Suppr超能文献

Rho激酶抑制剂Y-27632下调PC12细胞中去甲肾上腺素的合成与释放。

Rho kinase inhibitor Y-27632 down-regulates norepinephrine synthesis and release in PC12 cells.

作者信息

Duan Wei-Gang, Shang Jing, Jiang Zhen-Zhou, Yao Jin-Cheng, Yun Yu, Yan Ming, Shu Bin, Lin Qing, Yu Ze-Pu, Zhang Lu-Yong

机构信息

Jiangsu Center for Drug Screening, Jiangsu Center for Pharmacodynamics Research and Evaluation, China Pharmaceutical University, Nanjing, China.

出版信息

Basic Clin Pharmacol Toxicol. 2009 Jun;104(6):434-40. doi: 10.1111/j.1742-7843.2008.00314.x.

Abstract

Rho kinase inhibition is beneficial for neurite outgrowth and nerve disorders, and the Rho kinase inhibitors have been regarded as promising agents to treat neural diseases. The main aim of the study was to elucidate how Rho kinase inhibitor Y-27632 regulates neurotransmitter norepinephrine synthesis and release in PC12 cells when neurite outgrowth was induced. PC12 cells were treated with Y-27632 for 6 days. The amount of norepinephrine synthesized in PC12 cells and the amount released evoked by acetylcholine or by KCl were determined by norepinephrine enzyme-linked immunosorbent assay kits. The results showed that the amount of norepinephrine both synthesized and released was down-regulated with a concentration-dependent relationship. Further results of Western blotting found that the protein expression of tyrosine hydroxylase and synapsin I (especially its active form, synapsin I phosphoSer603) was also down-regulated, which were directly related to synthesis and release of norepinephrine, respectively. All the results suggest that Y-27632 is able to down-regulate norepinephrine synthesis and release, the direct mechanism of which may be associated with down-regulation on expression of some proteins, including tyrosine hydroxylase and synapsin I.

摘要

Rho激酶抑制作用对神经突生长和神经紊乱有益,Rho激酶抑制剂已被视为治疗神经疾病的有前景的药物。该研究的主要目的是阐明在诱导神经突生长时,Rho激酶抑制剂Y-27632如何调节PC12细胞中神经递质去甲肾上腺素的合成和释放。用Y-27632处理PC12细胞6天。通过去甲肾上腺素酶联免疫吸附测定试剂盒测定PC12细胞中合成的去甲肾上腺素量以及由乙酰胆碱或氯化钾诱发释放的量。结果表明,合成和释放的去甲肾上腺素量均呈浓度依赖性下调。蛋白质印迹的进一步结果发现,酪氨酸羟化酶和突触素I(尤其是其活性形式,突触素I磷酸化丝氨酸603)的蛋白质表达也下调,它们分别与去甲肾上腺素的合成和释放直接相关。所有结果表明,Y-27632能够下调去甲肾上腺素的合成和释放,其直接机制可能与包括酪氨酸羟化酶和突触素I在内的一些蛋白质表达的下调有关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验