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Regulatory effect of Panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2

Porcine circovirus type 2 (PCV2) exists widely in swine populations worldwide, and healthy PCV2 virus carriers have enhanced the severity of the infection, which is becoming more difficult to control. This study investigated the regulatory effect of Panax notoginseng saponins (PNS) on the oxidative...

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Autores principales: CAO, Mi-Xia, WANG, Xin-Rui, HU, Wen-Yue, YIN, Dan, REN, Chun-Zhi, CHEN, Si-Yu, YU, Mei-Ling, WEI, Ying-Yi, HU, Ting-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096040/
https://www.ncbi.nlm.nih.gov/pubmed/35125373
http://dx.doi.org/10.1292/jvms.21-0126
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author CAO, Mi-Xia
WANG, Xin-Rui
HU, Wen-Yue
YIN, Dan
REN, Chun-Zhi
CHEN, Si-Yu
YU, Mei-Ling
WEI, Ying-Yi
HU, Ting-Jun
author_facet CAO, Mi-Xia
WANG, Xin-Rui
HU, Wen-Yue
YIN, Dan
REN, Chun-Zhi
CHEN, Si-Yu
YU, Mei-Ling
WEI, Ying-Yi
HU, Ting-Jun
author_sort CAO, Mi-Xia
collection PubMed
description Porcine circovirus type 2 (PCV2) exists widely in swine populations worldwide, and healthy PCV2 virus carriers have enhanced the severity of the infection, which is becoming more difficult to control. This study investigated the regulatory effect of Panax notoginseng saponins (PNS) on the oxidative stress and histone acetylation modification induced by PCV2 in vitro and in mice. In vitro, PNS significantly increased the scavenging capacities of superoxide anion radicals (O(2)(•-)) and hydroxyl radicals ((•)OH) and reduced the content of hydrogen peroxide (H(2)O(2)) induced by PCV2 in porcine alveolar macrophages (3D4/2). In addition, PNS decreased the protein expression level of histone H4 acetylation (Ac-H4) by increasing the activity of histone deacetylase (HDAC) in PCV2-infected 3D4/2 cells. In vivo, PNS enhanced the scavenging capacities of (•)OH and O(2)(•−) and reduced the content of H(2)O(2) in the spleens of PCV2-infected mice. PNS also reduced the protein expression level of histone H3 acetylation (Ac-H3) by reducing the activity of histone acetylase (HAT) and increasing the activity of HDAC in the spleens of PCV2-infected mice. PCV2 infection activated oxidative stress and histone acetylation in vitro and in mice, but PNS ameliorated this oxidative stress. The research can provide experimental basis for exploring the antioxidant effect and the regulation of histone acetylation of PNS on PCV2-infected 3D4/2 cells and mice in vitro and in vivo, and provide new ideas for the treatment of PCV2 infection.
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spelling pubmed-90960402022-05-18 Regulatory effect of Panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2 CAO, Mi-Xia WANG, Xin-Rui HU, Wen-Yue YIN, Dan REN, Chun-Zhi CHEN, Si-Yu YU, Mei-Ling WEI, Ying-Yi HU, Ting-Jun J Vet Med Sci Pharmacology Porcine circovirus type 2 (PCV2) exists widely in swine populations worldwide, and healthy PCV2 virus carriers have enhanced the severity of the infection, which is becoming more difficult to control. This study investigated the regulatory effect of Panax notoginseng saponins (PNS) on the oxidative stress and histone acetylation modification induced by PCV2 in vitro and in mice. In vitro, PNS significantly increased the scavenging capacities of superoxide anion radicals (O(2)(•-)) and hydroxyl radicals ((•)OH) and reduced the content of hydrogen peroxide (H(2)O(2)) induced by PCV2 in porcine alveolar macrophages (3D4/2). In addition, PNS decreased the protein expression level of histone H4 acetylation (Ac-H4) by increasing the activity of histone deacetylase (HDAC) in PCV2-infected 3D4/2 cells. In vivo, PNS enhanced the scavenging capacities of (•)OH and O(2)(•−) and reduced the content of H(2)O(2) in the spleens of PCV2-infected mice. PNS also reduced the protein expression level of histone H3 acetylation (Ac-H3) by reducing the activity of histone acetylase (HAT) and increasing the activity of HDAC in the spleens of PCV2-infected mice. PCV2 infection activated oxidative stress and histone acetylation in vitro and in mice, but PNS ameliorated this oxidative stress. The research can provide experimental basis for exploring the antioxidant effect and the regulation of histone acetylation of PNS on PCV2-infected 3D4/2 cells and mice in vitro and in vivo, and provide new ideas for the treatment of PCV2 infection. The Japanese Society of Veterinary Science 2022-02-07 2022-04 /pmc/articles/PMC9096040/ /pubmed/35125373 http://dx.doi.org/10.1292/jvms.21-0126 Text en ©2022 The Japanese Society of Veterinary Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Pharmacology
CAO, Mi-Xia
WANG, Xin-Rui
HU, Wen-Yue
YIN, Dan
REN, Chun-Zhi
CHEN, Si-Yu
YU, Mei-Ling
WEI, Ying-Yi
HU, Ting-Jun
Regulatory effect of Panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2
title Regulatory effect of Panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2
title_full Regulatory effect of Panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2
title_fullStr Regulatory effect of Panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2
title_full_unstemmed Regulatory effect of Panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2
title_short Regulatory effect of Panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2
title_sort regulatory effect of panax notoginseng saponins on the oxidative stress and histone acetylation induced by porcine circovirus type 2
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096040/
https://www.ncbi.nlm.nih.gov/pubmed/35125373
http://dx.doi.org/10.1292/jvms.21-0126
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