Antagonistic interplay between hypocretin and leptin in the lateral hypothalamus regulates stress responses

被引:131
|
作者
Bonnavion, Patricia [1 ,2 ]
Jackson, Alexander C. [3 ,4 ]
Carter, Matthew E. [5 ]
de Lecea, Luis [1 ]
机构
[1] Stanford Univ, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[2] Univ Libre Bruxelles ULB UNI, Neurophysiol Lab, B-1070 Brussels, Belgium
[3] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
[4] Univ Connecticut, Dept Physiol & Neurobiol, Storrs, CT 06269 USA
[5] Williams Coll, Dept Biol, Williamstown, MA 01267 USA
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
基金
美国国家卫生研究院;
关键词
CORTICOTROPIN-RELEASING-FACTOR; PITUITARY-ADRENAL AXIS; MESOLIMBIC DOPAMINE SYSTEM; OREXIN NEURONS; NEUROPEPTIDE-Y; NEUROTENSIN NEURONS; ENERGY HOMEOSTASIS; GENE-EXPRESSION; HPA AXIS; RECEPTOR;
D O I
10.1038/ncomms7266
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
The hypothalamic-pituitary-adrenal (HPA) axis functions to coordinate behavioural and physiological responses to stress in a manner that depends on the behavioural state of the organism. However, the mechanisms through which arousal and metabolic states influence the HPA axis are poorly understood. Here using optogenetic approaches in mice, we show that neurons that produce hypocretin (Hcrt)/orexin in the lateral hypothalamic area (LHA) regulate corticosterone release and a variety of behaviours and physiological hallmarks of the stress response. Interestingly, we found that Hcrt neuronal activity and Hcrt-mediated stress responses were inhibited by the satiety hormone leptin, which acts, in part, through a network of leptin-sensitive neurons in the LHA. These data demonstrate how peripheral metabolic signals interact with hypothalamic neurons to coordinate stress and arousal and suggest one mechanism through which hyperarousal or altered metabolic states may be linked with abnormal stress responses.
引用
收藏
页数:14
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