Leptin downregulates ethanol-induced secretion of proinflammatory cytokines and growth factor

被引:8
作者
Balasubramaniyan, Vairappan
Murugaiyan, Gopal
Shukla, Ruchi
Bhonde, Ramachandra Ramesh
Nalini, Namasivayam [1 ]
机构
[1] Annamalai Univ, Dept Biochem & Biotechnol, Annamalainagar 608002, Tamil Nadu, India
[2] Natl Ctr Cell Sci, Dept Biotechnol, Pune, Maharashtra, India
关键词
cytokines; ethanol; in vitro; leptin and mice;
D O I
10.1016/j.cyto.2007.02.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inflammatory mediators, including cytokines and growth factors are associated with the pathology of chronic liver diseases. The aim of our present work was to study the effect of exogenous leptin and/or ethanol on the secretion of TNF-alpha, IL-6 and TGF-P I both in vivo and in vitro. Forty eight hours after the exposure to ethanol (500 mM) significantly elevated the secretion of TNF-alpha, IL-6 and TGF-PI in the cell-free culture supernatant (HepG2 and mouse HCC cell lines), which were decreased on leptin (31.2 nM) treatment. Similarly, leptin administration to ethanol (6.32 g kg(-1) body weight) fed mice for 45 days significantly lowered the concentration of these cytokines in the circulation; however, leptin alone (230 mu g kg(-1) body weight i.p. administered every alternate day for the last 15 days) had no such significant effect on cytokine secretion both in vivo and in vitro conditions. We conclude that leptin is involved in the protective mechanisms that allow an organism to cope with the potentially autoaggressive effects of its immune system in alcoholic liver disease. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:96 / 100
页数:5
相关论文
共 23 条
[1]   Leptin causes body weight loss in the absence of in vivo activities typical of cytokines of the IL-6 family [J].
Agnello, D ;
Meazza, C ;
Rowan, CG ;
Villa, P ;
Ghezzi, P ;
Senaldi, G .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1998, 275 (03) :R913-R919
[2]   Intraperitoneal leptin regulates lipid metabolism in ethanol supplemented Mus musculas heart [J].
Balasubramaniyan, V ;
Nalini, N .
LIFE SCIENCES, 2006, 78 (08) :831-837
[3]   Identification of SOCS-3 as a potential mediator of central leptin resistance [J].
Bjorbaek, C ;
Elmquist, JK ;
Frantz, JD ;
Shoelson, SE ;
Flier, JS .
MOLECULAR CELL, 1998, 1 (04) :619-625
[4]   Mechanisms of disease:: Role of transforming growth factor β in human disease. [J].
Blobe, GC ;
Schiemann, WP ;
Lodish, HF .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (18) :1350-1358
[5]   ENDOTOXEMIA IN PATIENTS WITH ALCOHOLIC AND NONALCOHOLIC CIRRHOSIS AND IN SUBJECTS WITH NO EVIDENCE OF CHRONIC LIVER-DISEASE FOLLOWING ACUTE ALCOHOL EXCESS [J].
BODE, C ;
KUGLER, V ;
BODE, JC .
JOURNAL OF HEPATOLOGY, 1987, 4 (01) :8-14
[6]   TRANSFORMING GROWTH FACTOR-BETA-1 AND FACTOR-ALPHA IN CHRONIC LIVER-DISEASE - EFFECTS OF INTERFERON ALFA THERAPY [J].
CASTILLA, A ;
PRIETO, J ;
FAUSTO, N .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (14) :933-940
[7]   Leptin deficiency enhances sensitivity to endotoxin-induced lethality [J].
Faggioni, R ;
Fantuzzi, G ;
Gabay, C ;
Moser, A ;
Dinarello, CA ;
Feingold, KR ;
Grunfeld, C .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 276 (01) :R136-R142
[8]   TUMOR-NECROSIS-FACTOR - CHARACTERIZATION AT THE MOLECULAR, CELLULAR AND INVIVO LEVEL [J].
FIERS, W .
FEBS LETTERS, 1991, 285 (02) :199-212
[9]   Transforming growth factor-beta enhances and pro-inflammatory cytokines inhibit OB gene expression in 3T3-L1 adipocytes [J].
Granowitz, EV .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 240 (02) :382-385
[10]   Leptin stimulates type I collagen production in db/db mesangial cells:: Glucose uptake and TGF-β type II receptor expression [J].
Han, DC ;
Isono, M ;
Chen, S ;
Casaretto, A ;
Hong, SW ;
Wolf, G ;
Ziyadeh, FN .
KIDNEY INTERNATIONAL, 2001, 59 (04) :1315-1323