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通过微阵列分析研究尼伐地平对RCS大鼠视网膜变性的药理作用

Study of pharmacological effects of nilvadipine on RCS rat retinal degeneration by microarray analysis.

作者信息

Sato Motoya, Ohguro Hiroshi, Ohguro Ikuyo, Mamiya Kazuhisa, Takano Yoshiko, Yamazaki Hitoshi, Metoki Tomomi, Miyagawa Yasuhiro, Ishikawa Fotoshi, Nakazawa Mitsuru

机构信息

Department of Ophthalmology, Hirosaki University School of Medicine, Hirosaki-shi, Aomori-ken, Japan.

出版信息

Biochem Biophys Res Commun. 2003 Jul 11;306(4):826-31. doi: 10.1016/s0006-291x(03)01092-1.

Abstract

In our recent study, we found that the Ca(2+) antagonist, nilvadipine caused significant preservation of photoreceptor cells in The Royal College of Surgeons (RCS) rats [Invest. Ophthalmol. Vis. Sci. 43 (2002) 919]. Here, to elucidate the mechanisms of nilvadipine-induced effects we analyzed altered gene expression of 1101 genes commonly expressed in rodent by DNA microarray analysis in the retinas of nilvadipine-treated and untreated RCS rats and SD rat. In the total number of genes, the expression of 30 genes was altered upon administration of nilvadipine to RCS rats, including several genes related to the apoptotic pathway and other mechanisms. Remarkably, neurotrophic factors, FGF-2 and Arc, known to suppress the apoptosis in the central nervous system, were up-regulated. These changes were also confirmed by real-time quantitative (Taqman) RT-PCR and Western blot analysis. Therefore, our present data suggested that administration of nilvadipine to RCS rats increases the expression of endogenous FGF-2 and Arc in retina, and potentially has a protective effect against retinal degeneration.

摘要

在我们最近的研究中,我们发现钙(2+)拮抗剂尼伐地平能显著保护皇家外科学院(RCS)大鼠的光感受器细胞[《Invest. Ophthalmol. Vis. Sci.》43(2002)919]。在此,为阐明尼伐地平诱导效应的机制,我们通过DNA微阵列分析,对经尼伐地平处理和未经处理的RCS大鼠及SD大鼠视网膜中1101个在啮齿动物中普遍表达的基因的表达变化进行了分析。在所有基因中,给RCS大鼠施用尼伐地平后,30个基因的表达发生了改变,包括几个与凋亡途径及其他机制相关的基因。值得注意的是,已知可抑制中枢神经系统凋亡的神经营养因子FGF - 2和Arc上调。这些变化也通过实时定量(Taqman)RT - PCR和蛋白质印迹分析得到了证实。因此,我们目前的数据表明,给RCS大鼠施用尼伐地平可增加视网膜中内源性FGF - 2和Arc的表达,并可能对视网膜变性具有保护作用。

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