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大鼠蛙皮素诱导胰腺炎期间及之后的血浆氨基酸消耗与胰腺分泌

Plasma amino acid consumption and pancreatic secretion during and after cerulein-induced pancreatitis in rats.

作者信息

Fischer H, Konturek J W, Szlachcic A, Konturek S J, Domschke W

机构信息

Department of Medicine B, University of Münster, Germany.

出版信息

Int J Pancreatol. 1995 Oct;18(2):127-34. doi: 10.1007/BF02785886.

Abstract

The decrease in pancreatic exocrine secretion during the course of acute pancreatitis is a well-documented process. However, the mechanisms underlying this reduced pancreatic function are not fully understood. To analyze pancreatic protein synthesis and secretion during and after cerulein-induced pancreatitis, we performed the plasma amino acid consumption test on conscious rats. After stimulation with 1 microgram cerulein/kg/h sc for 1 h, the control group with intact pancreas exhibited a decrease in plasma amino acid by about 15%, and this decrease could be abolished by the administration of the specific CCK-receptor antagonist, loxiglumide. Protein and amylase secretion were augmented by cerulein to about 400% of control values. Upon supramaximal stimulation of the pancreas with cerulein (20 micrograms/kg/h sc for 5 h), we observed a profound decrease of pancreatic secretion, which was accompanied by a more prolonged and more pronounced decrease of plasma amino acids (25%). Two hours after cessation of the supramaximal stimulation of pancreatic secretion (to induce pancreatitis), the administration of 1 microgram/kg/h of cerulein for 1 h resulted in a further decrease of amino plasma acid level, whereas no stimulation of exocrine pancreatic secretion was observed. Eighteen hours later, repeated administration of 1 microgram/kg/h of cerulein was still able to induce amino acid decrease by 20%, but again, no stimulation of exocrine pancreatic secretion was detectable. We conclude that, in the time course of acute cerulein-induced hyperstimulation, there might be an imbalance between synthesis of pancreatic enzymes (reflected by amino acid consumption) and the release of exocrine pancreatic secretion into the duodenum, which may be explained by leakage of proteolytic enzymes from damaged acinar cells into the extracellular space of the pancreas.

摘要

急性胰腺炎病程中胰腺外分泌分泌减少是一个有充分文献记载的过程。然而,这种胰腺功能降低的潜在机制尚未完全明了。为分析雨蛙肽诱导的胰腺炎期间及之后胰腺蛋白质的合成与分泌,我们对清醒大鼠进行了血浆氨基酸消耗试验。以1微克雨蛙肽/千克/小时的剂量皮下注射刺激1小时后,胰腺完整的对照组血浆氨基酸减少约15%,给予特异性CCK受体拮抗剂洛西肽胺可消除这种减少。雨蛙肽使蛋白质和淀粉酶分泌增加至对照值的约400%。用雨蛙肽(20微克/千克/小时皮下注射5小时)对胰腺进行超最大刺激后,我们观察到胰腺分泌显著减少,同时血浆氨基酸减少更持久、更明显(25%)。在超最大刺激胰腺分泌(以诱导胰腺炎)停止2小时后,给予1微克/千克/小时的雨蛙肽1小时导致血浆氨基酸水平进一步下降,而未观察到胰腺外分泌分泌受到刺激。18小时后,重复给予1微克/千克/小时的雨蛙肽仍能使氨基酸减少20%,但同样未检测到胰腺外分泌分泌受到刺激。我们得出结论,在急性雨蛙肽诱导的过度刺激过程中,胰腺酶的合成(以氨基酸消耗为指标)与胰腺外分泌向十二指肠的释放之间可能存在失衡,这可能是由于蛋白水解酶从受损的腺泡细胞渗漏到胰腺细胞外空间所致。

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