2006
DOI: 10.1016/j.nutres.2006.06.020
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Apolipoprotein E knockout mice have accentuated malnutrition with mucosal disruption and blunted insulin-like growth factor I responses to refeeding

Abstract: Apolipoprotein E (apoE) is synthesized mainly in the liver and in the brain and is critical for cholesterol metabolism and recovery from brain injury. However, although apoE mRNA increases at birth, during suckling, and after fasting in rat liver, little is known about its role in early postnatal development. Using an established postnatal malnutrition model and apoE knock-out (ko) mice, we examined the role of apoE in intestinal adaptation responses to early postnatal malnutrition. Wild-type and apoE-ko mice … Show more

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Cited by 13 publications
(17 citation statements)
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References 53 publications
(56 reference statements)
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“…As previously described [15], the undernourished non-infected mice showed profound crypt derangement and shortening, with almost complete mitotic blunting. Rarely Paneth and goblet cells were found within the crypt.…”
Section: Resultssupporting
confidence: 69%
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“…As previously described [15], the undernourished non-infected mice showed profound crypt derangement and shortening, with almost complete mitotic blunting. Rarely Paneth and goblet cells were found within the crypt.…”
Section: Resultssupporting
confidence: 69%
“…In an earlier study, we demonstrated that undernutrition caused by breastfeeding restriction during the suckling time in rodents could lead to severe stunting, poor weight gain [15] and much heavier cryptosporidial infections [10]. In the current study, we have evaluated the potential benefit of the conditional amino acid L-arginine during intestinal adaptations against C. parvum infection in suckling mice afflicted with early post-natal malnutrition.…”
Section: Discussionmentioning
confidence: 99%
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“…This may be caused by a disrupted growth factor signaling, since we had shown impaired intestinal adaptations during catch-up growth following re-feeding in severe undernourished ApoE knock-out mice, with poor intestinal IGF-1 expression [21]. …”
Section: Discussionmentioning
confidence: 99%
“…Most strikingly, the ApoEko malnourished mice fail to repair mucosal damage or recover from their growth faltering following refeeding, thus showing they have dramatically reduced intestinal adaptive responses. This appeared to be due, at least in part, to blunted IGF‐I expression 145 …”
Section: The Human Genetic Component: Thrifty Genes Evolution and Cmentioning
confidence: 99%