GLP-1 Neurons in the Nucleus of the Solitary Tract Project Directly to the Ventral Tegmental Area and Nucleus Accumbens to Control for Food Intake

被引:353
作者
Alhadeff, Amber L. [1 ]
Rupprecht, Laura E. [1 ]
Hayes, Matthew R. [1 ]
机构
[1] Univ Penn, Dept Psychiat, Translat Neurosci Program, Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
GLUCAGON-LIKE PEPTIDE-1; BODY-WEIGHT; GLUCAGON-LIKE-PEPTIDE-1; RECEPTOR; GASTRIC DISTENSION; GLYCEMIC CONTROL; REWARD; BRAIN; LIRAGLUTIDE; DOPAMINE; RAT;
D O I
10.1210/en.2011-1443
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Central glucagon-like-peptide-1 (GLP-1) receptor activation reduces food intake; however, brain nuclei and mechanism(s) mediating this effect remain poorly understood. Although central nervous system GLP-1 is produced almost exclusively in the nucleus of the solitary tract in the hindbrain, GLP-1 receptors (GLP-1R) are expressed throughout the brain, including nuclei in the mesolimbic reward system (MRS), e. g. the ventral tegmental area (VTA) and the nucleus accumbens (NAc). Here, we examine the MRS as a potential site of action for GLP-1-mediated control of food intake and body weight. Double immunohistochemistry for Fluorogold (monosynaptic retrograde tracer) and GLP-1 neuron immunoreactivity indicated that GLP-1-producing nucleus tractus solitarius neurons project directly to the VTA, the NAc core, and the NAc shell. Pharmacological data showed that GLP-1R activation in the VTA, NAc core, and NAc shell decreased food intake, especially of highly-palatable foods, and body weight. Moreover, blockade of endogenous GLP-1R signaling in the VTA and NAc core resulted in a significant increase in food intake, establishing a physiological relevance for GLP-1 signaling in the MRS. Current data highlight these nuclei within the MRS as novel sites for GLP-1R-mediated control of food intake and body weight. (Endocrinology 153: 647-658, 2012)
引用
收藏
页码:647 / 658
页数:12
相关论文
共 69 条
[31]   The physiology of glucagon-like peptide 1 [J].
Holst, Jens Juul .
PHYSIOLOGICAL REVIEWS, 2007, 87 (04) :1409-1439
[32]   Leptin receptor signaling in midbrain dopamine neurons regulates feeding [J].
Hommel, Jonathan D. ;
Trinko, Richard ;
Sears, Robert M. ;
Georgescu, Dan ;
Liu, Zong-Wu ;
Gao, Xiao-Bing ;
Thurmon, Jeremy J. ;
Marinelli, Michela ;
DiLeone, Ralph J. .
NEURON, 2006, 51 (06) :801-810
[33]   Leptin and the control of food intake: Neurons in the nucleus of the solitary tract are activated by both gastric distension and leptin [J].
Huo, Lihong ;
Maeng, Lisa ;
Bjorbaek, Christian ;
Grill, Harvey J. .
ENDOCRINOLOGY, 2007, 148 (05) :2189-2197
[34]   Peripheral and Central GLP-1 Receptor Populations Mediate the Anorectic Effects of Peripherally Administered GLP-1 Receptor Agonists, Liraglutide and Exendin-4 [J].
Kanoski, Scott E. ;
Fortin, Samantha M. ;
Arnold, Myrtha ;
Grill, Harvey J. ;
Hayes, Matthew R. .
ENDOCRINOLOGY, 2011, 152 (08) :3103-3112
[35]   Reward Mechanisms in Obesity: New Insights and Future Directions [J].
Kenny, Paul J. .
NEURON, 2011, 69 (04) :664-679
[36]   Opioid receptor subtype antagonists differentially alter GABA agonist-induced feeding elicited from either the nucleus accumbens shell or ventral tegmental area regions in rats [J].
Khaimova, E ;
Kandov, Y ;
Israel, Y ;
Cataldo, G ;
Hadjimarkou, MM ;
Bodnar, RJ .
BRAIN RESEARCH, 2004, 1026 (02) :284-294
[37]   Feeding association between the nucleus of the solitary tract and the ventral tegmental area [J].
Kim, Eun-Mee ;
Quinn, Joseph G. ;
Spanswick, David ;
O'Hare, Eugene .
APPETITE, 2009, 53 (03) :457-460
[38]  
Kinzig KP, 2002, J NEUROSCI, V22, P10470
[39]   Liraglutide: the therapeutic promise from animal models [J].
Knudsen, L. B. .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2010, 64 :4-11
[40]   Distribution of glucagon-like peptide-1 and other preproglucagon-derived peptides in the rat hypothalamus and brainstem [J].
Larsen, PJ ;
TangChristensen, M ;
Holst, JJ ;
Orskov, C .
NEUROSCIENCE, 1997, 77 (01) :257-270