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ACE2, Metformin, and COVID-19
被引:48
|作者:
Malhotra, Atul
[1
,2
]
Hepokoski, Mark
[1
,2
,5
]
McCowen, Karen C.
[1
,3
]
Shyy, John Y-J
[1
,4
]
机构:
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92023 USA
[2] Univ Calif San Diego, Div Pulm Crit Care & Sleep Med, La Jolla, CA 92023 USA
[3] Univ Calif San Diego, Div Endocrinol, La Jolla, CA 92023 USA
[4] Univ Calif San Diego, Div Cardiol, La Jolla, CA 92023 USA
[5] VA San Diego Hlth Syst, 9500 Gilman Dr, La Jolla, CA 92023 USA
来源:
关键词:
Endocrinology;
Virology;
D O I:
10.1016/j.isci.2020.101425
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
COVID-19 is becoming a leading cause of mortality throughout the world, and few effective therapies are currently available. Angiotensin converting enzyme 2 (ACE2) is essential to COVID-19 pathogenesis, as the binding of SARS-CoV-2 spike protein (S protein) is required for viral entry and development of COVID-19. AC72 regulates the protective arm of the renin-angiotensin-aldosterone system (RAAS) that endows anti-hypertensive and anti-inflammatory effects in the cardiovascular and pulmonary systems. Preclinical data suggest ACE2 might be downregulated after SARS-CoV-2 binding, and treatments that increase ACE2 may prevent cardiopulmonary injury. Development, testing, and mass production of novel ACE2 therapies may take years, whereas more effective treatments for COVID-19 are needed urgently. Metformin is a widely available anti-diabetic agent that has an excellent safety profile, and clinical and preclinical data suggest metformin may offer cardiopulmonary protection in COVID-19 via enhanced ACE2 expression.
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