Brown fat as a therapy for obesity and diabetes

被引:308
作者
Cypess, Aaron M. [1 ]
Kahn, C. Ronald [1 ]
机构
[1] Harvard Univ, Sch Med, Joslin Diabet Ctr, Boston, MA 02115 USA
关键词
adult humans; antiobesity therapy; brown adipose tissue; clinical and basic science research; PET/CT; BETA(3)-ADRENERGIC RECEPTOR AGONIST; BONE MORPHOGENETIC PROTEIN-7; DIET-INDUCED OBESITY; ADIPOSE-TISSUE; ENERGY-EXPENDITURE; WHITE ADIPOSE; ADULT HUMANS; PREADIPOCYTE DIFFERENTIATION; NONSHIVERING THERMOGENESIS; ADIPOCYTE DIFFERENTIATION;
D O I
10.1097/MED.0b013e328337a81f
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review Human fat consists of white and brown adipose tissue (WAT and BAT). Though most fat is energy-storing WAT, the thermogenic capacity of even small amounts of BAT makes it an attractive therapeutic target for inducing weight loss through energy expenditure. This review evaluates the recent discoveries regarding the identification of functional BAT in adult humans and its potential as a therapy for obesity and diabetes. Recent findings Over the past year, several independent research teams used a combination of positron-emission tomography and computed tomography (PET/CT) imaging, immunohistochemistry, and gene and protein expression assays to prove conclusively that adult humans have functional BAT. This has occurred against a backdrop of basic studies defining the origins of BAT, new components of its transcriptional regulation, and the role of hormones in stimulation of BAT growth and differentiation. Summary Adult humans have functional BAT, a new target for antiobesity and antidiabetes therapies focusing on increasing energy expenditure. Future studies will refine the methodologies used to measure BAT mass and activity, expand our knowledge of critical-control points in BAT regulation, and focus on testing pharmacological agents that increase BAT thermogenesis and help achieve long-lasting weight loss and an improved metabolic profile.
引用
收藏
页码:143 / 149
页数:7
相关论文
共 73 条
[1]
Ectopic brown adipose tissue in muscle provides a mechanism for differences in risk of metabolic syndrome in mice [J].
Almind, Katrine ;
Manieri, Monia ;
Sivitz, William I. ;
Cinti, Saverio ;
Kahn, C. Ronald .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (07) :2366-2371
[3]
IKK-β links inflammation to obesity-induced insulin resistance [J].
Arkan, MC ;
Hevener, AL ;
Greten, FR ;
Maeda, S ;
Li, ZW ;
Long, JM ;
Wynshaw-Boris, A ;
Poli, G ;
Olefsky, J ;
Karin, M .
NATURE MEDICINE, 2005, 11 (02) :191-198
[4]
Astrup A, 1986, Acta Endocrinol Suppl (Copenh), V278, P1
[5]
Effect of nicotine and ephedrine on the accumulation of 18F-FDG in brown adipose tissue [J].
Baba, Shingo ;
Tatsumi, Mitsuaki ;
Ishimori, Takayoshi ;
Lilien, David L. ;
Engles, James M. ;
Wahl, Richard L. .
JOURNAL OF NUCLEAR MEDICINE, 2007, 48 (06) :981-986
[6]
Badman MK, 2007, CELL METAB, V5, P426, DOI 10.1016/j.cmet.2007.05.002
[7]
Brown adipose tissue: Function and physiological significance [J].
Cannon, B ;
Nedergaard, J .
PHYSIOLOGICAL REVIEWS, 2004, 84 (01) :277-359
[8]
Brown Adipose Tissue -- When It Pays to Be Inefficient. [J].
Celi, Francesco S. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (15) :1553-1556
[9]
The adipose organ [J].
Cinti, S .
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS, 2005, 73 (01) :9-15
[10]
Thermogenic and metabolic antiobesity drugs: rationale and opportunities [J].
Clapham, J. C. ;
Arch, J. R. S. .
DIABETES OBESITY & METABOLISM, 2007, 9 (03) :259-275