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肿瘤坏死因子-α对家兔肠道D-果糖转运的影响。

The effect of tumor necrosis factor-alpha on D-fructose intestinal transport in rabbits.

作者信息

García-Herrera J, Navarro M A, Marca M C, de la Osada J, Rodríguez-Yoldi M J

机构信息

Department of Pharmacology and Physiology, Veterinary Faculty, University of Zaragoza, Miguel Servet 177, 50013 Zaragoza, Spain.

出版信息

Cytokine. 2004 Jan 7;25(1):21-30. doi: 10.1016/j.cyto.2003.09.005.

Abstract

Tumor necrosis factor-alpha (TNF-alpha) is an important immunoregulatory cytokine involved in septic responses during bacterial infection. The aim of this study was to examine the effect of TNF-alpha on the transport of D-fructose across rabbit jejunum. A sepsis condition was evoked by intravenous administration of this cytokine and hematological and plasma parameters were analyzed and body temperature was recorded. D-Fructose transport was assayed in rabbit jejunum. Sugar absorption in TNF-alpha treated rabbits was lower than in control animals. TNF-alpha decreased both the mucosal-to-serosal transepithelial flux and the transport across brush border membrane vesicles of D-fructose. The number of D-fructose transporters (GLUT5) was analyzed by Western blot in an attempt to explain this inhibition. TNF-alpha treated animals had lower levels of GLUT5, indicating a reduction in the expression of GLUT5 protein and therefore in transport capacity. The inhibition could also be related with the secretagogue effect of TNF-alpha on the gut since the intracellular tissue water was affected and the absence of chloride ion in the incubation medium partly removed the cytokine inhibition on sugar intestinal transport in treated rabbits. Finally, in terms of possible mediators involved in the TNF-alpha effect, nitric oxide and prostaglandins appeared to play a role in the inhibition of D-fructose intestinal uptake.

摘要

肿瘤坏死因子-α(TNF-α)是一种重要的免疫调节细胞因子,参与细菌感染期间的脓毒症反应。本研究的目的是检测TNF-α对兔空肠中D-果糖转运的影响。通过静脉注射这种细胞因子诱发脓毒症状态,分析血液学和血浆参数并记录体温。在兔空肠中测定D-果糖转运。经TNF-α处理的兔子的糖吸收低于对照动物。TNF-α降低了D-果糖从黏膜到浆膜的跨上皮通量以及通过刷状缘膜囊泡的转运。通过蛋白质免疫印迹分析D-果糖转运体(GLUT5)的数量,以试图解释这种抑制作用。经TNF-α处理的动物中GLUT5水平较低,表明GLUT5蛋白表达减少,从而转运能力降低。这种抑制作用也可能与TNF-α对肠道的促分泌作用有关,因为细胞内组织水分受到影响,并且孵育培养基中不存在氯离子部分消除了细胞因子对经处理兔子肠道糖转运的抑制作用。最后,就参与TNF-α作用的可能介质而言,一氧化氮和前列腺素似乎在抑制D-果糖肠道摄取中起作用。

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