Wilkes Jason J, Nelson Elizabeth, Osborne Melville, Demarest Keith T, Olefsky Jerrold M
Division of Endocrinology and Metabolism, Department of Medicine, University of California, San Diego, USA.
Am J Physiol Endocrinol Metab. 2005 Mar;288(3):E617-24. doi: 10.1152/ajpendo.00437.2004. Epub 2004 Nov 9.
We have studied the in vivo and in vitro effects of Topiramate (TPM) in female Zucker diabetic fatty (ZDF) rats. After weight matching, drug treatment had a marked effect to lower fasting glucose levels of relatively normoglycemic animals as well as during an oral glucose tolerance test. The glucose clamp studies revealed a approximately 30% increased glucose disposal, increased hepatic glucose output (HGO) suppression from approximately 30 to 60%, and an increased free fatty acid suppression from 40 to 75%. Therefore, TPM treatment led to enhanced insulin sensitivity at the level of tissue glucose disposal (increased ISGDR), liver (increased inhibition of HGO), and adipose tissue (enhanced suppression of lipolysis). When soleus muscle strips of control or TPM-treated ZDF rats were studied ex vivo, insulin-stimulated glucose transport was not enhanced in the drug-treated animals. In contrast, when isolated adipocytes were studied ex vivo, a marked increase (+55%) in insulin-stimulated glucose transport was observed. In vitro treatment of muscle strips and rat adipocytes showed no effect on glucose transport in muscle with a 40% increase in insulin-stimulated adipocyte glucose transport. In conclusion, 1) TPM treatment leads to a decrease in plasma glucose and increased in vivo insulin sensitivity; 2) insulin sensitization was observed in adipocytes, but not muscle, when tissues were studied ex vivo or in vitro; and 3) TPM directly enhances insulin action in insulin-resistant adipose cells in vitro. Thus the in vivo effects of TPM treatment appear to be exerted through adipose tissue.
我们研究了托吡酯(TPM)对雌性Zucker糖尿病脂肪大鼠(ZDF)的体内和体外作用。在体重匹配后,药物治疗对降低相对血糖正常动物的空腹血糖水平以及在口服葡萄糖耐量试验期间均有显著效果。葡萄糖钳夹研究显示,葡萄糖处置增加约30%,肝葡萄糖输出(HGO)抑制从约30%增加到60%,游离脂肪酸抑制从40%增加到75%。因此,TPM治疗导致在组织葡萄糖处置水平(增加ISGDR)、肝脏(增加对HGO的抑制)和脂肪组织(增强对脂解的抑制)方面胰岛素敏感性增强。当对对照或TPM治疗的ZDF大鼠的比目鱼肌条进行离体研究时,药物治疗的动物中胰岛素刺激的葡萄糖转运未增强。相反,当对分离的脂肪细胞进行离体研究时,观察到胰岛素刺激的葡萄糖转运显著增加(+55%)。对肌条和大鼠脂肪细胞的体外治疗显示,对肌肉中的葡萄糖转运无影响,而胰岛素刺激的脂肪细胞葡萄糖转运增加40%。总之,1)TPM治疗导致血浆葡萄糖降低和体内胰岛素敏感性增加;2)当对组织进行离体或体外研究时,在脂肪细胞中观察到胰岛素增敏作用,但在肌肉中未观察到;3)TPM在体外直接增强胰岛素抵抗脂肪细胞中的胰岛素作用。因此,TPM治疗的体内作用似乎是通过脂肪组织发挥的。