Brain adipocytokine action and metabolic regulation

被引:110
作者
Ahima, Rexford S.
Qi, Yong
Singhal, Neel S.
Jackson, Malaka B.
Scherer, Philipp E.
机构
[1] Univ Penn, Sch Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[3] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USA
[4] Albert Einstein Coll Med, Ctr Diabet Res & Training, Bronx, NY 10467 USA
关键词
D O I
10.2337/db06-S018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adipose tissue secretes factors that control various physiological systems. The fall in leptin during fasting mediates hyperphagia and suppresses thermogenesis, thyroid and reproductive hormones, and immune system. On the other hand, rising leptin levels in the fed state stimulate fatty acid oxidation, decrease appetite, and limit weight gain. These divergent effects of leptin occur through neuronal circuits in the hypothalamus and other brain areas. Leptin also regulates the activities of enzymes involved in lipid metabolism, e.g., AMP-activated protein kinase and stearoyl-CoA desaturase-1, and also interacts with insulin signaling in the brain. Adiponectin enhances fatty acid oxidation and insulin sensitivity, in part by stimulating AMP-activated protein kinase phosphorylation and activity in liver and muscle. Moreover, adiponectin decreases body fat by increasing energy expenditure and lipid catabolism. These effects involve peripheral and possibly central mechanisms. Adipose tissue mediates interconversion of steroid hormones and secretes proinflammatory cytokines, vasoactive peptides, and coagulation and complement proteins. Understanding the actions of these "adipocytokines" will provide insight into the pathogenesis and treatment of obesity and related diseases.
引用
收藏
页码:S145 / S154
页数:10
相关论文
共 99 条
[11]   STEROID-HORMONE INTERCONVERSIONS IN HUMAN ADIPOSE-TISSUE INVIVO [J].
BOULTON, KL ;
HUDSON, DU ;
COPPACK, SW ;
FRAYN, KN .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1992, 41 (05) :556-559
[12]   Trophic action of leptin on hypothalamic neurons that regulate feeding [J].
Bouret, SG ;
Draper, SJ ;
Simerly, RB .
SCIENCE, 2004, 304 (5667) :108-110
[13]  
Chan JL, 2003, J CLIN INVEST, V111, P1409, DOI 10.1172/JCI200317490
[14]   Heterozygosity for Lepob or Leprdb affects body composition and leptin homeostasis in adult mice [J].
Chung, WK ;
Belfi, K ;
Chua, M ;
Wiley, J ;
Mackintosh, R ;
Nicolson, M ;
Boozer, CN ;
Leibel, RL .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1998, 274 (04) :R985-R990
[15]  
Cinti S, 2000, Eat Weight Disord, V5, P132
[16]   Role for stearoyl-CoA desaturase-1 in leptin-mediated weight loss [J].
Cohen, P ;
Miyazaki, M ;
Socci, ND ;
Hagge-Greenberg, A ;
Liedtke, W ;
Soukas, AA ;
Sharma, R ;
Hudgins, LC ;
Ntambi, JM ;
Friedman, JM .
SCIENCE, 2002, 297 (5579) :240-243
[17]   Selective deletion of leptin receptor in neurons leads to obesity [J].
Cohen, P ;
Zhao, C ;
Cai, XL ;
Montez, JM ;
Rohani, SC ;
Feinstein, P ;
Mombaerts, P ;
Friedman, JM .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (08) :1113-1121
[18]   OBESITY GENES - BENEFICIAL-EFFECTS IN HETEROZYGOUS MICE [J].
COLEMAN, DL .
SCIENCE, 1979, 203 (4381) :663-665
[19]   EFFECTS OF PARABIOSIS OF OBESE WITH DIABETES AND NORMAL MICE [J].
COLEMAN, DL .
DIABETOLOGIA, 1973, 9 (04) :294-298
[20]   Leptin activates anorexigenic POMC neurons through a neural network in the arcuate nucleus [J].
Cowley, MA ;
Smart, JL ;
Rubinstein, M ;
Cordán, MG ;
Diano, S ;
Horvath, TL ;
Cone, RD ;
Low, MJ .
NATURE, 2001, 411 (6836) :480-484