Brown adipose tissue hyperplasia: a fundamental mechanism of adaptation to cold and hyperphagia.

Cold acclimation (4 degrees C) and "cafeteria diets" increased the thermic response of rats to catecholamines. This phenomenon was accompanied by six- to eightfold increases of interscapular brown adipose tissue (IBAT) weight, total tissue cytochrome oxidase activity, and total number of brown adipocytes. Quantitative radioautographic experiments using [3H]thymidine disclosed that cold exposure markedly enhanced the mitotic activity in blood capillaries and small-venule endothelial cells, adipose tissue interstitial cells, and preadipocytes rather than in fully differentiated brown adipocytes. IBAT mitotic index increased 70 times over control values after only 2 days of cold exposure. Thereafter, the proliferative activity progressively decreased. IBAT cell composition was modified during cold acclimation as the percentage of interstitial cells and preadipocytes increased over the other cellular types. Because brown adipose tissue is the principal site of norepinephrine-induced thermogenesis in homeothermal animals, it is suggested that brown adipocyte proliferation from precursor cells represents the fundamental phenomenon explaining the increased capacity of cold-acclimated animals to respond calorigenically to catecholamines.

[1]  N. Rothwell,et al.  Similarities between cold- and diet-induced thermogenesis in the rat , 1980 .

[2]  E. Horton,et al.  Characteristics of thyroid function in experimental protein malnutrition. , 1979, The Journal of nutrition.

[3]  Michael J. Stock,et al.  A role for brown adipose tissue in diet-induced thermogenesis , 1979, Nature.

[4]  I. Waheed,et al.  Human fat cell precursors. Morphologic and metabolic differentiation in culture. , 1973, Laboratory investigation; a journal of technical methods and pathology.

[5]  I. Waheed,et al.  Ultrastructural observations on differentiating human preadipocytes cultured in vitro. , 1976, Tissue & cell.

[6]  R. Sidman Histogenesis of brown adipose tissue in vivo and in organ culture , 1956, The Anatomical record.

[7]  B A Horwitz,et al.  Brown fat and thermogenesis. , 1969, Physiological reviews.

[8]  J. Leblanc,et al.  Beta-Adrenergic receptors in brown-adipose tissue. Characterization and alterations during acclimation of rats to cold. , 1978, European journal of biochemistry.

[9]  L. Landsberg,et al.  Fasting, feeding and regulation of the sympathetic nervous system. , 1978, The New England journal of medicine.

[10]  K. Iyama,et al.  Electron microscopical studies on the genesis of white adipocytes: Differentiation of immature pericytes into adipocytes in transplanted preadipose tissue , 1979, Virchows Archiv. B, Cell pathology including molecular pathology.

[11]  W. James,et al.  AN INTEGRATED VIEW OF THE METABOLIC AND GENETIC BASIS FOR OBESITY , 1976, The Lancet.

[12]  M. Frydman,et al.  Tissue distribution of cold-induced thermogenesis in conscious warm- or cold-acclimated rats reevaluated from changes in tissue blood flow: the dominant role of brown adipose tissue in the replacement of shivering by nonshivering thermogenesis. , 1979, Canadian journal of physiology and pharmacology.

[13]  J. Hirsch,et al.  Isotopic labeling of DNA in rat adipose tissue: evidence for proliferating cells associated with mature adipocytes. , 1979, Journal of lipid research.

[14]  I. Cameron,et al.  CYTOLOGICAL RESPONSES OF BROWN FAT TISSUE IN COLD-EXPOSED RATS , 1964, The Journal of cell biology.

[15]  T. E. Hunt,et al.  A radioautographic study of proliferation in brown fat of the rat after exposure to cold , 1967 .