Diabetes · 2002 · 836 citations · 38 references
MedicineEndocrinologyPhysiologyHormone BiochemistryMetabolic RegulationReproductive EndocrinologyAdipose TissueAndrogen PhysiologyHormonal Control Of MetabolismHormonal InfluencesHormonal RegulationInsulin ResistanceAdipose EndocrinologyAdipose Tissue EndocrinologyAndrogen MetabolismHormonal AlterationsImpaired Insulin SensitivityInsulin Sensitivity Adaptation
Adiponectin, an adipose‑specific secretory protein, exhibits antidiabetic and antiatherogenic properties. The study examined how sex hormones regulate adiponectin production. Men had lower plasma adiponectin than women, and in mice castration increased adiponectin while testosterone decreased it; castration also improved insulin sensitivity, indicating that androgens suppress adiponectin and may contribute to insulin resistance and atherosclerosis risk.
Adiponectin, an adipose-specific secretory protein, exhibits antidiabetic and antiatherogenic properties. In the present study, we examined the effects of sex hormones on the regulation of adiponectin production. Plasma adiponectin concentrations were significantly lower in 442 men (age, 52.6 +/- 11.9 years [mean +/- SD]) than in 137 women (53.2 +/- 12.0 years) but not different between pre- and postmenopausal women. In mice, ovariectomy did not alter plasma adiponectin levels. In contrast, high levels of plasma adiponectin were found in castrated mice. Testosterone treatment reduced plasma adiponectin concentration in both sham-operated and castrated mice. In 3T3-L1 adipocytes, testosterone reduced adiponectin secretion into the culture media, using pulse-chase study. Castration-induced increase in plasma adiponectin was associated with a significant improvement of insulin sensitivity. Our results indicate that androgens decrease plasma adiponectin and that androgen-induced hypoadiponectinemia may be related to the high risks of insulin resistance and atherosclerosis in men.
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Alan R. Saltiel, C. Ronald Kahn · Nature · 2001 · 5.3K citations · Full text