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人类胰腺和胆管对生理浓度八肽胆囊收缩素的反应。

Human pancreatic and biliary responses to physiological concentrations of cholecystokinin octapeptide.

作者信息

Anagnostides A A, Chadwick V S, Selden A C, Barr J, Maton P N

出版信息

Clin Sci (Lond). 1985 Sep;69(3):259-63. doi: 10.1042/cs0690259.

DOI:10.1042/cs0690259
PMID:4064569
Abstract

To determine the functional significance of physiological plasma concentrations of cholecystokinin, five volunteers each received graded doses of intravenous infusions of cholecystokinin octapeptide (CCK-8). At each dose plasma concentrations of CCK-8 were determined and pancreatic and biliary outputs were measured. Threshold plasma concentrations of CCK-8 for augmenting pancreatic trypsin secretion were undetectable (less than 3 pmol/l), and maximal trypsin output of 21.9 +/- 1.95 k-i.u./30 min was produced by 17.1 +/- 6.4 pmol of CCK-8/1. Calculated halfmaximal output was produced by 4.7 pmol of CCK-8/1. Maximal trypsin output during infusions of CCK-8 was significantly less than that after a combination of the CCK-like peptide, caerulein, and secretin (32.95 +/- 2.16 k-i.u./30 min, P less than 0.001). Biliary bile acid and bilirubin outputs were significantly augmented only when plasma concentrations of CCK-8 were greater than 5 pmol/l. Plasma concentrations of CCK-8 in the low picomolar range exert significant effects on pancreatic and biliary secretion. CCK-8 fulfills the criteria for a circulating hormone.

摘要

为了确定生理血浆浓度的胆囊收缩素的功能意义,五名志愿者每人接受了不同剂量的胆囊收缩素八肽(CCK-8)静脉输注。在每个剂量下,测定CCK-8的血浆浓度,并测量胰腺和胆汁的分泌量。增加胰腺胰蛋白酶分泌的CCK-8阈值血浆浓度无法检测到(低于3 pmol/l),17.1±6.4 pmol的CCK-8/1产生了21.9±1.95 k-i.u./30分钟的最大胰蛋白酶分泌量。计算得出,4.7 pmol的CCK-8/1产生了半数最大分泌量。输注CCK-8期间的最大胰蛋白酶分泌量显著低于CCK样肽、蛙皮素和促胰液素联合使用后的分泌量(32.95±2.16 k-i.u./30分钟,P<0.001)。仅当CCK-8的血浆浓度大于5 pmol/l时,胆汁酸和胆红素的胆汁分泌量才会显著增加。低皮摩尔范围内的CCK-8血浆浓度对胰腺和胆汁分泌有显著影响。CCK-8符合循环激素的标准。

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引用本文的文献

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Cholecystokinin-From Local Gut Hormone to Ubiquitous Messenger.胆囊收缩素——从局部肠道激素到广泛存在的信使
Front Endocrinol (Lausanne). 2017 Apr 13;8:47. doi: 10.3389/fendo.2017.00047. eCollection 2017.
2
Therapeutic potential for novel drugs targeting the type 1 cholecystokinin receptor.新型靶向胆囊收缩素 1 型受体药物的治疗潜力。
Br J Pharmacol. 2010 Mar;159(5):1009-21. doi: 10.1111/j.1476-5381.2009.00489.x. Epub 2009 Nov 18.
3
Light- and electron-microscopic immunocytochemistry of peptidergic neurons innervating thoracico-abdominal neurohaemal areas in the blowfly.
对家蝇中支配胸腹神经血器官区域的肽能神经元的光镜和电镜免疫细胞化学研究
Cell Tissue Res. 1988 Sep;253(3):583-95. doi: 10.1007/BF00219749.
4
Effects of a cholecystokinin receptor antagonist on intestinal phase of pancreatic and biliary responses in man.胆囊收缩素受体拮抗剂对人体胰腺和胆汁反应肠期的影响。
J Clin Invest. 1990 Mar;85(3):640-6. doi: 10.1172/JCI114486.