Herzig K H, Louie D S, Owyang C
Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109.
Am J Physiol. 1994 Jun;266(6 Pt 1):G1156-61. doi: 10.1152/ajpgi.1994.266.6.G1156.
We hypothesized that somatostatin exerts its inhibitory action on cholecystokinin (CCK) release and pancreatic secretion by inhibiting the secretion and/or action of a CCK-releasing peptide (CCK-RP) secreted from the small intestine. Our studies demonstrated that intravenous infusion of somatostatin (25 micrograms.kg-1.h-1) completely inhibited the increase in amylase output evoked by diversion of bile-pancreatic juice and 80 +/- 10% of the increase in plasma CCK. Intraduodenal administration of concentrated intestinal perfusate containing the CCK-RP collected from a donor rat with bile-pancreatic juice diversion raised amylase output by 2.3-fold and elevated plasma CCK levels to 7 +/- 0.8 pM in a recipient rat. The stimulatory effect of the concentrated intestinal washings was abolished when the "donor" rat was pretreated with somatostatin. In addition, in somatostatin-treated "recipient" rats, intraduodenal administration of intestinal washings containing CCK-RP also failed to elicit an increase in plasma CCK and amylase secretion. Furthermore, using duodenal mucosal explants, we demonstrated that the inhibitory action of somatostatin on CCK release evoked by CCK-RP was antagonized by pretreatment with pertussis toxin. These observations strongly suggest that somatostatin inhibits feedback regulation of pancreatic enzyme secretion by inhibiting both the secretion and action of CCK-RP.
我们推测,生长抑素通过抑制小肠分泌的胆囊收缩素释放肽(CCK-RP)的分泌和/或作用,对胆囊收缩素(CCK)释放和胰腺分泌发挥抑制作用。我们的研究表明,静脉输注生长抑素(25微克·千克⁻¹·小时⁻¹)可完全抑制胆汁胰液转流引起的淀粉酶分泌增加以及血浆CCK升高的80±10%。向十二指肠内注射含有从胆汁胰液转流的供体大鼠收集的CCK-RP的浓缩肠灌流液,可使受体大鼠的淀粉酶分泌增加2.3倍,并使血浆CCK水平升高至7±0.8皮摩尔。当“供体”大鼠用生长抑素预处理时,浓缩肠灌洗液的刺激作用消失。此外,在经生长抑素处理的“受体”大鼠中,十二指肠内注射含有CCK-RP的肠灌洗液也未能引起血浆CCK和淀粉酶分泌增加。此外,使用十二指肠黏膜外植体,我们证明百日咳毒素预处理可拮抗生长抑素对CCK-RP引起的CCK释放的抑制作用。这些观察结果强烈表明,生长抑素通过抑制CCK-RP的分泌和作用来抑制胰腺酶分泌的反馈调节。