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丙谷胺对胰腺消化酶导管分泌和基底外侧分泌的影响。

Effects of proglumide on ductal and basolateral secretion of pancreatic digestive enzymes.

作者信息

Niederau C, Grendell J H, Rothman S S

出版信息

Am J Physiol. 1985 Jul;249(1 Pt 1):G100-7. doi: 10.1152/ajpgi.1985.249.1.G100.

Abstract

Previous studies have shown that proglumide acts as a cholecystokinin (CCK) receptor antagonist in isolated pancreatic acini. To establish the effect of proglumide in the intact organ, its effects on both CCK-stimulated ductal and basolateral secretion of digestive enzymes were studied in the in vitro rabbit pancreas. CCK-stimulated ductal secretion of chymotrypsinogen, amylase, and total protein, as well as basolateral secretion of amylase, was inhibited by proglumide in a dose-dependent manner. Regression lines comparing ductal chymotrypsinogen and amylase outputs also were altered significantly by proglumide in a dose-dependent manner, with amylase secretion inhibited to a lesser degree. Similarly, the relative rates of amylase secretion across the ductal versus the basolateral cell surface were altered, with basolateral secretion inhibited to a lesser degree. The effects seen with increasing concentrations of proglumide at a given concentration of CCK mirrored the effects seen with decreasing the concentration of CCK in the absence of proglumide. Proglumide did not affect ductal or basolateral secretion stimulated by a cholinergic agonist and did not affect unstimulated pancreatic secretion. Thus, proglumide appears to act as a selective antagonist of CCK-stimulated secretion in the intact organ. The results further indicate that interactions of an agonist and an antagonist at the CCK receptor can alter not only the overall amount of enzymes secreted but their relative proportions as well.

摘要

先前的研究表明,丙谷胺在离体胰腺腺泡中作为胆囊收缩素(CCK)受体拮抗剂发挥作用。为了确定丙谷胺在完整器官中的作用,研究了其对体外培养的兔胰腺中CCK刺激的导管和基底外侧消化酶分泌的影响。丙谷胺以剂量依赖性方式抑制CCK刺激的胰凝乳蛋白酶原、淀粉酶和总蛋白的导管分泌以及淀粉酶的基底外侧分泌。比较导管胰凝乳蛋白酶原和淀粉酶分泌量的回归线也因丙谷胺而以剂量依赖性方式发生显著改变,其中淀粉酶分泌的抑制程度较小。同样,淀粉酶在导管与基底外侧细胞表面的相对分泌速率也发生了改变,基底外侧分泌的抑制程度较小。在给定CCK浓度下,随着丙谷胺浓度增加所观察到的效应与在无丙谷胺情况下降低CCK浓度所观察到的效应相似。丙谷胺不影响胆碱能激动剂刺激的导管或基底外侧分泌,也不影响未受刺激的胰腺分泌。因此,丙谷胺似乎在完整器官中作为CCK刺激分泌的选择性拮抗剂发挥作用。结果进一步表明,激动剂和拮抗剂在CCK受体处的相互作用不仅可以改变分泌的酶的总量,还可以改变它们的相对比例。

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