5-HT/CGRP pathway and Sumatriptan role in Covid-19.
Hayder M Al-KuraishyAli I Al-GareebAthanasios AlexiouNobendu MukherjeeSadiq Mohammed J Al-HamashThabat J Al-MaiahyGaber El-Saber BatihaPublished in: Biotechnology & genetic engineering reviews (2022)
Coronavirus disease 2019 (Covid-19) is a pandemic caused by severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2). In Covid-19, there is uncontrolled activation of immune cells with a massive release of pro-inflammatory cytokines and the development of cytokine storm. These inflammatory changes induce impairment of different organ functions, including the central nervous system (CNS), leading to acute brain injury and substantial changes in the neurotransmitters, including serotonin (5-HT) and calcitonin gene-related peptide (CGRP), which have immunomodulatory properties through modulation of central and peripheral immune responses. In Covid-19, 5-HT neurotransmitters and CGRP could contribute to abnormal and atypical vascular reactivity. Sumatriptan is a pre-synaptic 5-HT (5-HT1D and 5-HT1B) agonist and inhibits the release of CGRP. Both 5-HT and CGRP seem to be augmented in Covid-19 due to underlying activation of inflammatory signaling pathways and hyperinflammation. In virtue of its anti-inflammatory and antioxidant properties with inhibition release of 5-HT and CGRP, Sumatriptan may reduce Covid-19 hyperinflammation. Therefore, Sumatriptan might be a novel potential therapeutic strategy in managing Covid-19. In conclusion, Sumatriptan could be an effective therapeutic strategy in managing Covid-19 through modulation of 5-HT neurotransmitters and inhibiting CGRP.
Keyphrases
- coronavirus disease
- sars cov
- respiratory syndrome coronavirus
- brain injury
- anti inflammatory
- immune response
- signaling pathway
- oxidative stress
- toll like receptor
- gene expression
- inflammatory response
- dna methylation
- acute respiratory distress syndrome
- cell proliferation
- epithelial mesenchymal transition
- aortic dissection
- virtual reality
- extracorporeal membrane oxygenation