Serotonin reciprocally regulates melanocortin neurons to modulate food intake

被引:318
作者
Heisler, Lora K.
Jobst, Erin E.
Sutton, Gregory M.
Zhou, Ligang
Borok, Erzsebet
Thornton-Jones, Zoe
Liu, Hong Yan
Zigman, Jeffrey M.
Balthasar, Nina
Kishi, Toshiro
Lee, Charlotte E.
Aschkenasi, Carl J.
Zhang, Chen-Yu
Yu, Jia
Boss, Olivier
Mountjoy, Kathleen G.
Clifton, Peter G.
Lowell, Bradford B.
Friedman, Jeffrey M.
Horvath, Tamas
Butler, Andrew A.
Elmquist, Joel K. [1 ]
Cowley, Michael A.
机构
[1] Harvard Univ, Sch Med, Div Endocrinol Diabet & Metab, Dept Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Neurol, Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02215 USA
[4] Univ Cambridge, Addenbrookes Hosp, Dept Clin Biochem, Cambridge CB2 2QQ, England
[5] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Div Neurosci, Beaverton, OR 97006 USA
[6] Pacific Univ, Sch Phys Therapy, Forest Grove, OR 97116 USA
[7] Louisiana State Univ, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[8] Yale Univ, Sch Med, Dept Obstet & Gynecol, New Haven, CT 06520 USA
[9] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06520 USA
[10] Univ Sussex, Dept Psychol, Brighton BN1 9QG, E Sussex, England
[11] Rockefeller Univ, Howard Hughes Med Inst, Mol Genet Lab, New York, NY 10021 USA
[12] Shimane Med Univ, Sch Med, Dept Anat & Morphol Neurosci, Izumo, Shimane 6938501, Japan
[13] Univ Auckland, Fac Med & Hlth Sci, Dept Physiol, Auckland 1, New Zealand
[14] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
基金
英国惠康基金;
关键词
D O I
10.1016/j.neuron.2006.06.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The neural pathways through which central serotonergic systems regulate food intake and body weight remain to be fully elucidated. We report that serotonin, via action at serotonin1B receptors (5-HT(1B)Rs), modulates the endogenous release of both agonists and antagonists of the melanocortin receptors, which are a core component of the central circuitry controlling body weight homeostasis. We also show that serotonin-induced hypophagia requires downstream activation of melanocortin 4, but not melanocortin 3, receptors. These results identify a primary mechanism underlying the serotonergic regulation of energy balance and provide an example of a centrally derived signal that reciprocally regulates melanocortin receptor agonists and antagonists in a similar manner to peripheral adiposity signals.
引用
收藏
页码:239 / 249
页数:11
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