Effects of 6R-L-erythro-5,6,7,8-tetrahydrobiopterin on the dopaminergic and cholinergic receptors as evaluated by positron emission tomography in the Rhesus monkey.

Y Tani, T Ishihara, T Kanai, T Ohno, J Andersson, A Lilja, G Antoni, K J Fasth, P Bjurling, G Westerberg
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引用次数: 3

Abstract

The effects of 6R-L-erythro-5,6,7,8-tetrahydrobiopterin (R-THBP) on the central cholinergic and dopaminergic systems in the Rhesus monkey brain were investigated by positron emission tomography (PET) with the muscarinic cholinergic receptor ligands (N-[11C]methyl-benztropine) and dopaminergic receptor ligands selective for D1, D2, and D3 subtypes ([11C]SCH23390, N-[11C]methyl-spiperone, and (+)[11C]UH232, respectively). None of the doses (3, 10, and 30 mg/kg i.v.) of R-THBP used significantly affected the regional cerebral blood flow (rCBF as determined by Raichle's H(2)15O method), and 10 mg/kg of R-THBP had little effect on the regional cerebral metabolic rate of glucose (rCMRglc) in the Rhesus monkey brain, as assessed by the graphical [18F]fluoro-deoxyglucose method. The effect of R-THBP on the muscarinic cholinergic system was dose dependent; while 3 mg/kg of R-THBP did not significantly alter the uptake ratio of N-[11C]methylbenztropine in several brain regions to that in the cerebellum, 10 and 30 mg/kg of R-THBP significantly reduced the uptake ratio in the thalamus, as well as in the frontal and temporal cortices. None of the doses (3, 10, and 30 mg/kg i.v.) of R-THBP tested affected [11C]SCH23390 (dopamine D1 receptor) binding. However, the k3 value for N-[11C]methyl-spiperone (dopamine D2 receptor) binding, which represents the association rate X Bmax value, was significantly decreased in the striatum. The uptake ratio of (+)[11C]UH232 (dopamine D3 receptor) in the striatum to that in the cerebellum was also decreased by administration of R-THBP (3 and 30 mg/kg i.v.). These findings suggest that R-THBP acts on dopamine D2 and D3 receptors selectively without markedly affecting dopamine D1 receptor binding. Furthermore, the changes in cholinergic and dopamine D2 and D3 receptors in vivo can not be attributed to a change in rCBF but may depend on the action of R-THBP.

正电子发射断层扫描评估 6R-L-赤式-5,6,7,8-四氢生物蝶呤对恒河猴多巴胺能和胆碱能受体的影响。
正电子发射断层扫描(PET)研究了 6R-L-赤式-5,6,7,8-四氢生物蝶呤(R-THBP)对恒河猴大脑中枢胆碱能和多巴胺能系统的影响,研究中使用了毒蕈碱类胆碱能受体配体(N-[11C]甲基-苯托品)和选择性 D1、D2 和 D3 亚型的多巴胺能受体配体(分别为[11C]SCH23390、N-[11C]甲基-哌啶酮和 (+[11C]UH232 )、D2和D3亚型的多巴胺能受体配体(分别为[11C]SCH23390、N-[11C]甲基胡椒酮和(+)[11C]UH232)。使用的 R-THBP剂量(3、10 和 30 mg/kg i.v.)均未对区域脑血流量(rCBF,由 Raichle's H(2)15O 方法测定)产生显著影响,10 mg/kg R-THBP 对猕猴大脑区域葡萄糖代谢率(rCMRglc)影响甚微,由图形[18F]荧光脱氧葡萄糖法评估。R-THBP 对毒蕈碱胆碱能系统的影响与剂量有关;虽然 3 毫克/千克的 R-THBP 不会显著改变 N-[11C]甲基苯托品在多个脑区与小脑的摄取比率,但 10 毫克/千克和 30 毫克/千克的 R-THBP 会显著降低丘脑以及额叶和颞叶皮层的摄取比率。所有测试剂量(3、10 和 30 毫克/千克静脉注射)的 R-THBP 都不会影响 [11C]SCH23390(多巴胺 D1 受体)的结合。然而,N-[11C]甲基胡椒酮(多巴胺 D2 受体)结合的 k3 值(代表结合率 X Bmax 值)在纹状体中显著下降。R-THBP(3 毫克/千克和 30 毫克/千克静脉注射)也降低了纹状体和小脑对(+)[11C]UH232(多巴胺 D3 受体)的摄取比率。这些发现表明,R-THBP 可选择性地作用于多巴胺 D2 和 D3 受体,而不会明显影响多巴胺 D1 受体的结合。此外,体内胆碱能和多巴胺 D2 和 D3 受体的变化不能归因于 rCBF 的变化,而可能取决于 R-THBP 的作用。
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