Your browser doesn't support javascript.
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 32.574
Filtrar
Adicionar filtros

Intervalo de ano
3.
Geneva; World Health Organization; 2023-07-13.
em Inglês | WHOIRIS | ID: gwh-371096
4.
Копенгаген; Всемирная организация здравоохранения. Европейское региональное бюро; 2023. (WHO/2019-nCoV/Vaccines/SAGE/Prioritization/2023.1).
em Russo | WHOIRIS | ID: gwh-371051
6.
Geneva; World Health Organization; 2023-07-06.
em Inglês | WHOIRIS | ID: gwh-370545
9.
Geneva; World Health Organization; 2023-06-29.
em Inglês | WHOIRIS | ID: gwh-370351
11.
Geneva; World Health Organization; 2023-06-22.
em Inglês | WHOIRIS | ID: gwh-369787
12.
Postgrad Med J ; 96(1137): 403-407, 2020 Jul.
Artigo em Inglês | MEDLINE | ID: covidwho-20245306

RESUMO

This article reviews the correlation between ACE2 and COVID-19 and the resulting acute respiratory distress syndrome (ARDS). ACE2 is a crucial component of the renin-angiotensin system (RAS). The classical ACE-angiotensin Ⅱ (Ang II)-angiotensin type 1 receptor (AT1R) axis and the ACE2-Ang(1-7)-Mas counter-regulatory axis play an essential role in RAS system. ACE2 antagonises the activation of the classical RAS ACE-Ang II-AT1R axis and protects against lung injury. Similar to severe acute respiratory syndrome-related coronavirus, 2019 novel coronavirus (2019-nCoV) also uses ACE2 for cell entry. ARDS is a clinical high-mortality disease which is probably due to the excessive activation of RAS caused by 2019-nCoV infection, and ACE2 has a protective effect on ARDS caused by COVID-19. Because of these protective effects of ACE2 on ARDS, the development of drugs enhancing ACE2 activity may become one of the most promising approaches for the treatment of COVID-19 in the near future. In the meantime, however, the use of RAS blockers such as ACE inhibitors and angiotensin II receptor blockers that inhibit the damaging (ACE-Ang II) arm of the RAS cascade in the lung may also be promising. Trial registration number: NCT04287686.


Assuntos
Betacoronavirus/fisiologia , Infecções por Coronavirus/fisiopatologia , Peptidil Dipeptidase A/metabolismo , Pneumonia Viral/fisiopatologia , Receptores Virais/metabolismo , Síndrome do Desconforto Respiratório/fisiopatologia , Antagonistas de Receptores de Angiotensina/farmacologia , Enzima de Conversão de Angiotensina 2 , Betacoronavirus/efeitos dos fármacos , COVID-19 , Infecções por Coronavirus/tratamento farmacológico , Humanos , Pandemias , Pneumonia Viral/tratamento farmacológico , Sistema Renina-Angiotensina/efeitos dos fármacos , Sistema Renina-Angiotensina/fisiologia , Síndrome do Desconforto Respiratório/tratamento farmacológico , Síndrome do Desconforto Respiratório/virologia , SARS-CoV-2
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA