Is highly expressed ACE 2 in pregnant women �a curse� in times of COVID-19 pandemic?

dc.contributor.authorDhaundiyal, Ankit
dc.contributor.authorKumari, Puja
dc.contributor.authorJawalekar, Snehal Sainath
dc.contributor.authorChauhan, Gaurav
dc.contributor.authorKalra, Sourav
dc.contributor.authorNavik, Umashanker
dc.date.accessioned2024-01-21T10:54:56Z
dc.date.accessioned2024-08-14T07:44:17Z
dc.date.available2024-01-21T10:54:56Z
dc.date.available2024-08-14T07:44:17Z
dc.date.issued2020-10-28T00:00:00
dc.description.abstractAngiotensin-converting enzyme 2 (ACE 2) is a membrane-bound enzyme that cleaves angiotensin II (Ang II) into angiotensin (1�7). It also serves as an important binding site for SARS-CoV-2, thereby, facilitating viral entry into target host cells. ACE 2 is abundantly present in the intestine, kidney, heart, lungs, and fetal tissues. Fetal ACE 2 is involved in myocardium growth, lungs and brain development. ACE 2 is highly expressed in pregnant women to compensate preeclampsia by modulating angiotensin (1�7) which binds to the Mas receptor, having vasodilator action and maintain fluid homeostasis. There are reports available on Zika, H1N1 and SARS-CoV where these viruses have shown to produce fetal defects but very little is known about SARS-CoV-2 involvement in pregnancy, but it might have the potential to interact with fetal ACE 2 and enhance COVID-19 transmission to the fetus, leading to fetal morbidity and mortality. This review sheds light on a path of SARS-CoV-2 transmission risk in pregnancy and its possible link with fetal ACE 2. � 2020 Elsevier Inc.en_US
dc.identifier.doi10.1016/j.lfs.2020.118676
dc.identifier.issn243205
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/4283
dc.identifier.urlhttps://linkinghub.elsevier.com/retrieve/pii/S0024320520314296
dc.language.isoen_USen_US
dc.publisherElsevier Inc.en_US
dc.subjectACE 2en_US
dc.subjectPregnancy and fetal transmissionen_US
dc.subjectSARS-CoV-2en_US
dc.titleIs highly expressed ACE 2 in pregnant women �a curse� in times of COVID-19 pandemic?en_US
dc.title.journalLife Sciencesen_US
dc.typeReviewen_US
dc.type.accesstypeOpen Accessen_US

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