Increased uncoupling protein-2 gene expression in brain of lipopolysaccharide-injected mice:: role of tumour necrosis factor-α?

被引:20
作者
Busquets, S [1 ]
Alvarez, B [1 ]
Van Royen, M [1 ]
Figueras, MT [1 ]
López-Soriano, FJ [1 ]
Argilés, JM [1 ]
机构
[1] Univ Barcelona, Fac Biol, Unitat B, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2001年 / 1499卷 / 03期
关键词
lipopolysaccharide; brain; tumour necrosis factor-alpha; uncoupling protein-2; brain mitochondrial carrier protein-1; tumour;
D O I
10.1016/S0167-4889(00)00126-9
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
In order to understand the role of brain localized uncoupling proteins, we have examined the UCP2 and BMCP-1 gene expression in mice brain in two different catabolic states: administration of lipopolysaccharide (LPS) (2.5 mg/kg, i.p.) and tumour burden. Administration of LPS resulted in an increased UCP2 gene expression both in brain (208%) and cerebellum (77%). An increase in UCP2 gene expression was also observed after LPS treatment in double knockout mice for tumour necrosis factor-cc (TNF) receptors 1 and 2 (75% in brain and 33% in cerebellum). Tumour growth also resulted in increased brain UCP2 gene expression (80%) in mice bearing the Lewis lung carcinoma as compared with the non-tumour-bearing controls. No changes were observed in BMCP-1 mRNA levels of either LPS-injected or tumour-bearing mice. From the results presented it may be suggested that: (a) the brain may contribute significantly to the increase in energy expenditure associated with hypermetabolic states such as fever and tumour burden, and (b) the regulation of UCP2 gene expression in brain does not seem to be influenced by TNF; therefore the action of other cytokines cannot be discarded. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:249 / 256
页数:8
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