Beleslin D B, Terzić B, Samardzić R, Jovanović-Mićic D
Institut de Pharmacologie, Faculté de Médecine, Yougoslavie.
C R Seances Soc Biol Fil. 1988;182(2):202-7.
The inhibitory effect of the predominantly alpha-2 adrenoceptor agonist, guanabenz, on the peristaltic reflex and on the pendular movements of the rabbit isolated ileum was investigated. Guanabenz depressed or abolished the peristaltic reflex as well as the pendular movements. These effects were concentration-dependent. Guanabenz is much more potent inhibiting the peristaltic reflex (IC50 1 X 10(-7) M) than the pendular movements (IC50 1 X 10(-5) M). The choline ester, acetylcholine restored the peristaltic reflex and the anticholinesterase, eserine, restored the pendular movements previously abolished by guanabenz. During the blockade of the peristaltic reflex produced by guanabenz, the pendular movements were virtually not changed. It is therefore reasonable to suppose that the inhibitory effect of guanabenz reflects the different properties of alpha-2 adrenoceptors associated with cholinergic nerve terminals within the myenteric plexus and the longitudinal smooth muscle subserving the peristaltic reflex and the pendular movements.
研究了主要作为α-2肾上腺素能受体激动剂的胍那苄对兔离体回肠蠕动反射和摆动运动的抑制作用。胍那苄可抑制或消除蠕动反射以及摆动运动。这些作用呈浓度依赖性。胍那苄抑制蠕动反射(半数抑制浓度[IC50]为1×10⁻⁷M)比抑制摆动运动(IC50为1×10⁻⁵M)更有效。胆碱酯类物质乙酰胆碱可恢复蠕动反射,抗胆碱酯酶药毒扁豆碱可恢复先前被胍那苄消除的摆动运动。在胍那苄产生的蠕动反射阻断期间,摆动运动实际上未发生改变。因此可以合理推测,胍那苄的抑制作用反映了与肠肌丛内胆碱能神经末梢以及参与蠕动反射和摆动运动的纵行平滑肌相关的α-2肾上腺素能受体的不同特性。