Temperature-Acclimated Brown Adipose Tissue Modulates Insulin Sensitivity in Humans

被引:319
作者
Lee, Paul [1 ]
Smith, Sheila [1 ]
Linderman, Joyce [1 ]
Courville, Amber B. [2 ]
Brychta, Robert J. [1 ]
Dieckmann, William [3 ]
Werner, Charlotte D. [1 ]
Chen, Kong Y. [1 ]
Celi, Francesco S. [1 ,4 ]
机构
[1] NIDDK, Diabet Endocrinol & Obes Branch, Bethesda, MD 20892 USA
[2] NIH, Dept Nutr, Ctr Clin, Bethesda, MD 20892 USA
[3] NIH, PET Dept, Ctr Clin, Bethesda, MD 20892 USA
[4] Virginia Commonwealth Univ, Div Endocrinol & Metab, Richmond, VA USA
基金
英国医学研究理事会;
关键词
DIET-INDUCED THERMOGENESIS; ENERGY-EXPENDITURE; COLD-EXPOSURE; ADULT HUMANS; FAT; BEIGE; IDENTIFICATION; ADIPOGENESIS; ADIPOCYTES; PREVALENCE;
D O I
10.2337/db14-0513
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In rodents, brown adipose tissue (BAT) regulates cold- and diet-induced thermogenesis (CIT; DIT). Whether BAT recruitment is reversible and how it impacts on energy metabolism have not been investigated in humans. We examined the effects of temperature acclimation on BAT, energy balance, and substrate metabolism in a prospective crossover study of 4-month duration, consisting of four consecutive blocks of 1-month overnight temperature acclimation (24 degrees C [month 1] -> 19 degrees C [month 2] -> 24 degrees C [month 3] -> 27 degrees C [month 4]) of five healthy men in a temperature-controlled research facility. Sequential monthly acclimation modulated BAT reversibly, boosting and suppressing its abundance and activity in mild cold and warm conditions (P < 0.05), respectively, independent of seasonal fluctuations (P < 0.01). BAT acclimation did not alter CIT but was accompanied by DIT (P < 0.05) and postprandial insulin sensitivity enhancement (P < 0.05), evident only after cold acclimation. Circulating and adipose tissue, but not skeletal muscle, expression levels of leptin and adiponectin displayed reciprocal changes concordant with cold-acclimated insulin sensitization. These results suggest regulatory links between BAT thermal plasticity and glucose metabolism in humans, opening avenues to harnessing BAT for metabolic benefits.
引用
收藏
页码:3686 / 3698
页数:13
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