Cargando…
Selenadiazole Inhibited Adenovirus-Induced Apoptosis through the Oxidative-Damage-Mediated Bcl-2/Stat 3/NF-κB Signaling Pathway
Human adenovirus type 7 (HAdV7) infection causes severe pneumonia, yet there are still no breakthroughs in treatment options for adenovirus, and the road to antiviral drug development faces major challenges. We attempted to find new drugs and we stumbled upon one: selenadiazole. Selenadiazole has be...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610542/ https://www.ncbi.nlm.nih.gov/pubmed/37895944 http://dx.doi.org/10.3390/ph16101474 |
_version_ | 1785128280187207680 |
---|---|
author | Liu, Xia Lai, Jia Su, Jingyao Zhang, Kelan Li, Jiali Li, Chuqing Ning, Zhihui Wang, Chenyang Zhu, Bing Li, Yinghua Zhao, Mingqi |
author_facet | Liu, Xia Lai, Jia Su, Jingyao Zhang, Kelan Li, Jiali Li, Chuqing Ning, Zhihui Wang, Chenyang Zhu, Bing Li, Yinghua Zhao, Mingqi |
author_sort | Liu, Xia |
collection | PubMed |
description | Human adenovirus type 7 (HAdV7) infection causes severe pneumonia, yet there are still no breakthroughs in treatment options for adenovirus, and the road to antiviral drug development faces major challenges. We attempted to find new drugs and we stumbled upon one: selenadiazole. Selenadiazole has been shown to have significant anti-tumor effects due to its unique chemical structure and drug activity. However, its effectiveness against viruses has not been evaluated yet. In our study, selenadiazole also showed superior antiviral activity. In vitro experiments, selenadiazole was able to inhibit adenovirus-mediated mitochondrial-oxidative-damage-related apoptosis, and in in vivo experiments, selenadiazole was able to inhibit apoptosis by modulating the apoptotic signaling pathway Bcl-2/Stat3/NF-κB, etc., and was able to largely attenuate adenovirus-infection-induced pneumonia and lung injury in mice. This study aims to describe a new antiviral treatment option from the perspective of anti-adenovirus-mediated oxidative stress and its associated apoptosis and to provide theoretical guidance for the treatment of clinical adenovirus infection to a certain extent. |
format | Online Article Text |
id | pubmed-10610542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106105422023-10-28 Selenadiazole Inhibited Adenovirus-Induced Apoptosis through the Oxidative-Damage-Mediated Bcl-2/Stat 3/NF-κB Signaling Pathway Liu, Xia Lai, Jia Su, Jingyao Zhang, Kelan Li, Jiali Li, Chuqing Ning, Zhihui Wang, Chenyang Zhu, Bing Li, Yinghua Zhao, Mingqi Pharmaceuticals (Basel) Article Human adenovirus type 7 (HAdV7) infection causes severe pneumonia, yet there are still no breakthroughs in treatment options for adenovirus, and the road to antiviral drug development faces major challenges. We attempted to find new drugs and we stumbled upon one: selenadiazole. Selenadiazole has been shown to have significant anti-tumor effects due to its unique chemical structure and drug activity. However, its effectiveness against viruses has not been evaluated yet. In our study, selenadiazole also showed superior antiviral activity. In vitro experiments, selenadiazole was able to inhibit adenovirus-mediated mitochondrial-oxidative-damage-related apoptosis, and in in vivo experiments, selenadiazole was able to inhibit apoptosis by modulating the apoptotic signaling pathway Bcl-2/Stat3/NF-κB, etc., and was able to largely attenuate adenovirus-infection-induced pneumonia and lung injury in mice. This study aims to describe a new antiviral treatment option from the perspective of anti-adenovirus-mediated oxidative stress and its associated apoptosis and to provide theoretical guidance for the treatment of clinical adenovirus infection to a certain extent. MDPI 2023-10-16 /pmc/articles/PMC10610542/ /pubmed/37895944 http://dx.doi.org/10.3390/ph16101474 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liu, Xia Lai, Jia Su, Jingyao Zhang, Kelan Li, Jiali Li, Chuqing Ning, Zhihui Wang, Chenyang Zhu, Bing Li, Yinghua Zhao, Mingqi Selenadiazole Inhibited Adenovirus-Induced Apoptosis through the Oxidative-Damage-Mediated Bcl-2/Stat 3/NF-κB Signaling Pathway |
title | Selenadiazole Inhibited Adenovirus-Induced Apoptosis through the Oxidative-Damage-Mediated Bcl-2/Stat 3/NF-κB Signaling Pathway |
title_full | Selenadiazole Inhibited Adenovirus-Induced Apoptosis through the Oxidative-Damage-Mediated Bcl-2/Stat 3/NF-κB Signaling Pathway |
title_fullStr | Selenadiazole Inhibited Adenovirus-Induced Apoptosis through the Oxidative-Damage-Mediated Bcl-2/Stat 3/NF-κB Signaling Pathway |
title_full_unstemmed | Selenadiazole Inhibited Adenovirus-Induced Apoptosis through the Oxidative-Damage-Mediated Bcl-2/Stat 3/NF-κB Signaling Pathway |
title_short | Selenadiazole Inhibited Adenovirus-Induced Apoptosis through the Oxidative-Damage-Mediated Bcl-2/Stat 3/NF-κB Signaling Pathway |
title_sort | selenadiazole inhibited adenovirus-induced apoptosis through the oxidative-damage-mediated bcl-2/stat 3/nf-κb signaling pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10610542/ https://www.ncbi.nlm.nih.gov/pubmed/37895944 http://dx.doi.org/10.3390/ph16101474 |
work_keys_str_mv | AT liuxia selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT laijia selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT sujingyao selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT zhangkelan selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT lijiali selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT lichuqing selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT ningzhihui selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT wangchenyang selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT zhubing selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT liyinghua selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway AT zhaomingqi selenadiazoleinhibitedadenovirusinducedapoptosisthroughtheoxidativedamagemediatedbcl2stat3nfkbsignalingpathway |