Journal of Toxicology and Environmental Health, Part A最新文献_第5页

Jet fuel kerosene is not immunosuppressive in mice or rats following inhalation for 28 days. 喷射煤油在小鼠或大鼠体内吸入28天后没有免疫抑制作用。

IF 2.6

Journal of Toxicology and Environmental Health, Part A Pub Date : 2013-01-01 DOI: 10.1080/15287394.2013.819307

Kimber L White, Michael P DeLorme, Patrick W Beatty, Matthew J Smith, Vanessa L Peachee

{"title":"Jet fuel kerosene is not immunosuppressive in mice or rats following inhalation for 28 days.","authors":"Kimber L White, Michael P DeLorme, Patrick W Beatty, Matthew J Smith, Vanessa L Peachee","doi":"10.1080/15287394.2013.819307","DOIUrl":"https://doi.org/10.1080/15287394.2013.819307","url":null,"abstract":"Previous reports indicated that inhalation of JP-8 aviation turbine fuel is immunosuppressive. However, in some of those studies, the exposure concentrations were underestimated, and percent of test article as vapor or aerosol was not determined. Furthermore, it is unknown whether the observed effects are attributable to the base hydrocarbon fuel (jet fuel kerosene) or to the various fuel additives in jet fuels. The present studies were conducted, in compliance with Good Laboratory Practice (GLP) regulations, to evaluate the effects of jet fuel kerosene on the immune system, in conjunction with an accurate, quantitative characterization of the aerosol and vapor exposure concentrations. Two female rodent species (B6C3F1 mice and Crl:CD rats) were exposed by nose-only inhalation to jet fuel kerosene at targeted concentrations of 0, 500, 1000, or 2000 mg/m(3) for 6 h daily for 28 d. Humoral, cell-mediated, and innate immune functions were subsequently evaluated. No marked effects were observed in either species on body weights, spleen or thymus weights, the T-dependent antibody-forming cell response (plaque assay), or the delayed-type hypersensitivity (DTH) response. With a few exceptions, spleen cell numbers and phenotypes were also unaffected. Natural killer (NK) cell activity in mice was unaffected, while the NK assessment in rats was not usable due to an unusually low response in all groups. These studies demonstrate that inhalation of jet fuel kerosene for 28 d at levels up to 2000 mg/m(3) did not adversely affect the functional immune responses of female mice and rats. ","PeriodicalId":17418,"journal":{"name":"Journal of Toxicology and Environmental Health, Part A","volume":" ","pages":"778-97"},"PeriodicalIF":2.6,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15287394.2013.819307","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31726090","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 9

Effects of COREXIT dispersants on cytotoxicity parameters in a cultured human bronchial airway cells, BEAS-2B. COREXIT分散剂对培养的人支气管气道细胞BEAS-2B细胞毒性参数的影响。

IF 2.6

Journal of Toxicology and Environmental Health, Part A Pub Date : 2013-01-01 DOI: 10.1080/15287394.2013.821396

Yongli Shi, Astrid M Roy-Engel, He Wang

{"title":"Effects of COREXIT dispersants on cytotoxicity parameters in a cultured human bronchial airway cells, BEAS-2B.","authors":"Yongli Shi, Astrid M Roy-Engel, He Wang","doi":"10.1080/15287394.2013.821396","DOIUrl":"https://doi.org/10.1080/15287394.2013.821396","url":null,"abstract":"The objective of this study was to assess the cytotoxicity of COREXIT dispersants EC9500A, EC9527A, and EC9580A on human airway BEAS-2B epithelial cells. Cells were exposed to dispersants for 2 or 24 h at concentrations ranging from 0 to 300 ppm. COREXIT EC9527 at 100 ppm produced 50% viability loss as measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) at 24 h. COREXIT 9527 at 200 ppm produced 50% cell death at 2 h and 100% at 24 h. At 300 ppm COREXIT 9527 induced 100% cell death at 2 or 24 h. In the case of COREXIT 9500A 50% cell viability was noted with 200 ppm at 2 or 24 h, with a significant decrease in cell survival to 2% at 300 ppm. In contrast, no marked change in cell viability was observed in cells treated at any COREXIT 9580A concentration examined. Western blot analysis showed an increase in expression of LC3B, a marker of autophagy, in cells treated for 2 h with 300 ppm COREXIT EC9527A as well as 100 or 300 ppm Corexit EC9500A. No marked effect on LC3B expression was observed for any COREXIT 9580A concentration. Apoptosis markers as measured by cleaved caspase-3 and cleaved poly(ADP-ribose) polymerase (PARP) were detectable only in cells incubated with 300 ppm COREXIT EC9527A. Although all three dispersants induced enhanced generation of reactive oxygen species (ROS) after 2-h treatment at 300 ppm, Western blot analysis revealed that 2-h incubation was not sufficient to induce a significant change in the protein expression of superoxide dismutases SOD1, SOD2, and SOD3. Data thus indicate exposure to certain dispersants may be harmful to human airway epithelial cells in a concentration-dependent manner. ","PeriodicalId":17418,"journal":{"name":"Journal of Toxicology and Environmental Health, Part A","volume":" ","pages":"827-35"},"PeriodicalIF":2.6,"publicationDate":"2013-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15287394.2013.821396","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31726525","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 28

