mortality/aging
• mice begin to succumb to death at around 12 months of age
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renal/urinary system
• apoptosis is increased in the kidney thick ascending limb cells in 12-month-old mice but not in 1-month-old mice
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• 1-month old mice have more diluted urine, with lower osmolality and lower concentrations of all the electrolytes, including sodium, calcium, potassium, chloride, phosphorus, citrate, and magnesium
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• 12-month-old mice have a higher urine osmolality and lower 24-hour excretion of all the electrolytes
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• both young and old mice show increased serum uric acid levels
• both young and old mice show elevated levels of serum allantoin, the catabolic product of uric acid
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• sclerotic glomeruli are present in the cortex of 12-month-old mice
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• mice at 12 months of age exhibit interstitial fibrosis in medullary and papillary regions
• an increase in collagen deposition in the kidneys is seen in young (1 month of age) mice and more so in old (12 months of age) mice
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• mice at 12 months of age exhibit extensive atrophic tubules
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• 6- and 12-month-old mice show decreased creatinine clearance rate
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• by 6 months of age, mice have about 1/3 the urine output of wild-type mice and at 12 months of age, mice have about 1/5 of the urine volume of wild-type mice
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• urine volume of 1-month old mice is more than 2-fold higher than in wild-type mice
• however, this increase is reversed as early as 3 months of age
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cellular
• apoptosis is increased in the kidney thick ascending limb cells in 12-month-old mice but not in 1-month-old mice
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homeostasis/metabolism
• 1-month old mice have more diluted urine, with lower osmolality and lower concentrations of all the electrolytes, including sodium, calcium, potassium, chloride, phosphorus, citrate, and magnesium
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• 12-month-old mice have a higher urine osmolality and lower 24-hour excretion of all the electrolytes
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• both young and old mice show increased serum uric acid levels
• both young and old mice show elevated levels of serum allantoin, the catabolic product of uric acid
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
familial juvenile hyperuricemic nephropathy | DOID:0060062 |
OMIM:162000 OMIM:613092 OMIM:614227 |
J:252420 |