Bunnett N W, Mulvihill S J, Debas H T
Department of Surgery, University of California, San Francisco 94143-0104.
Exp Physiol. 1991 Jan;76(1):115-23. doi: 10.1113/expphysiol.1991.sp003473.
The mechanism by which calcitonin gene-related peptide (CGRP) inhibits exocrine secretion from the rat pancreas was examined in the isolated, vascularly perfused pancreas and in vitro using freshly isolated pancreatic acini. CGRP (10(-10)-10(-7) M) inhibited the volume and protein output from the perfused pancreas, stimulated by a mixture of the cholecystokinin octapeptide CCK8 (10(-10) M) and secretin (10(-8) M). The inhibition by CGRP was dose related and maximal at 10(-8) M (P less than 0.05). CGRP (10(-8) M) failed to inhibit amylase secretion from isolated pancreatic acini, stimulated by graded concentrations of CCK8 (10(-13)-10(-8) M). This implies an indirect mechanism of inhibition. The mechanism of inhibition was investigated in the isolated, vascularly perfused pancreas using tetrodotoxin, atropine and hexamethonium (all 10(-7) M). Tetrodotoxin and atropine but not hexamethonium prevented the inhibition of volume and protein secretion by CGRP (10(-8) M) (P less than 0.05). Tetrodotoxin, atropine and hexamethonium were without effect on exocrine secretion stimulated by CCK8 and secretin (controls). These results indicate that CGRP inhibits pancreatic exocrine secretion by an indirect, neurally mediated mechanism involving cholinergic-muscarinic transmission.
采用离体血管灌注胰腺及新鲜分离的胰腺腺泡进行体外实验,研究了降钙素基因相关肽(CGRP)抑制大鼠胰腺外分泌的机制。CGRP(10⁻¹⁰ - 10⁻⁷M)抑制了由八肽胆囊收缩素(CCK8,10⁻¹⁰M)和促胰液素(10⁻⁸M)混合物刺激引起的灌注胰腺的液体及蛋白质分泌。CGRP的抑制作用呈剂量依赖性,在10⁻⁸M时作用最强(P < 0.05)。CGRP(10⁻⁸M)未能抑制不同浓度CCK8(10⁻¹³ - 10⁻⁸M)刺激的离体胰腺腺泡淀粉酶分泌。这提示存在间接抑制机制。在离体血管灌注胰腺中,使用河豚毒素、阿托品和六甲铵(均为10⁻⁷M)研究抑制机制。河豚毒素和阿托品可阻止CGRP(10⁻⁸M)对液体和蛋白质分泌的抑制作用(P < 0.05),而六甲铵无此作用。河豚毒素、阿托品和六甲铵对CCK8和促胰液素刺激的外分泌(对照)无影响。这些结果表明,CGRP通过涉及胆碱能 - 毒蕈碱传递的间接神经介导机制抑制胰腺外分泌。