Abstract

Introduction: Aspirin has justifiably been called the first miracle drug. In this article, we highlight the history of Aspirin, a novel mechanism of action, and its use in cardiovascular and other diseases. Also included is a brief statement of emerging new applications. Objective: We highlight principal mechanisms by which Aspirin inhibits acute inflammation and alters platelet-biology; therefore, hypothesized that Aspirin might prove highly beneficial as a novel therapeutic drug for combating severe acute inflammation and thrombosis associated with the cytokine storm in COVID -19 patients. The communiqué also suggests possible strategies for maximizing the gain of Aspirin as a wonder-drug of the future. Discussion: Interestingly, some fascinating studies demonstrated Aspirin's superior benefits with dangerous side effects. Aspirin inhibits COX-1 (cyclooxygenase-1). Its impact on COX-2 is more delicate because it “turns off” COX-2's production of prostaglandins but “switches on” the enzymatic ability to produce novel protective lipid mediators. The established mechanism of action of Aspirin is the inhibition of prostaglandin synthesis. However, further evidence showed that aspirin-elicited nitric oxide exerts anti-inflammatory effects in the microcirculation by inhibiting leukocyte– endothelium interactions. Interestingly, aspirin-triggered lipoxin formation may provide a novel mechanism underlying Aspirin's clinical benefits. Interestingly, Aspirin reduces the risk of a cardiovascular event by about 30 percent. Also, Aspirin has been associated with a reduced risk of colorectal cancer, and possibly a few other digestive tract cancers. Conclusion: The current emerging interest is to conduct further study to provide evidence for Aspirin as the novel therapeutic drug for combating severe acute inflammation and thrombosis associated with the cytokine storm in COVID-19 patients. Besides, the most wanted is The RECOVERY II (Randomized Evaluation of COVID-19 Therapy II) trial to be established as a randomized clinical trial to test the effectiveness of low-dose Aspirin as an anti-inflammatory and antithrombotic treatment in COVID-19 patients.

Highlights

  • Aspirin has justifiably been called the first miracle drug

  • Aspirin has been associated with a reduced risk of colorectal cancer, and possibly a few other digestive tract cancers

  • Cytokine Storm: This is described as severe acute inflammation that arises from an exaggerated immune response to the presence of the SARS-CoV-2, which is considered as one of the most critical negative prognostic markers in COVID-19 disease [9,10,11,12]

Read more

Summary

Introduction

We highlight the history of Aspirin, a novel mechanism of action, and its use in cardiovascular and other diseases. Objective: We highlight principal mechanisms by which Aspirin inhibits acute inflammation and alters platelet-biology; hypothesized that Aspirin might prove highly beneficial as a novel therapeutic drug for combating severe acute inflammation and thrombosis associated with the cytokine storm in COVID -19 patients. The established mechanism of action of Aspirin is the inhibition of prostaglandin synthesis. Conclusion: The current emerging interest is to conduct further study to provide evidence for Aspirin as the novel therapeutic drug for combating severe acute inflammation and thrombosis associated with the cytokine storm in COVID-19 patients. The most wanted is The RECOVERY II (Randomized Evaluation of COVID-19 Therapy II) trial to be established as a randomized clinical trial to test the effectiveness of low-dose Aspirin as an anti-inflammatory and antithrombotic treatment in COVID-19 patients

INTRODUCTION
OBJECTIVES
HISTORICAL BACKGROUND
INDICATIONS FOR ASPIRIN
A NOVEL MECHANISM OF ACTION FOR ASPIRIN
PHASE ONE
PHASE TWO
ASPIRIN EFFECTIVE ROLE IN COVID-19 RELATED SIRS
ASPIRIN BENEFITS FOR THROMBOPROPHYLAXIS IN COVID-19
ASPIRIN MODULATION OF PLATELET ACTIVITY AND BIOLOGY
10. ASPIRIN MODULATION OF PLATELET ACTIVITY AND BIOLOGY
12. CONCLUSIONS AND FUTURE DIRECTIONS
Findings
13. REFERENCES
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call