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新型动力药 DA-9701 对大鼠应激性胃排空延迟及激素变化的影响。

Effect of DA-9701, a novel prokinetic agent, on stress-induced delayed gastric emptying and hormonal changes in rats.

机构信息

College of Pharmacy, Ajou University, Suwon, Korea.

出版信息

Neurogastroenterol Motil. 2013 Mar;25(3):254-9, e166. doi: 10.1111/nmo.12053. Epub 2012 Dec 6.

Abstract

BACKGROUND

DA-9701 is a novel prokinetic agent formulated with Pharbitis Semen and Corydalis Tuber. This study aimed to evaluate the effect of DA-9701 on stress-induced delay in gastric emptying and changes in plasma adrenocorticotropic hormone and ghrelin levels in rats.

METHODS

Changes in gastric emptying in response to different durations of stress were evaluated. Gastric emptying was compared between the following groups: (i) nonstressed vehicle- or DA-9701-treated group, (ii) nonstressed vehicle- or mosapride-treated group, (iii) 2-h stressed vehicle- or DA-9701-treated group, and (iv) 2-h stressed vehicle- or mosapride-treated group. Water immersion restraint stress was used as the stressor. DA-9701 or mosapride at 3 mg kg(-1) was administered to the rats after subjecting them to 2-h stress, and then gastric emptying was measured using the phenol red method.

KEY RESULTS

Gastric emptying was significantly delayed in the 2-h stressed group compared with the nonstressed group. Mosapride administration resulted in significant recovery from the stress-induced delay in gastric emptying. Gastric emptying in the rats that underwent 2-h stress followed by DA-9701 administration was not significantly different from that in the nonstressed group. The plasma adrenocorticotropic hormone and active ghrelin levels in the 2-h stressed group were significantly higher than those in the nonstressed group. These increases were significantly inhibited by DA-9701.

CONCLUSIONS & INFERENCES: The administration of DA-9701 improved delayed gastric emptying and inhibited the hormonal changes induced by stress, suggesting that DA-9701 can be used as a gastroprokinetic agent for the treatment of delayed gastric emptying, particularly that associated with stress.

摘要

背景

DA-9701 是一种新型的促动力药物,由菟丝子和延胡索组成。本研究旨在评估 DA-9701 对大鼠应激诱导胃排空延迟及血浆促肾上腺皮质激素和胃饥饿素水平变化的影响。

方法

评估不同持续时间的应激对胃排空的影响。比较了以下各组之间的胃排空情况:(i)非应激状态下给予载体或 DA-9701 处理组,(ii)非应激状态下给予载体或莫沙必利处理组,(iii)2 小时应激状态下给予载体或 DA-9701 处理组,和(iv)2 小时应激状态下给予载体或莫沙必利处理组。采用水浸束缚应激作为应激源。在给予大鼠 2 小时应激后,给予 DA-9701 或莫沙必利 3mg/kg,然后使用酚红法测量胃排空。

主要结果

与非应激组相比,2 小时应激组胃排空明显延迟。莫沙必利给药可显著恢复应激诱导的胃排空延迟。接受 2 小时应激后给予 DA-9701 处理的大鼠胃排空与非应激组无显著差异。2 小时应激组大鼠的血浆促肾上腺皮质激素和活性胃饥饿素水平明显高于非应激组。这些增加被 DA-9701 显著抑制。

结论和推论

DA-9701 的给药改善了胃排空延迟,并抑制了应激引起的激素变化,提示 DA-9701 可作为治疗胃排空延迟的胃肠动力药物,特别是与应激相关的胃排空延迟。

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