Kraus D, Jäger J, Meier B, Fasshauer M, Klein J
Department of Internal Medicine I, University of Lübeck, 23538 Lübeck, Germany.
Horm Metab Res. 2005 Jul;37(7):455-9. doi: 10.1055/s-2005-870240.
Aldosterone is a mineralocorticoid hormone that regulates blood pressure and salt/water balance. Increased aldosterone levels are found in states of disturbed energy balance such as the metabolic syndrome. Adipose tissue has been recognized to play a pivotal role in the regulation of energy homeostasis. We investigated direct aldosterone effects on brown adipocyte function. Aldosterone dose-dependently inhibited expression of uncoupling protein-1 (UCP-1) by 30% (p < 0.01). Furthermore, aldosterone dose-dependently impaired insulin-induced glucose uptake by about 25% (p < 0.01). On a transcriptional level, mRNA of the proinflammatory adipokines leptin and monocyte chemoattractant protein-1 (MCP-1) was increased by 5,000% and 40%, respectively, by aldosterone exposure (p < 0.05). This study demonstrates that aldosterone directly impacts on major adipose functions including stimulation of proinflammatory adipokines.
醛固酮是一种调节血压和盐/水平衡的盐皮质激素。在能量平衡紊乱的状态如代谢综合征中,醛固酮水平会升高。脂肪组织在能量稳态调节中发挥关键作用。我们研究了醛固酮对棕色脂肪细胞功能的直接影响。醛固酮以剂量依赖方式抑制解偶联蛋白-1(UCP-1)的表达达30%(p<0.01)。此外,醛固酮以剂量依赖方式使胰岛素诱导的葡萄糖摄取受损约25%(p<0.01)。在转录水平上,醛固酮暴露分别使促炎脂肪因子瘦素和单核细胞趋化蛋白-1(MCP-1)的mRNA增加了5000%和40%(p<0.05)。本研究表明,醛固酮直接影响主要的脂肪功能,包括刺激促炎脂肪因子。