The Central Nervous System Sites Mediating the Orexigenic Actions of Ghrelin

被引:57
作者
Mason, B. L. [1 ]
Wang, Q.
Zigman, J. M.
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Div Hypothalam Res, Dallas, TX 75390 USA
来源
ANNUAL REVIEW OF PHYSIOLOGY, VOL 76 | 2014年 / 76卷
关键词
GHSR; orexigenic; homeostatic; hedonic; GROWTH-HORMONE SECRETAGOGUE; RECEPTOR GHS-R; NEUROPEPTIDE-Y NEURONS; PITUITARY-ADRENAL AXIS; AGOUTI-RELATED PEPTIDE; BLOOD-BRAIN-BARRIER; ARCUATE NUCLEUS; FOOD-INTAKE; MESSENGER-RNA; PARAVENTRICULAR NUCLEUS;
D O I
10.1146/annurev-physiol-021113-170310
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The peptide hormone ghrelin is important for both homeostatic and hedonic eating behaviors, and its orexigenic actions occur mainly via binding to the only known ghrelin receptor, the growth hormone secretagogue receptor (GHSR). GHSRs are located in several distinct regions of the central nervous system. This review discusses those central nervous system sites that have been found to play critical roles in the orexigenic actions of ghrelin, including hypothalamic nuclei, the hippocampus, the amygdala, the caudal brain stem, and midbrain dopaminergic neurons. Hopefully, this review can be used as a stepping stone for the reader wanting to gain a clearer understanding of the central nervous system sites of direct ghrelin action on feeding behavior, and as inspiration for future studies to provide an even-more-detailed map of the neurocircuitry controlling eating and body weight.
引用
收藏
页码:519 / 533
页数:15
相关论文
共 129 条
[1]   Ghrelin modulates the activity and synaptic input organization of midbrain dopamine neurons while promoting appetite [J].
Abizaid, Alfonso ;
Liu, Zhong-Wu ;
Andrews, Zane B. ;
Shanabrough, Marya ;
Borok, Erzsebet ;
Elsworth, John D. ;
Roth, Robert H. ;
Sleeman, Mark W. ;
Picciotto, Marina R. ;
Tschop, Matthias H. ;
Gao, Xiao-Bing ;
Horvath, Tamas L. .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (12) :3229-3239
[2]   Physiological roles revealed by ghrelin and ghrelin receptor deficient mice [J].
Albarran-Zeckler, Rosie G. ;
Sun, Yuxiang ;
Smith, Roy G. .
PEPTIDES, 2011, 32 (11) :2229-2235
[3]   The Amygdala as a Neurobiological Target for Ghrelin in Rats: Neuroanatomical, Electrophysiological and Behavioral Evidence [J].
Alvarez-Crespo, Mayte ;
Skibicka, Karolina P. ;
Farkas, Imre ;
Molnar, Csilla S. ;
Egecioglu, Emil ;
Hrabovszky, Erik ;
Liposits, Zsolt ;
Dickson, Suzanne L. .
PLOS ONE, 2012, 7 (10)
[4]   UCP2 mediates ghrelin's action on NPY/AgRP neurons by lowering free radicals [J].
Andrews, Zane B. ;
Liu, Zhong-Wu ;
Walllingford, Nicholas ;
Erion, Derek M. ;
Borok, Erzsebet ;
Friedman, Jeffery M. ;
Tschop, Matthias H. ;
Shanabrough, Marya ;
Cline, Gary ;
Shulman, Gerald I. ;
Coppola, Anna ;
Gao, Xiao-Bing ;
Horvath, Tamas L. ;
Diano, Sabrina .
NATURE, 2008, 454 (7206) :846-851
[5]   AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training [J].
Aponte, Yexica ;
Atasoy, Deniz ;
Sternson, Scott M. .
NATURE NEUROSCIENCE, 2011, 14 (03) :351-355
[6]   Gut vagal afferents are not necessary for the eating-stimulatory effect of intraperitoneally injected Ghrelin in the rat [J].
Arnold, Myrtha ;
Mura, Anna ;
Langhans, Wolfgang ;
Geary, Nori .
JOURNAL OF NEUROSCIENCE, 2006, 26 (43) :11052-11060
[7]   Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin [J].
Asakawa, A ;
Inui, A ;
Kaga, T ;
Yuzuriha, H ;
Nagata, T ;
Ueno, N ;
Makino, S ;
Fujimiya, M ;
Niijima, A ;
Fujino, MA ;
Kasuga, M .
GASTROENTEROLOGY, 2001, 120 (02) :337-345
[8]  
Bagnol D, 1999, J NEUROSCI, V19
[9]   Divergence of melanocortin pathways in the control of food intake and energy expenditure [J].
Balthasar, N ;
Dalgaard, LT ;
Lee, CE ;
Yu, J ;
Funahashi, H ;
Williams, T ;
Ferreira, M ;
Tang, V ;
McGovern, RA ;
Kenny, CD ;
Christiansen, LM ;
Edelstein, E ;
Choi, B ;
Boss, O ;
Aschkenasi, C ;
Zhang, CY ;
Mountjoy, K ;
Kishi, T ;
Elmquist, JK ;
Lowell, BB .
CELL, 2005, 123 (03) :493-505
[10]   Extent and direction of ghrelin transport across the blood-brain barrier is determined by its unique primary structure [J].
Banks, WA ;
Tschöp, M ;
Robinson, SM ;
Heiman, ML .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 302 (02) :822-827