Erk1/2 Mediates Leptin Receptor Signaling in the Ventral Tegmental Area

被引:29
|
作者
Trinko, Richard [1 ]
Gan, Geliang [2 ]
Gao, Xiao-Bing [2 ]
Sears, Robert M. [1 ]
Guarnieri, Douglas J. [1 ]
DiLeone, Ralph J. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Psychiat, Div Mol Psychiat,Ribicoff Res Facil, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Obstet & Gynecol, New Haven, CT 06510 USA
来源
PLOS ONE | 2011年 / 6卷 / 11期
基金
美国国家卫生研究院;
关键词
MIDBRAIN DOPAMINE NEURONS; PROOPIOMELANOCORTIN NEURONS; INDUCED ANOREXIA; ARCUATE NUCLEUS; FOOD-INTAKE; INSULIN; HYPOTHALAMUS; EXPRESSION; RAT; TRANSCRIPTION-3;
D O I
10.1371/journal.pone.0027180
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Leptin acts on the ventral tegmental area (VTA) to modulate neuronal function and feeding behavior in rats and mice. To identify the intracellular effectors of the leptin receptor (Lepr), downstream signal transduction events were assessed for regulation by direct leptin infusion. Phosphorylated signal transducer and activator of transcription 3 (pSTAT3) and phosphorylated extracellular signal-regulated kinase-1 and -2 (pERK1/2) were increased in the VTA while phospho-AKT (pAKT) was unaffected. Pretreatment of brain slices with the mitogen-activated protein kinase kinase -1 and -2 (MEK1/2) inhibitor U0126 blocked the leptin-mediated decrease in firing frequency of VTA dopamine neurons. The anorexigenic effects of VTA-administered leptin were also blocked by pretreatment with U0126, which effectively blocked phosphorylation of ERK1/2 but not STAT3. These data demonstrate that pERK1/2 may have a critical role in mediating both the electrophysiogical and behavioral effects of leptin receptor signaling in the VTA.
引用
收藏
页数:6
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