Corticosterone binding to tissues of adrenalectomized lean and obese Zucker rats

被引:12
|
作者
Grasa, MM
Cabot, C
Balada, F
Virgili, J
Sanchis, D
Monserrat, C
Fernández-López, JA
Remesar, X
Alemany, M [1 ]
机构
[1] Univ Barcelona, Fac Biol, Dept Bioquim & Biol Mol, E-08028 Barcelona, Spain
[2] Ctr Invest Lab SAIVAT SA, Esplugas de Llobregat, Spain
关键词
glucocorticoid receptor; corticosterone-binding globulin; obesity; glucocorticoids; CBG;
D O I
10.1055/s-2007-978962
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The binding of corticosterone, dexamethasone and aldosterone was investigated in plasma and in homogenates of liver, kidney, brain, brown adipose tissue and visceral (periovaric) and subcutaneous white adipose tissues of Zucker lean and obese rats: intact controls, adrenalectomized and sham-operated. Corticosterone-binding globulin (CBG) accounted for most of the binding, whereas that of glucocorticoid and mineralocorticoid receptors was much lower. Plasma corticosterone levels increased in sham-operated and obviously decreased in the adrenalectomized animals. Sham-operated and adrenalectomized lean rats showed decreased plasma CBG; in the obese, CBG levels were lower than in controls and were not affected by either surgery, No variation with obesity or surgery was observed either in dexamethasone or aldosterone binding, the latter being practically zero in most samples. When expressed per unit of tissue protein, CBC activity was maximal in adipose tissues, with lowest values in brain and liver. In lean rats, tissue CBG activity decreased with either surgical treatment; no changes were observed in the obese, which also had lower CBG tissue levels. The relative lack of changes in CBG of obese rats suggests that they have lost - at least in part - the ability to counter-modulate the changes in glucocorticoid levels through CBG modulation, thus relying only on the control of corticosterone levels. This interpretation agrees with the postulated role of CBG modulating the availability of glucocorticoids to target cells.
引用
收藏
页码:699 / 704
页数:6
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