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金属硫蛋白(-I和-II)基因敲除小鼠中的肥胖和高瘦素血症。

Obesity and hyperleptinemia in metallothionein (-I and -II) null mice.

作者信息

Beattie J H, Wood A M, Newman A M, Bremner I, Choo K H, Michalska A E, Duncan J S, Trayhurn P

机构信息

Trace Element and Gene Expression Group, Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen AB21 9SB, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 1998 Jan 6;95(1):358-63. doi: 10.1073/pnas.95.1.358.

Abstract

Metallothionein (MT) has several putative roles in metal detoxification, in Zn and Cu homeostasis, in scavenging free radicals, and in the acute phase response. Mice of mixed 129/Ola and C57BL/6J background with targeted disruption of MT-I and MT-II genes are more sensitive to toxic metals and oxidative stress. We noted that these animals were larger than most strains of mice, and we systematically studied aspects of their physiology and biochemistry relating to energy metabolism. During the first 2 weeks after weaning, the growth rates of MT-null and C57BL/6J mice were similar, but the transgenic mice became significantly heavier at age 5-6 weeks. At age 14 weeks, the body weight and food intake of MT-null mice was 16 and 30% higher, respectively, compared with C57BL/6J mice. Most 22- to 39-week-old male MT-null mice were obese, as shown by increased fat accretion, elevated obese (ob) gene expression, and high plasma leptin levels, similar to those recorded in Zucker fatty (fa/fa) rats. Seven-week-old MT-null mice also had significantly higher levels of plasma leptin and elevated expression of ob, lipoprotein lipase, and CCAAT enhancer binding protein alpha genes as compared with age-matched C57BL/6J mice. These observations indicate that abnormal accretion of body fat and adipocyte maturation is initiated at 5-7 weeks of age, possibly coincident with sexual maturation. Targeted disruption of MT-I and MT-II genes seems to induce moderate obesity, providing a new obese animal model. A link between MT and the regulation of energy balance is implied.

摘要

金属硫蛋白(MT)在金属解毒、锌和铜的体内稳态、清除自由基以及急性期反应中具有多种假定作用。具有MT-I和MT-II基因靶向破坏的129/Ola和C57BL/6J混合背景小鼠对有毒金属和氧化应激更为敏感。我们注意到这些动物比大多数小鼠品系体型更大,并且我们系统地研究了它们与能量代谢相关的生理和生化方面。在断奶后的前2周,MT基因敲除小鼠和C57BL/6J小鼠的生长速率相似,但转基因小鼠在5 - 6周龄时体重显著增加。在14周龄时,与C57BL/6J小鼠相比,MT基因敲除小鼠的体重和食物摄入量分别高出16%和30%。如脂肪堆积增加、肥胖(ob)基因表达升高以及血浆瘦素水平升高所示,大多数22至39周龄的雄性MT基因敲除小鼠肥胖,这与在Zucker肥胖(fa/fa)大鼠中记录的情况相似。与年龄匹配的C57BL/6J小鼠相比,7周龄的MT基因敲除小鼠血浆瘦素水平也显著更高,并且ob、脂蛋白脂肪酶和CCAAT增强子结合蛋白α基因的表达升高。这些观察结果表明,在5 - 7周龄时开始出现异常的体脂堆积和脂肪细胞成熟,这可能与性成熟同时发生。MT-I和MT-II基因的靶向破坏似乎会诱发中度肥胖,从而提供一种新的肥胖动物模型。这暗示了MT与能量平衡调节之间的联系。

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