TY - JOUR
T1 - How could perfluorocarbon affect cytokine storm and angiogenesis in coronavirus disease 2019 (COVID-19): role of hypoxia-inducible factor 1 alpha
T2 - role of hypoxia-inducible factor 1α
AU - Moasefi, Narges
AU - Fouladi, Mehdi
AU - Norooznezhad, Amir Hossein
AU - Yarani, Reza
AU - Rahmani, Adibeh
AU - Mansouri, Kamran
N1 - © 2021. The Author(s), under exclusive licence to Springer Nature Switzerland AG.
PY - 2021/7
Y1 - 2021/7
N2 - Coronavirus disease 2019 (COVID-19) pandemic is still a world-class challenge. Inflammation, especially its severe form with excess release of pro-inflammatory cytokines (cytokine storm) which is a life-threatening condition, is among the most important suspects involved in COVID-19 pathogenesis. It has been shown that cytokine storm could cause notable morbidities such as acute respiratory distress syndrome (ARDS) which leads to hypoxia which is significantly associated with mortality of patients with COVID-19. Hypoxia-inducible factor 1α (HIF-1α) which activates following ARDS-induced hypoxia plays a crucial role in pathogenesis of cytokine storm. The expression of tumor necrosis factor α (TNF-α), interleukin 1 β (IL-1β), and IL-6 which are key elements of cytokine storm are by nuclear factor κβ (NFκB). Interestingly, during the hypoxia, HIF-1α activates NFκB to induce expression of pro-angiogenic and pro-inflammatory factors. These released factors starts a autocrine/paracrine loop and causes deterioration of their etiological pathways of expression: cytokine storm and ARDS. To sum up, it seems HIF-1α is an important target to hit to ameliorate the mentioned pathways. Herein, we suggest perfluorocarbons (PFCs) which are among the organofluorine compounds as a possible co-treatment to reduce hypoxemia and then hypoxia. These substances are known for their high gas solving potential that make them able to be used as a synthetic artificial blood product. Due to the potential of PFCs to affect the fountain of important physiopathological pathway such as inflammation a hypoxia through affecting NFκB, they could be considered as multi-target co-treatment for ARD individuals with COVID-19. It is highly suggested to evaluate this hypothesis in following researches.
AB - Coronavirus disease 2019 (COVID-19) pandemic is still a world-class challenge. Inflammation, especially its severe form with excess release of pro-inflammatory cytokines (cytokine storm) which is a life-threatening condition, is among the most important suspects involved in COVID-19 pathogenesis. It has been shown that cytokine storm could cause notable morbidities such as acute respiratory distress syndrome (ARDS) which leads to hypoxia which is significantly associated with mortality of patients with COVID-19. Hypoxia-inducible factor 1α (HIF-1α) which activates following ARDS-induced hypoxia plays a crucial role in pathogenesis of cytokine storm. The expression of tumor necrosis factor α (TNF-α), interleukin 1 β (IL-1β), and IL-6 which are key elements of cytokine storm are by nuclear factor κβ (NFκB). Interestingly, during the hypoxia, HIF-1α activates NFκB to induce expression of pro-angiogenic and pro-inflammatory factors. These released factors starts a autocrine/paracrine loop and causes deterioration of their etiological pathways of expression: cytokine storm and ARDS. To sum up, it seems HIF-1α is an important target to hit to ameliorate the mentioned pathways. Herein, we suggest perfluorocarbons (PFCs) which are among the organofluorine compounds as a possible co-treatment to reduce hypoxemia and then hypoxia. These substances are known for their high gas solving potential that make them able to be used as a synthetic artificial blood product. Due to the potential of PFCs to affect the fountain of important physiopathological pathway such as inflammation a hypoxia through affecting NFκB, they could be considered as multi-target co-treatment for ARD individuals with COVID-19. It is highly suggested to evaluate this hypothesis in following researches.
KW - Animals
KW - COVID-19/drug therapy
KW - Cytokine Release Syndrome/drug therapy
KW - Cytokines/biosynthesis
KW - Fluorocarbons/therapeutic use
KW - Humans
KW - Hypoxia-Inducible Factor 1, alpha Subunit/metabolism
KW - Hypoxia/drug therapy
KW - NF-kappa B/drug effects
KW - Neovascularization, Pathologic/drug therapy
KW - Protective Agents/therapeutic use
KW - Respiratory Distress Syndrome/drug therapy
UR - http://www.scopus.com/inward/record.url?scp=85108791018&partnerID=8YFLogxK
U2 - 10.1007/s00011-021-01469-8
DO - 10.1007/s00011-021-01469-8
M3 - Comment/debate
C2 - 34173853
SN - 1023-3830
VL - 70
SP - 749
EP - 752
JO - Inflammation research : official journal of the European Histamine Research Society ... [et al.]
JF - Inflammation research : official journal of the European Histamine Research Society ... [et al.]
IS - 7
ER -