tetano
Editor, Senior Moderator
Int Immunopharmacol
. 2023 Jan 11;115:109706.
doi: 10.1016/j.intimp.2023.109706. Online ahead of print.
Lidocaine inhibits influenza a virus replication by up-regulating IFNα4 via TBK1-IRF7 and JNK-AP1 signaling pathways
Xueer Liu[SUP] 1 [/SUP], Fengqing Zheng[SUP] 1 [/SUP], Lu Tian[SUP] 1 [/SUP], Tian Li[SUP] 1 [/SUP], Zelin Zhang[SUP] 1 [/SUP], Zhihui Ren[SUP] 1 [/SUP], Xiaoxuan Chen[SUP] 1 [/SUP], Weiqiang Chen[SUP] 2 [/SUP], Kangsheng Li[SUP] 3 [/SUP], Jiangtao Sheng[SUP] 4 [/SUP]
Affiliations
Abstract
Influenza A viruses (IAV), significant respiratory pathogenic agents, cause seasonal epidemics and global pandemics in intra- and interannual cycles. Despite effective therapies targeting viral proteins, the continuous generation of drug-resistant IAV strains is challenging. Therefore, exploring novel host-specific antiviral treatment strategies is urgently needed. Here, we found that lidocaine, widely used for local anesthesia and sedation, significantly inhibited H1N1(PR8) replication in macrophages. Interestingly, its antiviral effect did not depend on the inhibition of voltage-gated sodium channels (VGSC), the main target of lidocaine for anesthesia. Lidocaine significantly upregulated early IFN-I, interferon α4 (IFNα4) mRNA, and protein levels, but not those of early IFNβ in mouse RAW 264.7 cell line and human THP-1 derived macrophages. Knocking out IFNα4 by CRISPR-Cas9 partly reversed lidocaine's inhibition of PR8 replication in macrophages. Mechanistically, lidocaine upregulated IFNα4 by activating TANK-binding kinase 1 (TBK1)-IRF7 and JNK-AP1 signaling pathways. These findings indicate that lidocaine has an incredible antiviral potential by enhancing IFN-I signaling in macrophages. In conclusion, our results indicate the potential auxiliary role of lidocaine for anti-influenza A virus therapy and even for anti-SARS-CoV-2 virus therapy, especially in the absence of a specific medicine.
Keywords: Antiviral drugs; Influenza A viruses; JNK-AP1; Lidocaine; TBK1-IRF7; Type I interferon.
. 2023 Jan 11;115:109706.
doi: 10.1016/j.intimp.2023.109706. Online ahead of print.
Lidocaine inhibits influenza a virus replication by up-regulating IFNα4 via TBK1-IRF7 and JNK-AP1 signaling pathways
Xueer Liu[SUP] 1 [/SUP], Fengqing Zheng[SUP] 1 [/SUP], Lu Tian[SUP] 1 [/SUP], Tian Li[SUP] 1 [/SUP], Zelin Zhang[SUP] 1 [/SUP], Zhihui Ren[SUP] 1 [/SUP], Xiaoxuan Chen[SUP] 1 [/SUP], Weiqiang Chen[SUP] 2 [/SUP], Kangsheng Li[SUP] 3 [/SUP], Jiangtao Sheng[SUP] 4 [/SUP]
Affiliations
- PMID: 36638664
- DOI: 10.1016/j.intimp.2023.109706
Abstract
Influenza A viruses (IAV), significant respiratory pathogenic agents, cause seasonal epidemics and global pandemics in intra- and interannual cycles. Despite effective therapies targeting viral proteins, the continuous generation of drug-resistant IAV strains is challenging. Therefore, exploring novel host-specific antiviral treatment strategies is urgently needed. Here, we found that lidocaine, widely used for local anesthesia and sedation, significantly inhibited H1N1(PR8) replication in macrophages. Interestingly, its antiviral effect did not depend on the inhibition of voltage-gated sodium channels (VGSC), the main target of lidocaine for anesthesia. Lidocaine significantly upregulated early IFN-I, interferon α4 (IFNα4) mRNA, and protein levels, but not those of early IFNβ in mouse RAW 264.7 cell line and human THP-1 derived macrophages. Knocking out IFNα4 by CRISPR-Cas9 partly reversed lidocaine's inhibition of PR8 replication in macrophages. Mechanistically, lidocaine upregulated IFNα4 by activating TANK-binding kinase 1 (TBK1)-IRF7 and JNK-AP1 signaling pathways. These findings indicate that lidocaine has an incredible antiviral potential by enhancing IFN-I signaling in macrophages. In conclusion, our results indicate the potential auxiliary role of lidocaine for anti-influenza A virus therapy and even for anti-SARS-CoV-2 virus therapy, especially in the absence of a specific medicine.
Keywords: Antiviral drugs; Influenza A viruses; JNK-AP1; Lidocaine; TBK1-IRF7; Type I interferon.