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Osthole protects sepsis-induced acute kidney injury via down-regulating NF-κB signal pathway

BACKGROUND AND PURPOSE: As a natural coumarin derivative from the Cnidium monnieri(L)Cusson fruit, osthole consists of 7-methoxy-8-isopentenoxy-coumarin. The purpose of this research is to study the mechanism and effect of osthole on sepsis-induced acute kidney injury. EXPERIMENTAL APPROACH: The pro...

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Autores principales: Yu, Chen, Li, Peng, Qi, Dong, Wang, Lei, Qu, Hong-lin, Zhang, Yue-juan, Wang, Xue-kai, Fan, Hua-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354872/
https://www.ncbi.nlm.nih.gov/pubmed/27902475
http://dx.doi.org/10.18632/oncotarget.13592
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author Yu, Chen
Li, Peng
Qi, Dong
Wang, Lei
Qu, Hong-lin
Zhang, Yue-juan
Wang, Xue-kai
Fan, Hua-Ying
author_facet Yu, Chen
Li, Peng
Qi, Dong
Wang, Lei
Qu, Hong-lin
Zhang, Yue-juan
Wang, Xue-kai
Fan, Hua-Ying
author_sort Yu, Chen
collection PubMed
description BACKGROUND AND PURPOSE: As a natural coumarin derivative from the Cnidium monnieri(L)Cusson fruit, osthole consists of 7-methoxy-8-isopentenoxy-coumarin. The purpose of this research is to study the mechanism and effect of osthole on sepsis-induced acute kidney injury. EXPERIMENTAL APPROACH: The protective effect of osthole on mouse macrophage RAW 264.7 and HK-2 cells induced by LPS in vitro and on acute kidney injury model induced by sepsis and established by puncture and cecal ligation (CLP) in vivo were tested. KEY RESULTS: Osthole (20, 40 mg·kg(−1)) group can greatly attenuate the changes of the score and kidney histopathology damage and enhance the survival time of septic mice. After the CLP surgery, degrees of SCr and BUN related to kidney injury were upregulated. The concentrations of SCr and BUN can be greatly reduced by treatment with osthole. Furthermore, osthole could increase bacterial killing activity and phagocytic activities of macrophages impaired after CLP partly and attenuate blood bacterial counts and leukocyte infiltration markedly. Furthermore, osthole can suppress NF-κB signal pathway through the inhibition of the nuclear translocation by regulating phosphorylation of IκBα and IKKβ and hinder the production of chemoattractant (MCP-1 and IL-8) and proinflammatory cytokines (TNF-α, IL-1β and IL-6). CONCLUSION AND IMPLICATIONS: Mainly because of its immunomodulatory properties and anti-inflammatory activity, which might be closely associated with suppression of the stimulation of the NF-κB signal pathway, osthole has protective effect on sepsis-induced kidney injury. It can be seen from such evidence that osthole can be potentially applied in the treatment of acute kidney injury.
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spelling pubmed-53548722017-04-24 Osthole protects sepsis-induced acute kidney injury via down-regulating NF-κB signal pathway Yu, Chen Li, Peng Qi, Dong Wang, Lei Qu, Hong-lin Zhang, Yue-juan Wang, Xue-kai Fan, Hua-Ying Oncotarget Research Paper BACKGROUND AND PURPOSE: As a natural coumarin derivative from the Cnidium monnieri(L)Cusson fruit, osthole consists of 7-methoxy-8-isopentenoxy-coumarin. The purpose of this research is to study the mechanism and effect of osthole on sepsis-induced acute kidney injury. EXPERIMENTAL APPROACH: The protective effect of osthole on mouse macrophage RAW 264.7 and HK-2 cells induced by LPS in vitro and on acute kidney injury model induced by sepsis and established by puncture and cecal ligation (CLP) in vivo were tested. KEY RESULTS: Osthole (20, 40 mg·kg(−1)) group can greatly attenuate the changes of the score and kidney histopathology damage and enhance the survival time of septic mice. After the CLP surgery, degrees of SCr and BUN related to kidney injury were upregulated. The concentrations of SCr and BUN can be greatly reduced by treatment with osthole. Furthermore, osthole could increase bacterial killing activity and phagocytic activities of macrophages impaired after CLP partly and attenuate blood bacterial counts and leukocyte infiltration markedly. Furthermore, osthole can suppress NF-κB signal pathway through the inhibition of the nuclear translocation by regulating phosphorylation of IκBα and IKKβ and hinder the production of chemoattractant (MCP-1 and IL-8) and proinflammatory cytokines (TNF-α, IL-1β and IL-6). CONCLUSION AND IMPLICATIONS: Mainly because of its immunomodulatory properties and anti-inflammatory activity, which might be closely associated with suppression of the stimulation of the NF-κB signal pathway, osthole has protective effect on sepsis-induced kidney injury. It can be seen from such evidence that osthole can be potentially applied in the treatment of acute kidney injury. Impact Journals LLC 2016-11-25 /pmc/articles/PMC5354872/ /pubmed/27902475 http://dx.doi.org/10.18632/oncotarget.13592 Text en Copyright: © 2017 Yu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Yu, Chen
Li, Peng
Qi, Dong
Wang, Lei
Qu, Hong-lin
Zhang, Yue-juan
Wang, Xue-kai
Fan, Hua-Ying
Osthole protects sepsis-induced acute kidney injury via down-regulating NF-κB signal pathway
title Osthole protects sepsis-induced acute kidney injury via down-regulating NF-κB signal pathway
title_full Osthole protects sepsis-induced acute kidney injury via down-regulating NF-κB signal pathway
title_fullStr Osthole protects sepsis-induced acute kidney injury via down-regulating NF-κB signal pathway
title_full_unstemmed Osthole protects sepsis-induced acute kidney injury via down-regulating NF-κB signal pathway
title_short Osthole protects sepsis-induced acute kidney injury via down-regulating NF-κB signal pathway
title_sort osthole protects sepsis-induced acute kidney injury via down-regulating nf-κb signal pathway
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5354872/
https://www.ncbi.nlm.nih.gov/pubmed/27902475
http://dx.doi.org/10.18632/oncotarget.13592
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