Ghrelin and immunity: A young player in an old field

被引:87
作者
Dixit, VD [1 ]
Taub, DD [1 ]
机构
[1] US HHS Natl Inst Hlth, Gerontol Res Ctr, Immunol Lab, Clin Immunol Sect,Intramural Res Program, Baltimore, MD 21224 USA
关键词
ghrelin; GHS-R; inflammation; thymus; cytokines; IL-6; frailty; aging;
D O I
10.1016/j.exger.2005.09.003
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
There is increasing evidence of the coupling of immune status to the metabolic system. The communication between the state of systemic and cellular energy balance to immune compartment is mediated via a complex array of cytokines, hormones and neuropeptides. Ghrelin, a recently described orexigenic peptide hormone, is predominantly produced by the stomach and functions as a positive regulator of the somatotropic axis and a peripheral signal of negative energy balance. Apart from its well-studied metabolic effects, ghrelin also exerts multiple regulatory effects on several other organ systems including the cardiovascular, central nervous and immune systems. Here, we summarize the growing evidence of ghrelin as a significant player in the regulation of inflamtnation and the immune function and the potential therapeutic targeting of ghrelin or its receptor, the growth hormone secretagogue receptor (GHS-R), in various inflammatory and cachexic disease states. Published by Elsevier Inc.
引用
收藏
页码:900 / 910
页数:11
相关论文
共 117 条
[1]   Pharmacokinetics, safety, and endocrine and appetite effects of ghrelin administration in young healthy subjects [J].
Akamizu, T ;
Takaya, K ;
Irako, T ;
Hosoda, H ;
Teramukai, S ;
Matsuyama, A ;
Tada, H ;
Miura, K ;
Shimizu, A ;
Fukushima, M ;
Yokode, M ;
Tanaka, K ;
Kangawa, K .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2004, 150 (04) :447-455
[2]   Intermittent fasting dissociates beneficial effects of dietary restriction on glucose metabolism and neuronal resistance to injury from calorie intake [J].
Anson, RM ;
Guo, ZH ;
de Cabo, R ;
Iyun, T ;
Rios, M ;
Hagepanos, A ;
Ingram, DK ;
Lane, MA ;
Mattson, MP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (10) :6216-6220
[3]   Transgenic mice overexpressing des-acyl ghrelin show small phenotype [J].
Ariyasu, H ;
Takaya, K ;
Iwakura, H ;
Hosoda, H ;
Akamizu, T ;
Arai, Y ;
Kangawa, K ;
Nakao, K .
ENDOCRINOLOGY, 2005, 146 (01) :355-364
[4]   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
[5]   Antagonism of ghrelin receptor reduces food intake and body weight gain in mice [J].
Asakawa, A ;
Inui, A ;
Kaga, T ;
Katsuura, G ;
Fujimiya, M ;
Fujino, MA ;
Kasuga, M .
GUT, 2003, 52 (07) :947-952
[6]   The gut and energy balance: Visceral allies in the obesity wars [J].
Badman, MK ;
Flier, JS .
SCIENCE, 2005, 307 (5717) :1909-1914
[7]   Genetic linkage and association of the growth hormone secretagogue receptor (Ghrelin receptor) gene in human obesity [J].
Baessler, A ;
Hasinoff, MJ ;
Fischer, M ;
Reinhard, W ;
Sonnenberg, GE ;
Olivier, M ;
Erdmann, J ;
Schunkert, H ;
Doering, A ;
Jacob, HJ ;
Comuzzie, AG ;
Kissebah, AH ;
Kwitek, AE .
DIABETES, 2005, 54 (01) :259-267
[8]   Ghrelin and des-acyl ghrelin inhibit cell death in cardiomyocytes and endothelial cells through ERK1/2 and PI 3-kinase/AKT [J].
Baldanzi, G ;
Filigheddu, N ;
Cutrupi, S ;
Catapano, F ;
Bonissoni, S ;
Fubini, A ;
Malan, D ;
Baj, G ;
Granata, R ;
Broglio, F ;
Papotti, M ;
Surico, N ;
Bussolino, F ;
Isgaard, J ;
Deghenghi, R ;
Sinigaglia, F ;
Prat, M ;
Muccioli, G ;
Ghigo, E ;
Graziani, A .
JOURNAL OF CELL BIOLOGY, 2002, 159 (06) :1029-1037
[9]   Ghrelin inhibits the proliferative activity of immature Leydig cells in vivo and regulates stem cell factor messenger ribonucleic acid expression in rat testis [J].
Barreiro, ML ;
Gaytan, F ;
Castellano, JM ;
Suominen, JS ;
Roa, J ;
Gaytan, M ;
Aguilar, E ;
Dieguez, C ;
Toppari, J ;
Tena-Sempere, M .
ENDOCRINOLOGY, 2004, 145 (11) :4825-4834
[10]   Bacterial lipopolysaccharide shifts fasted plasma ghrelin to postprandial levels in rats [J].
Basa, NR ;
Wang, LX ;
Arteaga, JR ;
Heber, D ;
Livingston, EH ;
Taché, Y .
NEUROSCIENCE LETTERS, 2003, 343 (01) :25-28