Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2007-10-15
pubmed:abstractText
Inhalation of multiwalled carbon nanotubes (MWCNTs) at particle concentrations ranging from 0.3 to 5 mg/m3 did not result in significant lung inflammation or tissue damage, but caused systemic immune function alterations. C57BL/6 adult (10- to 12-week) male mice were exposed by whole-body inhalation to control air or 0.3, 1, or 5 mg/m3 respirable aggregates of MWCNTs for 7 or 14 days (6 h/day). Histopathology of lungs from exposed animals showed alveolar macrophages containing black particles; however, there was no inflammation or tissue damage observed. Bronchial alveolar lavage fluid also demonstrated particle-laden macrophages; however, white blood cell counts were not increased compared to controls. MWCNT exposures to 0.3 mg/m3 and higher particle concentrations caused nonmonotonic systemic immunosuppression after 14 days but not after 7 days. Immunosuppression was characterized by reduced T-cell-dependent antibody response to sheep erythrocytes as well as T-cell proliferative ability in presence of mitogen, Concanavalin A. Assessment of nonspecific natural killer (NK) cell activity showed that animals exposed to 1 mg/m(3) had decreased NK cell function. Gene expression analysis of selected cytokines and an indicator of oxidative stress were assessed in lung tissue and spleen. No changes in gene expression were observed in lung; however, interleukin-10 (IL-10) and NAD(P)H oxidoreductase 1 mRNA levels were increased in spleen.
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1096-6080
pubmed:author
pubmed:issnType
Print
pubmed:volume
100
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
203-14
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:17660506-Aerosols, pubmed-meshheading:17660506-Animals, pubmed-meshheading:17660506-Bronchoalveolar Lavage Fluid, pubmed-meshheading:17660506-Cells, Cultured, pubmed-meshheading:17660506-Dose-Response Relationship, Drug, pubmed-meshheading:17660506-Gene Expression Regulation, pubmed-meshheading:17660506-Immune System, pubmed-meshheading:17660506-Inhalation Exposure, pubmed-meshheading:17660506-Interleukin-10, pubmed-meshheading:17660506-Interleukin-6, pubmed-meshheading:17660506-Killer Cells, Natural, pubmed-meshheading:17660506-Leukocyte Count, pubmed-meshheading:17660506-Lung, pubmed-meshheading:17660506-Lymphocyte Activation, pubmed-meshheading:17660506-Macrophages, Alveolar, pubmed-meshheading:17660506-Male, pubmed-meshheading:17660506-Mice, pubmed-meshheading:17660506-Mice, Inbred C57BL, pubmed-meshheading:17660506-NAD(P)H Dehydrogenase (Quinone), pubmed-meshheading:17660506-NADPH Dehydrogenase, pubmed-meshheading:17660506-Nanotubes, Carbon, pubmed-meshheading:17660506-Oxidative Stress, pubmed-meshheading:17660506-Particle Size, pubmed-meshheading:17660506-RNA, Messenger, pubmed-meshheading:17660506-Spleen, pubmed-meshheading:17660506-T-Lymphocytes, pubmed-meshheading:17660506-Time Factors
pubmed:year
2007
pubmed:articleTitle
Pulmonary and systemic immune response to inhaled multiwalled carbon nanotubes.
pubmed:affiliation
College of Pharmacy, University of New Mexico, Albuquerque, New Mexico 87131-0001, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, N.I.H., Extramural