The advantage of using positron emission tomography in drug research

被引:80
作者
Farde, L
机构
[1] Psychiatry Section, Dept. of Clinical Neuroscience, Karolinska Institutet
关键词
D O I
10.1016/0166-2236(96)40002-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A large problem in drug discovery is to find relevant in vitro or in vivo animal models and to be able to extrapolate the results obtained to humans. Drug research now benefits from the fast development of imaging technologies that trace radiolabelled molecules directly in the human brain. Positron emission tomography (PET) and allied techniques use molecules that are labelled with short-lived radioisotopes and injected intravenously. The most straightforward approach is to radiolabel a new potential drug and then to trace its anatomical distribution and binding in the brain. An indirect approach is to study how the unlabelled drug inhibits specific radioligand binding. The demonstration of quantitative relationships between drug binding in vivo and drug effects in patients is used to validate targets for drug action and to optimize clinical treatment.
引用
收藏
页码:211 / 214
页数:4
相关论文
共 30 条
  • [1] D-1 RECEPTOR ANTAGONISTS IN SCHIZOPHRENIA
    BARNES, TRE
    GERLACH, J
    [J]. PSYCHOPHARMACOLOGY, 1995, 121 (03) : 287 - 288
  • [2] STRIATAL DOPAMINE RECEPTOR OCCUPANCY DURING AND FOLLOWING WITHDRAWAL FROM NEUROLEPTIC TREATMENT - CORRELATIVE EVALUATION BY POSITRON EMISSION TOMOGRAPHY AND PLASMA PROLACTIN LEVELS
    BARON, JC
    MARTINOT, JL
    CAMBON, H
    BOULENGER, JP
    POIRIER, MF
    CAILLARD, V
    BLIN, J
    HURET, JD
    LOCH, C
    MAZIERE, B
    [J]. PSYCHOPHARMACOLOGY, 1989, 99 (04) : 463 - 472
  • [3] THE RELATIONSHIP BETWEEN LOCOMOTOR DISABILITY, AUTONOMIC DYSFUNCTION, AND THE INTEGRITY OF THE STRIATAL DOPAMINERGIC SYSTEM IN PATIENTS WITH MULTIPLE SYSTEM ATROPHY, PURE AUTONOMIC FAILURE, AND PARKINSONS-DISEASE, STUDIED WITH PET
    BROOKS, DJ
    SALMON, EP
    MATHIAS, CJ
    QUINN, N
    LEENDERS, KL
    BANNISTER, R
    MARSDEN, CD
    FRACKOWIAK, RSJ
    [J]. BRAIN, 1990, 113 : 1539 - 1552
  • [4] CHIPKIN RE, 1988, J PHARMACOL EXP THER, V247, P1093
  • [5] STRIATAL BINDING OF THE PET LIGAND C-11 RACLOPRIDE IS ALTERED BY DRUGS THAT MODIFY SYNAPTIC DOPAMINE LEVELS
    DEWEY, SL
    SMITH, GS
    LOGAN, J
    BRODIE, JD
    FOWLER, JS
    WOLF, AP
    [J]. SYNAPSE, 1993, 13 (04) : 350 - 356
  • [6] DISTRIBUTION OF REMOXIPRIDE TO THE HUMAN BRAIN AND CENTRAL D2-DOPAMINE RECEPTOR-BINDING EXAMINED INVIVO BY PET
    FARDE, L
    VONBAHR, C
    [J]. ACTA PSYCHIATRICA SCANDINAVICA, 1990, 82 : 67 - &
  • [7] FARDE L, 1988, ARCH GEN PSYCHIAT, V45, P71
  • [8] POSITRON EMISSION TOMOGRAPHY STUDIES ON D-2 AND 5-HT2 RECEPTOR-BINDING IN RISPERIDONE-TREATED SCHIZOPHRENIC-PATIENTS
    FARDE, L
    NYBERG, S
    OXENSTIERNA, G
    NAKASHIMA, Y
    HALLDIN, C
    ERICSSON, B
    [J]. JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 1995, 15 (01) : S19 - S23
  • [9] QUANTITATIVE-ANALYSIS OF D2 DOPAMINE RECEPTOR-BINDING IN THE LIVING HUMAN-BRAIN BY PET
    FARDE, L
    HALL, H
    EHRIN, E
    SEDVALL, G
    [J]. SCIENCE, 1986, 231 (4735) : 258 - 261
  • [10] FARDE L, 1992, ARCH GEN PSYCHIAT, V49, P538