Abstract
Replication of measles virus in BSC cells was studied in the presence of enflurane (2-chloro-1,1,2-trifluoroethyl difluoromethyl ether), a commonly used volatile anesthetic agent, and its isomer, isoflurane (1-chloro-2,2,2-trifluoroethyl difluoromethyl ether). At clinical concentrations of the anesthetics (up to 4%), cell division was retarded, whereas only minimal toxic cellular effects were observed. The appearance of progeny virus from the cell cultures exposed to these anesthetics was decreased in a dose-related manner. Incorporation of [3H]uridine into measles virus nucleocapsids also decreased progressively with increasing anesthetic concentrations. In comparing the inhibition of measles virus replication in the presence of halothane (2-bromo-2-chloro,1,1,1-trifluoroethane), enflurane, or isoflurane, it was found that both inhibition of the appearance of infectious virus at 48 h postinfection and incorporation of [3H]uridine into measles virus nucleocapsids were proportional to the anesthetic concentrations. An equivalent degree of effect was produced by anesthetically equivalent concentrations of the three anesthetics (minimal alveolar concentration) but not by absolute concentrations. In addition, recovery of infectious virus synthesis from the inhibition encountered during exposure of infected BSC cells to halothane or isoflurane was also investigated. In cultures exposed to halothane or enflurane, recovery of infectious virus synthesis was rapid and complete. Recovery of virus synthesis was slower after isoflurane removal and did not reach the peak control titers of infected cultures not exposed to the anesthetic. Treatment with halothane resulted in the formation of a preponderance of slowly sedimenting virus nucleocapsid particles which contained less than full-length ribonucleic acids after anesthetic removal. Neither enflurane nor isoflurane treatment of BSC cultures resulted in the formation of significant levels of these slowly sedimenting particles with short genomes after anesthetic removal.
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Selected References
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- Bedows E., Payne F. E. Host cell factors involved in the production of slowly sedimenting nucleocapsids in measles virus-infected cells. J Virol. 1981 Jan;37(1):103–108. doi: 10.1128/jvi.37.1.103-108.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Conklin K. A., Lau S. S. Enflurane effects on cell division and macromolecular synthesis in Tetrahymena pyriformis: comparison with halothane. Anesthesiology. 1980 Oct;53(4):287–292. doi: 10.1097/00000542-198010000-00004. [DOI] [PubMed] [Google Scholar]
- Donovan C. A. The influence of diethyl ether inhalation on experimental canine distemper. Vet Med Small Anim Clin. 1968 Apr;63(4):345–347. [PubMed] [Google Scholar]
- Hall W. W., Martin S. J. Purification and characterization of measles virus. J Gen Virol. 1973 May;19(2):175–188. doi: 10.1099/0022-1317-19-2-175. [DOI] [PubMed] [Google Scholar]
- Halsey M. J., Wardley-Smith B., Green C. J. Pressure reversal of general anaesthesia--a multi-site expansion hypothesis. Br J Anaesth. 1978 Nov;50(11):1091–1097. doi: 10.1093/bja/50.11.1091. [DOI] [PubMed] [Google Scholar]
- Haspel M. V., Knight P. R., Duff R. G., Rapp F. Activation of a latent measles virus infection in hamster cells. J Virol. 1973 Oct;12(4):690–695. doi: 10.1128/jvi.12.4.690-695.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jackson S. H. The metabolic effects of halothane on mammalian hepatoma cells in vitro. II. Inhibition of DNA synthesis. Anesthesiology. 1973 Oct;39(4):405–409. doi: 10.1097/00000542-197310000-00013. [DOI] [PubMed] [Google Scholar]
- Kiley M. P., Gray R. H., Payne F. E. Replication of measles virus: distinct species of short nucleocapsids in cytoplasmic extracts of infected cells. J Virol. 1974 Mar;13(3):721–728. doi: 10.1128/jvi.13.3.721-728.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Knight P. R., Nahrwold M. L., Bedows E. Anesthetic action and virus replication: inhibition of measles virus replication in cells exposed to halothane. Antimicrob Agents Chemother. 1980 May;17(5):890–896. doi: 10.1128/aac.17.5.890. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Morgan E. M., Rapp F. Measles virus and its associated diseases. Bacteriol Rev. 1977 Sep;41(3):636–666. doi: 10.1128/br.41.3.636-666.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nahrwold M. L., Cohen P. J. Anesthetics and mitochondrial respiration. Clin Anesth. 1975;11(1):25–44. [PubMed] [Google Scholar]
- Rima B. K., Davidson W. B., Martin S. J. The role of defective interfering particles in persistent infection of Vero cells by measles virus. J Gen Virol. 1977 Apr;35(1):89–97. doi: 10.1099/0022-1317-35-1-89. [DOI] [PubMed] [Google Scholar]
- Rima R. K., Martin S. J. Persistent infection of tissue culture cells by RNA viruses. Med Microbiol Immunol. 1976 Jun 1;162(2):89–119. doi: 10.1007/BF02121320. [DOI] [PubMed] [Google Scholar]
- Trudell J. R. A unitary theory of anesthesia based on lateral phase separations in nerve membranes. Anesthesiology. 1977 Jan;46(1):5–10. doi: 10.1097/00000542-197701000-00003. [DOI] [PubMed] [Google Scholar]
- Welsh M. J., Dedman J. R., Brinkley B. R., Means A. R. Tubulin and calmodulin. Effects of microtubule and microfilament inhibitors on localization in the mitotic apparatus. J Cell Biol. 1979 Jun;81(3):624–634. doi: 10.1083/jcb.81.3.624. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wiklund R. A., Allison A. C. The effects of anaesthetics on the motility of Dictyostelium discoideum: evidence for a possible mechanism of anaesthesia. Br J Anaesth. 1972 Jun;44(6):622–622. [PubMed] [Google Scholar]
