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高脂饮食在缺乏强直性肌营养不良蛋白激酶的小鼠中诱发肥胖和胰岛素抵抗。

High-fat diet induced adiposity and insulin resistance in mice lacking the myotonic dystrophy protein kinase.

作者信息

Llagostera Esther, Carmona Mari Carmen, Vicente Meritxell, Escorihuela Rosa María, Kaliman Perla

机构信息

Departament de Bioquímica i Biologia Molecular, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.

出版信息

FEBS Lett. 2009 Jun 18;583(12):2121-5. doi: 10.1016/j.febslet.2009.05.043. Epub 2009 May 29.

Abstract

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.

摘要

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。

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