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BSB:一种多基因肥胖的新型小鼠模型。

BSB: a new mouse model of multigenic obesity.

作者信息

Fisler J S, Warden C H, Pace M J, Lusis A J

机构信息

Department of Medicine, University of California, Los Angeles, CA 90024, USA.

出版信息

Obes Res. 1993 Jul;1(4):271-80. doi: 10.1002/j.1550-8528.1993.tb00621.x.

Abstract

We report here a new mouse model of multigenic obesity. Backcross progeny ((C57BL/6J x Mus spretus)F1 x C57BL/6J), designated as BSB mice, range from 1% to 50% body fat. Since both parental strains are relatively lean, the wide range of the phenotype in the BSB mice indicates the involvement of multiple genes to produce obesity. Obesity in BSB mice results from increases in both intra-abdominal and subcutaneous fat and is associated with hyperinsulinemia, hyperglycemia, and hyperlipidemia. Female and male BSB mice do not differ in the degree of obesity obtained. Stimulated plasma corticosterone levels are reduced in obese male and female mice. The development of appropriate genetic markers and statistical methods have made it feasible to analyze quantitative polygenic traits in animal models by employing F2 or backcross progeny. Thus, this BSB model is uniquely suited to the genetic analysis of the multifactorial quantitative trait of obesity and its associated phenotypes.

摘要

我们在此报告一种新的多基因肥胖小鼠模型。回交后代((C57BL/6J×小家鼠)F1×C57BL/6J),命名为BSB小鼠,体脂率在1%至50%之间。由于两个亲本品系都相对较瘦,BSB小鼠广泛的表型范围表明多个基因参与导致肥胖。BSB小鼠的肥胖是由腹内脂肪和皮下脂肪增加所致,并且与高胰岛素血症、高血糖症和高脂血症相关。肥胖的雌性和雄性BSB小鼠在肥胖程度上没有差异。肥胖的雄性和雌性小鼠刺激后的血浆皮质酮水平降低。合适的遗传标记和统计方法的发展使得通过使用F2或回交后代来分析动物模型中的数量多基因性状成为可能。因此,这个BSB模型特别适合对肥胖及其相关表型的多因素数量性状进行遗传分析。

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