首页> 外文期刊>European Journal of Pharmacology: An International Journal >Pregabalin inhibits accelerated defecation and decreased colonic nociceptive threshold in sensitized rats.
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Pregabalin inhibits accelerated defecation and decreased colonic nociceptive threshold in sensitized rats.

机译:普瑞巴林抑制致敏大鼠的排便加速和结肠伤害感受性阈值降低。

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摘要

Pregabalin, a ligand of alpha(2)delta subunits of voltage-gated calcium channels, reduces visceral hypersensitivity associated with irritable bowel syndrome. However, effects of pregabalin on bowel function are not well described. We investigated the effects of pregabalin on bowel dysfunction and colonic nociceptive threshold in sensitized rats. Increased fecal pellet output was evoked by non-ulcerogenic stress. Decreased colonic nociceptive threshold was induced in separate rats by administration of 2,4,6-trinitrobenzene sulfonic acid (TNBS) into the lumen of the proximal colon. Fecal pellet output was significantly increased during 2h restraint stress. Oral pregabalin (10-100mg/kg, p.o.) inhibited this increased fecal output dose-dependently, but did not change fecal output in naive rats. The response threshold to distension of the non-inflamed distal colon was significantly decreased seven days after TNBS administration. An anti-hyperalgesic effect of pregabalin (30-100mg/kg, p.o.) that opposed the decreased colonic nociceptive threshold in TNBS-sensitized rats was observed, but nociceptive thresholds were not changed in naive rats. Moreover, pregabalin was more potent in reducing disturbed defecation compared with reduction in nociceptive threshold to distension in TNBS-sensitized rats. This is the first report that pregabalin modulates stress-induced defecation in rats. These data indicate that pregabalin can ameliorate both altered defecation and decreases in colonic nociceptive threshold, suggesting that pregabalin might warrant investigation for the treatment of irritable bowel syndrome.
机译:普瑞巴林是电压门控钙通道的α(2)δ亚基的配体,可减少与肠易激综合征相关的内脏超敏反应。但是,普瑞巴林对肠功能的影响尚未很好地描述。我们调查了普瑞巴林对致敏大鼠肠功能障碍和结肠伤害感受性阈值的影响。非溃疡性应激引起粪便颗粒产量增加。通过将2,4,6-三硝基苯磺酸(TNBS)注入近端结肠腔,在单独的大鼠中诱导降低结肠伤害感受性阈值。在2h的约束压力下粪便颗粒的产量显着增加。口服普瑞巴林(10-100mg / kg,p.o.)剂量依赖性地抑制了这种排便量的增加,但在未实验的大鼠中并未改变排便量。 TNBS给药7天后,对非发炎的远端结肠扩张的反应阈值显着降低。观察到普瑞巴林(30-100mg / kg,p.o.)的抗痛觉过敏作用与在TNBS致敏的大鼠中降低的结肠伤害感受性阈值相反,但在未治疗的大鼠中伤害感受性阈值没有改变。而且,与TNBS致敏大鼠的扩张性伤害阈值降低相比,普瑞巴林在减少不便排便方面更有效。这是普瑞巴林调节大鼠应激性排便的第一个报道。这些数据表明,普瑞巴林可以改善排便改变和结肠伤害感受性阈值的降低,这表明普瑞巴林可能需要研究肠易激综合征的治疗方法。

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