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Human Sensory LTP Predicts Memory Performance and Is Modulated by the BDNF Val66Met Polymorphism.
Spriggs, Meg J; Thompson, Chris S; Moreau, David; McNair, Nicolas A; Wu, C Carolyn; Lamb, Yvette N; McKay, Nicole S; King, Rohan O C; Antia, Ushtana; Shelling, Andrew N; Hamm, Jeff P; Teyler, Timothy J; Russell, Bruce R; Waldie, Karen E; Kirk, Ian J.
Afiliação
  • Spriggs MJ; Faculty of Science, School of Psychology, University of Auckland, Auckland, New Zealand.
  • Thompson CS; Centre for Brain Research, University of Auckland, Auckland, New Zealand.
  • Moreau D; Brain Research New Zealand, Auckland, New Zealand.
  • McNair NA; Psychedelic Research Group, Division of Brain Sciences, Centre for Psychiatry, Imperial College London, London, United Kingdom.
  • Wu CC; Faculty of Science, School of Psychology, University of Auckland, Auckland, New Zealand.
  • Lamb YN; Centre for Brain Research, University of Auckland, Auckland, New Zealand.
  • McKay NS; Faculty of Science, School of Psychology, University of Auckland, Auckland, New Zealand.
  • King ROC; Centre for Brain Research, University of Auckland, Auckland, New Zealand.
  • Antia U; Faculty of Science, School of Psychology, University of Auckland, Auckland, New Zealand.
  • Shelling AN; School of Psychology, University of Sydney, Sydney, NSW, Australia.
  • Hamm JP; Faculty of Science, School of Psychology, University of Auckland, Auckland, New Zealand.
  • Teyler TJ; Department of Psychology, University of Trier, Trier, Germany.
  • Russell BR; Faculty of Science, School of Psychology, University of Auckland, Auckland, New Zealand.
  • Waldie KE; Centre for Brain Research, University of Auckland, Auckland, New Zealand.
  • Kirk IJ; Faculty of Science, School of Psychology, University of Auckland, Auckland, New Zealand.
Front Hum Neurosci ; 13: 22, 2019.
Article em En | MEDLINE | ID: mdl-30828292
ABSTRACT

Background:

Long-term potentiation (LTP) is recognised as a core neuronal process underlying long-term memory. However, a direct relationship between LTP and human memory performance is yet to be demonstrated. The first aim of the current study was thus to assess the relationship between LTP and human long-term memory performance. With this also comes an opportunity to explore factors thought to mediate the relationship between LTP and long-term memory. The second aim of the current study was to explore the relationship between LTP and memory in groups differing with respect to brain-derived neurotrophic factor (BDNF) Val66Met; a single-nucleotide polymorphism (SNP) implicated in memory function.

Methods:

Participants were split into three genotype groups (Val/Val, Val/Met, Met/Met) and were presented with both an EEG paradigm for inducing LTP-like enhancements of the visually-evoked response, and a test of visual memory.

Results:

The magnitude of LTP 40 min after induction was predictive of long-term memory performance. Additionally, the BDNF Met allele was associated with both reduced LTP and reduced memory performance.

Conclusions:

The current study not only presents the first evidence for a relationship between sensory LTP and human memory performance, but also demonstrates how targeting this relationship can provide insight into factors implicated in variation in human memory performance. It is anticipated that this will be of utility to future clinical studies of disrupted memory function.
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Hum Neurosci Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Nova Zelândia

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Hum Neurosci Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Nova Zelândia