endocrine/exocrine glands
• small and disorganized
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digestive/alimentary system
• enterocyte differentiation is impaired
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• decrease in thickness of the mucosa
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• decrease in the number of goblet cells in the ileum
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• at 2 weeks, the intestine is more fragile than in wild-type mice
• intestinal size and length of crypt-villus units are reduced compared to in wild-type mice
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• reduction in villus height that results from a decrease in the number of epithelial cells per crypt-villus axis
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• at 2 weeks, the intestine is shorter than in wild-type mice
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• enterocytes show a large decrease in lactase and sucrase enzyme activity
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• number of proliferating epithelial cells per crypt is reduced in the distal small intestine
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cardiovascular system
• time to peak tension and time to 50% relaxation are prolonged compared to in wild-type mice
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• QRS duration is increased compared to in wild-type mice
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skeleton
• prior to hypothyroidy, mice exhibit impaired development of epiphyseal bone centers characterized by hypertrophied cartilage associated with low ossification unlike in wild-type mice
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homeostasis/metabolism
• enterocytes show a large decrease in lactase and sucrase enzyme activity
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muscle
• time to peak tension and time to 50% relaxation are prolonged compared to in wild-type mice
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cellular
• decrease in the number of goblet cells in the ileum
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• number of proliferating epithelial cells per crypt is reduced in the distal small intestine
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