| DOI | Resolve DOI: https://doi.org/10.1016/0014-5793(86)81109-7 |
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| Author | Search for: Cheeseman, K.H.; Search for: Collins, M.; Search for: Maddix, S.; Search for: Milia, A.; Search for: Proudfoot, K.; Search for: Slater, T.F.; Search for: Burton, G.W.1; Search for: Webb, A.1; Search for: Ingold, K. U.1 |
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| Affiliation | - National Research Council of Canada
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| Format | Text, Article |
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| Subject | lipid peroxide; thymidine kinase; animal cell; dna synthesis; liver; liver regeneration; microsome; rat; Cytochrome P-450 Enzyme System; Fatty Acids, Unsaturated; Kinetics; Lipid Peroxides; Liver; Liver Regeneration; Male; Microsomes, Liver; NADPH-Ferrihemoprotein Reductase; Rats; Rats, Inbred Strains; Thymidine Kinase; Vitamin E; Animalia |
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| Abstract | Rats entrained to a strictly regulated lighting and feeding schedule have been subjected to partial hepatectomy or a sham operation. In the partially hepatectomised animals the period of liver regeneration is characterised by regular bursts of thymidine kinase activity. Liver microsomes from rats, at times corresponding to maximum thymidine kinase activity, have much reduced rates of lipid peroxidation compared to control preparations: this is due in part to increased levels of lipid-soluble antioxidant at times of maximal DNA synthesis. This temporal relationship between thymidine kinase and lipid peroxidation is consistent with the view that lipid peroxidation is decreased prior to cell division. © 1986. |
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| Publication date | 1986 |
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| In | |
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| Language | English |
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| Peer reviewed | Yes |
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| NPARC number | 21276534 |
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| Export citation | Export as RIS |
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| Report a correction | Report a correction (opens in a new tab) |
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| Record identifier | 6d8c72d4-210a-4690-bbe9-bd5b75f7064b |
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| Record created | 2015-10-13 |
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| Record modified | 2020-03-17 |
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