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亚叶酸、左旋多巴和5-羟色氨酸在二氢蝶啶还原酶缺乏症中的单胺能作用。

Monoaminergic effects of folinic acid, L-DOPA, and 5-hydroxytryptophan in dihydropteridine reductase deficiency.

作者信息

Goldstein D S, Hahn S H, Holmes C, Tifft C, Harvey-White J, Milstien S, Kaufman S

机构信息

Clinical Neuroscience Branch, National Institute of Neurological Disorders and Stroke, NIH, Bethesda, MD 20892, USA.

出版信息

J Neurochem. 1995 Jun;64(6):2810-3. doi: 10.1046/j.1471-4159.1995.64062810.x.

Abstract

Plasma and CSF concentrations of endogenous L-DOPA, catecholamines, and metabolites of monoamines were assayed in a patient with atypical phenylketonuria due to absent dihydropteridine reductase (DHPR), before and during treatment with folinic acid, Sinemet, and 5-hydroxytryptophan. The patient had low but detectable levels of L-DOPA, 3,4-dihydroxyphenylacetic acid (DOPAC), and 3,4-dihydroxyphenylglycol (DHPG) in plasma and low but detectable levels of these compounds and of homovanillic acid (HVA) and 5-hydroxyindoleacetic acid (5-HIAA) in CSF, with approximately normal plasma and CSF levels of norepinephrine [noradrenaline (NA)]. Folinic acid treatment approximately doubled plasma levels of L-DOPA, NA, DOPAC, and DHPG, compared with values during dietary phenylalanine restriction alone. Detection of L-DOPA, catecholamines, and monoamine metabolites in this patient indicates that monoamine synthesis in humans does not absolutely require DHPR. The results are consistent with the existence of an alternative biochemical pathway, with folinic acid treatment augmenting activity along this pathway. Low plasma levels of L-DOPA, DOPAC, and DHPG may reflect decreased catecholamine synthesis and turnover in sympathetic nerves, with compensatory increases in exocytotic release normalizing plasma NA levels.

摘要

在一名因二氢蝶啶还原酶(DHPR)缺乏导致非典型苯丙酮尿症的患者中,在使用亚叶酸、息宁和美多巴治疗前及治疗期间,测定了内源性左旋多巴、儿茶酚胺和单胺代谢物的血浆和脑脊液浓度。该患者血浆中左旋多巴、3,4-二羟基苯乙酸(DOPAC)和3,4-二羟基苯乙二醇(DHPG)水平较低但可检测到,脑脊液中这些化合物以及高香草酸(HVA)和5-羟吲哚乙酸(5-HIAA)水平较低但可检测到,血浆和脑脊液中去甲肾上腺素[去甲肾上腺素(NA)]水平大致正常。与仅进行饮食苯丙氨酸限制时的值相比,亚叶酸治疗使血浆中左旋多巴、NA、DOPAC和DHPG水平增加了约一倍。该患者中左旋多巴、儿茶酚胺和单胺代谢物的检测表明,人类单胺合成并非绝对需要DHPR。结果与存在替代生化途径一致,亚叶酸治疗增强了该途径的活性。血浆中左旋多巴、DOPAC和DHPG水平较低可能反映交感神经中儿茶酚胺合成和周转减少,胞吐释放的代偿性增加使血浆NA水平正常化。

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