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肥胖基因表达:在瘦小鼠中,禁食可使其降低,胰岛素和葡萄糖可使其升高;而在后天性(饮食诱导)肥胖和遗传性(黄刺鼠)肥胖中则持续升高。

Obese gene expression: reduction by fasting and stimulation by insulin and glucose in lean mice, and persistent elevation in acquired (diet-induced) and genetic (yellow agouti) obesity.

作者信息

Mizuno T M, Bergen H, Funabashi T, Kleopoulos S P, Zhong Y G, Bauman W A, Mobbs C V

机构信息

Fishberg Center for Neurobiology, Mt. Sinai School of Medicine, New York, NY 10029, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Apr 16;93(8):3434-8. doi: 10.1073/pnas.93.8.3434.

DOI:10.1073/pnas.93.8.3434
PMID:8622953
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC39626/
Abstract

Mutations in the obese (ob) gene lead to obesity. This gene has been recently cloned, but the factors regulating its expression have not been elucidated. To address the regulation of the ob gene with regard to body weight and nutritional factors, Northern blot analysis was used to assess ob mRNA in adipose tissue from mice [lean, obese due to diet, or genetically (yellow agouti) obese] under different nutritional conditions. ob mRNA was elevated in both forms of obesity, compared to lean controls, correlated with elevations in plasma insulin and body weight, but not plasma glucose. In lean C57BL/6J mice, but not in mice with diet-induced obesity, ob mRNA decreased after a 48-hr fast. Similarly, in lean C57BL/6J controls, but not in obese yellow mice, i.p. glucose injection significantly increased ob mRNA. For up to 30 min after glucose injection, ob mRNA in lean mice significantly correlated with plasma glucose, but not with plasma insulin. In a separate study with only lean mice, ob mRNA was inhibited >90% by fasting, and elevated approximately 2-fold 30 min after i.p. injection of either glucose or insulin. These results suggest that in lean animals glucose and insulin enhance ob gene expression. In contrast to our results in lean mice, in obese animals ob mRNA is elevated and relatively insensitive to nutritional state, possibly due to chronic exposure to elevated plasma insulin and/or glucose.

摘要

肥胖(ob)基因突变会导致肥胖。该基因最近已被克隆,但调节其表达的因素尚未阐明。为了研究ob基因在体重和营养因素方面的调节作用,采用Northern印迹分析来评估不同营养条件下小鼠(瘦小鼠、饮食诱导肥胖小鼠或遗传性黄褐毛肥胖小鼠)脂肪组织中的ob mRNA。与瘦对照相比,两种肥胖形式下ob mRNA均升高,且与血浆胰岛素和体重升高相关,但与血浆葡萄糖无关。在瘦的C57BL/6J小鼠中,而不是在饮食诱导肥胖的小鼠中,禁食48小时后ob mRNA下降。同样,在瘦的C57BL/6J对照小鼠中,而不是在肥胖的黄色小鼠中,腹腔注射葡萄糖显著增加ob mRNA。在葡萄糖注射后长达30分钟内,瘦小鼠中的ob mRNA与血浆葡萄糖显著相关,但与血浆胰岛素无关。在一项仅针对瘦小鼠的单独研究中,禁食使ob mRNA抑制>90%,腹腔注射葡萄糖或胰岛素30分钟后ob mRNA升高约2倍。这些结果表明,在瘦动物中葡萄糖和胰岛素增强ob基因表达。与我们在瘦小鼠中的结果相反,在肥胖动物中ob mRNA升高且对营养状态相对不敏感,这可能是由于长期暴露于升高的血浆胰岛素和/或葡萄糖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d6a/39626/1fd47b40c443/pnas01515-0287-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d6a/39626/4e72437b005a/pnas01515-0286-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d6a/39626/1fd47b40c443/pnas01515-0287-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d6a/39626/4e72437b005a/pnas01515-0286-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d6a/39626/1fd47b40c443/pnas01515-0287-a.jpg

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