Achard F, Denavit M, Roche M
C R Seances Soc Biol Fil. 1985;179(4):462-70.
The electrical activity of the sphincter of Oddi and gastro-intestinal tract had been recorded on 21 negative atropineesterase conscious rabbits by means of chronically implanted electrodes located in the digestive wall. An analysis of the action of different spasmolytic and analgesic drugs was realized. Electromyograms of the sphincter of Oddi presented (a) isolated or in series spike potentials occurring independently of electrical activities of the duodenum (b) recurring spike potentials correlated with intestine spikes. The independent activity of the sphincter of Oddi was not controlled by the cholinergic system, contrary to the intestine-dependent activity (effect of the fempiverinium, atropine like drug). The pitofenone had inhibited the spike potentials of both the sphincter and intestine because its papaverinic effect. The noramidopyrine, analgesic drug without morphine-like effects, had induced activation and inhibition at low and high posology respectively.
通过长期植入位于消化壁的电极,记录了21只阴性阿托品酯酶清醒兔的Oddi括约肌和胃肠道的电活动。对不同解痉和镇痛药的作用进行了分析。Oddi括约肌的肌电图表现为:(a) 独立于十二指肠电活动出现的孤立或串联的尖峰电位;(b) 与肠尖峰相关的反复出现的尖峰电位。与依赖肠的活动(芬维铵,一种阿托品样药物的作用)相反,Oddi括约肌的独立活动不受胆碱能系统控制。匹托非诺因其罂粟碱样作用而抑制了括约肌和肠的尖峰电位。非那吡啶,一种无吗啡样作用的镇痛药,在低剂量和高剂量时分别引起激活和抑制。