Literature DB >> 9267542

Naltrexone biotransformation and incidence of subjective side effects: a preliminary study.

A C King1, J R Volpicelli, M Gunduz, C P O'Brien, M J Kreek.   

Abstract

When administered orally, naltrexone undergoes extensive biotransformation and is metabolized to 6 beta-naltrexol and other minor metabolites. Naltrexone has been recently approved by the Food and Drug Administration for the treatment of alcohol dependence. An important clinical issue with naltrexone treatment is predicting patient compliance, which may be influenced by adverse side effects experienced during the medication. We investigated whether subjective side effects were related to urinary concentrations of naltrexone and its metabolite 6 beta-naltrexol 3 hr after administration of 50 mg po naltrexone in 24 male moderate-to-heavy social drinkers. The results showed significantly higher levels of urinary 6 beta-naltrexol (p < 0.05) in those subjects who experienced one or more side effect (i.e., headache, nausea, anxiety, or erection). Urinary naltrexone levels did not differ between the groups. Results also showed an approximate 10:1 ratio of 6 beta-naltrexol to naltrexone levels and a significant positive correlation between the parent compound and metabolite, suggesting parallel renal clearance. The results of this study suggest a possible mechanism for the side effects observed after acute administration of naltrexone.

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Year:  1997        PMID: 9267542

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  15 in total

1.  Naltrexone alters the processing of social and emotional stimuli in healthy adults.

Authors:  Margaret C Wardle; Anya K Bershad; Harriet de Wit
Journal:  Soc Neurosci       Date:  2016-01-22       Impact factor: 2.083

2.  Kinetics and inhibition of the formation of 6beta-naltrexol from naltrexone in human liver cytosol.

Authors:  S J Porter; A A Somogyi; J M White
Journal:  Br J Clin Pharmacol       Date:  2000-11       Impact factor: 4.335

3.  Dual efficacy of delta opioid receptor-selective ligands for ethanol drinking and anxiety.

Authors:  Richard M van Rijn; Daniela I Brissett; Jennifer L Whistler
Journal:  J Pharmacol Exp Ther       Date:  2010-07-06       Impact factor: 4.030

4.  In vitro/in vivo correlation of transdermal naltrexone prodrugs in hairless guinea pigs.

Authors:  Satyanarayana Valiveti; Kalpana S Paudel; Dana C Hammell; Mohamed O Hamad; Jianhong Chen; Peter A Crooks; Audra L Stinchcomb
Journal:  Pharm Res       Date:  2005-06-08       Impact factor: 4.200

Review 5.  Safety and Tolerability of Pharmacological Treatment of Alcohol Dependence: Comprehensive Review of Evidence.

Authors:  Julia M A Sinclair; Sophia E Chambers; Celia J Shiles; David S Baldwin
Journal:  Drug Saf       Date:  2016-07       Impact factor: 5.606

6.  Naltrexone alters alcohol self-administration behaviors and hypothalamic-pituitary-adrenal axis activity in a sex-dependent manner in rats.

Authors:  Steven J Nieto; Cana B Quave; Therese A Kosten
Journal:  Pharmacol Biochem Behav       Date:  2018-02-24       Impact factor: 3.533

Review 7.  Improving clinical outcomes for naltrexone as a management of problem alcohol use.

Authors:  Gary K Hulse
Journal:  Br J Clin Pharmacol       Date:  2013-11       Impact factor: 4.335

8.  Microneedles permit transdermal delivery of a skin-impermeant medication to humans.

Authors:  Daniel P Wermeling; Stan L Banks; David A Hudson; Harvinder S Gill; Jyoti Gupta; Mark R Prausnitz; Audra L Stinchcomb
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-04       Impact factor: 11.205

9.  Naltrexone decreases heavy drinking rates in smoking cessation treatment: an exploratory study.

Authors:  Andrea King; Dingcai Cao; Catherine Vanier; Tracie Wilcox
Journal:  Alcohol Clin Exp Res       Date:  2009-03-19       Impact factor: 3.455

10.  Effects of naltrexone on pain sensitivity and mood in fibromyalgia: no evidence for endogenous opioid pathophysiology.

Authors:  Jarred W Younger; Alex J Zautra; Eric T Cummins
Journal:  PLoS One       Date:  2009-04-13       Impact factor: 3.240

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