mortality/aging
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• 4 of 34 mice fed normal chow die between 8 and 12 weeks of severe metabolic disorders (extreme hyperglycemia, dark yellow urine and very low body weight)
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homeostasis/metabolism
| N |
• mice fed normal chow exhibit the same skeletal muscle triglycerides and plasma free glycerol and free fatty acid levels as in Lepob homozygotes
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• in mice fed normal chow compared with Lepob homozygotes
• extreme in 4 of 34 mice fed normal chow that die between 8 and 12 weeks
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• in mice fed normal chow compared to in Lepob homozygotes
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• in mice fed normal chow compared with Lepob homozygotes
• in white adipose tissue of mice fed normal chow compared with Lepob homozygotes
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• in mice fed normal chow compared to in Lepob homozygotes
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• dark yellow urine in 4 of 34 mice fed normal chow that die between 8 and 12 weeks
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adipose tissue
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• in mice fed normal chow compared with Lepob homozygotes
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• impaired adipogenesis as determined by expression of adipogenic and anti-oxidant response genes compared with Lepob homozygotes
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• fewer small adipocytes in mice fed normal chow compared to in Lepob homozygotes
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growth/size/body
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• from 5 through 11 weeks in mice fed normal chow compared with Lepob homozygotes
• very low body weight in 4 of 34 mice fed normal chow that die between 8 and 12 weeks
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• in mice fed normal chow compared with Lepob homozygotes
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behavior/neurological
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• in female mice fed normal chow after 10 weeks compared with Lepob homozygotes
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liver/biliary system
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• in mice fed normal chow compared to in Lepob homozygotes
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• mild with fewer, smaller lipid droplets in mice fed normal chow compared to in Lepob homozygotes
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renal/urinary system
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• dark yellow urine in 4 of 34 mice fed normal chow that die between 8 and 12 weeks
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Analysis Tools