mortality/aging
• mice exhibit non-ischemic heart failure and die at 5-30 weeks of age
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cardiovascular system
• the heart/body weight ratio is about 1.5-fold higher at 6 weeks of age
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• global chamber dilatation with marked wall thinning
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• mice develop non-ischemic dilated cardiomyopathy
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• mice exhibit decreased fractional shortening
• 8 week old mice intravenously infused with wild-type bone marrow-derived mononuclear cells (BMMNC) show improved fractional shortening 3 days after infusion, however this effect is lost by 14 days after infusion
• BMMNC infusion repeated every 2 weeks results in improved cardiac function for more than 50 days
• mice injected intraperitoneally for 2 weeks with an anti-activin A antibody show improved fractional shortening and +dp/dt
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• echocardiography indicates a decrease in fractional shortening together with chamber dilatation
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• mice succumb to non-ischemic heart failure
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homeostasis/metabolism
• serum activin A levels are increased
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• decrease in growth hormone concentration in serum
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muscle
• mice develop non-ischemic dilated cardiomyopathy
|
• mice exhibit decreased fractional shortening
• 8 week old mice intravenously infused with wild-type bone marrow-derived mononuclear cells (BMMNC) show improved fractional shortening 3 days after infusion, however this effect is lost by 14 days after infusion
• BMMNC infusion repeated every 2 weeks results in improved cardiac function for more than 50 days
• mice injected intraperitoneally for 2 weeks with an anti-activin A antibody show improved fractional shortening and +dp/dt
|
growth/size/body
• the heart/body weight ratio is about 1.5-fold higher at 6 weeks of age
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
dilated cardiomyopathy | DOID:12930 |
OMIM:PS115200 |
J:182337 |