Selective inactivation of rat and bovine olfactory cytochrome P450 by three haloethanes
Toxicology Letters, ISSN: 0378-4274, Vol: 124, Issue: 1, Page: 83-90
2001
- 3Citations
- 1Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations3
- Citation Indexes3
- CrossRef3
- Captures1
- Readers1
Article Description
The effects of halothane, 1,1-dichloro-2,2,2-trifluoroethane (HCFC-123) and 1,1-dichloro-1-fluoroethane (HCFC-141b) on the P450 system in olfactory and hepatic microsomes of bovine and rat have been investigated. In the in vitro experiments, all three compounds decreased olfactory CYP-dependent activities in microsomes from both species, especially under anaerobic conditions, halothane showing the greatest effect. Hepatic activities were not affected. A selective olfactory CYP depletion was also observed in vivo after treatment with halothane, but not with HCFC-123 or HCFC-141b. A loss of olfactory ethoxycoumarin- O -deethylase activity was also found both in vitro and in vivo experiments, suggesting that a CYP2A isoform may be the main target of inactivation. The present results therefore suggest that CYP2A, the major isoform expressed in the olfactory tissue of mammals, may be particularly prone to catalyze the reductive metabolism of halothane both in anaerobic and aerobic conditions.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S037842740100323X; http://dx.doi.org/10.1016/s0378-4274(01)00323-x; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0035887028&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/11684360; https://linkinghub.elsevier.com/retrieve/pii/S037842740100323X; http://dx.doi.org/10.1016/s0378-4274%2801%2900323-x; https://dx.doi.org/10.1016/s0378-4274%2801%2900323-x
Elsevier BV
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