digestive/alimentary system
• cultured crypts from tamoxifen-tested mice exhibit poor organoid growth compared with control cells
• crypts of tamoxifen-treated mice exhibit increased DNA damage from cloxP cleavage compared with control crypts
• however, mice exhibit normal enterocyte proliferation and apoptosis and restored regeneration after 7 days following irradiation
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• delayed intestine regeneration in tamoxifen-treated mice following challenge with 12 Gy irradiation
• however, mice not treated with tamoxifen exhibit normal response to irradiation
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growth/size/body
• increased weight loss in tamoxifen-treated mice following challenge with 12 Gy irradiation
• however, mice not treated with tamoxifen exhibit normal response to irradiation
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homeostasis/metabolism
• following challenge with 12 Gy irradiation, tamoxifen-treated mice exhibit increased weight loss and intestinal damage with extensive decellularization of crypts, few crypt structures, and delayed regeneration compared with control mice
• however, mice not treated with tamoxifen exhibit normal response to irradiation
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