Evaluation of carbon-11-labeled KF17837:: A potential CNS adenosine A2a receptor ligand

被引:0
作者
Noguchi, J
Ishiwata, K
Wakabayashi, S
Nariai, T
Shumiya, S
Ishii, S
Toyama, H
Endo, K
Suzuki, F
Senda, M
机构
[1] Tokyo Metropolitan Inst Gerontol, Positron Med Ctr, Tokyo 173, Japan
[2] Tokyo Metropolitan Inst Gerontol, Lab Anim Sci, Tokyo 173, Japan
[3] Showa Coll Pharmaceut Sci, Tokyo, Japan
[4] Tokyo Med & Dent Univ, Dept Neurosurg, Tokyo 113, Japan
[5] Kyowa Hakko Kogyo Co Ltd, Pharmaceut Res Labs, Shizuoka, Japan
关键词
carbon-11-KF17837; xanthine; adenosine A(2a) receptor; central nervous system; PET;
D O I
暂无
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The C-11-labeled KF17837 ([7-methyl-C-11](E)-8-(3,4-dimethoxy-styryl)-1, 3-dipropyl-7-methylxanthine) was evaluated as a PET ligand for mapping adenosine A(2a) receptors in the central nervous system (CNS). Methods: The regional brain distribution of [C-11]KF17837 and the effect of adenosine antagonists on the distribution were measured in mice by the tissue sampling method. In rats, the regional brain uptake of [C-11]KF17837 and the effect of carrier KF17837 was visualized by autoradiography. Imaging of the monkey brain with [C-11]KF17837 was performed by PET, Results: In mice, a high uptake of [C-11]KF17837 was found in the striatum in which A,, receptors were highly enriched. The uptake was decreased by co-injection of carrier KF17837 or a xanthine-type A(2a), antagonist CSC but not by nonxanthine-type A(2a) antagonists ZM 241385 or SCH 58261, or an A(1) antagonist KF15372, In the rat brain, [C-11]KF17837 was accumulated higher in the striatum than in other brain regions, and the uptake was blocked by co-injection of carrier KF17837. In a monkey PET study, a high striatal uptake of radioactivity was observed. Conclusion: Carbon-11-KF17837 binds to adenosine A(2a), receptors in the striatum. However, the presence of an unknown but specific binding site for xanthine-type compounds also was suggested in the other brain regions. The results also suggested that the in vivo receptor-binding sites of xanthine-type ligands are slightly different from those of nonxanthine-type A(2a) antagonists.
引用
收藏
页码:498 / 503
页数:6
相关论文
共 34 条
  • [1] BRUNS RF, 1986, MOL PHARMACOL, V29, P331
  • [2] ANALOGS OF CAFFEINE AND THEOPHYLLINE - EFFECT OF STRUCTURAL ALTERATIONS ON AFFINITY AT ADENOSINE RECEPTORS
    DALY, JW
    PADGETT, WL
    SHAMIM, MT
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1986, 29 (07) : 1305 - 1308
  • [3] THE DISTRIBUTION OF ADENOSINE-A1-RECEPTORS AND 5'-NUCLEOTIDASE IN THE BRAIN OF SOME COMMONLY USED EXPERIMENTAL-ANIMALS
    FASTBOM, J
    PAZOS, A
    PALACIOS, JM
    [J]. NEUROSCIENCE, 1987, 22 (03) : 813 - 826
  • [4] ADENOSINE-A1-RECEPTORS IN THE HUMAN-BRAIN - A QUANTITATIVE AUTORADIOGRAPHIC STUDY
    FASTBOM, J
    PAZOS, A
    PROBST, A
    PALACIOS, JM
    [J]. NEUROSCIENCE, 1987, 22 (03) : 827 - 839
  • [5] ADENOSINE DOPAMINE INTERACTIONS IN THE BRAIN
    FERRE, S
    FUXE, K
    VONEULER, G
    JOHANSSON, B
    FREDHOLM, BB
    [J]. NEUROSCIENCE, 1992, 51 (03) : 501 - 512
  • [6] MOLECULAR-CLONING OF THE RAT ADENOSINE-A2 RECEPTOR - SELECTIVE COEXPRESSION WITH D2-DOPAMINE RECEPTORS IN RAT STRIATUM
    FINK, JS
    WEAVER, DR
    RIVKEES, SA
    PETERFREUND, RA
    POLLACK, AE
    ADLER, EM
    REPPERT, SM
    [J]. MOLECULAR BRAIN RESEARCH, 1992, 14 (03): : 186 - 195
  • [7] FREDHOLM BB, 1994, PHARMACOL REV, V46, P143
  • [8] Furuta R, 1996, J NUCL MED, V37, P1203
  • [9] GOODMAN RR, 1982, J NEUROSCI, V2, P1230
  • [10] SYNTHESIS AND PRELIMINARY EVALUATION OF [C-11] KF15372, A SELECTIVE ADENOSINE A(1) ANTAGONIST
    ISHIWATA, K
    FURUTA, R
    SHIMADA, J
    ISHII, S
    ENDO, K
    SUZUKI, F
    SENDA, M
    [J]. APPLIED RADIATION AND ISOTOPES, 1995, 46 (10) : 1009 - 1013