Mir S S, Mason G R, Ormsbee H S
Gastroenterology. 1977 Aug;73(2):432-4.
Our aim was to investigate the existence of an inhibitory innervation at the gastroduodenal junction (GDJ) in the whole animal. Motility induced by vagal stimulation was monitored with strain force transducers on the gastric antrum, pylorus and duodenum. The experiments were carried out in two phases: the control phase following vagotomy (TV), and the treated phase where atropine sulfate (1 mg/Kg) was injected intravenously (TV+A). After TV, antral, pyloric and duodenal contractile activity was significantly increased (P less than 0.01) during the period of vagal stimulation. After (TV+A), spontaneous activity in the antrum and duodenum was abolished and vagal stimulation did not increase motility in these organs. Spontaneous pyloric activity present after atropine administration was inhibited by stimulation, and a concomitant relaxation of the pylorus was also demonstrated. Following the termination of the stimulus, a significant increase in contractions was noted on the pylorus. These experiments demonstrate the existence of an atropine-resistant inhibitory innervation at the GDJ in the anesthetized dog.
我们的目的是研究在完整动物的胃十二指肠连接处(GDJ)是否存在抑制性神经支配。通过应变力传感器监测胃窦、幽门和十二指肠上由迷走神经刺激诱导的运动。实验分两个阶段进行:迷走神经切断术后(TV)的对照阶段,以及静脉注射硫酸阿托品(1毫克/千克)后的处理阶段(TV + A)。TV后,在迷走神经刺激期间,胃窦、幽门和十二指肠的收缩活动显著增加(P小于0.01)。(TV + A)后,胃窦和十二指肠的自发活动消失,迷走神经刺激未增加这些器官的运动。阿托品给药后出现的幽门自发活动受到刺激抑制,同时还证实幽门出现了松弛。刺激终止后,幽门的收缩显著增加。这些实验证明了在麻醉犬的GDJ处存在对阿托品耐药的抑制性神经支配。