Acetylcholine receptors in dementia and mild cognitive impairment

Eur J Nucl Med Mol Imaging. 2008 Mar:35 Suppl 1:S30-45. doi: 10.1007/s00259-007-0701-1.

Abstract

Purpose: To clarify whether changes in the cholinergic transmission occur early in the course of Alzheimer's disease (AD), we carried out positron emission tomography (PET) with the radioligand 2-[(18)F]F-A-85380, which is supposed to be specific for alpha4beta2 nicotinic acetylcholine receptors (nAChRs).

Method: We included patients with moderate to severe AD and patients with amnestic mild cognitive impairment (MCI), presumed to present preclinical AD.

Results: Both patients with AD and MCI showed significant reductions in alpha4beta2 nAChRs in brain regions typically affected by AD pathology. These findings indicate that a reduction in alpha4beta2 nAChRs occurs during early symptomatic stages of AD. The alpha4beta2 nAChR availability in these regions correlated with the severity of cognitive impairment, indicating a stage sensitivity of the alpha4beta2 nAChR status.

Conclusion: Together, our results provide evidence for the potential of 2-[(18)]F-A-85380 nAChR PET in the diagnosis of patients at risk for AD. Because of the extraordinary long acquisition time with 2-[(18)F]F-A-85380, we developed the new alpha4beta2 nAChR-specific radioligands (+)- and (-)-[(18)F]norchloro-fluoro-homoepibatidine (NCFHEB) and evaluated them preclinically. (-)-[(18)F]NCFHEB shows twofold higher brain uptake and significantly shorter acquisition times. Therefore, (-)-[(18)F]NCFHEB should be a suitable radioligand for larger clinical investigations.

Publication types

  • Review

MeSH terms

  • Brain / diagnostic imaging*
  • Brain / metabolism*
  • Cognition Disorders / complications
  • Cognition Disorders / diagnostic imaging*
  • Cognition Disorders / metabolism*
  • Dementia / complications
  • Dementia / diagnostic imaging*
  • Dementia / metabolism*
  • Humans
  • Molecular Probe Techniques
  • Positron-Emission Tomography / methods
  • Receptors, Cholinergic / metabolism*
  • Tissue Distribution

Substances

  • Receptors, Cholinergic