Glasgow I, Mattar K, Krantis A
Digestive Diseases Research Group, University of Ottawa, Ottawa, Ontario, Canada K1H 8M5.
Am J Physiol. 1998 Nov;275(5):G889-96. doi: 10.1152/ajpgi.1998.275.5.G889.
Our studies of fasted anesthetized rats have shown that all spontaneous relaxations of the antrum are nitric oxide (NO) dependent. Duodenal motility is patterned into propagating "grouped" motor activity interposed with "intergroup" periods of nonpropagating motor activity; in the duodenum, only intergroup relaxations are NO dependent. We examined the involvement of NO and ATP in spontaneous motor activities of the gastroduodenum in vivo: contractions and relaxations were recorded and analyzed simultaneously from the antrum (S1) and proximal duodenum (D1) of anesthetized Sprague-Dawley rats (n = 10/group), using extraluminal foil strain gauges. Treatment with the NO synthase inhibitor NG-nitro-L-arginine methyl ester (L-NAME; 10 mg/kg iv) attenuated (P < 0.05) antral and intergroup relaxations, whereas grouped relaxations were enhanced (P < 0.05). These effects were reversed with L-arginine (300 mg/kg iv). L-NAME also increased (P < 0.05) the amplitude of duodenal contractions. ATP (8 mg. kg-1. min-1 iv) stimulated relaxations at S1 and D1 that were blocked by the P2-purinoceptor antagonist suramin (60 mg/kg iv). This treatment did not affect spontaneous antral relaxations; however, duodenal grouped relaxations were attenuated. Desensitization to the P2x-purinoceptor agonist alpha,beta-methylene ATP (300 micrograms/kg iv) gave results similar to suramin. In contrast, the P2y-purinoceptor agonist 2-methylthio-ATP (2-MeS-ATP; 360 micrograms/kg iv) evoked duodenal relaxations that were attenuated by L-NAME, and desensitization to 2-MeS-ATP attenuated intergroup relaxations. Spontaneous relaxations of the rat antrum and duodenal intergroup relaxations are NO dependent. Both gut regions relax in response to systemically administered ATP; this response is sensitive to suramin. Grouped duodenal relaxations display functional sensitivity to suramin and P2x- purinoceptor desensitization, indicative of the involvement of ATP and P2x purinoceptors. P2y purinoceptors must also be present; however, these occur on elements releasing NO. Although NO does not mediate grouped relaxations or duodenal contractions, the sensitivity of these responses to L-NAME indicates that the pathway(s) controlling these responses is modulated by NO.
我们对禁食麻醉大鼠的研究表明,胃窦的所有自发性舒张均依赖于一氧化氮(NO)。十二指肠运动模式为传播性的“成组”运动活动,其间穿插着非传播性运动活动的“组间”期;在十二指肠中,只有组间舒张依赖于NO。我们研究了NO和ATP在体内胃十二指肠自发性运动活动中的作用:使用腔外箔应变片,同时记录并分析麻醉的Sprague-Dawley大鼠(每组n = 10)胃窦(S1)和十二指肠近端(D1)的收缩和舒张。用NO合酶抑制剂NG-硝基-L-精氨酸甲酯(L-NAME;10 mg/kg静脉注射)处理可减弱(P < 0.05)胃窦和组间舒张,而成组舒张增强(P < 0.05)。这些作用可被L-精氨酸(300 mg/kg静脉注射)逆转。L-NAME还增加了(P < 0.05)十二指肠收缩的幅度。ATP(8 mg·kg-1·min-1静脉注射)刺激S1和D1处的舒张,该作用被P2嘌呤受体拮抗剂苏拉明(60 mg/kg静脉注射)阻断。该处理不影响胃窦自发性舒张;然而,十二指肠成组舒张减弱。对P2x嘌呤受体激动剂α,β-亚甲基ATP(300 μg/kg静脉注射)脱敏得到了与苏拉明相似的结果。相反,P2y嘌呤受体激动剂2-甲硫基-ATP(2-MeS-ATP;360 μg/kg静脉注射)诱发的十二指肠舒张被L-NAME减弱,对2-MeS-ATP脱敏减弱了组间舒张。大鼠胃窦的自发性舒张和十二指肠组间舒张依赖于NO。两个肠道区域对全身给药的ATP均有舒张反应;该反应对苏拉明敏感。十二指肠成组舒张对苏拉明和P2x嘌呤受体脱敏表现出功能敏感性,表明ATP和P2x嘌呤受体参与其中。P2y嘌呤受体也必定存在;然而,它们存在于释放NO的细胞成分上。虽然NO不介导成组舒张或十二指肠收缩,但这些反应对L-NAME的敏感性表明,控制这些反应的信号通路受NO调节。