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细胞色素P-450与电离辐射的关系 被引量:5

Relation between cytochrome P-450and ionizing radiation
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摘要 电离辐射可以改变细胞色素P-450(主要有CYP1B1、CYP1A1、CYP4A11、CYP2E1等)的活性和(或)mRNA、蛋白含量,从而影响药物代谢和有毒化学物的生物转化过程及其生物学作用。细胞色素P-450参与了生物还原活性物TMQ、AQ4N在机体内的还原。动物实验和已有的临床研究表明,调节P-450可以提高生物还原活性物的辐射增敏作用和抗肿瘤作用。 Ionizing radiation can change the activity and/or the expression of mRNA,protein of Cytochrome P-450(CYP1B1,1A1,4A11,2E1),consequently influence the biotransformation and biological effects of the drugs and toxi-coid metabolization.Cytochrome P-450participated in the reduction of bioreductive drugs(including TMQ,AQ4N).Ani-mal experiments and clinical trials show Cytochrome P-450can be taken advantage to exert well sensitization for radio-therapy and chemotherapy.
出处 《国外医学(放射医学核医学分册)》 2003年第2期77-79,83,共4页 Foreign Medical Sciences(Section of Radiation Medicine and Nuclear Medicine)
基金 国家自然科学基金资助项目(编号:30100042)
关键词 细胞色素P—450 电离辐射 生物还原活性物 药物代谢 cytochrome P-450 radiation bioreductive drugs
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参考文献9

  • 1Katiyar SK, Matsui MS, Mukhtar H. Ultraviolet-B exposure of human skin induces cytochromes P450 1A1 and 1BI[J]. J Invest Dermatol,2000,114(2):328-333. 被引量:1
  • 2Villard PH, Sampol E, Elkaim JL,et al. Increase of CYP1B1 transcription in human keratinocytes and HaCaT cells after UV-B exposure[J]. Toxicol Appl Pharmacol,2002, 178(3):137-143. 被引量:1
  • 3Gonzalez MC, Marteau C, Franchi J, et al. Cytochrome P450 4A11 expression in human keratinocytes: effects of ultraviolet irradiation[J]. Br J Dermatol,2001,145(5):749-757. 被引量:1
  • 4Chandra D, Kale RK. Influence of gamma-rays on the mouse liver cytochrome P450 system and its modulation by phenothiazine drugs[J]. Int J Radiat Bio1,1999,75 (3):335-349. 被引量:1
  • 5Chung HC, Kim SH, Lee MG, et al. Mitochondrial dysfunction by gamma-irradiation accompanies the induction of cytochrome P450 2El (CYP2E1) in rat liver[J]. Toxicology,2001,161(1-2):79-91. 被引量:1
  • 6Goeptar AR, te Koppele JM, van Maanen JM, et al.Oneelectron reductive bioactivation of 2,3,5,6-tetramethylbenzoquinone by cytochrome P450 [J].Biochem Pharmacol,1992,43(2):343-352. 被引量:1
  • 7Patterson LH.Rationale for the use of aliphatic N-oxides of cytotoxic anthraquinones as prodrug DNA binding agents: a new class of, bioreductive agent [J].Cancer Metastasis Rev,1993,12(2):119-134. 被引量:1
  • 8Raleigh SM, Wanogho E, Burke MD, et al.Rat cytochromes P450 (CYP) specifically contribute to the reductive bioactivation of AQ4N, an alkylaminoanthraquinone-di-N-oxide anticancer prodrug[J].Xenobiotica, 1999,29( 11): 1115-1122. 被引量:1
  • 9Patterson LH, Murray GI.Tumour cytochrome P450 and drug activation[J].Curr Pharm Des, 2002,8(15): 1335-1347. 被引量:1

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