Decreased rates of cerebral protein synthesis in conscious young adults with fragile X syndrome demonstrated by L-[1-11C]leucine PET

J Cereb Blood Flow Metab. 2022 Sep;42(9):1666-1675. doi: 10.1177/0271678X221090997. Epub 2022 Mar 29.

Abstract

Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. Fragile X mental retardation protein, a putative translation suppressor, is significantly reduced in FXS. The prevailing hypothesis is that rates of cerebral protein synthesis (rCPS) are increased by the absence of this regulatory protein. We have previously reported increased rCPS in the Fmr1 knockout mouse model of FXS. To address the hypothesis in human subjects, we measured rCPS in young men with FXS with L-[1-11C]leucine PET. In previous studies we had used sedation during imaging, and we did not find increases in rCPS as had been seen in the mouse model. Since mouse measurements were conducted in awake animals, we considered the possibility that sedation may have confounded our results. In the present study we used a modified and validated PET protocol that made it easier for participants with FXS to undergo the study awake. We compared rCPS in 10 fragile X participants and 16 healthy controls all studied while awake. Contrary to the prevailing hypothesis and findings in Fmr1 knockout mice, results indicate that rCPS in awake participants with FXS are decreased in whole brain and most brain regions by 13-21% compared to healthy controls.

Keywords: FMRP; Fragile X syndrome; PET; protein synthesis; translation.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Cerebrum* / metabolism
  • Disease Models, Animal
  • Fragile X Mental Retardation Protein / genetics
  • Fragile X Mental Retardation Protein / metabolism
  • Fragile X Syndrome* / diagnostic imaging
  • Fragile X Syndrome* / metabolism
  • Humans
  • Leucine / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Positron-Emission Tomography
  • Protein Biosynthesis*
  • Young Adult

Substances

  • FMR1 protein, human
  • Fmr1 protein, mouse
  • Fragile X Mental Retardation Protein
  • Leucine