The atypical antipsychotic olanzapine causes weight gain by targeting serotonin receptor 2C

被引:127
作者
Lord, Caleb C. [1 ]
Wyler, Steven C. [1 ]
Wan, Rong [1 ]
Castorena, Carlos M. [1 ]
Ahmed, Newaz [1 ]
Mathew, Dias [1 ]
Lee, Syann [1 ]
Liu, Chen [1 ,2 ]
Elmquist, Joel K. [1 ,3 ]
机构
[1] UT Southwestern Med Ctr, Dept Internal Med, Div Hypothalam Res, Dallas, TX USA
[2] UT Southwestern Med Ctr, Dept Neurosci, Dallas, TX USA
[3] UT Southwestern Med Ctr, Dept Pharmacol, Dallas, TX USA
关键词
NEURONS REGULATE ENERGY; DOUBLE-BLIND; HISTAMINE H-1; RISK; SCHIZOPHRENIA; HOMEOSTASIS; DRUGS; TRIAL; MICE;
D O I
10.1172/JCI93362
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Atypical antipsychotics such as olanzapine often induce excessive weight gain and type 2 diabetes. However, the mechanisms underlying these drug-induced metabolic perturbations remain poorly understood. Here, we used an experimental model that reproduces olanzapine-induced hyperphagia and obesity in female C57BL/6 mice. We found that olanzapine treatment acutely increased food intake, impaired glucose tolerance, and altered physical activity and energy expenditure in mice. Furthermore, olanzapine-induced hyperphagia and weight gain were blunted in mice lacking the serotonin 2C receptor (HTR2C). Finally, we showed that treatment with the HTR2C-specific agonist lorcaserin suppressed olanzapine-induced hyperphagia and weight gain. Lorcaserin treatment also improved glucose tolerance in olanzapine-fed mice. Collectively, our studies suggest that olanzapine exerts some of its untoward metabolic effects via antagonism of HTR2C.
引用
收藏
页码:3408 / 3412
页数:5
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