Acute benzodiazepine administration induces changes in homocysteine metabolism in young healthy volunteers

التفاصيل البيبلوغرافية
العنوان: Acute benzodiazepine administration induces changes in homocysteine metabolism in young healthy volunteers
المؤلفون: Pompeia, Sabine UNIFESP, Grego, Bruno H. C. UNIFESP, Pradella-Hallinan, Marcia UNIFESP, Hachul, Helena UNIFESP, Tufik, Sergio UNIFESP, D'Almeida, Vania UNIFESP
المساهمون: Universidade Federal de São Paulo (UNIFESP)
بيانات النشر: Elsevier B.V.
سنة النشر: 2009
المجموعة: Universidade Federal de São Paulo (UNIFESP): Repositório Institucional
مصطلحات موضوعية: Benzodiazepine, Cortisol, Cysteine, Gender, Homocysteine
الوصف: Purpose: High cortisol plasma concentrations have been shown to be associated with increases in homocysteine levels. Here we studied whether decreases in cortisol concentration, induced by an acute oral dose of a benzodiazepine, could decrease homocysteine, and if changes were similar in both genders.Methods: This was a double-blind, cross-over design study of acute oral flunitrazepam (1.2 mg) and placebo in young, healthy, male and female (n = 21) volunteers. Blood samples were collected 3 h after ingestion (after peak-plasma concentration of flunitrazepam was reached). Various biochemical parameters were analysed, such as plasma homocysteine, cysteine, folate, vitamins B6, B12, and sexual hormones.Results: Flunitrazepam reduced cortisol (p = 0.0011), cysteine (p = 0.014) and homocysteine (p = 0.028) concentrations, irrespective of gender. No correlations were found between cortisol and other biochemical markers (all r's<0.03). Concentration of cysteine and homocysteine were negatively correlated with plasma flunitrazepam concentration, suggesting that changes in these amino acids might be related to the metabolism of this benzodiazepine.Conclusion: Acute administration of flunitrazepam decreases plasma homocysteine and cysteine by mechanisms that seem unrelated to changes in cortisol. Given the importance of homocysteine as a market of life-threatening disorders, the mechanisms involved in the decrease of these amino acids are potential targets for clinical application. (C) 2009 Elsevier Inc. All rights reserved. ; Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) ; Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) ; AFIP ; Universidade Federal de São Paulo, Dept Psychobiol, BR-04024002 São Paulo, Brazil ; Universidade Federal de São Paulo, Dept Biosci, BR-04024002 São Paulo, Brazil ; Universidade Federal de São Paulo, Dept Psychobiol, BR-04024002 São Paulo, Brazil ; Universidade Federal de São Paulo, Dept Biosci, BR-04024002 São Paulo, Brazil ; FAPESP: 2005/03552-8 ; FAPESP: ...
نوع الوثيقة: review
وصف الملف: 933-938
اللغة: English
تدمد: 0278-5846
Relation: Progress in Neuro-psychopharmacology & Biological Psychiatry; http://dx.doi.org/10.1016/j.pnpbp.2009.04.017; Progress in Neuro-psychopharmacology & Biological Psychiatry. Oxford: Pergamon-Elsevier B.V., v. 33, n. 6, p. 933-938, 2009.; http://repositorio.unifesp.br/handle/11600/31750; WOS:000269300600003
DOI: 10.1016/j.pnpbp.2009.04.017
الاتاحة: http://repositorio.unifesp.br/handle/11600/31750
https://doi.org/10.1016/j.pnpbp.2009.04.017
Rights: Acesso restrito ; http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
رقم الانضمام: edsbas.8A9433C8
قاعدة البيانات: BASE
الوصف
تدمد:02785846
DOI:10.1016/j.pnpbp.2009.04.017