Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/31750
Title: Acute benzodiazepine administration induces changes in homocysteine metabolism in young healthy volunteers
Authors: Pompeia, Sabine [UNIFESP]
Grego, Bruno H. C. [UNIFESP]
Pradella-Hallinan, Marcia [UNIFESP]
Hachul, Helena [UNIFESP]
Tufik, Sergio [UNIFESP]
D'Almeida, Vania [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Keywords: Benzodiazepine
Cortisol
Cysteine
Gender
Homocysteine
Issue Date: 31-Aug-2009
Publisher: Elsevier B.V.
Citation: Progress in Neuro-psychopharmacology & Biological Psychiatry. Oxford: Pergamon-Elsevier B.V., v. 33, n. 6, p. 933-938, 2009.
Abstract: 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.
URI: http://repositorio.unifesp.br/handle/11600/31750
ISSN: 0278-5846
Other Identifiers: http://dx.doi.org/10.1016/j.pnpbp.2009.04.017
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