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鸟氨酸脱羧酶和多胺在卡莫司他(Foy - 305)诱导大鼠胰腺生长中的作用

Role of ornithine decarboxylase and polyamines in camostate (Foy-305)-induced pancreatic growth in rats.

作者信息

Löser C, Fölsch U R, Cleffmann U, Nustede R, Creutzfeldt W

机构信息

Department of Medicine, Georg-August University of Göttingen, FRG.

出版信息

Digestion. 1989;43(1-2):98-112. doi: 10.1159/000199867.

Abstract

This study was designed to investigate changes of ornithine decarboxylase and polyamines during pancreatic adaptation in response to feeding of the synthetic protease inhibitor camostate. alpha-Difluoromethylornithine, an irreversible and specific inhibitor of ornithine decarboxylase, was applied simultaneously to elucidate the essential role of polyamines in pancreatic growth. Cholecystokinin (CCK) plasma levels in camostate-fed rats increased from basal values of 3-4 pmol/l to a maximal level of 27.4 pmol/l after 2h; they then decreased up to 12 h but remained elevated above controls throughout the 30-day experiments. In the camostate group pancreatic ornithine decarboxylase activity was elevated after 2 h, reaching a maximum after 6 h (1,858.5 pmol 14CO2/h/mg DNA, about 200-fold above controls) followed by a significant increase in putrescine after 4 h and spermidine after 24 h while spermine remained unchanged. The trophic parameters increased in the following time sequence: thymidine kinase (12 h), DNA polymerase (12 h), protein (24 h), pancreatic weight (24 h) and DNA (5 days). alpha-Difluoromethylornithine significantly delayed and reduced the camostate-induced increase in ornithine decarboxylase activity and polyamine concentrations as well as the trophic parameters. Application of the CCK receptor antagonist L-364,718 resulted in complete inhibition of the increases in ornithine decarboxylase, polyamines and all trophic parameters. These data indicate an important role for ornithine decarboxylase and polyamines in camostate-induced pancreatic growth and hormonal mediated pancreatic adaptation in rats.

摘要

本研究旨在调查在给予合成蛋白酶抑制剂卡莫司他后胰腺适应过程中鸟氨酸脱羧酶和多胺的变化。同时应用α-二氟甲基鸟氨酸(一种不可逆且特异性的鸟氨酸脱羧酶抑制剂)以阐明多胺在胰腺生长中的重要作用。给予卡莫司他的大鼠血浆胆囊收缩素(CCK)水平从基础值3 - 4 pmol/l在2小时后升至最高水平27.4 pmol/l;随后在12小时内下降,但在整个30天实验中仍高于对照组。在卡莫司他组中,胰腺鸟氨酸脱羧酶活性在2小时后升高,6小时后达到最大值(1,858.5 pmol 14CO2/h/mg DNA,约为对照组的200倍),随后4小时腐胺显著增加,24小时亚精胺增加,而精胺保持不变。营养参数按以下时间顺序增加:胸苷激酶(12小时)、DNA聚合酶(12小时)、蛋白质(24小时)、胰腺重量(24小时)和DNA(5天)。α-二氟甲基鸟氨酸显著延迟并降低了卡莫司他诱导的鸟氨酸脱羧酶活性、多胺浓度以及营养参数的增加。应用CCK受体拮抗剂L-364,718导致鸟氨酸脱羧酶、多胺和所有营养参数的增加完全受到抑制。这些数据表明鸟氨酸脱羧酶和多胺在卡莫司他诱导的大鼠胰腺生长和激素介导的胰腺适应中起重要作用。

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