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阿扑吗啡、α-甲基对酪氨酸、氟哌啶醇和利血平对克隆细胞系(PC-12和N1E-115)中多巴生成的影响。

Effect of apomorphine, alpha-methylparatyrosine, haloperidol and reserpine on DOPA production in clonal cell lines (PC-12 and N1E-115).

作者信息

Bräutigam M, Laschinski G, Kittner B, Herken H

出版信息

Biochem Pharmacol. 1985 Apr 1;34(7):941-7. doi: 10.1016/0006-2952(85)90594-5.

Abstract

The effect of various drugs on DOPA production in the pheochromocytoma clone PC-12 and the neuroblastoma clone N1E-115 was studied. The N1E-115 cells contain only very low amounts of dopamine due to a lack of the aromatic L-amino acid decarboxylase, whereas the PC-12 cells are rich in dopamine. alpha-Methyl-p-tyrosine and apomorphine blocked DOPA production in both cell clones. Reserpine and haloperidol reduced the intracellular dopamine in the PC-12 cells and simultaneously induced a blockade of cellular DOPA production. The released dopamine was primarily recovered as 3,4-dihydroxyphenylacetic acid indicating a release of dopamine into the cytoplasm. This transient increase of cytoplasmic dopamine by reserpine or haloperidol brings about the inhibition of DOPA production in the PC-12 cells. Our results show that the PC-12 clone especially reacts to various drugs like other in vitro systems and may serve as an additional model for studying drug effects on catecholamine biosynthesis and metabolism.

摘要

研究了各种药物对嗜铬细胞瘤克隆PC-12和神经母细胞瘤克隆N1E-115中多巴产生的影响。由于缺乏芳香族L-氨基酸脱羧酶,N1E-115细胞仅含有极少量的多巴胺,而PC-12细胞富含多巴胺。α-甲基-p-酪氨酸和阿扑吗啡阻断了两个细胞克隆中的多巴产生。利血平和氟哌啶醇降低了PC-12细胞中的细胞内多巴胺水平,同时诱导细胞多巴产生的阻断。释放的多巴胺主要以3,4-二羟基苯乙酸的形式回收,表明多巴胺释放到细胞质中。利血平或氟哌啶醇引起的细胞质多巴胺的这种短暂增加导致PC-12细胞中多巴产生的抑制。我们的结果表明,PC-12克隆与其他体外系统一样,对各种药物有特殊反应,可作为研究药物对儿茶酚胺生物合成和代谢影响的额外模型。

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