Literature DB >> 7520379

Association of cerebrospinal fluid deficiency of 5-methyltetrahydrofolate, but not S-adenosylmethionine, with reduced concentrations of the acid metabolites of 5-hydroxytryptamine and dopamine.

R Surtees1, S Heales, A Bowron.   

Abstract

1. Folate deficiency, or inborn errors of folate metabolism, cause reduced turnover of 5-hydroxytryptamine (serotonin), and perhaps dopamine, in the central nervous system. The mechanism by which this occurs are not known. One possibility is that this is mediated by deficiency of the methyl-donor S-adenosylmethionine. 2. To test this in humans, we have measured cerebrospinal fluid concentrations of 5-hydroxyindoleacetic acid and homovanillic acid, metabolites of 5-hydroxytryptamine and dopamine, respectively, in children with inborn errors of the methyl-transfer pathway. These children are naturally deficient in 5-methyltetrahydrofolate, S-adenosylmethionine or both before treatment, and replete with S-adenosylmethionine, but not necessarily with 5-methyltetrahydrofolate, during treatment. 3. Children with subnormal cerebrospinal fluid concentrations of 5-methyltetrahydrofolate had significantly reduced concentrations of 5-hydroxyindoleacetic acid and homovanillic acid. Children with subnormal cerebrospinal fluid concentrations of S-adenosylmethionine did not have significantly reduced concentrations of these metabolites. 4. We conclude that the mechanism by which deficiency of 5-methyltetrahydrofolate causes reduced 5-hydroxytryptamine and dopamine turnover is unlikely to be mediated by S-adenosylmethionine.

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Year:  1994        PMID: 7520379     DOI: 10.1042/cs0860697

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  5 in total

1.  Folate and depression--a neglected problem.

Authors:  Simon N Young
Journal:  J Psychiatry Neurosci       Date:  2007-03       Impact factor: 6.186

2.  Long term treatment with betaine in methylenetetrahydrofolate reductase deficiency.

Authors:  E Ronge; B Kjellman
Journal:  Arch Dis Child       Date:  1996-03       Impact factor: 3.791

3.  Decreased cerebral spinal fluid neurotransmitter levels in Smith-Lemli-Opitz syndrome.

Authors:  S E Sparks; C A Wassif; H Goodwin; S K Conley; D C Lanham; L E Kratz; K Hyland; A Gropman; E Tierney; F D Porter
Journal:  J Inherit Metab Dis       Date:  2014-02-06       Impact factor: 4.982

4.  L-methylfolate Plus SSRI or SNRI from Treatment Initiation Compared to SSRI or SNRI Monotherapy in a Major Depressive Episode.

Authors:  Lawrence D Ginsberg; Alondra Y Oubre; Yahya A Daoud
Journal:  Innov Clin Neurosci       Date:  2011-01

5.  Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 gene.

Authors:  Belén Pérez-Dueñas; Claudio Toma; Aida Ormazábal; Jordi Muchart; Francesc Sanmartí; Georgina Bombau; Mercedes Serrano; Angels García-Cazorla; Bru Cormand; Rafael Artuch
Journal:  J Inherit Metab Dis       Date:  2010-09-21       Impact factor: 4.982

  5 in total

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