Department of Medical Physics and Engineering, Course of Health Science, Osaka University Graduate School of Medicine, 1-7 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Department of Biomedical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
Mol Imaging Biol. 2019 Apr;21(2):249-256. doi: 10.1007/s11307-018-1251-6.
Regulation of metabolic activity in adipose tissue is of great concern for treating obesity. This study aimed to evaluate the adrenergic regulation of glucose uptake and the thermogenic program in adipose tissues in mouse models of both type 1 and 2 diabetes mellitus (DM).
Male mice were treated with streptozotocin to induce type 1 (T1) DM, and obese ob/ob mice were used for the type 2 (T2) DM model. After selective β-adrenoreceptor stimulation by CL 316,243 (CL) treatment, 2-deoxy-D-[C]glucose ([C]DG) was administered to DM and corresponding control mice. Radioactivity and uncoupling protein 1 (UCP1) expression were measured and analyzed in adipose tissues.
In T1DM, [C]DG uptake in brown adipose tissue (BAT) decreased both at rest and upon CL stimulation, and UCP1 expression was preserved. However, CL treatment enhanced [C]DG uptake without impairing UCP1 expression in inguinal white adipose tissue (iWAT). In this model, CL could not alter blood glucose levels. In T2DM mice, the blood glucose level was significantly lowered by CL treatment. There was no decrease in CL-induced [C]DG uptake in BAT, and UCP1 expression was maintained. However, [C]DG uptake was not increased in iWAT and no UCP1 expression was observed in iWAT (browning).
The metabolic response against adrenergic stimulation varied depending on the type of adipose tissue and DM. This could be important for the therapeutic activation of adipose tissue metabolism in obese diabetic patients.
调节脂肪组织的代谢活性对于治疗肥胖症具有重要意义。本研究旨在评估肾上腺素能对 1 型和 2 型糖尿病(DM)小鼠模型脂肪组织葡萄糖摄取和生热程序的调节作用。
雄性小鼠用链脲佐菌素处理以诱导 1 型(T1)DM,肥胖 ob/ob 小鼠用于 2 型(T2)DM 模型。用 CL316,243(CL)选择性刺激β-肾上腺素受体后,给 DM 和相应的对照小鼠注射 2-脱氧-D-[C]葡萄糖([C]DG)。测量并分析脂肪组织中的放射性和解偶联蛋白 1(UCP1)表达。
在 T1DM 中,棕色脂肪组织(BAT)在休息和 CL 刺激时的 [C]DG 摄取均减少,而 UCP1 表达得到保留。然而,CL 处理增强了腹股沟白色脂肪组织(iWAT)中的 [C]DG 摄取,而不损害 UCP1 表达。在该模型中,CL 不能改变血糖水平。在 T2DM 小鼠中,CL 处理显著降低血糖水平。BAT 中 CL 诱导的 [C]DG 摄取没有减少,UCP1 表达得到维持。然而,iWAT 中的 [C]DG 摄取没有增加,iWAT 中也没有观察到 UCP1 表达(褐变)。
对肾上腺素能刺激的代谢反应因脂肪组织类型和 DM 类型而异。这对于肥胖糖尿病患者脂肪组织代谢的治疗性激活可能很重要。