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Early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)H-magnetic resonance spectroscopy of N-acetyl-aspartate
Increasing interest surrounds potential neuroprotective or neurotrophic actions of antidepressants. While growing evidence points to important early clinical and neuropsychological effects of antidepressants, the time-course of any effect on neuronal integrity is unclear. This study used magnetic re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496168/ https://www.ncbi.nlm.nih.gov/pubmed/22449253 http://dx.doi.org/10.1017/S1461145712000272 |
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author | Taylor, Matthew J. Godlewska, Beata R. Norbury, Ray Selvaraj, Sudhakar Near, Jamie Cowen, Philip J. |
author_facet | Taylor, Matthew J. Godlewska, Beata R. Norbury, Ray Selvaraj, Sudhakar Near, Jamie Cowen, Philip J. |
author_sort | Taylor, Matthew J. |
collection | PubMed |
description | Increasing interest surrounds potential neuroprotective or neurotrophic actions of antidepressants. While growing evidence points to important early clinical and neuropsychological effects of antidepressants, the time-course of any effect on neuronal integrity is unclear. This study used magnetic resonance spectroscopy to assess effects of short-term treatment with escitalopram on N-acetyl-aspartate (NAA), a marker of neuronal integrity. Thirty-nine participants with major depression were randomly assigned to receive either 10 mg escitalopram or placebo daily in a double-blind, parallel group design. On the seventh day of treatment, PRESS data were obtained from a 30×30×20 mm voxel placed in medial frontal cortex. Age and gender-matched healthy controls who received no treatment were also scanned. Levels of NAA were significantly higher in patients treated with escitalopram than in either placebo-treated patients (p<0.01) or healthy controls (p<0.01). Our findings are consistent with the proposition that antidepressant treatment in depressed patients can produce early changes in neuronal integrity. |
format | Online Article Text |
id | pubmed-3496168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34961682012-11-20 Early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)H-magnetic resonance spectroscopy of N-acetyl-aspartate Taylor, Matthew J. Godlewska, Beata R. Norbury, Ray Selvaraj, Sudhakar Near, Jamie Cowen, Philip J. Int J Neuropsychopharmacol Brief Report Increasing interest surrounds potential neuroprotective or neurotrophic actions of antidepressants. While growing evidence points to important early clinical and neuropsychological effects of antidepressants, the time-course of any effect on neuronal integrity is unclear. This study used magnetic resonance spectroscopy to assess effects of short-term treatment with escitalopram on N-acetyl-aspartate (NAA), a marker of neuronal integrity. Thirty-nine participants with major depression were randomly assigned to receive either 10 mg escitalopram or placebo daily in a double-blind, parallel group design. On the seventh day of treatment, PRESS data were obtained from a 30×30×20 mm voxel placed in medial frontal cortex. Age and gender-matched healthy controls who received no treatment were also scanned. Levels of NAA were significantly higher in patients treated with escitalopram than in either placebo-treated patients (p<0.01) or healthy controls (p<0.01). Our findings are consistent with the proposition that antidepressant treatment in depressed patients can produce early changes in neuronal integrity. Cambridge University Press 2012-11 2012-03-26 /pmc/articles/PMC3496168/ /pubmed/22449253 http://dx.doi.org/10.1017/S1461145712000272 Text en © CINP 2012 The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence <http://creativecommons.org/licenses/by-nc-sa/2.5/>. The written permission of Cambridge University Press must be obtained for commercial re-use. http://creativecommons.org/licenses/by-nc-sa/2.5/ The online version of this article is published within an Open Access environment subject to the conditions of the Creative Commons Attribution-NonCommercial-ShareAlike licence <http://creativecommons.org/licenses/by-nc-sa/2.5/>. (http://creativecommons.org/licenses/by-nc-sa/2.5/>) The written permission of Cambridge University Press must be obtained for commercial re-use. |
spellingShingle | Brief Report Taylor, Matthew J. Godlewska, Beata R. Norbury, Ray Selvaraj, Sudhakar Near, Jamie Cowen, Philip J. Early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)H-magnetic resonance spectroscopy of N-acetyl-aspartate |
title | Early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)H-magnetic resonance spectroscopy of N-acetyl-aspartate |
title_full | Early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)H-magnetic resonance spectroscopy of N-acetyl-aspartate |
title_fullStr | Early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)H-magnetic resonance spectroscopy of N-acetyl-aspartate |
title_full_unstemmed | Early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)H-magnetic resonance spectroscopy of N-acetyl-aspartate |
title_short | Early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)H-magnetic resonance spectroscopy of N-acetyl-aspartate |
title_sort | early increase in marker of neuronal integrity with antidepressant treatment of major depression: (1)h-magnetic resonance spectroscopy of n-acetyl-aspartate |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496168/ https://www.ncbi.nlm.nih.gov/pubmed/22449253 http://dx.doi.org/10.1017/S1461145712000272 |
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