Neurochemical alterations in Rett syndrome

Gary L. Wenk, Marina O'Leary, Charles B. Nemeroff, Garth Bissette, Hugo Moser, Saku Naidu

Research output: Contribution to journalArticle

42 Scopus citations

Abstract

The Rett syndrome (RS) is a neurological disorder associated with severe mental deficiency and neurological manifestations of cortical and extrapyramidal dysfunction. The present report is (1) a postmortem brain study that compares the levels of choline acetyltransferase (ChAT) activity and the binding density of selected neurotransmitter receptors in four cases of RS and five normal controls of similar age and (2) a study of cerebrospinal fluid (CSF) concentrations of the endogenous tridecapeptide neurotensin in 12 RS patients and 8 controls of similar age. The level of ChAT activity was lower in many cortical and subcortical regions in the RS brains as compared to control levels. The number of NMDA, AMPA, μ opioid and neurotensin binding sites, as well as CSF concentrations of neurotensin, did not differ significantly from control levels. The results suggest that changes in specific neurotransmitter systems, particularly cholinergic neurons, in the thalamus, cerebellum and basal ganglia may underlie the progressive deterioration in motor and cognitive function characteristic of this disorder.

Original languageEnglish (US)
Pages (from-to)67-72
Number of pages6
JournalDevelopmental Brain Research
Volume74
Issue number1
DOIs
StatePublished - Jul 16 1993
Externally publishedYes

Keywords

  • Acetylcholine
  • Glutamate
  • Neurotensin
  • Opiate
  • Post-mortem analysis
  • Rett syndrome

ASJC Scopus subject areas

  • Developmental Biology
  • Developmental Neuroscience

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    Wenk, G. L., O'Leary, M., Nemeroff, C. B., Bissette, G., Moser, H., & Naidu, S. (1993). Neurochemical alterations in Rett syndrome. Developmental Brain Research, 74(1), 67-72. https://doi.org/10.1016/0165-3806(93)90084-N