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建立慢性胰腺炎动物模型。长期用细胞色素P450化学诱导剂处理的仓鼠的胰胆分泌。

Toward an animal model of chronic pancreatitis. Pancreatobiliary secretion in hamsters on long-term treatment with chemical inducers of cytochromes P450.

作者信息

Rutishauser S C, Ali A E, Jeffrey I J, Hunt L P, Braganza J M

机构信息

Department of Biological Sciences, University of Manchester, UK.

出版信息

Int J Pancreatol. 1995 Oct;18(2):117-26. doi: 10.1007/BF02785885.

Abstract

There is currently no reproducible model of the painful and lithogenic disease, chronic pancreatitis. Its biphasic evolution, from acinar cell hyperplasia and hyperactivity toward effacement of enzyme as well as bicarbonate secretory parenchyma, would be rationalized if it was linked to induction of cytochrome P450 mono-oxygenases (CYP): the increased oxidant load from long-term CYP induction eventually erodes micronutrient antioxidant defenses to injure cells. This philosophy would also rationalize the reported hepatobiliary aberrations associated with the human disease, including increases in free radical oxidation products in bile. Accordingly, pancreatic and biliary secretions were studied in Syrian golden hamsters that were reared for 6 mo on low or high (16% corn oil) fat diets that were supplemented with a prototype inducer of CYP2 (200 ppm phenobarbitone) or CYP1 (100 ppm beta naphthoflavone) enzyme families, with or without a putative enzyme inhibitor (400 ppm cimetidine). The drugs did not alter the reduction in flow rate or bicarbonate concentration of pancreatic juice caused by the high fat diet alone, but, in contrast, evoked pancreatic protein hypersecretion in a number of animals. beta naphthoflavone, but not phenobarbitone, augmented the output of biliary lipid peroxidation products irrespective of dietary fat content, and cimetidine cotreatment with either inducer did the same. We conclude: (1) that drug modifiers of CYP magnify the deleterious pancreatobiliary effects of corn oil-enriched diets and draw them closer to those found in human chronic pancreatitis; (2) that these functional derangements are accompanied by pancreatic lipoatrophy; and (3) that long-term CYP induction does not, of its own, cause fibrosis or the ductal abnormalities that generally accompany loss of pancreatic acinar cells in the human disease and, also in contrast, the changes that are caused appear to be painless.

摘要

目前尚无慢性胰腺炎这种疼痛性致石疾病的可重复性模型。其双相演变过程,从腺泡细胞增生和功能亢进发展到酶以及碳酸氢盐分泌实质的消失,如果与细胞色素P450单加氧酶(CYP)的诱导有关,将会变得合理:长期CYP诱导导致的氧化负荷增加最终会侵蚀微量营养素抗氧化防御系统,从而损伤细胞。这种理念也能解释与人类疾病相关的已报道的肝胆异常情况,包括胆汁中自由基氧化产物的增加。因此,对叙利亚金黄地鼠的胰腺和胆汁分泌进行了研究,这些地鼠在低脂肪或高脂肪(16%玉米油)饮食中饲养6个月,饮食中添加了CYP2(200 ppm苯巴比妥)或CYP1(100 ppmβ-萘黄酮)酶家族的原型诱导剂,有或没有一种假定的酶抑制剂(400 ppm西咪替丁)。这些药物并没有改变仅由高脂肪饮食引起的胰液流速降低或碳酸氢盐浓度降低,但相反,在一些动物中诱发了胰腺蛋白分泌过多。β-萘黄酮而非苯巴比妥,无论饮食脂肪含量如何,都会增加胆汁脂质过氧化产物的输出,西咪替丁与任何一种诱导剂共同处理也会产生同样的效果。我们得出以下结论:(1)CYP的药物调节剂会放大富含玉米油饮食的有害胰胆效应,并使其更接近人类慢性胰腺炎中发现的效应;(2)这些功能紊乱伴随着胰腺脂肪萎缩;(3)长期CYP诱导本身不会导致纤维化或导管异常,而在人类疾病中,这些通常伴随着胰腺腺泡细胞的丧失,而且相反,所引起的变化似乎是无痛的。

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