Treating obesity: Pharmacology of energy expenditure

被引:25
作者
Clapham, JC [1 ]
机构
[1] AstraZeneca R&D, Dept Mol Pharmacol, S-41383 Molndal, Sweden
关键词
D O I
10.2174/1389450043490451
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacological treatment options for obesity are currently very limited but the prevalence of the disease is increasing rapidly. Obesity has many serious sequelae, the most common of which is type-2-diabetes. The benefits of weight loss on health are established but the major impediment to weight loss treatments is maintenance of weight lost over the long term. The reduced- or post-obese individual undergoes physiological changes that are geared towards energy storage and weight regain. One of the physiological changes is a reduced capacity to oxidise fatty acids pushing them through pathways of triacylglycerol synthesis. In this review, some of the past drug treatments aimed at increasing energy expenditure, such as dinitrophenol and ephedrine, are discussed. Current, or nearly current therapies such as sibutramine and rimonabant are also discussed in the context of increased energy expenditure. The main part of the review focuses on future prospects with discussion around a selection of targets with potential in energy expenditure that lie in pathways with AMP-kinase at their centre and ending at the mitochondrion.
引用
收藏
页码:309 / 323
页数:15
相关论文
共 182 条
[1]   Continuous fatty acid oxidation and reduced fat storage in mice lacking acetyl-CoA carboxylase 2 [J].
Abu-Elheiga, L ;
Matzuk, MM ;
Abo-Hashema, KAH ;
Wakil, SJ .
SCIENCE, 2001, 291 (5513) :2613-2616
[2]   Obesity and target organ damage: diabetes [J].
Adler, A .
INTERNATIONAL JOURNAL OF OBESITY, 2002, 26 (Suppl 4) :S11-S14
[3]   Obesity and disease management: Effects of weight loss on comorbid conditions [J].
Anderson, JW ;
Konz, EC .
OBESITY RESEARCH, 2001, 9 :326S-334S
[4]  
[Anonymous], [No title captured]
[5]   Lessons in obesity from transgenic animals [J].
Arch, JRS .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2002, 25 (10) :867-875
[6]   β3-adrenoceptor agonists:: potential, pitfalls and progress [J].
Arch, JRS .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2002, 440 (2-3) :99-107
[7]   Selective inhibition of sucrose and ethanol intake by SR 141716, an antagonist of central cannabinoid (CB1) receptors [J].
Arnone, M ;
Maruani, J ;
Chaperon, F ;
Thiebot, MH ;
Poncelet, M ;
Soubrie, P ;
LeFur, G .
PSYCHOPHARMACOLOGY, 1997, 132 (01) :104-106
[8]   THERMOGENIC SYNERGISM BETWEEN EPHEDRINE AND CAFFEINE IN HEALTHY-VOLUNTEERS - A DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY [J].
ASTRUP, A ;
TOUBRO, S ;
CANNON, S ;
HEIN, P ;
MADSEN, J .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1991, 40 (03) :323-329
[9]   CONTRIBUTION OF BAT AND SKELETAL-MUSCLE TO THERMOGENESIS INDUCED BY EPHEDRINE IN MAN [J].
ASTRUP, A ;
BULOW, J ;
MADSEN, J ;
CHRISTENSEN, NJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (05) :E507-E515
[10]  
ASTRUP A, 1990, CURR THER RES CLIN E, V48, P1087