Potential of human lung cells for predicting acute cytotoxicity
By Barile, F.A. - Alexander, D. - Sookhoo, A.
| Record number: | 2928370 |
|---|---|
| Category: | fibroblasts - cell culture - cytotoxicity - bioassays - animal use alternatives |
Human fetal lung fibroblasts (HFL1) were studied in culture to evaluate their potential as a screen for cytotoxicity. The cytotoxic concentrations determined in vitro were compared with established human and animal toxicity data. Confluent monolayers were incubated in the absence or presence of increasing concentrations of test chemicals for 24 hours, and the MTT assay was used to assess toxicity. Inhibitory concentrations were extrapolated from concentration-effect curves after linear regression analysis. Comparison of the cytotoxicity data with rodent lethal concentrations and human lethal concentrations obtained from the testing of 50 chemicals in human lung cells, suggests that the experimental IC50 values are as accurate as predictors of human toxicity as the equivalent toxic blood concentrations derived from rodent LD50 tests. In addition, evaluation of the first 15 chemicals reveals no significant differences between results from continuous cell lines of human and rodent origin. Together with a related battery of tests, cell culture procedures have the potential to supplement or replace current animal protocols in screening chemicals for human toxicity.
Issued: July/Aug 1995
Journal Title: Alternatives to laboratory animals
ISSN: 0261-1929
Volume issue: 23 v. 4 no.
Pages: 461 - 468
Notes:
Paper presented at the Twelfth Congress on In Vitro Toxicology of the Scandinavian Society for Cell Toxicology, September 22-25, 1994, Ustaoset, Norway.
AGRICOLA identifier: IND20569729
Takk for din tilbakemelding! Vær oppmerksom på at vi ikke kan kontakte deg hvis ikke du oppgir din epostadresse.
Hva lette du etter?
Gi oss gjerne en tilbakemelding slik at vi kan forbedre informasjonen på siden. På forhånd takk for hjelpen! Vennligst skriv inn din epostadresse hvis du vil ha et svar.
Kontakt oss gjerne på e-post hvis du har spørsmål.