Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
The ACE-2 in COVID-19: Foe or Friend? / Dalan, Rinkoo; Bornstein, Stefan R. ; El-Armouche, Ali ; Rodionov, Roman N ; Markov, Alexander G; Wielockx, Ben; Beuschlein, Felix ; Boehm, Bernhard O. .
в: Hormone and Metabolic Research, Том 52, № 5, 01.05.2020, стр. 257-263.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - The ACE-2 in COVID-19: Foe or Friend?
AU - Dalan, Rinkoo
AU - Bornstein, Stefan R.
AU - El-Armouche, Ali
AU - Rodionov, Roman N
AU - Markov, Alexander G
AU - Wielockx, Ben
AU - Beuschlein, Felix
AU - Boehm, Bernhard O.
N1 - Publisher Copyright: © 2020 Georg Thieme Verlag. All rights reserved.
PY - 2020/5/1
Y1 - 2020/5/1
N2 - COVID-19 is a rapidly spreading outbreak globally. Emerging evidence demonstrates that older individuals and people with underlying metabolic conditions of diabetes mellitus, hypertension, and hyperlipidemia are at higher risk of morbidity and mortality. The SARS-CoV-2 infects humans through the angiotensin converting enzyme (ACE-2) receptor. The ACE-2 receptoris a part of the dual system renin-angiotensin-system (RAS) consisting of ACE-Ang-II-AT 1 R axis and ACE-2-Ang-(1–7)-Mas axis. In metabolic disorders and with increased age, it is known that there is an upregulation of ACE-Ang-II-AT 1 R axis with a downregulation of ACE-2-Ang-(1–7)-Mas axis. The activated ACE-Ang-II-AT1R axis leads to pro-infl ammatory and pro-fibrotic eff ects in respiratory system, vascular dysfunction, myocardialfi brosis, nephropathy, and insulin secretory defects with increased insulin resistance. On the other hand, the ACE-2-Ang-(1–7)-Mas axis has anti-inflammatory and antifi brotic effects on the respiratory system and anti-inflammatory, antioxidative stress, and protective eff ects on vascular function, protects against myocardial fi brosis, nephropathy, pancreatitis, andinsulin resistance. In eff ect, the balance between these two axes may determine the prognosis. The already strained ACE-2-Ang-(1–7)-Mas in metabolic disorders is further stressed due to the use of the ACE-2 by the virus for entry, which aff ects the prognosis in terms of respiratory compromise. Further evidence needs to be gathered on whether modulation of the renin angiotensin system would be advantageous due to upregulationof Mas activation or harmful due to the concomitant ACE-2 receptor upregulation in the acute management of COVID-19.
AB - COVID-19 is a rapidly spreading outbreak globally. Emerging evidence demonstrates that older individuals and people with underlying metabolic conditions of diabetes mellitus, hypertension, and hyperlipidemia are at higher risk of morbidity and mortality. The SARS-CoV-2 infects humans through the angiotensin converting enzyme (ACE-2) receptor. The ACE-2 receptoris a part of the dual system renin-angiotensin-system (RAS) consisting of ACE-Ang-II-AT 1 R axis and ACE-2-Ang-(1–7)-Mas axis. In metabolic disorders and with increased age, it is known that there is an upregulation of ACE-Ang-II-AT 1 R axis with a downregulation of ACE-2-Ang-(1–7)-Mas axis. The activated ACE-Ang-II-AT1R axis leads to pro-infl ammatory and pro-fibrotic eff ects in respiratory system, vascular dysfunction, myocardialfi brosis, nephropathy, and insulin secretory defects with increased insulin resistance. On the other hand, the ACE-2-Ang-(1–7)-Mas axis has anti-inflammatory and antifi brotic effects on the respiratory system and anti-inflammatory, antioxidative stress, and protective eff ects on vascular function, protects against myocardial fi brosis, nephropathy, pancreatitis, andinsulin resistance. In eff ect, the balance between these two axes may determine the prognosis. The already strained ACE-2-Ang-(1–7)-Mas in metabolic disorders is further stressed due to the use of the ACE-2 by the virus for entry, which aff ects the prognosis in terms of respiratory compromise. Further evidence needs to be gathered on whether modulation of the renin angiotensin system would be advantageous due to upregulationof Mas activation or harmful due to the concomitant ACE-2 receptor upregulation in the acute management of COVID-19.
KW - covid
KW - рецептор
KW - инфекция
KW - вирус
KW - ангиотензин-превращающий фактор
KW - ACE-2
KW - COVID-19
KW - renin angiotensin system
KW - Pneumonia, Viral/physiopathology
KW - Pandemics
KW - Prognosis
KW - Peptidyl-Dipeptidase A/genetics
KW - Humans
KW - Coronavirus Infections/physiopathology
KW - Angiotensin-Converting Enzyme 2
KW - Betacoronavirus/isolation & purification
KW - Renin-Angiotensin System/genetics
KW - SARS-CoV-2
KW - Metabolic Diseases/physiopathology
KW - CONVERTING ENZYME 2
KW - SARS CORONAVIRUS
KW - RECEPTOR
KW - RENIN-ANGIOTENSIN SYSTEM
KW - INFLAMMATION
KW - DIFFERENTIATION
KW - STRESS
UR - http://www.scopus.com/inward/record.url?scp=85084617426&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/db7e36ad-b309-3c42-b02c-ddee7d1a8f00/
U2 - 10.1055/a-1155-0501
DO - 10.1055/a-1155-0501
M3 - Article
C2 - 32340044
VL - 52
SP - 257
EP - 263
JO - Hormone and Metabolic Research
JF - Hormone and Metabolic Research
SN - 0018-5043
IS - 5
ER -
ID: 53164745