Cargando…

Adrenomedullin protects Leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via MAPK/NF-κB signalling pathways

This study aimed to explore the possible benefits of adrenomedullin (ADM) in preventing oxidative stress and inflammation by using an in vitro primary culture model of rat Leydig cells exposed to lipopolysaccharide (LPS). Cell proliferation was detected through CCK-8 and BrdU incorporation assays. R...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Wei, Shi, Lei, Li, Ming-yong, Zhou, Pang-hu, Qiu, Bo, Yin, Ke, Zhang, Hui-hui, Gao, Yong, Kang, Ran, Qin, Song-lin, Ning, Jin-zhuo, Wang, Wei, Zhang, Li-jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705677/
https://www.ncbi.nlm.nih.gov/pubmed/29184072
http://dx.doi.org/10.1038/s41598-017-16008-x
_version_ 1783282069408841728
author Hu, Wei
Shi, Lei
Li, Ming-yong
Zhou, Pang-hu
Qiu, Bo
Yin, Ke
Zhang, Hui-hui
Gao, Yong
Kang, Ran
Qin, Song-lin
Ning, Jin-zhuo
Wang, Wei
Zhang, Li-jun
author_facet Hu, Wei
Shi, Lei
Li, Ming-yong
Zhou, Pang-hu
Qiu, Bo
Yin, Ke
Zhang, Hui-hui
Gao, Yong
Kang, Ran
Qin, Song-lin
Ning, Jin-zhuo
Wang, Wei
Zhang, Li-jun
author_sort Hu, Wei
collection PubMed
description This study aimed to explore the possible benefits of adrenomedullin (ADM) in preventing oxidative stress and inflammation by using an in vitro primary culture model of rat Leydig cells exposed to lipopolysaccharide (LPS). Cell proliferation was detected through CCK-8 and BrdU incorporation assays. ROS were determined with a DCFDA kit, and cytokine concentrations were measured with ELISA assay kits. Protein production was examined by immunohistochemical staining and Western blot, and gene expression was observed through RT-qPCR. Results revealed that ADM significantly reduced LPS-induced cytotoxicity, and pretreatment with ADM significantly suppressed ROS overproduction and decreased 4-HNE and 8-OHdG expression levels and concentrations. ADM pretreatment also significantly attenuated the overactivation of enzymatic antioxidants, namely, superoxide dismutase, catalase, thioredoxin reductase, glutathione peroxidase, glutathione reductase and glutathione-S-transferase. ADM supplementation reversed the significantly increased gene expression levels and concentrations of TNF-α, IL-1β, TGF-β1, MCP-1 and MIF. ADM pretreatment significantly inhibited the gene expression and protein production of TLR-2 and 4. Furthermore, ADM pretreatment markedly reduced the phosphorylation of JNK, ERK 1/2 and p38, phosphorylation and degradation of IκBα and nuclear translocation of p65. Our findings demonstrated that ADM protects Leydig cells from LPS-induced oxidative stress and inflammation, which might be associated with MAPK/NF-κB signalling pathways.
format Online
Article
Text
id pubmed-5705677
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-57056772017-12-05 Adrenomedullin protects Leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via MAPK/NF-κB signalling pathways Hu, Wei Shi, Lei Li, Ming-yong Zhou, Pang-hu Qiu, Bo Yin, Ke Zhang, Hui-hui Gao, Yong Kang, Ran Qin, Song-lin Ning, Jin-zhuo Wang, Wei Zhang, Li-jun Sci Rep Article This study aimed to explore the possible benefits of adrenomedullin (ADM) in preventing oxidative stress and inflammation by using an in vitro primary culture model of rat Leydig cells exposed to lipopolysaccharide (LPS). Cell proliferation was detected through CCK-8 and BrdU incorporation assays. ROS were determined with a DCFDA kit, and cytokine concentrations were measured with ELISA assay kits. Protein production was examined by immunohistochemical staining and Western blot, and gene expression was observed through RT-qPCR. Results revealed that ADM significantly reduced LPS-induced cytotoxicity, and pretreatment with ADM significantly suppressed ROS overproduction and decreased 4-HNE and 8-OHdG expression levels and concentrations. ADM pretreatment also significantly attenuated the overactivation of enzymatic antioxidants, namely, superoxide dismutase, catalase, thioredoxin reductase, glutathione peroxidase, glutathione reductase and glutathione-S-transferase. ADM supplementation reversed the significantly increased gene expression levels and concentrations of TNF-α, IL-1β, TGF-β1, MCP-1 and MIF. ADM pretreatment significantly inhibited the gene expression and protein production of TLR-2 and 4. Furthermore, ADM pretreatment markedly reduced the phosphorylation of JNK, ERK 1/2 and p38, phosphorylation and degradation of IκBα and nuclear translocation of p65. Our findings demonstrated that ADM protects Leydig cells from LPS-induced oxidative stress and inflammation, which might be associated with MAPK/NF-κB signalling pathways. Nature Publishing Group UK 2017-11-28 /pmc/articles/PMC5705677/ /pubmed/29184072 http://dx.doi.org/10.1038/s41598-017-16008-x Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hu, Wei
Shi, Lei
Li, Ming-yong
Zhou, Pang-hu
Qiu, Bo
Yin, Ke
Zhang, Hui-hui
Gao, Yong
Kang, Ran
Qin, Song-lin
Ning, Jin-zhuo
Wang, Wei
Zhang, Li-jun
Adrenomedullin protects Leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via MAPK/NF-κB signalling pathways
title Adrenomedullin protects Leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via MAPK/NF-κB signalling pathways
title_full Adrenomedullin protects Leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via MAPK/NF-κB signalling pathways
title_fullStr Adrenomedullin protects Leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via MAPK/NF-κB signalling pathways
title_full_unstemmed Adrenomedullin protects Leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via MAPK/NF-κB signalling pathways
title_short Adrenomedullin protects Leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via MAPK/NF-κB signalling pathways
title_sort adrenomedullin protects leydig cells against lipopolysaccharide-induced oxidative stress and inflammatory reaction via mapk/nf-κb signalling pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705677/
https://www.ncbi.nlm.nih.gov/pubmed/29184072
http://dx.doi.org/10.1038/s41598-017-16008-x
work_keys_str_mv AT huwei adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT shilei adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT limingyong adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT zhoupanghu adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT qiubo adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT yinke adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT zhanghuihui adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT gaoyong adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT kangran adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT qinsonglin adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT ningjinzhuo adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT wangwei adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways
AT zhanglijun adrenomedullinprotectsleydigcellsagainstlipopolysaccharideinducedoxidativestressandinflammatoryreactionviamapknfkbsignallingpathways