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D-Limonene Is a Potential Monoterpene to Inhibit PI3K/Akt/IKK-α/NF-κB p65 Signaling Pathway in Coronavirus Disease 2019 Pulmonary Fibrosis

At the time of the prevalence of coronavirus disease 2019 (COVID-19), pulmonary fibrosis (PF) related to COVID-19 has become the main sequela. However, the mechanism of PF related to COVID (COVID-PF) is unknown. This study aimed to explore the key targets in the development of COVID-PF and the mecha...

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Autores principales: Yang, Fan, Chen, Ru, Li, Wan-yang, Zhu, Hao-yue, Chen, Xiao-xuan, Hou, Zhen-feng, Cao, Ren-shuang, Zang, GuoDong, Li, Yu-xuan, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985179/
https://www.ncbi.nlm.nih.gov/pubmed/33768100
http://dx.doi.org/10.3389/fmed.2021.591830
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author Yang, Fan
Chen, Ru
Li, Wan-yang
Zhu, Hao-yue
Chen, Xiao-xuan
Hou, Zhen-feng
Cao, Ren-shuang
Zang, GuoDong
Li, Yu-xuan
Zhang, Wei
author_facet Yang, Fan
Chen, Ru
Li, Wan-yang
Zhu, Hao-yue
Chen, Xiao-xuan
Hou, Zhen-feng
Cao, Ren-shuang
Zang, GuoDong
Li, Yu-xuan
Zhang, Wei
author_sort Yang, Fan
collection PubMed
description At the time of the prevalence of coronavirus disease 2019 (COVID-19), pulmonary fibrosis (PF) related to COVID-19 has become the main sequela. However, the mechanism of PF related to COVID (COVID-PF) is unknown. This study aimed to explore the key targets in the development of COVID-PF and the mechanism of d-limonene in the COVID-PF treatment. The differentially expressed genes of COVID-PF were downloaded from the GeneCards database, and their pathways were analyzed. d-Limonene was molecularly docked with related proteins to screen its pharmacological targets, and a rat lung fibrosis model was established to verify d-limonene's effect on COVID-PF-related targets. The results showed that the imbalance between collagen breakdown and metabolism, inflammatory response, and angiogenesis are the core processes of COVID-PF; and PI3K/AKT signaling pathways are the key targets of the treatment of COVID-PF. The ability of d-limonene to protect against PF induced by bleomycin in rats was reported. The mechanism is related to the binding of PI3K and NF-κB p65, and the inhibition of PI3K/Akt/IKK-α/NF-κB p65 signaling pathway expression and phosphorylation. These results confirmed the relationship between the PI3K–Akt signaling pathway and COVID-PF, showing that d-limonene has a potential therapeutic value for COVID-PF.
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spelling pubmed-79851792021-03-24 D-Limonene Is a Potential Monoterpene to Inhibit PI3K/Akt/IKK-α/NF-κB p65 Signaling Pathway in Coronavirus Disease 2019 Pulmonary Fibrosis Yang, Fan Chen, Ru Li, Wan-yang Zhu, Hao-yue Chen, Xiao-xuan Hou, Zhen-feng Cao, Ren-shuang Zang, GuoDong Li, Yu-xuan Zhang, Wei Front Med (Lausanne) Medicine At the time of the prevalence of coronavirus disease 2019 (COVID-19), pulmonary fibrosis (PF) related to COVID-19 has become the main sequela. However, the mechanism of PF related to COVID (COVID-PF) is unknown. This study aimed to explore the key targets in the development of COVID-PF and the mechanism of d-limonene in the COVID-PF treatment. The differentially expressed genes of COVID-PF were downloaded from the GeneCards database, and their pathways were analyzed. d-Limonene was molecularly docked with related proteins to screen its pharmacological targets, and a rat lung fibrosis model was established to verify d-limonene's effect on COVID-PF-related targets. The results showed that the imbalance between collagen breakdown and metabolism, inflammatory response, and angiogenesis are the core processes of COVID-PF; and PI3K/AKT signaling pathways are the key targets of the treatment of COVID-PF. The ability of d-limonene to protect against PF induced by bleomycin in rats was reported. The mechanism is related to the binding of PI3K and NF-κB p65, and the inhibition of PI3K/Akt/IKK-α/NF-κB p65 signaling pathway expression and phosphorylation. These results confirmed the relationship between the PI3K–Akt signaling pathway and COVID-PF, showing that d-limonene has a potential therapeutic value for COVID-PF. Frontiers Media S.A. 2021-03-09 /pmc/articles/PMC7985179/ /pubmed/33768100 http://dx.doi.org/10.3389/fmed.2021.591830 Text en Copyright © 2021 Yang, Chen, Li, Zhu, Chen, Hou, Cao, Zang, Li and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Yang, Fan
Chen, Ru
Li, Wan-yang
Zhu, Hao-yue
Chen, Xiao-xuan
Hou, Zhen-feng
Cao, Ren-shuang
Zang, GuoDong
Li, Yu-xuan
Zhang, Wei
D-Limonene Is a Potential Monoterpene to Inhibit PI3K/Akt/IKK-α/NF-κB p65 Signaling Pathway in Coronavirus Disease 2019 Pulmonary Fibrosis
title D-Limonene Is a Potential Monoterpene to Inhibit PI3K/Akt/IKK-α/NF-κB p65 Signaling Pathway in Coronavirus Disease 2019 Pulmonary Fibrosis
title_full D-Limonene Is a Potential Monoterpene to Inhibit PI3K/Akt/IKK-α/NF-κB p65 Signaling Pathway in Coronavirus Disease 2019 Pulmonary Fibrosis
title_fullStr D-Limonene Is a Potential Monoterpene to Inhibit PI3K/Akt/IKK-α/NF-κB p65 Signaling Pathway in Coronavirus Disease 2019 Pulmonary Fibrosis
title_full_unstemmed D-Limonene Is a Potential Monoterpene to Inhibit PI3K/Akt/IKK-α/NF-κB p65 Signaling Pathway in Coronavirus Disease 2019 Pulmonary Fibrosis
title_short D-Limonene Is a Potential Monoterpene to Inhibit PI3K/Akt/IKK-α/NF-κB p65 Signaling Pathway in Coronavirus Disease 2019 Pulmonary Fibrosis
title_sort d-limonene is a potential monoterpene to inhibit pi3k/akt/ikk-α/nf-κb p65 signaling pathway in coronavirus disease 2019 pulmonary fibrosis
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985179/
https://www.ncbi.nlm.nih.gov/pubmed/33768100
http://dx.doi.org/10.3389/fmed.2021.591830
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