Brown adipose tissue-a new role in humans?

被引:101
作者
Lidell, Martin E. [1 ]
Enerback, Sven [1 ]
机构
[1] Univ Gothenburg, Dept Med & Clin Genet, Inst Biomed, SE-40530 Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
DIET-INDUCED THERMOGENESIS; MITOCHONDRIAL UNCOUPLING-PROTEIN; WHITE FAT; INSULIN-RESISTANCE; TRANSCRIPTIONAL CONTROL; ADULT HUMANS; ADAPTIVE THERMOGENESIS; BODY-WEIGHT; OBESITY; MICE;
D O I
10.1038/nrendo.2010.64
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
New targets for pharmacological interventions are of great importance to combat the epidemic of obesity. Brown adipose tissue could potentially represent one such target. Unlike white adipose tissue, brown adipose tissue has the ability to dissipate energy by producing heat rather than storing it as triglycerides. In small mammals, the presence of active brown adipose tissue is pivotal for the maintenance of body temperature and possibly to protect against the detrimental effects of surplus energy intake. Animal studies have shown that expansion and/or activation of brown adipose tissue counteracts diet-induced weight gain and related disorders such as type 2 diabetes mellitus. Several independent studies have now confirmed the presence of functional brown adipose tissue in adult humans, for whom this tissue is probably metabolically beneficial given its association with both low BMI and low total adipose tissue content. Over the past few years, knowledge of the transcriptional control and development of brown adipose tissue has increased substantially. Thus, several possible targets that may be useful for the expansion and/or activation of this tissue by pharmacological means have been identified. Whether or not brown adipose tissue will be useful in the battle against obesity remains to be seen. However, this possibility is certainly well worth exploring.
引用
收藏
页码:319 / 325
页数:7
相关论文
共 79 条
[1]   ENDOCRINE ACTIVITY IN A LARGE HIBERNOMA [J].
ALLEGRA, SR ;
GMUER, C ;
OLEARY, GP .
HUMAN PATHOLOGY, 1983, 14 (12) :1044-1052
[2]   ATYPICAL BETA-ADRENOCEPTOR ON BROWN ADIPOCYTES AS TARGET FOR ANTI-OBESITY DRUGS [J].
ARCH, JRS ;
AINSWORTH, AT ;
CAWTHORNE, MA ;
PIERCY, V ;
SENNITT, MV ;
THODY, VE ;
WILSON, C ;
WILSON, S .
NATURE, 1984, 309 (5964) :163-165
[3]   β-catenin activation is necessary and sufficient to specify the dorsal dermal fate in the mouse [J].
Atit, Radhika ;
Sgaier, Sema K. ;
Mohamed, Othman A. ;
Taketo, Makoto M. ;
Dufort, Daniel ;
Joyner, Alexandra L. ;
Niswander, Lee ;
Conlon, Ronald A. .
DEVELOPMENTAL BIOLOGY, 2006, 296 (01) :164-176
[4]   Brown Adipose Tissue and Seasonal Variation in Humans [J].
Au-Yong, Iain T. H. ;
Thorn, Natasha ;
Ganatra, Rakesh ;
Perkins, Alan C. ;
Symonds, Michael E. .
DIABETES, 2009, 58 (11) :2583-2587
[5]   βAR signaling required for diet-induced thermogenesis and obesity resistance [J].
Bachman, ES ;
Dhillon, H ;
Zhang, CY ;
Cinti, S ;
Bianco, AC ;
Kobilka, BK ;
Lowell, BB .
SCIENCE, 2002, 297 (5582) :843-845
[6]   BETA-ADRENERGIC CONTROL OF LIPOLYSIS IN PRIMATE WHITE FAT-CELLS - A COMPARATIVE-STUDY WITH NONPRIMATE MAMMALS [J].
BOUSQUETMELOU, A ;
GALITZKY, J ;
CARPENE, C ;
LAFONTAN, M ;
BERLAN, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (01) :R115-R123
[7]   BROWN ADIPOSE-TISSUE HYPERPLASIA - A FUNDAMENTAL MECHANISM OF ADAPTATION TO COLD AND HYPERPHAGIA [J].
BUKOWIECKI, L ;
COLLET, AJ ;
FOLLEA, N ;
GUAY, G ;
JAHJAH, L .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 242 (06) :E353-E359
[8]   Brown adipose tissue: Function and physiological significance [J].
Cannon, B ;
Nedergaard, J .
PHYSIOLOGICAL REVIEWS, 2004, 84 (01) :277-359
[9]   FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance [J].
Cederberg, A ;
Gronning, LM ;
Ahrén, B ;
Taskén, K ;
Carlsson, P ;
Enerbäck, S .
CELL, 2001, 106 (05) :563-573
[10]   Reversal of hypermetabolic brown adipose tissue in F-18FDG PET imaging [J].
Christensen, CR ;
Clark, RB ;
Morton, KA .
CLINICAL NUCLEAR MEDICINE, 2006, 31 (04) :193-196