Llagostera Esther, Carmona Mari Carmen, Vicente Meritxell, Escorihuela Rosa María, Kaliman Perla
Departament de Bioquímica i Biologia Molecular, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
FEBS Lett. 2009 Jun 18;583(12):2121-5. doi: 10.1016/j.febslet.2009.05.043. Epub 2009 May 29.
Myotonic dystrophy 1 (MD1) is caused by a CTG expansion in the 3'-unstranslated region of the myotonic dystrophy protein kinase (DMPK) gene. MD1 patients frequently present insulin resistance and increased visceral adiposity. We examined whether DMPK deficiency is a genetic risk factor for high-fat diet-induced adiposity and insulin resistance using the DMPK knockout mouse model. We found that high-fat fed DMPK knockout mice had significantly increased body weights, hypertrophic adipocytes and whole-body insulin resistance compared with wild-type mice. This nutrient-genome interaction should be considered by physicians given the cardiometabolic risks and sedentary lifestyle associated with MD1 patients.
强直性肌营养不良1型(MD1)是由强直性肌营养不良蛋白激酶(DMPK)基因3'非翻译区的CTG重复扩增引起的。MD1患者常出现胰岛素抵抗和内脏脂肪增多。我们使用DMPK基因敲除小鼠模型研究了DMPK缺乏是否是高脂饮食诱导肥胖和胰岛素抵抗的遗传风险因素。我们发现,与野生型小鼠相比,高脂喂养的DMPK基因敲除小鼠体重显著增加,脂肪细胞肥大,且存在全身胰岛素抵抗。考虑到与MD1患者相关的心脏代谢风险和久坐不动的生活方式,医生应重视这种营养-基因组相互作用。