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debrisoquin and Metabolism, Inborn Errors

debrisoquin has been researched along with Metabolism, Inborn Errors in 8 studies

Debrisoquin: An adrenergic neuron-blocking drug similar in effects to GUANETHIDINE. It is also noteworthy in being a substrate for a polymorphic cytochrome P-450 enzyme. Persons with certain isoforms of this enzyme are unable to properly metabolize this and many other clinically important drugs. They are commonly referred to as having a debrisoquin 4-hydroxylase polymorphism.

Metabolism, Inborn Errors: Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.

Research Excerpts

ExcerptRelevanceReference
"Debrisoquine was a weak, noncompetitive inhibitor of alfentanil metabolism and of the formation of its major metabolites, with Ki values between 2."1.27Is the metabolism of alfentanil subject to debrisoquine polymorphism? A study using human liver microsomes. ( Hendrickx, JJ; Heykants, JJ; Lauwers, W; Lavrijsen, KL; Meuldermans, WE; Van Dyck, DM; Van Houdt, JM; Woestenborghs, RJ, 1988)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19907 (87.50)18.7374
1990's1 (12.50)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Roots, I1
Dick, B1
Küpfer, A1
Molnàr, J1
Braunschweig, S1
Preisig, R1
Danhof, M1
Idle, JR3
Teunissen, MW1
Sloan, TP1
Breimer, DD1
Smith, RL2
Mahgoub, A1
Dring, LG1
Lancaster, R1
Du, YL1
Lou, YQ1
Vesell, ES1
Lavrijsen, KL1
Van Houdt, JM1
Van Dyck, DM1
Hendrickx, JJ1
Woestenborghs, RJ1
Lauwers, W1
Meuldermans, WE1
Heykants, JJ1

Other Studies

8 other studies available for debrisoquin and Metabolism, Inborn Errors

ArticleYear
[Genetic causes for the variability of effects and side effects of drugs].
    Der Internist, 1982, Volume: 23, Issue:11

    Topics: Debrisoquin; Drug-Related Side Effects and Adverse Reactions; Female; Humans; Hydroxylation; Kinetic

1982
[Drug hydroxylation disorders (debrisoquin type) in a random sample of the Swiss population].
    Schweizerische medizinische Wochenschrift, 1982, Jul-24, Volume: 112, Issue:30

    Topics: Adolescent; Adult; Aged; Debrisoquin; Female; Homozygote; Humans; Hydroxylation; Isoquinolines; Male

1982
Influence of the genetically controlled deficiency in debrisoquine hydroxylation on antipyrine metabolite formation.
    Pharmacology, 1981, Volume: 22, Issue:6

    Topics: Aging; Antipyrine; Body Weight; Debrisoquin; Female; Half-Life; Humans; Hydroxylation; Isoquinolines

1981
Polymorphic hydroxylation of Debrisoquine in man.
    Lancet (London, England), 1977, Sep-17, Volume: 2, Issue:8038

    Topics: Administration, Oral; Adolescent; Adult; Alleles; Biological Availability; Chemical Phenomena; Chemi

1977
Polymorphism of debrisoquine 4-hydroxylation and family studies of poor metabolizers in Chinese population.
    Zhongguo yao li xue bao = Acta pharmacologica Sinica, 1990, Volume: 11, Issue:1

    Topics: Adolescent; Adult; Asian People; China; Debrisoquin; Female; Humans; Incidence; Isoquinolines; Male;

1990
Poor metabolisers of debrisoquine reveal their true colours.
    Lancet (London, England), 1989, Nov-04, Volume: 2, Issue:8671

    Topics: Alleles; Debrisoquin; Humans; Isoquinolines; Metabolism, Inborn Errors; Polymorphism, Restriction Fr

1989
Pharmacogenetic approaches to the prediction of drug response.
    NIDA research monograph, 1986, Volume: 66

    Topics: Debrisoquin; Disease Susceptibility; Drug Hypersensitivity; Drug-Related Side Effects and Adverse Re

1986
Is the metabolism of alfentanil subject to debrisoquine polymorphism? A study using human liver microsomes.
    Anesthesiology, 1988, Volume: 69, Issue:4

    Topics: Alfentanil; Chromatography, High Pressure Liquid; Debrisoquin; Fentanyl; Humans; Hydroxylation; Isoq

1988