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通过反复皮下注射胆囊收缩素八肽诱导大鼠急性间质性胰腺炎的病程及消退情况。

Course and regression of acute interstitial pancreatitis induced in rats by repeated serial subcutaneous cholecystokinin-octapeptide injections.

作者信息

Lászik G Z, Berger Z, Pap A, Tóth G K, Varró V

机构信息

Department of Pathology, Albert Szent-Györgyi Medical University, Szeged, Hungary.

出版信息

Int J Pancreatol. 1989 Dec;5(4):347-58. doi: 10.1007/BF02924299.

Abstract

The aim of this study was to examine histologic and biochemical alterations in experimental acute interstitial pancreatitis (AIP) induced by serial repeated supramaximal cholecystokinin-octapeptide (CCK-OP) stimulation in rats. High doses of CCK-OP (60 micrograms/kg body wt) were administered subcutaneously (sc) six times at hourly intervals for 1 d (Group I) or for 3, 5, or 7 d (Group II). Rats were killed after 1, 3, 5, 7, and 10 d in both groups and also after 13, 20, and 27 d in Group II. During the course of the AIP, the morphological alterations were more pronounced in the repeatedly treated rats, but their appearance and disappearance essentially occurred in parallel in the two groups. Increased mitotic activity of the centroacinar and acinar cells were observed in d 5 and rose further even in Group II. The pancreatic weight and the protein and DNA contents reached a minimum on d 5 in both groups. The lowest enzyme activities did not occur in parallel. Thereafter, functional regeneration occurred despite continuing CCK-OP overstimulation in Group II. The toxicity of repeated CCK-OP hyperstimulation, thus, was limited: after its fifth administration, it failed to further aggravate the acute pancreatic damage or prevent the regeneration. This might be explained by a decreased CCK-OP sensitivity of the preexisting acinar cells, and/or increased CCK-OP tolerance of newly-formed ones.

摘要

本研究旨在检测大鼠在连续重复给予超最大剂量胆囊收缩素八肽(CCK-OP)刺激诱导的实验性急性间质性胰腺炎(AIP)中的组织学和生化改变。高剂量的CCK-OP(60微克/千克体重)以皮下注射(sc)方式,每小时给药1次,共6次,持续1天(I组)或3、5或7天(II组)。两组大鼠分别在1、3、5、7和10天处死,II组还在13、20和27天处死。在AIP病程中,反复给药组大鼠的形态学改变更明显,但两组中这些改变的出现和消失基本同步。在第5天观察到腺泡中心细胞和腺泡细胞的有丝分裂活性增加,在II组中甚至进一步升高。两组大鼠的胰腺重量以及蛋白质和DNA含量在第5天达到最低值。最低酶活性并非同时出现。此后,尽管II组持续存在CCK-OP过度刺激,但仍发生了功能再生。因此,反复CCK-OP过度刺激的毒性是有限的:在第5次给药后,它未能进一步加重急性胰腺损伤或阻止再生。这可能是由于原有腺泡细胞对CCK-OP的敏感性降低,和/或新形成的腺泡细胞对CCK-OP的耐受性增加所致。

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