A concise review on the therapeutics of obesity

被引:99
作者
Bray, GA [1 ]
机构
[1] Louisiana State Univ, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
关键词
sibutramine; orlistat; ephedrine; thermogenic; monoamine; peptides; leptin;
D O I
10.1016/S0899-9007(00)00424-X
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Drugs to treat obesity can be divided into three groups: those that reduce food intake; those that alter metabolism; and those that increase thermogenesis. Monoamines acting on noradrenergic receptors, serotonin receptors, dopamine receptors, and histamine receptors can reduce food intake. A number of peptides also affect food intake. The noradrenergic drugs phentermine, diethylpropion, mazindol, benzphetamine, and phendimetrazine are approved only for short-term use. Sibutramine, a norepinephrine-serotonin reuptake inhibitor, is approved for long-term use. Orlistat inhibits pancreatic Lipase and can block 30% of the triacylglycerol hydrolysis in subjects eating a 30% fat diet. The only thermogenic drug combination that has been tested is ephedrine and caffeine, but this treatment has not been approved by regulatory agencies. In clinical trials other drugs that may modulate peptide-feeding systems are being developed. Nutrition 2000;16:953-960. (C) Elsevier Science Inc. 2000.
引用
收藏
页码:953 / 960
页数:8
相关论文
共 15 条
[1]   Long-term maintenance of weight loss after a very-low-calorie diet: A randomized blinded trial of the efficacy and tolerability of sibutramine [J].
Apfelbaum, M ;
Vague, P ;
Ziegler, O ;
Hanotin, C ;
Thomas, F ;
Leutenegger, E .
AMERICAN JOURNAL OF MEDICINE, 1999, 106 (02) :179-184
[2]  
ASTRUP A, 1992, INT J OBESITY, V16, P269
[3]   Sibutramine produces dose-related weight loss [J].
Bray, GA ;
Blackburn, GL ;
Ferguson, JM ;
Greenway, FL ;
Jain, AK ;
Mendel, CM ;
Mendels, J ;
Ryan, DH ;
Schwartz, SL ;
Scheinbaum, ML ;
Seaton, TB .
OBESITY RESEARCH, 1999, 7 (02) :189-198
[4]   Evaluation of drugs for treating obesity [J].
Bray, GA .
OBESITY RESEARCH, 1995, 3 :S425-S434
[5]   Current and potential drugs for treatment of obesity [J].
Bray, GA ;
Greenway, FL .
ENDOCRINE REVIEWS, 1999, 20 (06) :805-875
[6]   USE AND ABUSE OF APPETITE-SUPPRESSANT DRUGS IN THE TREATMENT OF OBESITY [J].
BRAY, GA .
ANNALS OF INTERNAL MEDICINE, 1993, 119 (07) :707-713
[7]   Valvular heart disease associated with fenfluramine-phentermine [J].
Connolly, HM ;
Crary, JL ;
McGoon, MD ;
Hensrud, DD ;
Edwards, BS ;
Edwards, WD ;
Schaff, HV .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (09) :581-588
[8]   Effects of recombinant leptin therapy in a child with congenital leptin deficiency [J].
Farooqi, IS ;
Jebb, SA ;
Langmack, G ;
Lawrence, E ;
Cheetham, CH ;
Prentice, AM ;
Hughes, IA ;
McCamish, MA ;
O'Rahilly, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (12) :879-884
[9]   Glucagon-like peptide 1 promotes satiety and suppresses energy intake in humans [J].
Flint, A ;
Raben, A ;
Astrup, A ;
Holst, JJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (03) :515-520
[10]   Recombinant leptin for weight loss in obese and lean adults - A randomized, controlled, dose-escalation trial [J].
Heymsfield, SB ;
Greenberg, AS ;
Fujioka, K ;
Dixon, RM ;
Kushner, R ;
Hunt, T ;
Lubina, JA ;
Patane, J ;
Self, B ;
Hunt, P ;
McCamish, M .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (16) :1568-1575