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国家自然科学基金(81070752)

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Retinoic acid metabolic change in retina and choroid of the guinea pig with lens-induced myopia被引量:9
2012年
AIM: To investigate the role of retinoic add (RA) and retinaldehyde dehydrogenase-2 (RALDH(2)) of retina and choroid in the guinea pig lens-induced myopic eyes. METHODS: Totally 45 guinea pigs, at age of three weeks, were randomly assigned into three groups: the normal control, the lens-induced group and the recovering group. Out of focus was induced by the -6.00D concave lens on the left eye, and lasted for 15 days. All animals underwent biometric measurement (corneal radius of curvature, refraction and axial length). Subsequently, RA content in the retina and RPE/choriod complex was detected by reversed-phase high-performance liquid chromatography. RALDH(2) protein in the retina and RPE/choriod complex was evaluated by the immunohistochemical staining and Western blotting. RESULTS: After wearing -6.00D lens for 15 days, axial length of the lens-induced eye extends and myopia was formed, with RA contents increasing in both the neural retina and RPE/choroid complex. Comparing with the lens-induced group, myopic degree significantly relieved, and its RA contents in both the neural retina and RPE/choroid complex decreased in the recovering group. In the normal control, RALDH(2) protein was expressed positively in the retinal nerve fiber layer (RNFL), inner plexiform layer (IPL) and lateral border of outer nuclear layer (ONL). Retinal RALDH(2) protein increased in the lens-induced group, and was also positive in the outer plexiform layer (OPL). In the recovering group, retinal RALDH(2) protein attenuated the expression in the OPL turns to negative. RALDH(2) protein was not expressed in the choroid of any group. CONCLUSION: RA of retina and chorid participates in the regulation of the lens-induced myopia in guinea pigs, which may be related with retinal RALDH(2) protein.
Jun-Feng MaoShuang-Zhen LiuXiu-Qiong Dou
视黄酸对豚鼠离焦性近视眼视网膜色素上皮通透性的调控被引量:1
2013年
背景视网膜视黄酸在离焦性近视形成中起重要作用,但目前尚不清楚其如何通过视网膜色素上皮(RPE)屏障向脉络膜传递近视信号。目的研究全反式视黄酸(atRA)对离焦性近视眼RPE屏障功能的影响。方法21日龄清洁级三色豚鼠30只,用随机数字表法分为正常对照组和离焦组,一6D凹透镜缝合于离焦组豚鼠左眼15d以制备离焦性近视模型,每天光照与黑暗周期为12h/12h。用角膜曲率计测量各组豚鼠的角膜曲率半径,行复方托吡卡胺滴眼液扩瞳检影验光以测量豚鼠眼球屈光度,应用A型超声法测量各组豚鼠的眼轴长度。于造模15d时处死动物并分离视网膜,体外培养RPE细胞并传代,将第3代RPE细胞用于实验,制备视网膜铺片,接种于Millcell—PET微孔滤膜插入式培养池,分别加入1×10-6、1×10-7、1×10-8和1×10-9mol/LatRA培养RPE细胞24h,以加入等体积atRA溶剂的培养孔作为阴性对照,以完全培养基加MTT溶液的无细胞孔作为空白对照。采用MTT比色法检测各组RPE细胞的存活率,用CN10一EVOM2型电阻测量仪测定单层细胞跨上皮电阻(TER),计算RPE细胞的TER值,采用FM1-43型荧光染色技术检测得出RPE细胞FM1-43阳性荧光染色的相对强度值,评价RPE细胞膜泡运输变化。结果豚鼠模型眼屈光度为(-2.20±O.95)D,对照组为(+1.15±0.30)D,差异有统计学意义(t=14.57,P〈0.01);豚鼠模型眼的眼轴长度为(8.24±0.09)mm,明显长于对照组的(7.81±0.05)mm,差异有统计学意义(t=17.20,P〈0.01)。原代培养豚鼠近视眼的RPE细胞,取第3代细胞用于实验。RPE细胞接种于Millcell培养池1周后细胞长满滤膜,呈单层生长。加入atRA干预24h,RPE细胞的存活率随药物浓度的升高而逐渐降低,1×10^-9 mol/LatRA组RPE细胞存活率为93.3%,1×10-8mol/LatRA组为88.2%,1×10-6mol/LatRA组和1�
毛俊峰刘双珍豆秀琼王沙谭星平
关键词:视黄酸近视视网膜色素上皮
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