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通过瘦素基因疗法纠正遗传性肥胖小鼠的肥胖和糖尿病

Correction of obesity and diabetes in genetically obese mice by leptin gene therapy.

作者信息

Muzzin P, Eisensmith R C, Copeland K C, Woo S L

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Proc Natl Acad Sci U S A. 1996 Dec 10;93(25):14804-8. doi: 10.1073/pnas.93.25.14804.

Abstract

The ob/ob mouse is genetically deficient in leptin and exhibits both an obese and a mild non-insulin-dependent diabetic phenotype. To test the hypothesis that correction of the obese phenotype by leptin gene therapy will lead to the spontaneous correction of the diabetic phenotype, the ob/ob mouse was treated with a recombinant adenovirus expressing the mouse leptin cDNA. Treatment resulted in dramatic reductions in both food intake and body weight, as well as the normalization of serum insulin levels and glucose tolerance. The subsequent diminishment in serum leptin levels resulted in the rapid resumption of food intake and a gradual gain of body weight, which correlated with the gradual return of hyperinsulinemia and insulin resistance. These results not only demonstrated that the obese and diabetic phenotypes in the adult ob/ob mice are corrected by leptin gene treatment but also provide confirming evidence that body weight control may be critical in the long-term management of non-insulin-dependent diabetes mellitus in obese patients.

摘要

ob/ob小鼠在瘦素方面存在基因缺陷,表现出肥胖和轻度非胰岛素依赖型糖尿病表型。为了验证瘦素基因疗法纠正肥胖表型会导致糖尿病表型自发纠正这一假设,用表达小鼠瘦素cDNA的重组腺病毒对ob/ob小鼠进行治疗。治疗导致食物摄入量和体重显著降低,同时血清胰岛素水平和葡萄糖耐量恢复正常。随后血清瘦素水平的下降导致食物摄入量迅速恢复和体重逐渐增加,这与高胰岛素血症和胰岛素抵抗的逐渐恢复相关。这些结果不仅证明了成年ob/ob小鼠的肥胖和糖尿病表型可通过瘦素基因治疗得到纠正,还提供了确证证据,即体重控制对于肥胖患者非胰岛素依赖型糖尿病的长期管理可能至关重要。

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Manipulation of adenovirus vectors.腺病毒载体的操控
Methods Mol Biol. 1991;7:109-28. doi: 10.1385/0-89603-178-0:109.
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Trends Genet. 1994 Jul;10(7):253-7. doi: 10.1016/0168-9525(94)90173-2.
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Preventing non-insulin-dependent diabetes.预防非胰岛素依赖型糖尿病。
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