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促胰液素与八肽胆囊收缩素在大鼠胰腺外分泌中的体内及体外相互作用

Interaction between secretin and cholecystokinin-octapeptide in the exocrine rat pancreas in vivo and in vitro.

作者信息

Singh J, Lennard R, Salido G M, Wisdom D, Render C L, Pozo M J, Pariente J A, Camello P J

机构信息

Department of Applied Biology, Lancashire Polytechnic, Preston.

出版信息

Exp Physiol. 1992 Jan;77(1):191-204. doi: 10.1113/expphysiol.1992.sp003573.

Abstract

This study investigates the interaction between physiological doses of the synthetic gut hormones, cholecystokinin-octapeptide (CCK8) and secretin on pancreatic juice secretion in the anaesthetized rat and on amylase secretion and Ca2+ and Mg2+ mobilization in isolated pancreatic segments and acinar cells. CCK8 (150 pmol kg-1 h-1) and secretin (100 pmol kg-1 h-1) evoked marked time course increases in pancreatic juice flow, total protein output and amylase secretion in the anaesthetized rat when administered separately compared to saline controls. Simultaneous intravenous infusion of CCK8 and secretin did not yield either an additive response or a potentiation but instead it caused a decrease in secretory responses. Administration of either polymyxin B (10(-8) mol kg-1 h-1) or staurosporine (10(-8) mol kg-1 h-1), two protein kinase C inhibitors, simultaneously with both CCK8 and secretin caused a further decrease in all secretory parameters. Superfusing pancreatic segments with either CCK8 (10(-11) M) or secretin (10(-11) M) elevated amylase output compared to the smaller response with a combination of CCK8 and secretin. Combining staurosporine (10(-6) M) with CCK8 and secretin resulted in a further decrease in amylase output. CCK8 (10(-11) M) evoked a large increase in radiolabelled Ca2+ influx into pancreatic segments and elevated cytosolic free Ca2+ concentration ([Ca2+]i) in acinar cells loaded with the fluorescent dye, Fura-2. Secretin (10(-11) M) alone had no significant effect on Ca2+ mobilization but it markedly attenuated the increases in radiolabelled Ca2+ influx and [Ca2+]i elicited by CCK8. In superfused pancreatic segments CCK8 (10(-11) M) evoked a net efflux of Mg2+ whereas secretin (10(-11) M) induced a net uptake of Mg2+. Combining secretin with CCK8 also resulted in a net uptake of Mg2+. The results indicate that both Ca2+ and Mg2+ mobilization may be associated with the interaction between CCK8 and secretin in the rat pancreas.

摘要

本研究调查了生理剂量的合成肠道激素——胆囊收缩素八肽(CCK8)和促胰液素对麻醉大鼠胰液分泌以及对分离的胰腺节段和腺泡细胞淀粉酶分泌、Ca2+和Mg2+动员的相互作用。与生理盐水对照组相比,单独给予CCK8(150 pmol kg-1 h-1)和促胰液素(100 pmol kg-1 h-1)时,麻醉大鼠的胰液流量、总蛋白输出量和淀粉酶分泌随时间显著增加。同时静脉输注CCK8和促胰液素既未产生相加反应也未产生增强作用,反而导致分泌反应降低。与两种蛋白激酶C抑制剂多粘菌素B(10(-8) mol kg-1 h-1)或星形孢菌素(10(-8) mol kg-1 h-1)同时给予CCK8和促胰液素,会使所有分泌参数进一步降低。与CCK8和促胰液素联合使用时较小的反应相比,用CCK8(10(-11) M)或促胰液素(10(-11) M)灌注胰腺节段可提高淀粉酶输出量。将星形孢菌素(10(-6) M)与CCK8和促胰液素联合使用会导致淀粉酶输出量进一步降低。CCK8(10(-11) M)引起放射性标记的Ca2+大量流入胰腺节段,并使加载荧光染料Fura-2的腺泡细胞胞质游离Ca2+浓度([Ca2+]i)升高。单独的促胰液素(10(-11) M)对Ca2+动员无显著影响,但它显著减弱了CCK8引起的放射性标记的Ca2+流入和[Ca2+]i的增加。在灌注的胰腺节段中,CCK8(10(-11) M)引起Mg2+的净流出,而促胰液素(10(-11) M)诱导Mg2+的净摄取。促胰液素与CCK8联合使用也导致Mg2+的净摄取。结果表明,Ca2+和Mg2+的动员可能与大鼠胰腺中CCK8和促胰液素之间的相互作用有关。

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