP), and by the inhibitory factor extracted from the bovine retractor penis muscle. Of the three putative transmitters, the inhibitory factor produced responses that most closely resembled those to field stimulation. Haemoglobin, which blocks non‐adrenergic, non‐cholinergic inhibitory transmission in the bovine and canine retractor penis muscles, did not impair the vasodilatations produced by ATP or VIP, but slowly reduced or abolished those produced by field stimulation or by the inhibitory factor. Haemoglobin itself produced a powerful constriction of the isolated penile arteries. The results are compatable with the possibility that the inhibitory factor from the bovine retractor penis muscle (which may be the inhibitory transmitter in that muscle) is, or closely resembles, the transmitter of non‐adrenergic, non‐cholinergic vasodilator fibres in the penile arteries of dog and ox.