Leptin action on nonneuronal cells in the CNS: potential clinical applications

被引:37
作者
Pan, Weihong [1 ]
Hsuchou, Hung [1 ]
Jayaram, Bhavaani [1 ]
Khan, Reas S. [1 ]
Huang, Eagle Yi-Kung [2 ]
Wu, Xiaojun [1 ]
Chen, Chu [3 ]
Kastin, Abba J. [1 ]
机构
[1] Pennington Biomed Res Ctr, Blood Brain Barrier Grp, Baton Rouge, LA 70808 USA
[2] Natl Def Med Ctr, Dept Pharmacol, Taipei, Taiwan
[3] Louisiana State Univ, Hlth Sci Ctr, Neurosci Ctr Excellence, New Orleans, LA USA
来源
BRAIN AND OBESITY | 2012年 / 1264卷
关键词
leptin; CNS; obesity; astrocytes; blood-brain barrier; RECEPTOR MESSENGER-RNA; NUCLEUS-TRACTUS-SOLITARIUS; CEREBROSPINAL FLUID BARRIER; RAT HIPPOCAMPAL-NEURONS; BLOOD-BRAIN-BARRIER; MOUSE-BRAIN; GLUCOSE DEPRIVATION; INDUCED SEIZURES; CHOROID-PLEXUS; EXPRESSION;
D O I
10.1111/j.1749-6632.2012.06472.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Leptin, an adipocyte-derived cytokine, crosses the blood-brain barrier to act on many regions of the central nervous system (CNS). It participates in the regulation of energy balance, inflammatory processes, immune regulation, synaptic formation, memory condensation, and neurotrophic activities. This review focuses on the newly identified actions of leptin on astrocytes. We first summarize the distribution of leptin receptors in the brain, with a focus on the hypothalamus, where the leptin receptor is known to mediate essential feeding suppression activities, and on the hippocampus, where leptin facilitates memory, reduces neurodegeneration, and plays a dual role in seizures. We will then discuss regulation of the nonneuronal leptin system in obesity. Its relationship with neuronal leptin signaling is illustrated by in vitro assays in primary astrocyte culture and by in vivo studies on mice after pretreatment with a glial metabolic inhibitor or after cell-specific deletion of intracellular signaling leptin receptors. Overall, the glial leptin system shows robust regulation and plays an essential role in obesity. Strategies to manipulate this nonneuronal leptin signaling may have major clinical impact.
引用
收藏
页码:64 / 71
页数:8
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