Géloën A, Trayhurn P
Department of Medicine, University of Alberta, Edmonton, Canada.
Am J Physiol. 1990 Feb;258(2 Pt 2):R418-24. doi: 10.1152/ajpregu.1990.258.2.R418.
The role of insulin in the regulation of the thermogenic activity and capacity (uncoupling protein content) of brown adipose tissue (BAT) has been investigated using mice made diabetic with streptozotocin and then subsequently infused with different doses of insulin. After 12 days of diabetes, the animals received either 0, 8, 16, or 32 units of insulin.kg body wt-1.day-1 delivered by osmotic minipumps implanted subcutaneously for 12 days. After 12 days of diabetes, body weight, interscapular BAT, and epididymal white adipose tissue weights were each reduced. In BAT, significant decreases (P less than 0.05) in the mitochondrial protein content (63%), cytochrome oxidase activity (79%), mitochondrial GDP binding (51%), and the specific mitochondrial concentration and total tissue content of uncoupling protein (71 and 89%, respectively) were obtained, indicating that the thermogenic activity and capacity of the tissue were reduced in diabetes. The infusion of insulin at a dose of 8 units.kg-1.day-1 normalized mitochondrial GDP binding and doubled the concentration of uncoupling protein. Body weight, epididymal white adipose tissue weight, and the mitochondrial protein content of BAT were restored with 16 units of insulin.kg-1.day-1. Higher doses of insulin did not further increase the specific mitochondrial concentration of uncoupling protein, but the mitochondrial content (and thereby the total uncoupling protein content) of BAT was increased and blood glucose normalized. There was a significant correlation between the dose of insulin replacement and several of the parameters measured in BAT: mitochondrial protein content (r = 0.68, P less than 0.001), cytochrome oxidase activity (r = 0.54, P less than 0.001), and total uncoupling protein content (r = 0.68, P less than 0.001).(ABSTRACT TRUNCATED AT 250 WORDS)
利用链脲佐菌素使小鼠患糖尿病,随后给其注射不同剂量的胰岛素,研究了胰岛素在调节棕色脂肪组织(BAT)产热活性和能力(解偶联蛋白含量)中的作用。糖尿病12天后,动物接受皮下植入渗透微型泵持续12天输送的0、8、16或32单位胰岛素·千克体重⁻¹·天⁻¹。糖尿病12天后,体重、肩胛间BAT和附睾白色脂肪组织重量均降低。在BAT中,线粒体蛋白含量(63%)、细胞色素氧化酶活性(79%)、线粒体GDP结合(51%)以及解偶联蛋白的特定线粒体浓度和总组织含量(分别为71%和89%)均显著降低(P<0.05),表明糖尿病时该组织的产热活性和能力降低。以8单位·千克⁻¹·天⁻¹的剂量输注胰岛素可使线粒体GDP结合正常化,并使解偶联蛋白浓度增加一倍。16单位胰岛素·千克⁻¹·天⁻¹可恢复体重、附睾白色脂肪组织重量以及BAT的线粒体蛋白含量。更高剂量的胰岛素并未进一步增加解偶联蛋白的特定线粒体浓度,但BAT的线粒体含量(从而总解偶联蛋白含量)增加且血糖正常化。胰岛素替代剂量与BAT中测量的几个参数之间存在显著相关性:线粒体蛋白含量(r = 0.68,P<0.001)、细胞色素氧化酶活性(r = 0.54,P<0.001)和总解偶联蛋白含量(r = 0.68,P<0.001)。(摘要截短于250字)