mortality/aging
• following treatment with J0-2 to induce fulminant hepatitis, fewer mice survive than in similarly treated wild-type mice
• following partial hepatectomy, mice exhibit increased mortality compared to similarly treated wild-type mice
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liver/biliary system
• following two thirds partial hepatectomy, hepatocytes exhibit reduced proliferation associated with extended S phase and fewer mitotic cells compared to in wild-type cells
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• following partial hepatectomy, mice exhibit increased mortality and delayed liver mass restoration compared to similarly treated wild-type mice
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homeostasis/metabolism
• following facial nerve lesion, mice fail to exhibit rescue of nerve loss when treated with ciliary neurotrophic factor unlike wild-type mice
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• mice are more susceptible to fulminant hepatitis induced by J0-2 than wild-type mice as indicated by decreased survival, increased serum levels of alanine transaminase and aspartate transaminase and increased apoptosis
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nervous system
N |
• mice exhibit normal motor neurons
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• at P5, myelination of the hypoglossal nerve is delayed compared to in wild-type mice
• however, myelination of the hypoglossal nerve is normal by P21
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behavior/neurological
• mice exhibit impaired suckling behavior compared to wild-type mice
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cellular
• following partial hepatectomy, mice exhibit increased sensitivity to Fas induced oxidative stress compared to similarly treated wild-type mice
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• following two thirds partial hepatectomy, hepatocytes exhibit reduced proliferation associated with extended S phase and fewer mitotic cells compared to in wild-type cells
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