Literature DB >> 6990798

The clinical application of tricyclic antidepressant pharmacokinetics and plasma levels.

J Amsterdam, D Brunswick, J Mendels.   

Abstract

The authors present a clinical approach for predicting and using plasma concentrations of tricyclic antidepressants in the treatment of depressed patients. They review the pharmacokinetics of this group of drugs and their side effects and toxicity. There is a suggested therapeutic range for plasma concentrations of imipramine, amitriptyline, and nortriptyline; more definitive studies are needed to determine the necessary plasma levels for achieving clinical response with the other tricyclic antidepressants (desmethylimipramine, protriptyline, doxepin, clomipramine, impiramine N-oxide, and butriptyline). A more thorough knowledge of the clinical pharmacokinetics of tricyclic antidepressants should lead to more rational use of these drugs, with a higher response rate and fewer adverse reactions.

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Year:  1980        PMID: 6990798     DOI: 10.1176/ajp.137.6.653

Source DB:  PubMed          Journal:  Am J Psychiatry        ISSN: 0002-953X            Impact factor:   18.112


  26 in total

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Review 2.  Pharmacokinetic and pharmacodynamic principles of illicit drug use and treatment of illicit drug users.

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Journal:  Clin Pharmacokinet       Date:  1997-11       Impact factor: 6.447

3.  Acute versus repeated administration of desipramine in rats and mice: relationships between brain concentrations and reduction of immobility in the swimming test.

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Journal:  Psychopharmacology (Berl)       Date:  1986       Impact factor: 4.530

Review 4.  Guide to drug dosage in renal failure.

Authors:  W M Bennett
Journal:  Clin Pharmacokinet       Date:  1988-11       Impact factor: 6.447

5.  Absolute bioavailability of imipramine: influence of food.

Authors:  D R Abernethyl; M Divoll; D J Greenblatt; J S Harmatz; R I Shader
Journal:  Psychopharmacology (Berl)       Date:  1984       Impact factor: 4.530

6.  Doxepin plasma concentrations in clinical practice. Could there be a pharmacokinetic explanation for low concentrations?

Authors:  P R Joyce; J R Sharman
Journal:  Clin Pharmacokinet       Date:  1985 Jul-Aug       Impact factor: 6.447

7.  Imipramine inhibition of transient K+ current: an external open channel blocker preventing fast inactivation.

Authors:  C C Kuo
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

8.  Cimetidine-induced alterations in desipramine plasma concentrations.

Authors:  J D Amsterdam; D J Brunswick; L Potter; M J Kaplan
Journal:  Psychopharmacology (Berl)       Date:  1984       Impact factor: 4.530

Review 9.  Drug therapy for geriatric depression.

Authors:  R Bressler; M D Katz
Journal:  Drugs Aging       Date:  1993 May-Jun       Impact factor: 3.923

10.  Antidepressant interactions with the NMDA NR1-1b subunit.

Authors:  Richard Raabe; Lisa Gentile
Journal:  J Biophys       Date:  2008-06-05
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