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胃泌素释放肽对大鼠胃排空的抑制作用。

Inhibitory effects of gastrin releasing peptide on gastric emptying in rats.

作者信息

Yeğen B C, Gürbüz V, Coşkun T, Bozkurt A, Kurtel H, Alican I, Dockray G J

机构信息

Department of Physiology, Marmara University, Faculty of Medicine, Istanbul, Turkey.

出版信息

Regul Pept. 1996 Mar 22;61(3):175-80. doi: 10.1016/0167-0115(95)00151-4.

Abstract

Gastrin-releasing peptide (GRP) has a wide range of biological actions, including stimulation of the frequency of antral contractions and delaying gastric emptying. The present study was designed to evaluate the role of GRP in the control of gastric emptying of liquid test meals in the rat. The emptying of methyl cellulose given by gavage to fasted rats, or of saline given via the fistula to conscious gastric fistula rats was not influenced by the GRP antagonists, NC-8-89 (Leu13-psi-(CH2NH)-Leu14-bombesin) and 2258U89 ((de-NH2)Phe19, D-Ala24, D-Pro26 psi (CH2NH)Phe27(-GRP (19-27)), at 2 mg/kg, s.c. However, both antagonists (0.02, 0.2 and 2 mg/kg) reversed the inhibitory effect of HCI on gastric emptying in gastric fistula rats (P < 0.05-0.001). When peptone was administered after a preload, but not otherwise, the inhibition of emptying was also partly reversed by both antagonists at all doses used (P < 0.05-0.001). Interestingly, the delay in the emptying of hyperosmolal saline compared to saline, was enhanced at a dose of 0.2 mg/kg of both antagonists (P < 0.05 and P < 0.01). Food intake did not change significantly with the two lower doses of antagonists, but was decreased by the highest dose of NC 8-89. We conclude that GRP specifically inhibits gastric emptying of acid and peptone solutions in the conscious rat.

摘要

胃泌素释放肽(GRP)具有广泛的生物学作用,包括刺激胃窦收缩频率和延缓胃排空。本研究旨在评估GRP在大鼠液体试验餐胃排空控制中的作用。给禁食大鼠灌胃甲基纤维素,或给清醒胃瘘大鼠经瘘管注入生理盐水,其排空不受GRP拮抗剂NC - 8 - 89(Leu13 - psi - (CH2NH) - Leu14 - 蛙皮素)和2258U89((de - NH2)Phe19, D - Ala24, D - Pro26 psi (CH2NH)Phe27(-GRP (19 - 27)))的影响,皮下注射剂量为2mg/kg。然而,两种拮抗剂(0.02、0.2和2mg/kg)均可逆转盐酸对胃瘘大鼠胃排空的抑制作用(P < 0.05 - 0.001)。当在预负荷后给予蛋白胨时(其他情况则不然),所有使用剂量的两种拮抗剂均可部分逆转排空抑制作用(P < 0.05 - 0.001)。有趣的是,与生理盐水相比,高渗盐水排空延迟在两种拮抗剂剂量为0.2mg/kg时增强(P < 0.05和P < 0.01)。两种较低剂量的拮抗剂对食物摄入量无显著影响,但最高剂量的NC 8 - 89可使其降低。我们得出结论,GRP特异性抑制清醒大鼠胃内酸和蛋白胨溶液的排空。

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