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首页> 外文期刊>BMC Gastroenterology >The oxytocin/vasopressin receptor antagonist atosiban delays the gastric emptying of a semisolid meal compared to saline in human
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The oxytocin/vasopressin receptor antagonist atosiban delays the gastric emptying of a semisolid meal compared to saline in human

机译:与人类盐水相比,催产素/加压素受体拮抗剂阿托西班延迟了半固体食物的胃排空

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Background Oxytocin is released in response to a meal. Further, mRNA for oxytocin and its receptor have been found throughout the gastrointestinal (GI) tract. The aim of this study was therefore to examine whether oxytocin, or the receptor antagonist atosiban, influence the gastric emptying. Methods Ten healthy volunteers (five men) were examined regarding gastric emptying at three different occasions: once during oxytocin stimulation using a pharmacological dose; once during blockage of the oxytocin receptors (which also blocks the vasopressin receptors) and thereby inhibiting physiological doses of oxytocin; and once during saline infusion. Gastric emptying rate (GER) was assessed and expressed as the percentage reduction in antral cross-sectional area from 15 to 90 min after ingestion of rice pudding. The assessment was performed by real-time ultrasonography. At the same time, the feeling of satiety was registered using visual satiety scores. Results Inhibition of the binding of endogenous oxytocin by the receptor antagonist delayed the GER by 37 % compared to saline (p = 0.037). In contrast, infusion of oxytocin in a dosage of 40 mU/min did not affect the GER (p = 0.610). Satiation scores areas in healthy subjects after receiving atosiban or oxytocin did not show any significant differences. Conclusion Oxytocin and/or vasopressin seem to be regulators of gastric emptying during physiological conditions, since the receptor antagonist atosiban delayed the GER. However, the actual pharmacological dose of oxytocin in this study had no effect. The effect of oxytocin and vasopressin on GI motility has to be further evaluated.
机译:背景催产素是根据膳食而释放的。此外,在整个胃肠道(GI)中都发现了催产素及其受体的mRNA。因此,本研究的目的是检查催产素或受体拮抗剂阿托西班是否影响胃排空。方法在10种健康的志愿者(5名男性)中,在3种不同的情况下进行了胃排空的检查:一次在催产素刺激期间使用药理剂量;一次在一次催产素刺激下进行。一次在催产素受体(也能阻断血管加压素受体)受阻期间,从而抑制催产素的生理剂量;并在输注盐水时一次。评估胃排空率(GER),并表示为摄取大米布丁后15至90分钟的肛门横截面积减少的百分比。该评估通过实时超声检查进行。同时,使用视觉饱腹感评分来记录饱腹感。结果与盐水相比,受体拮抗剂抑制内源性催产素的结合使GER延迟了37%(p = 0.037)。相反,以40 mU / min的剂量注入催产素不会影响GER(p = 0.610)。健康受试者接受阿托西班或催产素后的满意度得分区域无明显差异。结论催产素和/或加压素似乎在生理条件下是胃排空的调节剂,因为受体拮抗剂阿托西班延迟了GER。但是,该研究中催产素的实际药理剂量没有影响。催产素和加压素对胃肠动力的影响有待进一步评估。

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