Leptin regulates interleukin-1β expression in the brain via the STAT3-independent mechanisms

被引:52
作者
Hosoi, T [1 ]
Okuma, Y [1 ]
Nomura, Y [1 ]
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Dept Pharmacol, Kita Ku, Sapporo, Hokkaido 0600812, Japan
基金
日本学术振兴会;
关键词
neuroimmunology; leptin receptor; db/db mouse; inflammation; interleukin-1; beta;
D O I
10.1016/S0006-8993(02)02974-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Leptin is known to be an important circulating signal for regulation of food intake and body weight. These effects were suggested to be mediated through the hypothalamic center via the Ob-Rb receptor (long isoform of leptin receptor). Although short isoforms of leptin receptor exist in many regions of the brain, there has been little in vivo functional study of these areas such as for leptin's target site. We report here that peripherally applied leptin increased interleukin (IL)-1beta transcripts in many regions of the brain such as the hypothalamus, the hippocampus, the cortex, the cerebellum and the brainstem. Although leptin did not induce STAT3 activation or suppressor of cytokine signaling3 (SOCS3) expression in the hypothalamus of the db/db mice, which lack a functional Ob-Rb receptor, leptin increased the IL-1beta levels to similar extents as normal mice. Therefore, a novel function of leptin is suggested as the induction of IL-1beta expression in many regions of the brain via STAT3-independent mechanisms. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:139 / 146
页数:8
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