Perfluorocarbon restrains inflammation and cell apoptosis in rats with lung ischemia reperfusion injury via down regulation of TLR4/NF κB signaling pathway

Purpose: To exaluate the effect of perfluorocarbon on lung ischemia-reperfusion injury in rats, and to unravel the potential underlying mechanism.Methods: A total of 36 Sprague-Dawley (SD) rats were randomly assigned to sham group, model group, and perfluorocarbon group (12 rats per group). The leve...

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Veröffentlicht in:Tropical journal of pharmaceutical research 2022-12, Vol.21 (12), p.2533-2539
Hauptverfasser: Liu, Li, Gou, Dan, Song, Yanyan, Li, Mingliang, Gu, Jiwei, Zhang, Yujing, Qu, Chengliang, Wang, Yun
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container_end_page 2539
container_issue 12
container_start_page 2533
container_title Tropical journal of pharmaceutical research
container_volume 21
creator Liu, Li
Gou, Dan
Song, Yanyan
Li, Mingliang
Gu, Jiwei
Zhang, Yujing
Qu, Chengliang
Wang, Yun
description Purpose: To exaluate the effect of perfluorocarbon on lung ischemia-reperfusion injury in rats, and to unravel the potential underlying mechanism.Methods: A total of 36 Sprague-Dawley (SD) rats were randomly assigned to sham group, model group, and perfluorocarbon group (12 rats per group). The levels of inflammatory factors (TNF-α and IL1β) were determined using enzyme-linked immunosorbent assay (ELISA). Cell apoptosis was evaluated by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay, while Western blotting was conducted to determine the protein expressions of TLR4 and NF-κB.Results: The levels of inflammatory factors in the model and perfluorocarbon groups were significantly higher than those in operation group (p < 0.05), while their levels in perfluorocarbon group were significantly lower than in model group (p < 0.05). The mRNA expression levels of TNF-α and IL-1β in lung tissues rose significantly in both model and perfluorocarbon groups when compared with those in sham group (p < 0.05), but declined significantly in the perfluorocarbon group in comparison with those in model group (p < 0.05). Furthermore, the perfluorocarbon group exhibited a significantly lower cell apoptosis than model group (p < 0.05). The relative protein expression levels of TLR4 and NF-κBdeclined significantly in perfluorocarbon group than in model group.Conclusions: Perfluorocarbon down-regulates the TLR4/NF-κB signaling pathway, and inhibits inflammation an
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The levels of inflammatory factors (TNF-α and IL1β) were determined using enzyme-linked immunosorbent assay (ELISA). Cell apoptosis was evaluated by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay, while Western blotting was conducted to determine the protein expressions of TLR4 and NF-κB.Results: The levels of inflammatory factors in the model and perfluorocarbon groups were significantly higher than those in operation group (p &lt; 0.05), while their levels in perfluorocarbon group were significantly lower than in model group (p &lt; 0.05). The mRNA expression levels of TNF-α and IL-1β in lung tissues rose significantly in both model and perfluorocarbon groups when compared with those in sham group (p &lt; 0.05), but declined significantly in the perfluorocarbon group in comparison with those in model group (p &lt; 0.05). Furthermore, the perfluorocarbon group exhibited a significantly lower cell apoptosis than model group (p &lt; 0.05). The relative protein expression levels of TLR4 and NF-κBdeclined significantly in perfluorocarbon group than in model group.Conclusions: Perfluorocarbon down-regulates the TLR4/NF-κB signaling pathway, and inhibits inflammation an</description><identifier>ISSN: 1596-5996</identifier><identifier>EISSN: 1596-9827</identifier><identifier>DOI: 10.4314/tjpr.v21i12.5</identifier><language>eng</language><ispartof>Tropical journal of pharmaceutical research, 2022-12, Vol.21 (12), p.2533-2539</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c237t-fbfca0a298405b4eaef66a90469c8b3324cef6b63b04a5922bea0b1e23f2a9803</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27923,27924</link.rule.ids></links><search><creatorcontrib>Liu, Li</creatorcontrib><creatorcontrib>Gou, Dan</creatorcontrib><creatorcontrib>Song, Yanyan</creatorcontrib><creatorcontrib>Li, Mingliang</creatorcontrib><creatorcontrib>Gu, Jiwei</creatorcontrib><creatorcontrib>Zhang, Yujing</creatorcontrib><creatorcontrib>Qu, Chengliang</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><title>Perfluorocarbon restrains inflammation and cell apoptosis in rats with lung ischemia reperfusion injury via down regulation of TLR4/NF κB signaling pathway</title><title>Tropical journal of pharmaceutical research</title><description>Purpose: