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胰高血糖素样肽-1对小肠运动的抑制作用。禁食状态下而非进食状态下的运动通过一氧化氮被抑制,且与胰岛素和生长抑素无关。

Inhibitory effect of glucagon-like peptide-1 on small bowel motility. Fasting but not fed motility inhibited via nitric oxide independently of insulin and somatostatin.

作者信息

Tolessa T, Gutniak M, Holst J J, Efendic S, Hellström P M

机构信息

Department of Medicine, Karolinska Hospital, Karolinska Institute, SE-171 76 Stockholm, Sweden.

出版信息

J Clin Invest. 1998 Aug 15;102(4):764-74. doi: 10.1172/JCI942.

Abstract

Effects of glucagon-like peptide-1 (GLP-1)(7-36)amide on fasted and fed motility in the rat small intestine were investigated in relation to its dependence on nitric oxide (NO), insulin, and somatostatin. Small bowel electromyography was performed using bipolar electrodes implanted 15, 25, and 35 cm distal to pylorus, and transit was studied with a radioactive marker. In the fasted state, GLP-1 (5-20 pmol kg-1min-1), reaching physiological plasma levels, prolonged the migrating myoelectric complex (MMC) cycle length along with slowed transit. This effect was antagonized by exendin(9-39)amide. The NO synthase inhibitor Nomega-nitro- L-arginine (L-NNA) also blocked the response to GLP-1, whereas L-arginine restored the response. Insulin (80-200 pmol kg-1min-1) induced irregular spiking, whereas somatostatin (100-500 pmol kg-1min-1) increased the MMC cycle length, independently of NO. In the fed state, GLP-1 (20-40 pmol kg-1min-1) reduced motility, an inhibition unaffected by L-NNA, whereas motility was stimulated by exendin(9-39)amide. Infusion of GLP-1 (20-100 pmol kg-1min-1) did not affect plasma insulin, but somatostatin was increased. In conclusion, GLP-1 seems to inhibit small bowel motility directly via the GLP-1 receptor. Inhibition of fasting motility is dependent of NO and not mediated via insulin or somatostatin, whereas inhibition of fed motility is independent of NO.

摘要

研究了胰高血糖素样肽-1(GLP-1)(7-36)酰胺对大鼠小肠禁食和进食状态下运动的影响,并探讨了其对一氧化氮(NO)、胰岛素和生长抑素的依赖性。使用植入幽门远端15、25和35厘米处的双极电极进行小肠肌电图检查,并用放射性标记物研究转运情况。在禁食状态下,达到生理血浆水平的GLP-1(5-20 pmol kg-1min-1)延长了移行性肌电复合波(MMC)的周期长度,同时转运减慢。艾塞那肽(9-39)酰胺可拮抗此作用。NO合酶抑制剂Nω-硝基-L-精氨酸(L-NNA)也可阻断对GLP-1的反应,而L-精氨酸可恢复该反应。胰岛素(80-200 pmol kg-1min-1)诱导不规则的尖峰活动,而生长抑素(100-500 pmol kg-1min-1)增加MMC周期长度,且与NO无关。在进食状态下,GLP-1(20-40 pmol kg-1min-1)降低运动性,这种抑制不受L-NNA影响,而艾塞那肽(9-39)酰胺可刺激运动性。输注GLP-1(20-100 pmol kg-1min-1)不影响血浆胰岛素,但生长抑素增加。总之,GLP-1似乎通过GLP-1受体直接抑制小肠运动。禁食状态下的运动抑制依赖于NO,而非通过胰岛素或生长抑素介导,而进食状态下的运动抑制则与NO无关。

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