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XMetA, an allosteric monoclonal antibody to the insulin receptor, improves glycaemic control in mice with diet-induced obesity

机译:XMetA是一种针对胰岛素受体的变构单克隆抗体,可改善饮食诱发的肥胖小鼠的血糖控制

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摘要

XMetA, a high-affinity, fully human monoclonal antibody, allosterically binds to and activates the insulin receptor (INSR). Previously, we found that XMetA normalized fasting glucose and glucose tolerance in insulinopenic mice. To determine whether XMetA is also beneficial for reducing hyperglycaemia due to the insulin resistance of obesity, we have now evaluated XMetA in hyperinsulinemic mice with diet-induced obesity. XMetA treatment of these mice normalized fasting glucose for 4weeks without contributing to weight gain. XMetA also corrected glucose tolerance and improved non-high density lipoprotein cholesterol. These studies indicate, therefore, that monoclonal antibodies that allosterically activate the INSR, such as XMetA, have the potential to be novel agents for the treatment of hyperglycaemia in conditions associated with the insulin resistance of obesity.
机译:XMetA是一种高亲和力的完全人源单克隆抗体,与胰岛素受体(INSR)发生变构结合并激活。以前,我们发现XMetA可以使胰岛素缺乏症小鼠的空腹血糖和葡萄糖耐量正常化。为了确定XMetA是否也对降低由于肥胖症的胰岛素抵抗引起的高血糖症有益,我们现在对饮食引起的肥胖症的高胰岛素小鼠评估了XMetA。对这些小鼠的XMetA治疗可使空腹血糖正常化4周,而无助于体重增加。 XMetA还纠正了葡萄糖耐量并改善了非高密度脂蛋白胆固醇。因此,这些研究表明,变构激活INSR的单克隆抗体,例如XMetA,有可能成为治疗与肥胖症胰岛素抵抗相关的高血糖症的新型药物。

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