Influence of cytochrome P-450 inhibitors on the inhalative uptake of methyl chloride and methylene chloride in male B6C3F1 mice


Autoria(s): Ottenwalder, H.; Jager, R.; Thier, R.; Bolt, H. M.
Data(s)

1989

Resumo

Dichloromethane (DCM) is thought to be metabolized in vivo by two independent pathways: a glutathione (GSH) dependent pathway that yields CO2 and a cytochrome P-450 mediated one that yields both CO and CO2 (Gargas et al 1986). With a physiologically based pharmacokinetic (PB-PK) model, Andersen et al (1987) calculate the quantitative parameters for both metabolic pathways. Using the kinetic parameters thus obtained and the results of two carcinogenicity studies with rodents (Serota et al 1986; NTP 1985), the authors then estimate the tumour risk for humans.

Identificador

http://eprints.qut.edu.au/77469/

Publicador

Springer Verlag

Relação

DOI:10.1007/978-3-642-74117-3_45

Ottenwalder, H., Jager, R., Thier, R., & Bolt, H. M. (1989) Influence of cytochrome P-450 inhibitors on the inhalative uptake of methyl chloride and methylene chloride in male B6C3F1 mice. Archives of Toxicology, 13, pp. 258-261.

Direitos

Copyright 1989 Springer Verlag

Fonte

School of Clinical Sciences; Faculty of Health

Palavras-Chave #cytochrome p450 #dichloromethane #diethyldithiocarbamic acid #methyl chloride #pyrazole #chlorinated hydrocarbon #Cytochrome P 450 Enzyme System #glutathione #pyrazole derivative #abstract report #animal experiment #enzyme inhibition #inhalation #intraperitoneal drug administration #male #mouse #nonhuman #priority journal #animal #article #inhalational drug administration #liver #lung #metabolism #mouse strain #Administration #Inhalation #Cytochrome P-450 Enzyme System #Ditiocarb #Hydrocarbons #Chlorinated #Methylene Chloride #Mice #Mice #Inbred Strains #Pyrazoles
Tipo

Journal Article