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急性应激导致大鼠结肠释放黏蛋白:促肾上腺皮质激素释放因子和肥大细胞的作用。

Acute stress causes mucin release from rat colon: role of corticotropin releasing factor and mast cells.

作者信息

Castagliuolo I, Lamont J T, Qiu B, Fleming S M, Bhaskar K R, Nikulasson S T, Kornetsky C, Pothoulakis C

机构信息

Division of Gastroenterology, Beth Israel Hospital, Harvard Medical School, Boston 02215, USA.

出版信息

Am J Physiol. 1996 Nov;271(5 Pt 1):G884-92. doi: 10.1152/ajpgi.1996.271.5.G884.

Abstract

We determined the effects of immobilization stress on rat colonic mucus release and mast cell degranulation and examined whether corticotropin releasing factor (CRF) was involved in these responses. After 30-min immobilization, rats were killed, colonic mucosal explants were cultured, and levels of rat mast cell protease II (RMCP II) and prostaglandin E2 (PGE2) were measured. Mucin release from explants was assayed by incorporation of [3H]glucosamine into colonic mucin and by histological evaluation of goblet cell depletion. Stress caused significant increases of colonic RMCP II, PGE2, and mucin release and fecal pellet output and caused an approximately 10-fold increase in colonic mucosal levels of cyclooxygenase-2 (COX-2) mRNA. These stress-associated changes were reproduced by intravenous or intracerebral injection of CRF in conscious, nonstressed rats. Pretreatment of rats with the CRF antagonist alpha-helical-CRF9-41, hexamethonium, atropine, or bretylium, or the mast cell stabilizer lodoxamide inhibited stress-induced release of RMCP II, PGE2, and mucin, whereas indomethacin prevented mucin release but not mast cell degranulation. Hexamethonium and CP-96,345, a substance P antagonist, inhibited fecal pellet output caused by stress. We conclude that CRF released during immobilization stress increases colonic transit via a neuronal pathway and stimulates colonic mucin secretion via activation of neurons and mast cells.

摘要

我们确定了制动应激对大鼠结肠黏液释放和肥大细胞脱颗粒的影响,并研究促肾上腺皮质激素释放因子(CRF)是否参与了这些反应。制动30分钟后,处死大鼠,培养结肠黏膜外植体,测定大鼠肥大细胞蛋白酶II(RMCP II)和前列腺素E2(PGE2)的水平。通过将[3H]葡萄糖胺掺入结肠黏蛋白以及对杯状细胞耗竭进行组织学评估来测定外植体的黏蛋白释放。应激导致结肠RMCP II、PGE2和黏蛋白释放以及粪便颗粒输出显著增加,并使结肠黏膜中环氧合酶-2(COX-2)mRNA水平增加约10倍。在清醒、未应激的大鼠中,静脉内或脑室内注射CRF可重现这些与应激相关的变化。用CRF拮抗剂α-螺旋-CRF9-41、六甲铵、阿托品或溴苄铵,或肥大细胞稳定剂洛度沙胺预处理大鼠,可抑制应激诱导的RMCP II、PGE2和黏蛋白释放,而吲哚美辛可阻止黏蛋白释放,但不能抑制肥大细胞脱颗粒。六甲铵和P物质拮抗剂CP-96,345可抑制应激引起的粪便颗粒输出。我们得出结论,制动应激期间释放的CRF通过神经元途径增加结肠转运,并通过激活神经元和肥大细胞刺激结肠黏蛋白分泌。

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