Evaluation of S-[11C]citalopram as a radioligand for in vivo labelling of 5-hydroxytryptamine uptake sites

Int J Rad Appl Instrum B. 1992 Nov;19(8):851-5. doi: 10.1016/0883-2897(92)90171-t.

Abstract

The biologically active S-enantiomer of [N-methyl-11C]citalopram was evaluated as a radioligand for in vivo labelling of the 5-hydroxytryptamine uptake site in brain, using ex vivo tissue counting in rats and positron emission tomography in man. In rats, the maximal signal for total versus non-specific binding was approx. 2 at 60-120 min after radioligand injection. Subsequent studies in man failed to identify a specific signal over a 90 min scanning period, due to prolonged retention of non-specific label.

MeSH terms

  • Animals
  • Brain / metabolism
  • Carbon Radioisotopes*
  • Citalopram / metabolism*
  • Male
  • Radioligand Assay
  • Rats
  • Rats, Sprague-Dawley
  • Serotonin / metabolism*
  • Stereoisomerism
  • Tomography, Emission-Computed

Substances

  • Carbon Radioisotopes
  • Citalopram
  • Serotonin