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3
Interactions between levodopa and other drugs: significance in the treatment of Parkinson's disease.左旋多巴与其他药物的相互作用:在帕金森病治疗中的意义
Drugs. 1973;6(5):364-88. doi: 10.2165/00003495-197306050-00004.
4
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[18F]fluoro-dopa, an analogue of dopa, and its use in direct external measurements of storage, degradation, and turnover of intracerebral dopamine.[18F]氟多巴,一种多巴类似物,及其在直接体外测量脑内多巴胺的储存、降解和周转中的应用。
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本文引用的文献

1
IN-VITRO DECARBOXYLATION OF NEW PHENYLALANINE DERIVATIVES.新型苯丙氨酸衍生物的体外脱羧作用
Biochem Pharmacol. 1964 May;13:798-801. doi: 10.1016/0006-2952(64)90018-8.
2
Metabolic fate of l-[14C] DOPA in cerebrospinal fluid and blood plasma of humans.l-[14C]多巴在人体脑脊液和血浆中的代谢命运。
Brain Res. 1967 Feb;4(1):106-9. doi: 10.1016/0006-8993(67)90154-0.
3
Drug-induced changes of extracerebral dopa metabolism in man.
Arch Neurol. 1969 Feb;20(2):187-90. doi: 10.1001/archneur.1969.00480080087010.
4
Cerebral accumulation and metabolism of C14-dopa after selective inhibition of peripheral decarboxylase.外周脱羧酶选择性抑制后C14 - 多巴的脑内蓄积与代谢
J Pharmacol Exp Ther. 1968 May;161(1):14-20.
5
L-dopa-induced accumulation of 3-O-metyldopa in brain and heart.左旋多巴诱导的3 - O - 甲基多巴在脑和心脏中的蓄积。
Eur J Pharmacol. 1970 May;10(2):189-92. doi: 10.1016/0014-2999(70)90272-4.

L-3-O-甲基多巴在大鼠体内的分布与代谢

Distribution and metabolism of L-3-O-methyldopa in rats.

作者信息

Bartholini G, Kuruma I, Pletscher A

出版信息

Br J Pharmacol. 1970 Nov;40(3):461-7. doi: 10.1111/j.1476-5381.1970.tb10627.x.

DOI:10.1111/j.1476-5381.1970.tb10627.x
PMID:5497794
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1703137/
Abstract
  1. After intraperitoneal administration of L-2-(14)C-3-O-methyldopa ((14)C-O-methyldopa) to rats, the amino-acid was distributed evenly in blood, brain, heart, adipose tissue and liver, whereas it accumulated more in the kidney and the pancreas. (14)C-O-methyldopa showed a biological half-life of about 12-13 h in blood, brain and heart.2. The concentration curve of (14)C-O-methyldopa in brain (after increasing doses of the amino-acid) was linear if measured 2 h after administration, but seemed to reach a plateau at the higher doses if determined after 16 h.3. The concentrations of (14)C-O-methyldopa metabolites (mainly homovanillic acid and 4-hydroxy-3-methoxyphenyllactic acid) were low, except in the kidney, and varied according to the tissue.4. Twenty-four hours after administration of (14)C-O-methyldopa, 33% of the injected radioactivity appeared in the urine. This radioactivity consisted of about 95% of metabolites (probably in the main (14)C-homovanillic acid and (14)C-4-hydroxy-3-methoxyphenyllactic acid) and of 5% of unchanged (14)C-O-methyldopa. In the faeces, 10% of the radioactivity appeared, mainly as metabolic end-products.5. It is concluded that (14)C-O-methyldopa easily penetrates from the blood into various tissues, including brain, and that the majority of the amino-acid undergoes a slow metabolism. The different shape of the concentration curves for (14)C-O-methyldopa in the brain after 2 and 16 h might indicate the presence of two tissue pools of the amino-acid.
摘要
  1. 给大鼠腹腔注射L-2-(14)C-3-O-甲基多巴((14)C-O-甲基多巴)后,该氨基酸在血液、脑、心脏、脂肪组织和肝脏中分布均匀,而在肾脏和胰腺中积累较多。(14)C-O-甲基多巴在血液、脑和心脏中的生物半衰期约为12 - 13小时。

  2. 如果在给药后2小时测量,脑内(14)C-O-甲基多巴的浓度曲线(在增加氨基酸剂量后)呈线性,但如果在16小时后测定,在较高剂量时似乎达到平台期。

  3. (14)C-O-甲基多巴代谢物(主要是高香草酸和4-羟基-3-甲氧基苯乳酸)的浓度较低,肾脏除外,且因组织而异。

  4. 给予(14)C-O-甲基多巴24小时后,33%的注入放射性出现在尿液中。这种放射性约95%由代谢物组成(可能主要是(14)C-高香草酸和(14)C-4-羟基-3-甲氧基苯乳酸),5%由未变化的(14)C-O-甲基多巴组成。在粪便中,10%的放射性出现,主要为代谢终产物。

  5. 得出结论:(14)C-O-甲基多巴容易从血液进入包括脑在内的各种组织,且该氨基酸的大部分经历缓慢代谢。给药后2小时和16小时后脑内(14)C-O-甲基多巴浓度曲线的不同形状可能表明该氨基酸存在两个组织池。