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Nerve pathways involved in adrenergic regulation of electrical and mechanical activities in the chicken rectum
Author(s) -
Komori Seiichi,
Ohashi Hidenori
Publication year - 1987
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1987.tb16831.x
Subject(s) - phentolamine , cholinergic , rectum , adrenergic , stimulation , hexamethonium , endocrinology , medicine , atropine , biology , anatomy , receptor
1 Peripheral nerve pathways responsible for adrenergic inhibition of mechanical and electrical activities in the chicken rectum and receptors mediating the adrenergic inhibition were investigated in isolated extrinsically‐innervated rectum of the chicken. 2 Electrical stimulation of the anal end (Ra) or the ileal cut end (Ri) of Remak's nerve, or perivascular nerves (P) elicited relaxation of the rectum pretreated with atropine (0.5 μ m ) and hexamethonium (0.3 m m ) to block the cholinergic and non‐cholinergic, non‐adrenergic excitatory innervations. Ri stimulation was much less effective than Ra and P stimulations. The relaxation was shown to be related to cessation of spontaneous spike discharge of the longitudinal muscle which was accompanied by membrane hyperpolarization. 3 The inhibitory effects elicited by Ra and P stimulations, which were prolonged beyond the period of the stimulation, were converted to transient ones by propranolol (3.4 μ m ). Phentolamine (2.6 μ m ) reduced effectively the residual effects. In contrast, the effects of Ri stimulation were little affected by these drugs. 4 The present results provide evidence for the existence of two nerve pathways responsible for direct adrenergic inhibitory innervation to the chicken rectum, one running orally in Remak's nerve trunk, leaving it and descending in the branches to the rectum, and the other running as the perivascular nerves along the arterial supplies of the rectum. The direct innervation is mediated predominantly by β‐adrenoceptors.