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生长抑素sst(2)受体抑制大鼠和小鼠空肠的蠕动。

Somatostatin sst(2) receptors inhibit peristalsis in the rat and mouse jejunum.

作者信息

Abdu Faiza, Hicks Gareth A, Hennig Grant, Allen Jeremy P, Grundy David

机构信息

Department of Biomedical Science, Alfred Denny Building, University of Sheffield, Western Bank, Sheffield S10 2TN, United Kingdom.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2002 Apr;282(4):G624-33. doi: 10.1152/ajpgi.00354.2001.

Abstract

Somatostatin [somatotropin release-inhibitory factor (SRIF)] has widespread actions throughout the gastrointestinal tract, but the receptor mechanisms involved are not fully characterized. We have examined the effect of selective SRIF-receptor ligands on intestinal peristalsis by studying migrating motor complexes (MMCs) in isolated segments of jejunum from rats, mice, and sst(2)-receptor knockout mice. MMCs were recorded in 4- to 5-cm segments of jejunum mounted horizontally in vitro. MMCs occurred in rat and mouse jejunum with intervals of 104.4 +/- 10 and 131.2 +/- 8 s, respectively. SRIF, octreotide, and BIM-23027 increased the interval between MMCs, an effect fully or partially antagonized by the sst(2)-receptor antagonist Cyanamid154806. A non-sst(2) receptor-mediated component was evident in mouse as confirmed by the observation of an inhibitory action of SRIF in sst(2) knockout tissue. Blocking nitric oxide generation abolished the response to SRIF in rat but not mouse jejunum. sst(2) Receptors mediate inhibition of peristalsis in both rat and mouse jejunum, but a non-sst(2) component also exists in the mouse. Nitrergic mechanisms are differentially involved in rat and mouse jejunum.

摘要

生长抑素[促生长激素释放抑制因子(SRIF)]在整个胃肠道具有广泛作用,但所涉及的受体机制尚未完全明确。我们通过研究大鼠、小鼠及sst(2)受体基因敲除小鼠空肠分离段中的移行性运动复合波(MMC),来检测选择性SRIF受体配体对肠道蠕动的影响。MMC记录于体外水平安装的4至5厘米长的空肠段。MMC分别以104.4±10秒和131.2±8秒的间隔出现在大鼠和小鼠空肠中。生长抑素、奥曲肽和BIM-23027增加了MMC之间的间隔,该作用被sst(2)受体拮抗剂Cyanamid154806完全或部分拮抗。如在sst(2)基因敲除组织中观察到生长抑素的抑制作用所证实,在小鼠中存在非sst(2)受体介导的成分。阻断一氧化氮生成消除了大鼠空肠对生长抑素的反应,但未消除小鼠空肠的反应。sst(2)受体介导大鼠和小鼠空肠蠕动的抑制,但小鼠中也存在非sst(2)成分。一氧化氮能机制在大鼠和小鼠空肠中的参与情况不同。

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