Hirata Y, Nagatsu T
Brain Res. 1985 Jun 24;337(1):193-6. doi: 10.1016/0006-8993(85)91631-2.
1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), a nigrostriatal neurotoxin in humans and primates, at 10(-5) M inhibited hydroxylation of tyrosine to 3,4-dihydrophenylalanine (DOPA), the rate-limiting step of dopamine synthesis, in tissue slices of the striatum and nucleus accumbens of the rat. Nomifensine, an inhibitor of dopamine uptake, reversed the inhibition but sulpiride, a dopamine receptor antagonist, did not affect the inhibition. MPTP at 10(-5) M inhibited neither the purified tyrosine hydroxylase nor dihydropteridine reductase in vitro. The level of total biopterin did not change significantly, but the tetrahydrobiopterin level was decreased in the striatal slices incubated in the presence of MPTP. These results suggest that MPTP inhibits dopamine synthesis in situ at the tyrosine hydroxylase step probably through inhibition of dihydropteridine reductase.
1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)是一种对人类和灵长类动物具有黑质纹状体毒性的神经毒素,在10^(-5) M浓度时可抑制大鼠纹状体和伏隔核组织切片中酪氨酸羟化生成3,4-二羟基苯丙氨酸(DOPA)的过程,而这是多巴胺合成的限速步骤。去甲替林,一种多巴胺摄取抑制剂,可逆转这种抑制作用,但舒必利,一种多巴胺受体拮抗剂,则不影响这种抑制作用。10^(-5) M浓度的MPTP在体外既不抑制纯化的酪氨酸羟化酶,也不抑制二氢蝶啶还原酶。总生物蝶呤水平没有显著变化,但在MPTP存在下孵育的纹状体切片中,四氢生物蝶呤水平降低。这些结果表明,MPTP可能通过抑制二氢蝶啶还原酶,在酪氨酸羟化酶步骤原位抑制多巴胺合成。