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结肠短链脂肪酸通过增加胃泌素介导空肠生长。

Colonic short chain fatty acids mediate jejunal growth by increasing gastrin.

作者信息

Reilly K J, Frankel W L, Bain A M, Rombeau J L

机构信息

Harrison Department of Surgical Research Hospital, University of Pennsylvania, Philadelphia 19104, USA.

出版信息

Gut. 1995 Jul;37(1):81-6. doi: 10.1136/gut.37.1.81.

Abstract

Colonic infusion of short chain fatty acids (SCFAs) is trophic to rat jejunum and is associated with raised jejunal gastrin concentration. This study examined the hypothesis that the jejunal trophic effects of colonic SCFAs are mediated in part by gastrin. Forty six adult rats underwent caecectomy to reduce endogenous production of SCFA, ileocolonic anastomosis, and placement of a colonic infusion catheter. SCFA (70 mM acetate, 35 mM propionate, 20 mM butyrate) or saline were continuously infused into the colon for seven days. Rats received either a gastrin receptor blocker (L-365,260) or a control solution and animals were killed on day 8. SCFA infused into the colon acted systemically to significantly improve jejunal structure and increase jejunal gastrin concentrations. Gastrin receptor blockade abolished effects of SCFA on jejunal DNA, protein, crypt cell proliferation, and gastrin. Gastrin blockade did not reduce SCFA induced augmentation of villous height or crypt depth. It is concluded that the jejunal trophic effects of colonically infused SCFA are mediated in part by gastrin.

摘要

向结肠内输注短链脂肪酸(SCFAs)对大鼠空肠具有营养作用,并与空肠胃泌素浓度升高有关。本研究检验了结肠SCFAs对空肠的营养作用部分由胃泌素介导这一假说。46只成年大鼠接受盲肠切除术以减少内源性SCFA的产生、回结肠吻合术以及放置结肠输注导管。将SCFA(70 mM乙酸盐、35 mM丙酸盐、20 mM丁酸盐)或生理盐水持续输注到结肠中7天。大鼠接受胃泌素受体阻滞剂(L-365,260)或对照溶液,并在第8天处死动物。输注到结肠中的SCFA发挥全身作用,显著改善空肠结构并增加空肠胃泌素浓度。胃泌素受体阻断消除了SCFA对空肠DNA、蛋白质、隐窝细胞增殖和胃泌素的作用。胃泌素阻断并未降低SCFA诱导的绒毛高度或隐窝深度增加。得出的结论是,结肠输注SCFA对空肠的营养作用部分由胃泌素介导。

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本文引用的文献

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The gastrin-receptor antagonist L-365,260 inhibits stimulated acid secretion in humans.
Clin Pharmacol Ther. 1993 Nov;54(5):533-9. doi: 10.1038/clpt.1993.185.
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Gut. 1981 Sep;22(9):763-79. doi: 10.1136/gut.22.9.763.

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