Mandell A J, Bullard W P, Yellin J B, Russo P V
J Pharmacol Exp Ther. 1980 Jun;213(3):569-74.
Rat brain striatal reduced biopterin (BH4) levels vary diurnally by 2-fold, oscillating around a concentration of 3 micrometer. D-Amphetamine consistently induced a decrease in BH4 levels that did not exceed 25 to 30% with increasing doses; recovery of control levels required several hours. A large number of other psychotropic drugs, including other stimulants and phenylethylamine congeners, failed to induce a similar change. The amphetamine effect was blocked by methylphenidate and reserpine. The prolonged time for BH4 recovery could be explained by an amphetamine-induced functional uncoupling of quinonoid dihydropteridine reductase from striatal tyrosine hydroxylase as reported for various cofactor analogs, leading to spontaneous isomerization of the partially reduced pterin to its nonquinonoid form, which is not a substrate for the BH4 regenerating enzyme. If relevant to dopamine biosynthesis, such an uncoupling phenomenon might account for a unique neuropharmacology of the postamphetamine state.
大鼠脑纹状体中还原型生物蝶呤(BH4)水平呈昼夜变化,波动幅度为2倍,围绕3微摩尔的浓度振荡。随着剂量增加,右旋苯丙胺持续诱导BH4水平降低,但降幅不超过25%至30%;恢复到对照水平需要数小时。大量其他精神药物,包括其他兴奋剂和苯乙胺同系物,未能诱导类似变化。苯丙胺的作用被哌甲酯和利血平阻断。BH4恢复所需的延长时间可以用苯丙胺诱导的醌型二氢蝶啶还原酶与纹状体酪氨酸羟化酶的功能解偶联来解释,这与各种辅因子类似物的情况相同,导致部分还原的蝶呤自发异构化为其非醌型形式,而这不是BH4再生酶的底物。如果与多巴胺生物合成相关,这种解偶联现象可能解释了苯丙胺后状态独特的神经药理学。