## Abstract The metabolism of tritiated benzo[a]pyrene (B[a]P) by primary mouse embryo cells in culture was studied. At concentrations of B[a]P in the medium below about 2–3 mμ moles/ml, metabolism was exponential with time, but at higher concentrations a period of rapid metabolism was followed by
Metabolism and binding to cellular macromolecules of a series of hydrocarbons by mouse embryo cells in culture
✍ Scribed by Margaret Duncan; P. Brookes; A. Dipple
- Publisher
- John Wiley and Sons
- Year
- 1969
- Tongue
- French
- Weight
- 517 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
A series of eight tritium-labelled polycyclic hydrocarbons were incubated in the presence of monolayer cultures of primary mouse embryo cells, and the time-course of their metabolism to water-soluble derivatives was studied. All the hydrocarbons, both carcinogenic and non-carcinogenic, were metabolized at approximately the same rate when a low concenrratiotz of the order of 0.05 p M was used. The binding of the various hydrocarbons to cellular DNA, R N A and protein was determined and a " binding index " calculated, i.e., the extent of reaction of the hydrocarbon with the particular macromolecule resulting from the metabolism of I mpmole of hydrocarbon per ml of medium to which the cells were exposed. While no very significant difference between the various hydrocarbons was found for the protein binding index, the D N A and R N A binding indices divided the compounds into two groups. One group with a high binding index consisted of potent carcinogens while the other group had much lower (one tenth) values for the binding index. With the exception of dibenz [a,h]anthracene, this latter group consisted of non-carcinogens.
📜 SIMILAR VOLUMES
## Abstract The metabolism and consequent macromolecular binding of dibenz(a,c)anthracene and dibenz(a,h) anthracene by mouse embryo cells in culture was compared at approximately equal, low doses of hydrocarbon in the medium. Both hydrocarbons were metabolized more slowly than other hydrocarbons t
## Abstract The DNA of mouse embryo cells was specifically labelled in the purine moieties with (G^3^H)‐deoxyadenosine or in the cytosine moieties with (5^3^H)‐deoxycytidine. These cells were then treated with 7‐methylbenz (__a__) anthracene (__7MBA__) or benzo (__a__)‐pyrene (B(__a__)P) and the DN
## Abstract The marked localization of a carcinogenic polycyclic aromatic hydrocarbon, benzo(__a__)pyrene, and its metabolites and a carcinogenic alkylating agent, N‐methyl‐N'‐nitro‐N‐nitrosoguanidine, to a specific subnuclear fraction (fraction I) from AKR‐2B mouse embryo cells in culture is descr
## Abstract The extents of reaction of seven ^3^H‐labelled polycyclic hydrocarbons with DNA in mouse skin following their topical application have been studied. DNA isolated from the treated areas was hydrolysed enzymically to deoxyribonucleosides and the products chromatographed on Sephadex LH20 c
## Abstract Three potycyclic hydrocarbons, benz(__a__)anthracene, 3‐methylcholanthrene and 7,12‐dimethyl‐benz(__a__)anthracene, have been studied in a cell‐mediated mutagenesis system using BHK 21 cells to metabolize the hydrocarbons and V‐79 cells as targets for detecting induced cytotoxicity and