scholarly journals Can Melatonin Be a Potential “Silver Bullet” in Treating COVID-19 Patients?

Diseases ◽  
2020 ◽  
Vol 8 (4) ◽  
pp. 44
Author(s):  
Daniel P. Cardinali ◽  
Gregory M. Brown ◽  
Seithikurippu R. Pandi-Perumal

The therapeutic potential of melatonin as a chronobiotic cytoprotective agent to counteract the consequences of COVID-19 infections has been advocated. Because of its wide-ranging effects as an antioxidant, anti-inflammatory, and immunomodulatory compound, melatonin could be unique in impairing the consequences of SARS-CoV-2 infection. Moreover, indirect evidence points out to a possible antiviral action of melatonin by interfering with SARS-CoV-2/angiotensin-converting enzyme 2 association. Melatonin is also an effective chronobiotic agent to reverse the circadian disruption of social isolation and to control delirium in severely affected patients. As a cytoprotector, melatonin serves to combat several comorbidities such as diabetes, metabolic syndrome, and ischemic and non-ischemic cardiovascular diseases, which aggravate COVID-19 disease. In view of evidence on the occurrence of neurological sequels in COVID-19-infected patients, another putative application of melatonin emerges based on its neuroprotective properties. Since melatonin is an effective means to control cognitive decay in minimal cognitive impairment, its therapeutic significance for the neurological sequels of SARS-CoV-2 infection should be considered. Finally, yet importantly, exogenous melatonin can be an adjuvant capable of augmenting the efficacy of anti-SARS-CoV-2 vaccines. We discuss in this review the experimental evidence suggesting that melatonin is a potential “silver bullet” in the COVID 19 pandemic.

2016 ◽  
Vol 34 (Supplement 1) ◽  
pp. e222
Author(s):  
Li-Juan Min ◽  
Masaki Mogi ◽  
Xiao-Li Wang ◽  
Kana Tsukuda ◽  
Akinori Higaki ◽  
...  

2004 ◽  
Vol 22 (Suppl. 2) ◽  
pp. S317-S318
Author(s):  
J. Zhong ◽  
Z. Zhu ◽  
T. Cao ◽  
Z. Yan ◽  
C. Shen ◽  
...  

Author(s):  
Jiandong Huo ◽  
Yuguang Zhao ◽  
Jingshan Ren ◽  
Daming Zhou ◽  
Helen ME Duyvesteyn ◽  
...  

SummaryThere are as yet no licenced therapeutics for the COVID-19 pandemic. The causal coronavirus (SARS-CoV-2) binds host cells via a trimeric Spike whose receptor binding domain (RBD) recognizes angiotensin-converting enzyme 2 (ACE2), initiating conformational changes that drive membrane fusion. We find that monoclonal antibody CR3022 binds the RBD tightly, neutralising SARS-CoV-2 and report the crystal structure at 2.4 Å of the Fab/RBD complex. Some crystals are suitable for screening for entry-blocking inhibitors. The highly conserved, structure-stabilising, CR3022 epitope is inaccessible in the prefusion Spike, suggesting that CR3022 binding would facilitate conversion to the fusion-incompetent post-fusion state. Cryo-EM analysis confirms that incubation of Spike with CR3022 Fab leads to destruction of the prefusion trimer. Presentation of this cryptic epitope in an RBD-based vaccine might advantageously focus immune responses. Binders at this epitope may be useful therapeutically, possibly in synergy with an antibody blocking receptor attachment.HighlightsCR3022 neutralises SARS-CoV-2Neutralisation is by destroying the prefusion SPIKE conformationThis antibody may have therapeutic potential alone or with one blocking receptor attachment


2016 ◽  
Vol 34 ◽  
pp. e75
Author(s):  
J. Iwanami ◽  
M. Mogi ◽  
X.L. Wang ◽  
K. Tsukuda ◽  
A. Higaki ◽  
...  

2012 ◽  
Vol 108 (12) ◽  
pp. 1089-1096 ◽  
Author(s):  
Rodrigo Fraga-Silva ◽  
Danielle Da Silva ◽  
Fabrizio Montecucco ◽  
François Mach ◽  
Nikolaos Stergiopulos ◽  
...  

SummaryDespite many therapeutic advances leading to increasingly effective drug treatments, thrombotic events (such as ischaemic stroke, pulmonary embolism, deep venous thrombosis and acute myocardial infarction) still represent a major worldwide cause of morbidity and mortality. Remarkable effort has been made to identify new drug targets. There is growing evidence indicating that the recently described counter-regulator axis of the renin-angiotensin system (RAS), composed of Angiotensin-Converting Enzyme 2 (ACE2), Angiotensin-(1–7) and the Mas receptor, has protective effects against thrombosis. In addition, it could be considered as a promising target for treating or preventing this disease. In this narrative review, we focused on the recent findings of the role of the ACE2/Angiotensin-(1–7)/Mas axis on the haemostatic process and its therapeutic potential.


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