Symposium Proceedings--Occupational Lung Disease in Response to Mixed Exposures: Approaches to Identify the Toxicity of Process-Dependent Contaminants 研讨会论文集——混合暴露引起的职业性肺病:确定过程相关污染物毒性的方法

Journal of Toxicology and Environmental Health, Part A Pub Date : 2003-06-01 DOI: 10.1080/716100655

V. Castranova

引用次数: 0

Assessing the health risks of benzene: a report on the benzene state-of-the-science workshop. 评估苯的健康风险:关于苯科学状况讲习班的报告。

Journal of Toxicology and Environmental Health, Part A Pub Date : 2000-11-01 DOI: 10.1080/00984100050166325

D. Krewski, R. Snyder, P. Beatty, G. Granville, B. Meek, B. Sonawane

引用次数: 51

Appendix A : Health Risk Assessment for the Nerve Agent GA 附录A: GA神经毒剂的健康风险评估

Journal of Toxicology and Environmental Health, Part A Pub Date : 2000-01-01 DOI: 10.1080/009841000156826

K. Bakshi, Susan N. J. Pang, R. Snyder

引用次数: 4

Appendix E : Health Risk Assessment for Sulfur Mustard (HD) 附录E:硫芥菜的健康风险评估

Journal of Toxicology and Environmental Health, Part A Pub Date : 2000-01-01 DOI: 10.1080/009841000156862

K. Bakshi, Susan N. J. Pang, R. Snyder

引用次数: 1

Appendix C : Health Risk Assessment for the Nerve Agent GD (Soman) 附录C: GD(索曼)神经毒剂的健康风险评估

Journal of Toxicology and Environmental Health, Part A Pub Date : 2000-01-01 DOI: 10.1080/009841000156844

K. Bakshi, Susan N. J. Pang, R. Snyder

引用次数: 3

Appendix G : Inhibition of cholinesterases and an evaluation of the methods used to measure cholinesterase activity 附录G:胆碱酯酶的抑制和测定胆碱酯酶活性方法的评价

Journal of Toxicology and Environmental Health, Part A Pub Date : 2000-01-01 DOI: 10.1080/009841000156880

K. Bakshi, Susan N. J. Pang, R. Snyder

引用次数: 4

Invited Review POTENTIAL BIOMARKERS OF BENZENE EXPOSURE 应邀评论苯暴露的潜在生物标志物

Journal of Toxicology and Environmental Health, Part A Pub Date : 1997-08-01 DOI: 10.1080/009841097159818

A. Medeiros, M. Bird, G. Witz

引用次数: 3

A Review of “LOOMIS'S ESSENTIALS OF TOXICOLOGY” Edited by Ted A. Loomis and A. Wallace Hayes Academic Press, London, 1996, 282 pp. 泰德·A·卢米斯和A·华莱士·海耶斯学术出版社编辑的《卢米斯毒理学要点》书评，伦敦，1996年，282页。

Journal of Toxicology and Environmental Health, Part A Pub Date : 1997-08-01 DOI: 10.1080/00984109708984041

Ram P. Gupta

引用次数: 0