Savoye Guillaume, Jemaa Yassine, Mosni Grégory, Savoye-Collet Céline, Morcamp Paola, Déchelotte Pierre, Bouin Mickael, Denis Philippe, Ducrotté Philippe
ADEN EA 3234, Department of Gastroenterology and Nutrition, Rouen University, Hospital C Nicolle, 1 rue de Germont, 76031, Rouen Cedex, France.
Dig Dis Sci. 2006 Dec;51(12):2147-53. doi: 10.1007/s10620-006-9393-9. Epub 2006 Nov 14.
Nitric oxide (NO) plays an important role as a nonadrenergic, noncholinergic inhibitory neurotransmitter in the GI tract. Our study aims were to investigate the effect of a single intragastric L-arginine (L-Arg) administration, as a source of NO, on proximal stomach tone in basal and postintragastric administration of a polymeric diet in humans and to evaluate concomitantly the effect on antral area as an indirect assessment of gastric emptying. Eight healthy volunteers were studied in a randomized double-blind crossover study after, respectively, 15 g L-Arg, 30 g L-Arg, or placebo administered in the stomach through a gastric tube. The drug administration was followed by a polymeric diet infusion (500 ml/500 kcal) at a rate of 250 ml/hr. Gastric tone variations were recorded with an electronic barostat, gastric emptying was concomitantly estimated by repeated ultrasound measurements of antral area, and symptoms were recorded throughout the experiment.L-Arg administration was associated with significantly higher increases in barostat bag volumes at both dosages, 30 g (117+/-16 ml) and 15 g (67+/-15 ml), compared to placebo (46+/-11 ml; P < 0.05). In response to the polymeric diet the 30-g L-Arg challenge was associated with a smaller increase in intrabag volume, whereas postinfusion final volumes did not differ in the three treatment conditions. Antral areas were not different at any time of measurement among the three challenges. Bloating and diarrhea were observed after 30-g L-Arg administration in five subjects of eight. Short-term L-Arg administration was able to induce proximal stomach relaxation that allowed a secondary response to enteral feeding only at the 15-g dosage. This 15-g dosage was as well tolerated as the placebo and was associated with no significant changes in gastric emptying patterns.
一氧化氮(NO)作为胃肠道中一种非肾上腺素能、非胆碱能的抑制性神经递质发挥着重要作用。我们的研究目的是调查单次胃内给予L-精氨酸(L-Arg)作为NO的来源,对人体基础状态下以及给予聚合饮食后近端胃张力的影响,并同时评估对胃窦面积的影响,以此作为胃排空的间接评估指标。在一项随机双盲交叉研究中,对8名健康志愿者分别通过胃管给予15 g L-Arg、30 g L-Arg或安慰剂。给药后以250 ml/小时的速度输注聚合饮食(500 ml/500千卡)。用电子恒压器记录胃张力变化,通过重复超声测量胃窦面积同时评估胃排空情况,并在整个实验过程中记录症状。与安慰剂组(46±11 ml;P<0.05)相比,给予30 g(117±16 ml)和15 g(67±16 ml)L-Arg剂量时,恒压器气囊容积均显著增加。在给予聚合饮食后,30 g L-Arg激发试验时气囊内体积增加较小,而在三种治疗条件下输注后的最终体积没有差异。在三次激发试验的任何测量时间点,胃窦面积均无差异。在8名受试者中有5名在给予30 g L-Arg后出现腹胀和腹泻。短期给予L-Arg能够诱导近端胃松弛,仅在15 g剂量时对肠内喂养有继发反应。15 g剂量与安慰剂耐受性相当,且胃排空模式无显著变化。