Suppr超能文献

大鼠细胞内蛋白酶与全胃肠外营养诱导的肠黏膜萎缩及黏膜大分子通透性增加的相互关系。

Interrelation of intracellular proteases with total parenteral nutrition-induced gut mucosal atrophy and increase of mucosal macromolecular transmission in rats.

作者信息

Kishibuchi M, Tsujinaka T, Iijima S, Yano M, Ebisui C, Kan K, Morimoto T, Mori T

机构信息

Department of Surgery II, Osaka University Medical School, Japan.

出版信息

JPEN J Parenter Enteral Nutr. 1995 May-Jun;19(3):187-92. doi: 10.1177/0148607195019003187.

Abstract

Total parenteral nutrition (TPN) is known to induce mucosal atrophy and to increase macromolecular transmission of the small intestine. The potential participation of various proteases in that process was investigated. Male Wistar rats were randomly divided into two groups: the TPN group (n = 11) received a standard TPN (250 kcal/kg per day, 1.78 g nitrogen/kg per day) and the FED group (n = 10) received a standard rat food for 1 week. This was followed by an examination of gut macromolecular transmission of fluorescein isothiocyanate dextran 70,000 (FITC-dextran) after intragastric injection and of the activities of gut mucosal cathepsins B, H, and L and of proteasome. Mucosal wet weight and protein content decreased significantly by TPN for 1 week. In both groups, the activities of all proteases in the ileum were significantly greater than in the jejunum. In the TPN group, cathepsin L and H activities in the ileum, and cathepsin B activity in both the jejunum and the ileum, were greater than those in the FED group. The portal concentration of FITC-dextran was higher than arterial and venous concentrations in the both groups. In the TPN group, the portal FITC-dextran concentration increased significantly compared with the FED group. In conclusion, active proteolysis is not associated with TPN-induced mucosal atrophy. Cathepsins activities in the ileum increase as a result of TPN. Interrelationship is implicated between increase of lysosomal protease activity and the deterioration of the intestinal barrier function, which permits macromolecular transmission.

摘要

全胃肠外营养(TPN)已知可导致黏膜萎缩并增加小肠的大分子通透性。本研究调查了各种蛋白酶在该过程中的潜在作用。将雄性Wistar大鼠随机分为两组:TPN组(n = 11)接受标准TPN(每天250 kcal/kg,每天1.78 g氮/kg),FED组(n = 10)接受标准大鼠饲料1周。随后,在胃内注射异硫氰酸荧光素葡聚糖70,000(FITC-葡聚糖)后检测肠道大分子通透性,并检测肠道黏膜组织蛋白酶B、H和L以及蛋白酶体的活性。TPN处理1周后,黏膜湿重和蛋白质含量显著降低。两组中,回肠中所有蛋白酶的活性均显著高于空肠。在TPN组中,回肠中的组织蛋白酶L和H活性以及空肠和回肠中的组织蛋白酶B活性均高于FED组。两组中,门静脉中FITC-葡聚糖的浓度均高于动脉和静脉中的浓度。在TPN组中,门静脉FITC-葡聚糖浓度与FED组相比显著升高。总之,活跃的蛋白水解作用与TPN诱导的黏膜萎缩无关。TPN导致回肠中的组织蛋白酶活性增加。溶酶体蛋白酶活性增加与肠道屏障功能恶化之间存在关联,肠道屏障功能恶化会导致大分子通透性增加。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验