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Naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress

BACKGROUND: Naja naja atra venom (NNAV) displays diverse pharmacological actions including analgesia, anti-inflammation and immune regulation. In this study, we investigated the effects of NNAV on pulmonary fibrosis and its mechanisms of action. METHODS: To determine if Naja naja atra venom (NNAV) c...

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Autores principales: Cui, Kui, Kou, Jian-Qun, Gu, Jin-Hua, Han, Rong, Wang, Guanghui, Zhen, Xuechu, Qin, Zheng-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258260/
https://www.ncbi.nlm.nih.gov/pubmed/25465226
http://dx.doi.org/10.1186/1472-6882-14-461
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author Cui, Kui
Kou, Jian-Qun
Gu, Jin-Hua
Han, Rong
Wang, Guanghui
Zhen, Xuechu
Qin, Zheng-Hong
author_facet Cui, Kui
Kou, Jian-Qun
Gu, Jin-Hua
Han, Rong
Wang, Guanghui
Zhen, Xuechu
Qin, Zheng-Hong
author_sort Cui, Kui
collection PubMed
description BACKGROUND: Naja naja atra venom (NNAV) displays diverse pharmacological actions including analgesia, anti-inflammation and immune regulation. In this study, we investigated the effects of NNAV on pulmonary fibrosis and its mechanisms of action. METHODS: To determine if Naja naja atra venom (NNAV) can produce beneficial effects on pulmonary fibrosis, two marine models of pulmonary fibrosis were produced with bleomycin (BLM) and lipopolysaccharide (LPS). NNAV (30, 90, 270 μg/kg) was orally administered once a day started five days before BLM and LPS until to the end of experiment. The effects of NNAV treatment on pulmonary injury were evaluated with arterial blood gas analysis, hydroxyproline (HYP) content assessment and HE/Masson staining. The effects of NNAV treatment on inflammatory related cytokines, fibrosis related TGF-β/Smad signaling pathway and oxidative stress were examined. RESULTS: The results showed that NNAV improved the lung gas-exchange function and attenuated the fibrotic lesions in lung. NNAV decreased IL-1β and TNF-α levels in serum in both pulmonary fibrosis models. NNAV inhibited the activation of NF-κB in LPS-induced and TGF-β/Smad pathway in BLM-induced pulmonary fibrosis. Additionally, NNAV also increased the levels of SOD and GSH and reduced the levels of MDA in BLM-induced pulmonary fibrosis model. CONCLUSIONS: The present study indicates that NNAV attenuates LPS- and BLM-induced lung fibrosis. Its mechanisms of action are associated with inhibiting inflammatory response and oxidative stress. The study suggests that NNAV might be a potential therapeutic drug for treatment of pulmonary fibrosis.
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spelling pubmed-42582602014-12-08 Naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress Cui, Kui Kou, Jian-Qun Gu, Jin-Hua Han, Rong Wang, Guanghui Zhen, Xuechu Qin, Zheng-Hong BMC Complement Altern Med Research Article BACKGROUND: Naja naja atra venom (NNAV) displays diverse pharmacological actions including analgesia, anti-inflammation and immune regulation. In this study, we investigated the effects of NNAV on pulmonary fibrosis and its mechanisms of action. METHODS: To determine if Naja naja atra venom (NNAV) can produce beneficial effects on pulmonary fibrosis, two marine models of pulmonary fibrosis were produced with bleomycin (BLM) and lipopolysaccharide (LPS). NNAV (30, 90, 270 μg/kg) was orally administered once a day started five days before BLM and LPS until to the end of experiment. The effects of NNAV treatment on pulmonary injury were evaluated with arterial blood gas analysis, hydroxyproline (HYP) content assessment and HE/Masson staining. The effects of NNAV treatment on inflammatory related cytokines, fibrosis related TGF-β/Smad signaling pathway and oxidative stress were examined. RESULTS: The results showed that NNAV improved the lung gas-exchange function and attenuated the fibrotic lesions in lung. NNAV decreased IL-1β and TNF-α levels in serum in both pulmonary fibrosis models. NNAV inhibited the activation of NF-κB in LPS-induced and TGF-β/Smad pathway in BLM-induced pulmonary fibrosis. Additionally, NNAV also increased the levels of SOD and GSH and reduced the levels of MDA in BLM-induced pulmonary fibrosis model. CONCLUSIONS: The present study indicates that NNAV attenuates LPS- and BLM-induced lung fibrosis. Its mechanisms of action are associated with inhibiting inflammatory response and oxidative stress. The study suggests that NNAV might be a potential therapeutic drug for treatment of pulmonary fibrosis. BioMed Central 2014-12-02 /pmc/articles/PMC4258260/ /pubmed/25465226 http://dx.doi.org/10.1186/1472-6882-14-461 Text en © Cui et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Cui, Kui
Kou, Jian-Qun
Gu, Jin-Hua
Han, Rong
Wang, Guanghui
Zhen, Xuechu
Qin, Zheng-Hong
Naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress
title Naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress
title_full Naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress
title_fullStr Naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress
title_full_unstemmed Naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress
title_short Naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress
title_sort naja naja atra venom ameliorates pulmonary fibrosis by inhibiting inflammatory response and oxidative stress
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258260/
https://www.ncbi.nlm.nih.gov/pubmed/25465226
http://dx.doi.org/10.1186/1472-6882-14-461
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