Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/102642
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dc.contributorDepartment of Civil and Environmental Engineering-
dc.creatorYan, Ben_US
dc.creatorLi, Jen_US
dc.creatorGuo, Jen_US
dc.creatorMa, Pen_US
dc.creatorWu, Zen_US
dc.creatorLing, Zen_US
dc.creatorGuo, Hen_US
dc.creatorHiroshi, Yen_US
dc.creatorYanagi, Uen_US
dc.creatorYang, Xen_US
dc.creatorZhu, Sen_US
dc.creatorChen, Men_US
dc.date.accessioned2023-10-26T07:20:05Z-
dc.date.available2023-10-26T07:20:05Z-
dc.identifier.issn0260-437Xen_US
dc.identifier.urihttp://hdl.handle.net/10397/102642-
dc.language.isoenen_US
dc.publisherJohn Wiley & Sonsen_US
dc.rightsCopyright © 2015 John Wiley & Sons, Ltd.en_US
dc.rightsThis is the peer reviewed version of the following article: Yan, B., Li, J., Guo, J., Ma, P., Wu, Z., Ling, Z., Guo, H., Hiroshi, Y., Yanagi, U., Yang, X., Zhu, S., and Chen, M. (2016) The toxic effects of indoor atmospheric fine particulate matter collected from allergic and non-allergic families in Wuhan on mouse peritoneal macrophages. J. Appl. Toxicol., 36(4): 596–608, which has been published in final form at https://doi.org/10.1002/jat.3217. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited.en_US
dc.subjectAllergyen_US
dc.subjectCytokinesen_US
dc.subjectMacrophagesen_US
dc.subjectOxidative stressen_US
dc.subjectPM2.5en_US
dc.titleThe toxic effects of indoor atmospheric fine particulate matter collected from allergic and non-allergic families in Wuhan on mouse peritoneal macrophagesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage596en_US
dc.identifier.epage608en_US
dc.identifier.volume36en_US
dc.identifier.issue4en_US
dc.identifier.doi10.1002/jat.3217en_US
dcterms.abstractRecent studies have shown that fine particulate matter (PM2.5) is associated with multiple adverse health outcomes and PM2.5-induced oxidative stress is now commonly known as a proposed mechanism of PM2.5-mediated toxicity. However, the association between allergic symptoms in children and exposure to PM2.5 has not been fully elucidated, particularly the role of PM2.5 on the indoor environment involved in allergy or non-allergy is unknown. The aim of the present study was to explore whether indoor PM2.5 from the homes of children with allergic symptoms had more increased risks of allergy than that of healthy ones and then compare the toxicity and inflammatory response of them. In this study, indoor PM2.5 was collected from the homes of schoolchildren with allergic symptoms and those of healthy ones respectively, and components of PM2.5 were analyzed. PM2.5-mediated oxidative damage and inflammatory response were further evaluated in mouse peritoneal macrophages based on its effects on the levels of reactive oxygen species accumulation, lipid peroxidation, DNA damage or cytokine production. It seems that oxidative stress may contribute to PM2.5-induced toxicity, and PM2.5 from the allergic indoor environment produced more serious toxic effects and an inflammatory response on mouse peritoneal macrophages than that from a non-allergic indoor environment.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of applied toxicology, Apr. 2016, v. 36, no. 4, p. 596-608en_US
dcterms.isPartOfJournal of applied toxicologyen_US
dcterms.issued2016-04-
dc.identifier.scopus2-s2.0-84958927806-
dc.identifier.pmid26304222-
dc.description.validate202310 bcch-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberCEE-2529-
dc.description.fundingSourceSelf-fundeden_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6618738-
dc.description.oaCategoryGreen (AAM)en_US
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