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Toxicological implications of polymorphic drug metabolism.

作者信息

Ritchie J C, Sloan T P, Idle J R, Smith R L

出版信息

Ciba Found Symp. 1980;76:219-44. doi: 10.1002/9780470720592.ch12.

DOI:10.1002/9780470720592.ch12
PMID:6906263
Abstract

The occurrence of genetic polymorphisms of drug metabolism means that populations contain subgroups (phenotypes) that differ sharply in their abilities to effect a number of metabolic reactions. Because of this, major interphenotype differences occur in responsiveness to drugs and toxic substances. The well established genetic polymorphisms of acetylation and hydrolysis illustrate the important association that exists between phenotype and propensity to develop toxic and exaggerated responses to some substances. Recently, for metabolic oxidation, a new genetic polymorphism of drug metabolism has been described and it promises to provide a better understanding of inter-individual variability in the metabolic handling of, and responsiveness to, drugs and toxic substances. The following effects of the polymorphism are described here: (a) its influence in determining variable presystemic metabolism and hence systemic drug availability; (b) its role in determining alternative toxic pathways of metabolism in individuals who have a genetically determined impairment of oxidative capacity and (c) its influence on the development of agranulocytosis associated with metiamide administration.

摘要

相似文献

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Toxicological implications of polymorphic drug metabolism.
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引用本文的文献

1
Proceedings of the British Pharmacological Society. 16--18th December, 1980.英国药理学会会议记录。1980年12月16日至18日。
Br J Pharmacol. 1981 May;73(1):175P-318P. doi: 10.1111/j.1476-5381.1981.tb16787.x.
2
Evidence for an enzymatic defect in the 4-hydroxylation of debrisoquine by human liver.人体肝脏中去甲丙咪嗪4-羟化酶缺陷的证据。
Br J Clin Pharmacol. 1981 Jan;11(1):89-91. doi: 10.1111/j.1365-2125.1981.tb01108.x.
3
Genetically determined oxidation capacity and the disposition of debrisoquine.遗传决定的氧化能力与异喹胍的代谢
Br J Clin Pharmacol. 1983 Apr;15(4):443-50. doi: 10.1111/j.1365-2125.1983.tb01528.x.
4
Antipyrine metabolism in relation to polymorphic oxidations of sparteine and debrisoquine.安替比林代谢与司巴丁和异喹胍多态性氧化的关系。
Br J Clin Pharmacol. 1983 Mar;15(3):317-21. doi: 10.1111/j.1365-2125.1983.tb01505.x.
5
Impaired oxidation of debrisoquine in patients with perhexiline neuropathy.患有哌克昔林神经病变患者的异喹胍氧化受损。
Br Med J (Clin Res Ed). 1982 Jan 30;284(6312):295-9. doi: 10.1136/bmj.284.6312.295.
6
Assessment of the drug metabolism capacity of the liver.肝脏药物代谢能力的评估。
Br J Clin Pharmacol. 1982 Nov;14(5):631-51. doi: 10.1111/j.1365-2125.1982.tb04950.x.
7
Inhibitory effects of neuroleptics on debrisoquine oxidation in man.抗精神病药物对人体中异喹胍氧化的抑制作用。
Br J Clin Pharmacol. 1986 Jul;22(1):89-92.
8
Genetically determined variability in acetylation and oxidation. Therapeutic implications.乙酰化和氧化的基因决定变异性。治疗意义。
Drugs. 1985 Apr;29(4):342-75. doi: 10.2165/00003495-198529040-00003.