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八肽胆囊收缩素、胃泌素和促胰液素在体外对猫胆囊的相互作用。

Interaction between octapeptide-cholecystokinin, gastrin, and secretin on cat gallbladder in vitro.

作者信息

Chowdhury J R, Berkowitz J M, Praissman M, Fara J W

出版信息

Am J Physiol. 1975 Nov;229(5):1311-5. doi: 10.1152/ajplegacy.1975.229.5.1311.

DOI:10.1152/ajplegacy.1975.229.5.1311
PMID:1200149
Abstract

Effects of OP-CCK, gastrin, and secretin were studied on isometric tension development in strips of cat gallbladder. Effective molar concentrations were 2.2 X 10(-10) to 5.3 X 10(-9) for OP-CCK, and 1.13 X 10(-7) to 1.5 X 10(-6) for gastrin. The maximal response to gastrin averaged 66% the maximal response to OP-CCK and effects were not blocked by atropine. Secretin was weakly stimulatory or ineffective by itself. Prior addition of submaximal doses of gastrin shifted the dose-response curve of OP-CCK to the right, but neither the slope nor the calculated maximal response (CMR) was significantly changed. This suggests that gastrin and OP-CCK compete for a common receptor on cat gallbladder. On the other hand, a background dose of secretin shifted the dose-response curves for both OP-CCK and gastrin to the left and increased the slopes significantly with increase in the respective CMRs. The combined action of OP-CCK (or gastrin) and secretin are supra-additive. These experiments suggest that OP-CCK and gastrin act at a common receptor site which is different from the secretin-receptor site.

摘要

研究了蛙皮胆囊收缩素(OP-CCK)、胃泌素和促胰液素对猫胆囊条等长张力发展的影响。OP-CCK的有效摩尔浓度为2.2×10⁻¹⁰至5.3×10⁻⁹,胃泌素的有效摩尔浓度为1.13×10⁻⁷至1.5×10⁻⁶。胃泌素的最大反应平均为OP-CCK最大反应的66%,且其作用不受阿托品阻断。促胰液素本身的刺激作用较弱或无作用。预先加入次最大剂量的胃泌素可使OP-CCK的剂量反应曲线右移,但斜率和计算出的最大反应(CMR)均无明显变化。这表明胃泌素和OP-CCK在猫胆囊上竞争共同受体。另一方面,促胰液素的背景剂量可使OP-CCK和胃泌素的剂量反应曲线左移,并随着各自CMR的增加而显著增加斜率。OP-CCK(或胃泌素)与促胰液素的联合作用具有超相加性。这些实验表明,OP-CCK和胃泌素作用于一个与促胰液素受体位点不同的共同受体位点。

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Interaction between octapeptide-cholecystokinin, gastrin, and secretin on cat gallbladder in vitro.八肽胆囊收缩素、胃泌素和促胰液素在体外对猫胆囊的相互作用。
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