Tsukada H, Lindner K J, Hartvig P, Tani Y, Valtysson J, Bjurling P, Kihlberg T, Westerberg G, Watanabe Y, Långström B
Central Research Laboratory, Hamamatsu Photonics K.K., Shizuoka, Japan.
Brain Res. 1996 Mar 25;713(1-2):92-8. doi: 10.1016/0006-8993(95)01489-6.
The effect of 6R-L-erythro-5,6,7,8-tetrahydrobiopterin (6R-BH4) and L-tyrosine infusion on [11C]dopamine synthesis was analyzed in the striatum of Rhesus using positron emission tomography (PET). The rate for decarboxylation from L-[beta-11C]DOPA to [11C]dopamine was calculated using a graphical method with cerebellum as a reference region. Although the peripheral administration of 6R-BH4 at low dose (2 mg/kg) did not provide a significant increase in the rate of dopamine biosynthesis, a high dose of 6R-BH4 (20 mg/kg) induced an elevation of the rate. This 6R-BH4-induced elevation of the dopamine synthesis rate was further dose-dependently enhanced by the continuous infusion of L-tyrosine (0.2 and 1.0 mumol/min/kg). L-Tyrosine infusion with a rate of 1.0 mumol/min/kg caused an enhancement of the rate even during low dose administration of 6R-BH4 (2 mg/kg). L-Tyrosine infusion alone did not induce any elevation of the dopamine biosynthesis rate. The analysis of plasma indicated that the metabolic ratios of L-[beta-11C]DOPA to each metabolite were not affected by 6R-BH4 and/or L-tyrosine infusion. The results suggest that the low dose loading of tyrosine facilitates the activity of 6R-BH4 on the presynaptic dopamine biosynthesis, and also that the combined effects can be monitored by PET using L-[beta-11C]DOPA as a biochemical probe.
利用正电子发射断层扫描(PET)技术,分析了6R-L-赤藓糖型-5,6,7,8-四氢生物蝶呤(6R-BH4)和L-酪氨酸输注对恒河猴纹状体中[11C]多巴胺合成的影响。以小脑作为参考区域,采用图像法计算L-[β-11C]多巴脱羧生成[11C]多巴胺的速率。虽然低剂量(2mg/kg)的6R-BH4外周给药并未使多巴胺生物合成速率显著增加,但高剂量(20mg/kg)的6R-BH4可使其速率升高。持续输注L-酪氨酸(0.2和1.0μmol/min/kg)可进一步剂量依赖性地增强6R-BH4诱导的多巴胺合成速率升高。即使在低剂量(2mg/kg)6R-BH4给药期间,以1.0μmol/min/kg的速率输注L-酪氨酸也会导致速率增强。单独输注L-酪氨酸不会引起多巴胺生物合成速率的任何升高。血浆分析表明,L-[β-11C]多巴与各代谢产物的代谢比不受6R-BH4和/或L-酪氨酸输注的影响。结果表明,低剂量的酪氨酸负荷可促进6R-BH4对突触前多巴胺生物合成的作用,并且还表明可以使用L-[β-11C]多巴作为生化探针,通过PET监测联合效应。