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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1990-5-18
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pubmed:abstractText |
We investigated the effects of silica (SiO2) and titanium dioxide (TiO2) on the pulmonary recruitment of inflammatory cells and the ability of alveolar macrophages (AMs) to release the pro-inflammatory cytokines, interleukin 1 (IL-1) and tumor necrosis factor alpha (TNF). Rats were intratracheally instilled with 5 to 100 mg/kg of the materials, and bronchoalveolar lavage cell populations and AM cytokine release were characterized on days 1, 7, 14, and 28. Both dusts elicited dose-related increases in neutrophils, lymphocytes, and AMs; however, this response was more pronounced and persistent with SiO2. SiO2 at greater than or equal to 50 mg/kg increased AM release of IL-1 and TNF at all time points; lower SiO2 doses had either a transient or no effect on AM-derived cytokines. TiO2 did not result in AM IL-1 release and increased TNF release transiently at doses greater than or equal to 50 mg/kg. Both dusts primed AMs to release increased levels of IL-1 and TNF upon in vitro stimulation with lipopolysaccharide. Histopathology (day 28) demonstrated dose-related interstitial inflammation associated with SiO2 exposure, an effect that was less severe with TiO2. SiO2 doses of greater than or equal to 50 mg/kg elicited a granulomatous response. Development of granulomatous inflammation only at SiO2 doses for which persistent AM IL-1 release occurred suggests involvement of this cytokine in the formation of SiO2-induced granulomas. The ability of SiO2 to activate AM release of IL-1 and TNF in a more pronounced and persistent manner than TiO2 is likely responsible, at least in part, for the greater inflammation and pneumotoxicity associated with SiO2.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Silicon Dioxide,
http://linkedlifedata.com/resource/pubmed/chemical/Titanium,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/titanium dioxide
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1044-1549
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
2
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
381-90
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2157474-Animals,
pubmed-meshheading:2157474-Bronchoalveolar Lavage Fluid,
pubmed-meshheading:2157474-Interleukin-1,
pubmed-meshheading:2157474-Leukocyte Count,
pubmed-meshheading:2157474-Lipopolysaccharides,
pubmed-meshheading:2157474-Lung,
pubmed-meshheading:2157474-Lymphocytes,
pubmed-meshheading:2157474-Macrophages,
pubmed-meshheading:2157474-Male,
pubmed-meshheading:2157474-Neutrophils,
pubmed-meshheading:2157474-Pulmonary Alveoli,
pubmed-meshheading:2157474-Pulmonary Fibrosis,
pubmed-meshheading:2157474-Rats,
pubmed-meshheading:2157474-Rats, Inbred F344,
pubmed-meshheading:2157474-Silicon Dioxide,
pubmed-meshheading:2157474-Titanium,
pubmed-meshheading:2157474-Tumor Necrosis Factor-alpha
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pubmed:year |
1990
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pubmed:articleTitle |
Pulmonary response to silica or titanium dioxide: inflammatory cells, alveolar macrophage-derived cytokines, and histopathology.
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pubmed:affiliation |
Human and Environmental Safety Division, Procter & Gamble Company, Cincinnati, Ohio 45239-8707.
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pubmed:publicationType |
Journal Article,
Comparative Study
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