Kharitonenkov Alexei, Shiyanova Tatiyana L, Koester Anja, Ford Amy M, Micanovic Radmila, Galbreath Elizabeth J, Sandusky George E, Hammond Lisa J, Moyers Julie S, Owens Rebecca A, Gromada Jesper, Brozinick Joseph T, Hawkins Eric D, Wroblewski Victor J, Li De-Shan, Mehrbod Farrokh, Jaskunas S Richard, Shanafelt Armen B
Lilly Research Laboratories, Division of Eli Lilly and Co., Indianapolis, Indiana 46285, USA.
J Clin Invest. 2005 Jun;115(6):1627-35. doi: 10.1172/JCI23606. Epub 2005 May 2.
Diabetes mellitus is a major health concern, affecting more than 5% of the population. Here we describe a potential novel therapeutic agent for this disease, FGF-21, which was discovered to be a potent regulator of glucose uptake in mouse 3T3-L1 and primary human adipocytes. FGF-21-transgenic mice were viable and resistant to diet-induced obesity. Therapeutic administration of FGF-21 reduced plasma glucose and triglycerides to near normal levels in both ob/ob and db/db mice. These effects persisted for at least 24 hours following the cessation of FGF-21 administration. Importantly, FGF-21 did not induce mitogenicity, hypoglycemia, or weight gain at any dose tested in diabetic or healthy animals or when overexpressed in transgenic mice. Thus, we conclude that FGF-21, which we have identified as a novel metabolic factor, exhibits the therapeutic characteristics necessary for an effective treatment of diabetes.
糖尿病是一个主要的健康问题,影响着超过5%的人口。在此我们描述一种针对该疾病的潜在新型治疗药物,即FGF-21,它被发现是小鼠3T3-L1和原代人脂肪细胞中葡萄糖摄取的有效调节剂。FGF-21转基因小鼠能够存活,并且对饮食诱导的肥胖具有抗性。对ob/ob和db/db小鼠进行FGF-21治疗性给药可将血浆葡萄糖和甘油三酯降低至接近正常水平。在停止FGF-21给药后,这些作用至少持续24小时。重要的是,在糖尿病或健康动物中测试的任何剂量下,或在转基因小鼠中过表达时,FGF-21均未诱导有丝分裂活性、低血糖或体重增加。因此,我们得出结论,我们已鉴定为新型代谢因子的FGF-21具有有效治疗糖尿病所需的治疗特性。