To exaluate the effect of perfluorocarbon on lung ischemia-reperfusion injury in rats, and to unravel the potential underlying mechanism.Methods: A total of 36 Sprague-Dawley (SD) rats were randomly assigned to sham group, model group, and perfluorocarbon group (12 rats per group). The levels of inflammatory factors (TNF-α and IL1β) were determined using enzyme-linked immunosorbent assay (ELISA). Cell apoptosis was evaluated by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assay, while Western blotting was conducted to determine the protein expressions of TLR4 and NF-κB.Results: The levels of inflammatory factors in the model and perfluorocarbon groups were significantly higher than those in operation group (p &lt; 0.05), while their levels in perfluorocarbon group were significantly lower than in model group (p &lt; 0.05). The mRNA expression levels of TNF-α and IL-1β in lung tissues rose significantly in both model and perfluorocarbon groups when compared with those in sham group (p &lt; 0.05), but declined significantly in the perfluorocarbon group in comparison with those in model group (p &lt; 0.05). Furthermore, the perfluorocarbon group exhibited a significantly lower cell apoptosis than model group (p &lt; 0.05). The relative protein expression levels of TLR4 and NF-κBdeclined significantly in perfluorocarbon group than in model group.Conclusions: Perfluorocarbon down-regulates the TLR4/NF-κB signaling pathway, and inhibits inflammation an</description><issn>1596-5996</issn><issn>1596-9827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNotkE1OwzAQRi0EEqWwZO8LpPgvabyEigJSBQiVdTR27daVG0d20qp34SQcgjORqF3N6H2aN9KH0D0lE8GpeGi3TZzsGXWUTfILNKK5LDJZsunlec-lLK7RTUpbQvJCSjpCP58mWt-FGDREFWocTWojuDphV1sPux20rsdQr7A23mNoQtOG5IYcR2gTPrh2g31Xr7FLemN2DnpJ02u7NFy6etvFI973eBUOw4N150_SYPFy8SUe3uf47_cJJ7euwbte1EC7OcDxFl1Z8MncnecYfc-fl7PXbPHx8jZ7XGSa8WmbWWU1EGCyFCRXwoCxRQGSiELqUnHOhO6JKrgiAnLJmDJAFDWMWwayJHyMspNXx5BSNLZqottBPFaUVEO11VBtdaq2yvk_I31zxQ</recordid><startdate>20221201</startdate><enddate>20221201</enddate><creator>Liu, Li</creator><creator>Gou, Dan</creator><creator>Song, Yanyan</creator><creator>Li, Mingliang</creator><creator>Gu, Jiwei</creator><creator>Zhang, Yujing</creator><creator>Qu, Chengliang</creator><creator>Wang, Yun</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20221201</creationdate><title>Perfluorocarbon restrains inflammation and cell apoptosis in rats with lung ischemia reperfusion injury via down regulation of TLR4/NF κB signaling pathway</title><author>Liu, Li ; Gou, Dan ; Song, Yanyan ; Li, Mingliang ; Gu, Jiwei ; Zhang, Yujing ; Qu, Chengliang ; Wang, Yun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c237t-fbfca0a298405b4eaef66a90469c8b3324cef6b63b04a5922bea0b1e23f2a9803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Li</creatorcontrib><creatorcontrib>Gou, Dan</creatorcontrib><creatorcontrib>Song, Yanyan</creatorcontrib><creatorcontrib>Li, Mingliang</creatorcontrib><creatorcontrib>Gu, Jiwei</creatorcontrib><creatorcontrib>Zhang, Yujing</creatorcontrib><creatorcontrib>Qu, Chengliang</creatorcontrib><creatorcontrib>Wang, Yun</creatorcontrib><collection>CrossRef</collection><jtitle>Tropical journal of pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Li</au><au>Gou, Dan</au><au>Song, Yanyan</au><au>Li, Mingliang</au><au>Gu, Jiwei</au><au>Zhang, Yujing</au><au>Qu, Chengliang</au><au>Wang, Yun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Perfluorocarbon restrains inflammation and cell apoptosis in rats with lung ischemia reperfusion injury via down regulation of TLR4/NF κB signaling pathway</atitle><jtitle>Tropical journal of pharmaceutical research</jtitle><date>2022-12-01</date><risdate>2022</risdate><volume>21</volume><issue>12</issue><spage>2533</spage><epage>2539</epage><pages>2533-2539</pages><issn>1596-5996</issn><eissn>1596-9827</eissn><abstract>Purpose: To exaluate the effect of perfluorocarbon on lung ischemia-reperfusion injury in rats, and to unravel the potential underlying mechanism.Methods: A total of 36 Sprague-Dawley (SD) rats were randomly assigned to sham group, model group, and perfluorocarbon group (12 rats per group). 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The relative protein expression levels of TLR4 and NF-κBdeclined significantly in perfluorocarbon group than in model group.Conclusions: Perfluorocarbon down-regulates the TLR4/NF-κB signaling pathway, and inhibits inflammation an</abstract><doi>10.4314/tjpr.v21i12.5</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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title Perfluorocarbon restrains inflammation and cell apoptosis in rats with lung ischemia reperfusion injury via down regulation of TLR4/NF κB signaling pathway
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