Interaction between the corticotropin-releasing factor system and hypocretins (Orexins): A novel circuit mediating stress response

被引:359
作者
Winsky-Sommerer, R
Yamanaka, A
Diano, S
Borok, E
Roberts, AJ
Sakurai, T
Kilduff, TS
Horvath, TL
de Lecea, L
机构
[1] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Neuropharmacol, La Jolla, CA 92037 USA
[3] SRI Int, Mol Neurobiol Lab, Menlo Pk, CA 94025 USA
[4] Univ Tsukuba, Inst Basic Med Sci, Dept Pharmacol, Tsukuba 3058575, Japan
[5] Yale Univ, Sch Med, Dept Obstet & Gynecol, New Haven, CT 06520 USA
[6] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06520 USA
关键词
hypocretin; orexin; corticotropin-releasing factor; hypothalamus; stress; homeostasis;
D O I
10.1523/JNEUROSCI.3459-04.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The hypothalamic neuropeptides hypocretins (orexins) play a crucial role in the stability of arousal and alertness. We tested whether the hypocretinergic system is a critical component of the stress response activated by the corticotropin-releasing factor (CRF). Our results show that CRF-immunoreactive terminals make direct contact with hypocretin-expressing neurons in the lateral hypothalamus and that numerous hypocretinergic neurons express the CRF-R1/2 receptors. We also demonstrate that application of CRF to hypothalamic slices containing identified hypocretin neurons depolarizes membrane potential and increases firing rate in a subpopulation of hypocretinergic cells. CRF-induced depolarization was tetrodotoxin insensitive and was blocked by the peptidergic CRF-R1 antagonist astressin. Moreover, activation of hypocretinergic neurons in response to acute stress was severely impaired in CRF-R1 knock-out mice. Together, our data provide evidence of a direct neuroanatomical and physiological input from CRF peptidergic system onto hypocretin neurons. We propose that, after stressor stimuli, CRF stimulates the release of hypocretins and that this circuit contributes to activation and maintenance of arousal associated with the stress response.
引用
收藏
页码:11439 / 11448
页数:10
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