Zhou Shi-Yi, Lu Yuan-Xu, Yao HongRen, Owyang Chung
Division of Gastroenterology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
Am J Physiol Gastrointest Liver Physiol. 2008 May;294(5):G1201-9. doi: 10.1152/ajpgi.00309.2006.
The dorsal motor nucleus of the vagus (DMV) contains preganglionic neurons that control gastric motility and secretion. Stimulation of different parts of the DMV results in a decrease or an increase in gastric motor activities, suggesting a spatial organization of vagal preganglionic neurons in the DMV. Little is known about how these preganglionic neurons in the DMV synapse with different groups of intragastric motor neurons to mediate contraction or relaxation of the stomach. We used pharmacological and immunohistochemical methods to characterize intragastric neural pathways involved in mediating gastric contraction and relaxation in rats. Microinjections of L-glutamate (L-Glu) into the rostral or caudal DMV produced gastric contraction and relaxation, respectively, in a dose-related manner. Intravenous infusion of hexamethonium blocked these actions, suggesting mediation via preganglionic cholinergic pathways. Atropine inhibited gastric contraction by 85.5 +/- 4.5%. Gastric relaxation was reduced by intravenous administration of N(G)-nitro-L-arginine methyl ester (L-NAME; 52.5 +/- 11.9%) or VIP antagonist (56.3 +/- 14.9%). Combined administration of L-NAME and VIP antagonist inhibited gastric relaxation evoked by L-Glu (87.8 +/- 4.3%). Immunohistochemical studies demonstrated choline acetyltransferase immunoreactivity in response to L-Glu microinjection into the rostral DMV in 88% of c-Fos-positive intragastric myenteric neurons. Microinjection of L-Glu into the caudal DMV evoked expression of nitric oxide (NO) synthase and VIP immunoreactivity in 81 and 39%, respectively, of all c-Fos-positive intragastric myenteric neurons. These data indicate spatial organization of the DMV. Depending on the location, microinjection of L-Glu into the DMV may stimulate intragastric myenteric cholinergic neurons or NO/VIP neurons to mediate gastric contraction and relaxation.
迷走神经背运动核(DMV)包含控制胃动力和分泌的节前神经元。刺激DMV的不同部位会导致胃运动活动减少或增加,这表明DMV中迷走神经节前神经元存在空间组织。关于DMV中的这些节前神经元如何与不同组的胃内运动神经元形成突触以介导胃的收缩或舒张,我们知之甚少。我们使用药理学和免疫组织化学方法来表征参与介导大鼠胃收缩和舒张的胃内神经通路。向DMV的头端或尾端微量注射L-谷氨酸(L-Glu)分别以剂量相关的方式引起胃收缩和舒张。静脉注射六甲铵可阻断这些作用,表明是通过节前胆碱能通路介导的。阿托品抑制胃收缩85.5±4.5%。静脉注射N(G)-硝基-L-精氨酸甲酯(L-NAME;抑制率为52.5±11.9%)或VIP拮抗剂(抑制率为56.3±14.9%)可减少胃舒张。联合使用L-NAME和VIP拮抗剂可抑制L-Glu引起的胃舒张(抑制率为87.8±4.3%)。免疫组织化学研究表明,在向DMV头端微量注射L-Glu后,88%的c-Fos阳性胃内肌间神经元中有胆碱乙酰转移酶免疫反应性。向DMV尾端微量注射L-Glu分别在81%和39%的所有c-Fos阳性胃内肌间神经元中诱发一氧化氮(NO)合酶和VIP免疫反应性表达。这些数据表明DMV存在空间组织。根据位置不同,向DMV微量注射L-Glu可能刺激胃内肌间胆碱能神经元或NO/VIP神经元以介导胃收缩和舒张。