Attie Alan D, Flowers Matthew T, Flowers Jessica B, Groen Albert K, Kuipers Folkert, Ntambi James M
Department of Biochemistry, University of Wisconsin, Madison, Wisconsin 53706-1544, USA.
Nutr Rev. 2007 Jun;65(6 Pt 2):S35-8. doi: 10.1111/j.1753-4887.2007.tb00326.x.
Previous studies showed that mice deficient in Scd1 had a reduced level of liver triglyceride and an improvement in insulin sensitivity. We studied Scd1(-/-) mice on a very low-fat, high-carbohydrate lipogenic diet. The animals were almost entirely devoid of high-density lipoprotein (HDL). Nonetheless, they were hypercholesterolemic and had cholestasis. These changes were reversible with oil containing both mono- and polyunsaturated fat, but not entirely reversible with just triolein, suggesting that Scd1 deficiency increased the requirement for polyunsaturated fat. We also found that the Scd1(-/-) mice on a normal chow diet had dramatically improved insulin sensitivity. However, leptin(ob/ob) Scd1(-/-) mice had worse diabetes than leptin(ob/ob) Scd1(wt/wt) mice.
先前的研究表明,缺乏硬脂酰辅酶A去饱和酶1(Scd1)的小鼠肝脏甘油三酯水平降低,胰岛素敏感性得到改善。我们研究了在极低脂肪、高碳水化合物生脂饮食条件下的Scd1基因敲除(Scd1(-/-))小鼠。这些动物几乎完全缺乏高密度脂蛋白(HDL)。尽管如此,它们仍患有高胆固醇血症和胆汁淤积。这些变化可通过含有单不饱和脂肪和多不饱和脂肪的油逆转,但仅用三油精不能完全逆转,这表明Scd1缺乏增加了对多不饱和脂肪的需求。我们还发现,正常饲料饮食的Scd1(-/-)小鼠胰岛素敏感性显著提高。然而,瘦素(ob/ob)Scd1(-/-)小鼠比瘦素(ob/ob)Scd1(野生型/野生型)小鼠的糖尿病病情更严重。