Division of Molecular Psychiatry, Ribicoff Research Facilities, Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut, United States of America.
PLoS One. 2011;6(11):e27180. doi: 10.1371/journal.pone.0027180. Epub 2011 Nov 4.
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.
瘦素作用于腹侧被盖区 (VTA),调节大鼠和小鼠的神经元功能和摄食行为。为了确定瘦素受体 (Lepr) 的细胞内效应物,评估了直接瘦素输注对下游信号转导事件的调节。磷酸化信号转导和转录激活因子 3 (pSTAT3) 和磷酸化细胞外信号调节激酶-1 和 -2 (pERK1/2) 在 VTA 中增加,而磷酸化 AKT (pAKT) 不受影响。用丝裂原活化蛋白激酶激酶 -1 和 -2 (MEK1/2) 抑制剂 U0126 预处理脑片可阻断瘦素介导的 VTA 多巴胺神经元放电频率的降低。U0126 预处理还阻断了 VTA 给予瘦素的厌食作用,它有效地阻断了 ERK1/2 的磷酸化,但不阻断 STAT3。这些数据表明,pERK1/2 可能在介导 VTA 中瘦素受体信号的电生理和行为效应中起关键作用。