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乙酰左旋肉碱增强PC12细胞对神经生长因子的反应。

Acetyl-L-carnitine enhances the response of PC12 cells to nerve growth factor.

作者信息

Taglialatela G, Angelucci L, Ramacci M T, Werrbach-Perez K, Jackson G R, Perez-Polo J R

机构信息

Department of Human Biological Chemistry and Genetics, University of Texas Medical Branch, Galveston 77550.

出版信息

Brain Res Dev Brain Res. 1991 Apr 24;59(2):221-30. doi: 10.1016/0165-3806(91)90102-o.

Abstract

We have demonstrated that treatment of rat pheochromocytoma (PC12) cells with acetyl-L-carnitine (ALCAR) stimulates the synthesis of nerve growth factor receptors (NGFR). ALCAR has also been reported to prevent some age-related impairments of the central nervous system (CNS). In particular, ALCAR reduces the loss of NGFR in the hippocampus and basal forebrain of aged rodents. On these bases, a study on the effect of NGF on the PC12 cells was carried out to ascertain whether ALCAR induction of NGFR resulted in an enhancement of NGF action. Treatment of PC12 cells for 6 days with ALCAR (10 mM) stimulated [125I]NGF PC12 cell uptake, consistent with increased NGFR levels. Also, neurite outgrowth elicited in PC12 cells by NGF (100 ng/ml) was greatly augmented by ALCAR pretreatment. When PC12 cells were treated with 10 mM ALCAR and then exposed to NGF (1 ng/ml), an NGF concentration that is insufficient to elicit neurite outgrowth under these conditions, there was an ALCAR effect on neurite outgrowth. The concentration of NGF necessary for survival of serum-deprived PC12 cells was 100-fold lower for ALCAR-treated cells as compared to controls. The minimal effective dose of ALCAR here was between 0.1 and 0.5 mM. This is similar to the reported minimal concentration of ALCAR that stimulates the synthesis of NGFR in these cells. The data here presented indicate that one mechanism by which ALCAR rescues aged neurons may be by increasing their responsiveness to neuronotrophic factors in the CNS.

摘要

我们已经证明,用乙酰-L-肉碱(ALCAR)处理大鼠嗜铬细胞瘤(PC12)细胞可刺激神经生长因子受体(NGFR)的合成。据报道,ALCAR还可预防中枢神经系统(CNS)的一些与年龄相关的损伤。特别是,ALCAR可减少老年啮齿动物海马体和基底前脑NGFR的丢失。基于这些,我们开展了一项关于NGF对PC12细胞作用的研究,以确定ALCAR诱导NGFR是否会增强NGF的作用。用ALCAR(10 mM)处理PC12细胞6天可刺激[125I]NGF对PC12细胞的摄取,这与NGFR水平的增加一致。此外,ALCAR预处理可极大增强NGF(100 ng/ml)诱导的PC12细胞神经突生长。当PC12细胞用10 mM ALCAR处理,然后暴露于NGF(1 ng/ml)(在此条件下该NGF浓度不足以引发神经突生长)时,ALCAR对神经突生长有影响。与对照组相比,经ALCAR处理的血清剥夺PC12细胞存活所需的NGF浓度低100倍。此处ALCAR的最小有效剂量在0.1至0.5 mM之间。这与报道的在这些细胞中刺激NGFR合成的ALCAR最小浓度相似。此处呈现的数据表明,ALCAR拯救衰老神经元的一种机制可能是增加它们对CNS中神经营养因子的反应性。

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