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缩胆囊素在大鼠60%远端胰腺切除术后胰腺再生中的重要作用。

Essential role of cholecystokinin in pancreatic regeneration after 60% distal resection in rats.

作者信息

Pap A, Boros L, Hajnal F

机构信息

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

出版信息

Pancreas. 1991 Jul;6(4):412-8. doi: 10.1097/00006676-199107000-00007.

Abstract

The essential role of cholecystokinin (CCK) in pancreatic regeneration after pancreatitis or resection has been supposed, but not yet clearly demonstrated. In rats, 6-8 weeks after 60% distal resection of the pancreas a gradual increase in pancreatic weight and contents of DNA, protein, trypsin, chymotrypsin and amylase, occurred (there was no increase in lipase); Pancreatic regeneration stopped thereafter. Nonparallel increases in enzyme values were similar to those seen after CCK administration. Indeed, basal CCK levels increased significantly by the 6th week and declined thereafter. A one month s.c. administration of CCK-octapeptide (CCK-8) (3 x 300 ng/kg/d) accelerated regeneration in the first month, but it had almost no effect during the second or third postoperative months. A two week s.c. administration of a specific CCK antagonist, CR 1409 (3 x 4 mg/kg/d) totally prevented regeneration by the fifth and sixth weeks, but did not diminish pancreatic weight or DNA and protein contents during the first two weeks. Alcohol administration (12 g/kg/d) reduced CCK release and prevented pancreatic regeneration during the three-month experimental period. These data indicate that CCK has an essential role in pancreatic regeneration and that the deleterious effect of alcohol on regeneration involves inhibition of CCK release.

摘要

胆囊收缩素(CCK)在胰腺炎或胰腺切除术后胰腺再生中的重要作用已被推测,但尚未得到明确证实。在大鼠中,胰腺远端60%切除术后6 - 8周,胰腺重量以及DNA、蛋白质、胰蛋白酶、糜蛋白酶和淀粉酶含量逐渐增加(脂肪酶含量未增加);此后胰腺再生停止。酶值的非平行增加与给予CCK后所见相似。实际上,基础CCK水平在第6周时显著升高,此后下降。皮下注射CCK - 八肽(CCK - 8)(3×300 ng/kg/d)持续1个月,在第一个月加速了再生,但在术后第二个月或第三个月几乎没有效果。皮下注射一种特异性CCK拮抗剂CR 1409(3×4 mg/kg/d)持续2周,到第5周和第6周时完全阻止了再生,但在前两周并未减轻胰腺重量或DNA和蛋白质含量。给予酒精(12 g/kg/d)在三个月的实验期内减少了CCK释放并阻止了胰腺再生。这些数据表明CCK在胰腺再生中起重要作用,并且酒精对再生的有害作用涉及抑制CCK释放。

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