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suck abstract from ncbi


10.1016/j.nut.2021.111226

http://scihub22266oqcxt.onion/10.1016/j.nut.2021.111226
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33965680!7937331!33965680
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suck abstract from ncbi

pmid33965680      Nutrition 2021 ; 90 (?): 111226
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  • Intestinal expression of ACE2 in mice with high-fat diet-induced obesity and neonates exposed to maternal high-fat diet #MMPMID33965680
  • Sun J; Chen L; Xiao XA; Jia MQ; Wang XY; Jiao H; Gao Y
  • Nutrition 2021[Oct]; 90 (?): 111226 PMID33965680show ga
  • OBJECTIVE: The 2019 novel coronavirus disease (COVID-19) is threatening global health and is especially pronounced in patients with chronic metabolic syndromes. Meanwhile, a significant proportion of patients present with digestive symptoms since angiotensin-converting enzyme 2 (ACE2), which is the receptor for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is highly expressed in the intestine. The aim of this study was to evaluate the effects of a high-fat diet (HFD) and a maternal HFD on the intestinal ACE2 levels in adults and neonates. METHODS: We examined intestinal ACE2 protein levels in mice with diet-induced obesity (DIO) and neonatal mice exposed to a maternal HFD. We also investigated Ace2 mRNA expression in intestinal macrophages. RESULTS: Intestinal ACE2 protein levels were increased in DIO mice but decreased in offspring exposed to a maternal HFD compared with chow-fed controls. Ace2 mRNA expression in intestinal macrophages was detected and downregulated in DIO mice. Additionally, higher intestinal ACE2 protein levels were observed in neonates than in adult mice. CONCLUSIONS: The influence of an HFD on intestinal ACE2 protein levels is opposite in adults and neonates. Macrophages might also be involved in SARS-CoV-2 intestinal infection. These findings provide some clues for the outcomes of patients with COVID-19 with metabolic syndromes.
  • |*COVID-19[MESH]
  • |*Diet, High-Fat/adverse effects[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Animals[MESH]
  • |Humans[MESH]
  • |Intestines[MESH]
  • |Mice[MESH]
  • |Obesity/etiology[MESH]
  • |Peptidyl-Dipeptidase A/genetics[MESH]


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