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首页> 外文期刊>European Journal of Nuclear Medicine and Molecular Imaging >(123)I)Iodobenzamide binding to the rat dopamine D(2) receptor in competition with haloperidol and endogenous dopamine-an in vivo imaging study with a dedicated small animal SPECT.
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(123)I)Iodobenzamide binding to the rat dopamine D(2) receptor in competition with haloperidol and endogenous dopamine-an in vivo imaging study with a dedicated small animal SPECT.

机译:(123)I)碘苯甲酰胺在与氟哌啶醇和内源性多巴胺竞争中与大鼠多巴胺D(2)受体结合-用专用小动物SPECT进行的体内成像研究。

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PURPOSE: This study assessed [(123)I]iodobenzamide binding to the rat dopamine D(2) receptor in competition with haloperidol and endogenous dopamine using a high-resolution small animal SPECT. METHODS: Subsequent to baseline quantifications of D(2) receptor binding, imaging studies were performed on the same animals after pre-treatment with haloperidol and methylphenidate, which block D(2) receptors and dopamine transporters, respectively. RESULTS: Striatal baseline equilibrium ratios (V(3)'') of [(123)I]iodobenzamide binding were 1.42+/-0.31 (mean+/-SD). After pre-treatment with haloperidol and methylphenidate, V(3)'' values decreased to 0.54+/-0.46 (p<0.0001) and 0.98+/-0.48 (p=0.009), respectively. CONCLUSION: The decrease in [(123)I]iodobenzamide binding induced by pre-treatment with haloperidol reflects D(2) receptor blockade, whereas the decrease in receptor binding induced by pre-treatment with methylphenidate can be interpreted in terms of competition between [(123)I]IBZM and endogenous dopamine. Findings show that multiple in vivo measurements of [(123)I]iodobenzamide binding to D(2) receptors in competition with exogenous and endogenous ligands are feasible in the same animal. This may be of future relevance for the in vivo evaluation of novel radioligands as well as for studying the interrelations between pre- and/or postsynaptic radioligand binding and different levels of endogenous dopamine.
机译:目的:本研究使用高分辨率的小动物SPECT评估了[(123)I]碘苯甲酰胺与氟哌啶醇和内源性多巴胺竞争时与大鼠多巴胺D(2)受体的结合。方法:在对D(2)受体结合进行基线定量之后,对氟哌啶醇和哌醋甲酯分别阻断D(2)受体和多巴胺转运蛋白的动物进行了影像学研究。结果:[(123)I]碘代苯甲酰胺结合的纹状体基线平衡比(V(3)'')为1.42 +/- 0.31(平均+/- SD)。用氟哌啶醇和哌醋甲酯进行预处理后,V(3)''值分别降至0.54 +/- 0.46(p <0.0001)和0.98 +/- 0.48(p = 0.009)。结论:氟哌啶醇预处理诱导的[(123)I]碘苯甲酰胺结合的减少反映了D(2)受体阻滞,而哌醋甲酯预处理诱导的受体结合的减少可以解释为[ (123)I] IBZM和内源性多巴胺。研究结果表明,在同一只动物中,与外源和内源配体竞争的[[123] I]碘代苯甲酰胺与D(2)受体结合的多种体内测量是可行的。这对于新型放射性配体的体内评估以及研究突触前和/或突触后放射性配体结合与不同水平的内源多巴胺之间的相互关系可能具有未来的意义。

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