| First Author | Allan MF | Year | 2004 |
| Journal | Obes Res | Volume | 12 |
| Issue | 9 | Pages | 1397-407 |
| PubMed ID | 15483204 | Mgi Jnum | J:357754 |
| Mgi Id | MGI:6758297 | Doi | 10.1038/oby.2004.176 |
| Citation | Allan MF, et al. (2004) The M16 mouse: an outbred animal model of early onset polygenic obesity and diabesity. Obes Res 12(9):1397-407 |
| abstractText | OBJECTIVE: To characterize the phenotypic consequences of long-term selective breeding for rapid weight gain, with an emphasis on obesity and obesity-induced diabetes (diabesity). RESEARCH METHODS AND PROCEDURES: M16 is the result of long-term selection for 3- to 6-week weight gain from an ICR base population. Experiment 1 characterized males from both lines for body weights (3, 6, and 8 weeks), feed (4 to 8 weeks) and H(2)O (6 to 8 weeks) consumption, and heat loss, body composition, and levels of several plasma proteins at 8 weeks of age. Experiment 2 characterized differences between lines for both sexes at three ages (6, 8, and 16 weeks) and fed two diets (high and normal fat). Body weight, composition, blood glucose, and plasma insulin and leptin levels were evaluated after an 8-hour fast. RESULTS: At all ages measured, M16 mice were heavier, fatter, hyperphagic, hyperinsulinemic, and hyperleptinemic relative to ICR. M16 males and females were hyperglycemic relative to ICR, with 56% and 22% higher fasted blood glucose levels at 8 weeks of age. DISCUSSION: M16 mice represent an outbred animal model to facilitate gene discovery and pathway regulation controlling early onset polygenic obesity and type 2 diabetic phenotypes. Phenotypes prevalent in the M16 model, with obesity and diabesity exhibited at a young age, closely mirror current trends in human populations. |
