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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.
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http://dx.doi.org/10.1016/j.nut.2021.111226 | DOI Listing |
Vet Microbiol
August 2025
College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China. Electronic address:
Transmissible gastroenteritis virus (TGEV) is one of the major pathogen causing swine diarrhea, inducing acute severe atrophic enteritis and lethal watery diarrhea in neonatal piglets with up to 100 % mortality, resulting in significant economic losses to the swine industry. Angiotensin-converting enzyme 2 (ACE2) is known as an invasion receptor for SARS-CoV-2, but its role in TGEV infection remains unclear, and the current understanding of TGEV infection mechanisms is incomplete. In this study, we identified an important role for porcine ACE2 (pACE2) in TGEV infection.
View Article and Find Full Text PDFJ Nutr Biochem
August 2025
Department of Pharmacology, Faculty of Medicine, University of Helsinki, 00014 Helsinki, Finland; Human Microbiome Research Program, Faculty of Medicine, University of Helsinki, 00014 Helsinki, Finland.
Inhibiting the overexpression of the renin-angiotensin-aldosterone system (RAAS) alleviates intestinal inflammation. Recently, we and others reported that a high-fat, low carbohydrate, ketogenic diet (KD), shown to downregulate the conventional RAAS components in rat lung and adipose tissue, can protect mice from experimental colitis. Here we assessed whether the proinflammatory angiotensin-converting enzyme - angiotensin receptor type 1 (ACE-AT1R) axis and the anti-inflammatory angiotensin-converting enzyme 2- MAS1 receptor (ACE2-MAS1) axis RAAS components are influenced by the consumption of a KD rich either in saturated fatty acids (SFA-KD) or polyunsaturated linoleic acid (LA-KD) in healthy and inflamed intestine of C57BL/6J male mice.
View Article and Find Full Text PDFCommun Biol
August 2025
Marine Synthetic Ecology Research Center, Guangdong Core Germplasm Bank for Marine Economic Animals, Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai)/State Key Laboratory for Biocontrol, Sun Yat-sen University, 519082, Zhuhai, China.
Angiotensin-converting enzyme 2 (Ace2) is a well-studied enzyme with important physiological functions in mammals. However, its roles in non-mammalian animals remain largely unexplored. This study investigates the function of Ace2 in zebrafish using CRISPR/Cas9-generated ace2 mutants (-/-).
View Article and Find Full Text PDFLife Sci
August 2025
Department of Histology and Cell Biology, Faculty of Medicine, Minia University, 61111 Minia, Egypt; Faculty of Physical therapy, Lotus University, 61768 Minia, Egypt; Department of Histology and Cell Biology, Faculty of Medicine, Minia National University, Minia, Egypt. Electronic address: Manar.fo
Aim: Intestinal ischemic reperfusion (I-I/R) injury is a serious clinical case with high death rate. This research assessed the influence of Angiotensin 1-7 (Ang-(1-7)) alone on the induced I-I/R injury or combined with each of nuclear factor erythroid 2 related factor 2 (Nrf-2) inhibitor (ML-385) or Mas receptor antagonist (A779). The primary objective of our study was to assess the role of Mas receptor and Nrf-2 pathway in mediating the probable protective effect of Ang-(1-7) against intestinal I/R injury.
View Article and Find Full Text PDFInt J Mol Sci
June 2025
College of Pharmacy, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait.
A growing body of evidence suggests the potent anti-inflammatory properties of the newly discovered arm of the renin-angiotensin-aldosterone system, ACE2/Ang-(1-7)/MasR, in various disease conditions. Our group was the first to report the anti-inflammatory properties of the Ang-(1-7) polypeptide in the murine dextran sulfate sodium (DSS) colitis model. Both its short half-life and high degradation rate limit the clinical use of Ang-(1-7).
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