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膳食多不饱和脂肪对乙醇诱导的肝星状细胞激活的影响。

Effects of dietary polyunsaturated fat on ethanol-induced Ito cell activation.

作者信息

Tsukamoto H, Cheng S, Blaner W S

机构信息

Department of Medicine, University of Southern California, Los Angeles 90033-4581, USA.

出版信息

Am J Physiol. 1996 Apr;270(4 Pt 1):G581-6. doi: 10.1152/ajpgi.1996.270.4.G581.

Abstract

Ito cells, vitamin A-storing perisinusoidal cells, are believed to undergo myofibroblastic transformation in liver fibrogenesis. Our previous studies have shown that a diet high in polyunsaturated fat was key for induction of experimental alcoholic liver fibrosis. To investigate the cellular basis for this fibrogenic effect of a high-fat diet, we analyzed the content of vitamin A and cellular retinol binding protein (CRBP), the steady-state mRNA levels of procollagen-alpha1(I), transforming growth factor-beta1 (TGF-beta1), interleukin-6 (IL-6), and smooth muscle alpha-actin (alpha-SM) in freshly isolated Ito cells from rats given isocaloric amounts of ethanol and a low- or high-fat diet. After 10 wk, the Ito cell content of retinyl palmitate was severely reduced in both the high- and low-fat diet-ethanol-fed animals to 13-17% of those measured in respective pair-fed controls. On the other hand, the content of CRBP was reduced in the high-fat-ethanol rats but not in the low-fat-ethanol group. The cells from the high-fat-ethanol but not low-fat ethanol rats showed an 18-fold increase in procollagen-alpha1(I) mRNA at 17 wk, which was accompanied by 2.8- and 2.3-fold enhancement of TGF-beta1 and alpha-SM transcripts. IL-6 mRNA was not detected in the cells from any groups. These results demonstrate 1) myofibroblastic activation of Ito cells is evident in rats given a high-fat diet and ethanol but not in the low-fat-ethanol animals; 2) vitamin A depletion of Ito cells is the early and general effect of chronic ethanol intake but does not necessarily predict subsequent myofibroblastic activation; 3) reduced CRBP level is more closely associated with the subsequent cellular activation seen under the high-fat-ethanol regimen; and 4) IL-6 is not expressed in vivo by Ito cells from either normal livers or livers with alcoholic liver fibrosis.

摘要

肝星状细胞,即储存维生素A的肝血窦周细胞,被认为在肝纤维化形成过程中会发生肌成纤维细胞转化。我们之前的研究表明,高多不饱和脂肪饮食是诱导实验性酒精性肝纤维化的关键因素。为了探究高脂饮食这种促纤维化作用的细胞基础,我们分析了给予等热量乙醇及低脂或高脂饮食的大鼠新鲜分离的肝星状细胞中维生素A和细胞视黄醇结合蛋白(CRBP)的含量、I型前胶原α1(procollagen-alpha1(I))、转化生长因子-β1(TGF-beta1)、白细胞介素-6(IL-6)和平滑肌α-肌动蛋白(α-SM)的稳态mRNA水平。10周后,高脂和低脂饮食-乙醇喂养动物的肝星状细胞中棕榈酸视黄酯含量均严重降低,降至各自配对喂养对照组测量值的13 - 17%。另一方面,高脂-乙醇组大鼠的CRBP含量降低,而低脂-乙醇组未降低。高脂-乙醇组大鼠而非低脂-乙醇组大鼠的细胞在17周时I型前胶原α1 mRNA增加了18倍,同时TGF-beta1和α-SM转录本分别增强了2.8倍和2.3倍。在任何组的细胞中均未检测到IL-6 mRNA。这些结果表明:1)给予高脂饮食和乙醇的大鼠肝星状细胞出现肌成纤维细胞活化,而给予低脂-乙醇的动物未出现;2)肝星状细胞维生素A耗竭是慢性乙醇摄入的早期普遍效应,但不一定预示随后的肌成纤维细胞活化;3)CRBP水平降低与高脂-乙醇方案下随后出现的细胞活化更密切相关;4)正常肝脏或酒精性肝纤维化肝脏的肝星状细胞在体内均不表达IL-6。

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