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TMT-based quantitative proteomics reveals the targets of andrographolide on LPS-induced liver injury

BACKGROUND: Andrographolide (Andro) is a diterpenoid derived from Andrographis paniculate, which has anti-inflammatory, antibacterial, antiviral and hepatoprotective activities. Gram-negative bacterial infections can cause varying degrees of liver injury in chickens, although Andro has been shown to...

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Autores principales: Ge, Shihao, Lian, Wenqi, Bai, Yongjiang, Wang, Linzheng, Zhao, Fuwei, Li, Houmei, Wang, Dongliang, Pang, Quanhai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563216/
https://www.ncbi.nlm.nih.gov/pubmed/37817228
http://dx.doi.org/10.1186/s12917-023-03758-2
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author Ge, Shihao
Lian, Wenqi
Bai, Yongjiang
Wang, Linzheng
Zhao, Fuwei
Li, Houmei
Wang, Dongliang
Pang, Quanhai
author_facet Ge, Shihao
Lian, Wenqi
Bai, Yongjiang
Wang, Linzheng
Zhao, Fuwei
Li, Houmei
Wang, Dongliang
Pang, Quanhai
author_sort Ge, Shihao
collection PubMed
description BACKGROUND: Andrographolide (Andro) is a diterpenoid derived from Andrographis paniculate, which has anti-inflammatory, antibacterial, antiviral and hepatoprotective activities. Gram-negative bacterial infections can cause varying degrees of liver injury in chickens, although Andro has been shown to have a protective effect on the liver, its underlying mechanism of action and effects on liver proteins are not known. METHODS: The toxicity of Andro on the viability of leghorn male hepatoma (LMH) cells at different concentrations and times was analyzed by CCK-8 assays. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities in the culture supernatants were measured using an automatic biochemical analyzer to evaluate the protective effect of androscopolide on LPS-induced injury of LMH cells. Subsequently, TMT proteomics analysis were performed on the negative control group (NC group), LPS, and LPS-Andro groups, and bioinformatics analysis was performed on the differentially expressed proteins (DEPs). RESULTS: It was found that Andro reduced ALT and AST levels in the cell supernatant and alleviated LPS-induced injury in LMH cells. Proteomic analysis identified 50 and 166 differentially expressed proteins in the LPS vs. NC group and LPS-Andro vs. LPS group, respectively. Andro may be involved in steroid metabolic processes, negative regulation of MAPK cascade, oxidative stress, and other processes to protect against LPS-induced liver injury. CONCLUSIONS: Andro protects against LPS-induced liver injury, HMGCS1, HMGCR, FDPS, PBK, CAV1, PRDX1, PRDX4, and PRDX6, which were identified by differential proteomics, may be the targets of Andro. Our study may provide new theoretical support for Andro protection against liver injury. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-023-03758-2.
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spelling pubmed-105632162023-10-11 TMT-based quantitative proteomics reveals the targets of andrographolide on LPS-induced liver injury Ge, Shihao Lian, Wenqi Bai, Yongjiang Wang, Linzheng Zhao, Fuwei Li, Houmei Wang, Dongliang Pang, Quanhai BMC Vet Res Research BACKGROUND: Andrographolide (Andro) is a diterpenoid derived from Andrographis paniculate, which has anti-inflammatory, antibacterial, antiviral and hepatoprotective activities. Gram-negative bacterial infections can cause varying degrees of liver injury in chickens, although Andro has been shown to have a protective effect on the liver, its underlying mechanism of action and effects on liver proteins are not known. METHODS: The toxicity of Andro on the viability of leghorn male hepatoma (LMH) cells at different concentrations and times was analyzed by CCK-8 assays. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities in the culture supernatants were measured using an automatic biochemical analyzer to evaluate the protective effect of androscopolide on LPS-induced injury of LMH cells. Subsequently, TMT proteomics analysis were performed on the negative control group (NC group), LPS, and LPS-Andro groups, and bioinformatics analysis was performed on the differentially expressed proteins (DEPs). RESULTS: It was found that Andro reduced ALT and AST levels in the cell supernatant and alleviated LPS-induced injury in LMH cells. Proteomic analysis identified 50 and 166 differentially expressed proteins in the LPS vs. NC group and LPS-Andro vs. LPS group, respectively. Andro may be involved in steroid metabolic processes, negative regulation of MAPK cascade, oxidative stress, and other processes to protect against LPS-induced liver injury. CONCLUSIONS: Andro protects against LPS-induced liver injury, HMGCS1, HMGCR, FDPS, PBK, CAV1, PRDX1, PRDX4, and PRDX6, which were identified by differential proteomics, may be the targets of Andro. Our study may provide new theoretical support for Andro protection against liver injury. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12917-023-03758-2. BioMed Central 2023-10-10 /pmc/articles/PMC10563216/ /pubmed/37817228 http://dx.doi.org/10.1186/s12917-023-03758-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ge, Shihao
Lian, Wenqi
Bai, Yongjiang
Wang, Linzheng
Zhao, Fuwei
Li, Houmei
Wang, Dongliang
Pang, Quanhai
TMT-based quantitative proteomics reveals the targets of andrographolide on LPS-induced liver injury
title TMT-based quantitative proteomics reveals the targets of andrographolide on LPS-induced liver injury
title_full TMT-based quantitative proteomics reveals the targets of andrographolide on LPS-induced liver injury
title_fullStr TMT-based quantitative proteomics reveals the targets of andrographolide on LPS-induced liver injury
title_full_unstemmed TMT-based quantitative proteomics reveals the targets of andrographolide on LPS-induced liver injury
title_short TMT-based quantitative proteomics reveals the targets of andrographolide on LPS-induced liver injury
title_sort tmt-based quantitative proteomics reveals the targets of andrographolide on lps-induced liver injury
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563216/
https://www.ncbi.nlm.nih.gov/pubmed/37817228
http://dx.doi.org/10.1186/s12917-023-03758-2
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