Gibb J W, Kogan F J
Naunyn Schmiedebergs Arch Pharmacol. 1979 Dec;310(2):185-7. doi: 10.1007/BF00500283.
Methamphetamine in large doses decreases striatal tyrosine hydroxylase activity. This effect is prevented by neuroleptic agents such as chlorpromazine and haloperidol which would suggest that released dopamine may be involved in the response. To test this hypothesis, we have altered dopamine synthesis with alpha-methyl-p-tyrosine and L-Dopa and found that dopamine synthesis is necessary for the observed depression of striatal TH activity by methamphetamine. In the adrenal gland, however, the increase in TH activity by methamphetamine is not prevented by inhibition of catecholamine synthesis. It is possible that released dopamine may be inhibiting TH activity by activation of pre- or postsynaptic dopamine receptors in the neostriatum resulting in activation of the neuronal feedback pathway or released dopamine may act on dendrodendritic autoreceptors in the substantia nigra.
大剂量甲基苯丙胺会降低纹状体酪氨酸羟化酶的活性。这种效应可被氯丙嗪和氟哌啶醇等抗精神病药物所阻止,这表明释放的多巴胺可能参与了该反应。为了验证这一假设,我们用α-甲基对酪氨酸和左旋多巴改变了多巴胺的合成,发现多巴胺合成对于甲基苯丙胺所观察到的纹状体酪氨酸羟化酶活性降低是必要的。然而,在肾上腺中,抑制儿茶酚胺合成并不能阻止甲基苯丙胺引起的酪氨酸羟化酶活性增加。有可能释放的多巴胺通过激活新纹状体中突触前或突触后多巴胺受体来抑制酪氨酸羟化酶活性,从而导致神经元反馈通路的激活,或者释放的多巴胺可能作用于黑质中的树-树状自身受体。