机构地区:[1]四川中医药高等专科学校中医学院,四川省绵阳市621000 [2]绵阳万江眼科医院中医眼科,四川省绵阳市621000 [3]绵阳市第三人民医院,四川省绵阳市621000
出 处:《眼科新进展》2023年第2期105-110,共6页Recent Advances in Ophthalmology
基 金:四川省科技厅一般项目(编号:2021YJ0252)。
摘 要:目的研究高良姜素对青光眼大鼠视网膜神经节细胞(RGC)的保护作用。方法取48只SD大鼠随机分为对照组、对照+高良姜素组、高眼压组和高眼压+高良姜素组,每组12只(12眼)。对照+高良姜素组和高眼压+高良姜素组大鼠接受高良姜素滴眼液治疗,对照组和高眼压组大鼠则接受相同剂量二甲基亚砜溶剂滴眼。于造模后第0~28天监测大鼠眼压,并于造模后第28天处死大鼠,收集各组大鼠右眼球,并采用HE染色观察大鼠视网膜形态变化,采用免疫组织化学染色分析各组大鼠视网膜中GFAP、Toll样受体4(TLR4)和NOD样受体3(NLRP3)表达。从4只4 d龄大鼠视网膜中分离RGC,分为空白组、光气组和CoCl 2+高良姜素组。光气组和光气+高良姜素组RGC与200μmol·L-1 CoCl 2一起孵育48 h,光气+高良姜素组RGC中加入20μmol·L-1高良姜素干预48 h。收集各组细胞,采用流式细胞术和Western blot检测RGC的凋亡率及相关蛋白的相对表达情况,并采用ELISA检测空白组、光气组和光气+高良姜素组RGC中IL-18和IL-1β蛋白表达。结果造模后第3~28天,与对照组比较,高眼压组大鼠眼压均显著升高(均为P<0.001),高眼压+高良姜素组大鼠眼压差异均有统计学意义(均为P<0.05)。造模后第0~28天,对照组与对照+高良姜素组大鼠眼压差异均无统计学意义(均为P>0.05)。造模后第18~28天,与高眼压组比较,高眼压+高良姜素组大鼠眼压均持续显著降低(均为P<0.05)。对照组大鼠视网膜厚度、RGC生存率与对照+高良姜素组相比差异均无统计学意义(均为P>0.05);与对照组比较,高眼压组大鼠视网膜厚度、RGC生存率均显著减少(均为P<0.01),高眼压+高良姜素组大鼠视网膜厚度、RGC生存率差异均无统计学意义(均为P>0.05);与高眼压组比较,高眼压+高良姜素组大鼠视网膜厚度、RGC生存率均显著增加(均为P<0.05)。Western blot检测结果显示,与对照组比较,高眼压组大鼠视网膜组Objective To investigate the protective effect of galangin on glaucoma rats with retinal ganglion cell(RGC)loss.Methods Forty-eight Sprague\|Dawley rats were randomly divided into the control group,control+galangin group,high intraocular pressure(IOP)group,and high IOP+galangin group with 12 rats(12 eyes)in each group.The rats in the control+galangin group and high IOP+galangin group were treated with galangin eye drops,while rats in the control group and the high IOP group were treated with the same dose of dimethyl sulfoxide eye drops.The IOP of rats was monitored from 0 d to 28 d after modeling.The rats were killed on the 28 d,and the right eyeballs of rats in each group were collected.The retinal morphological changes were observed by Hematoxylin and Eosin staining,and expression levels of glial fibrillary acidic protein(GFAP),Toll-like receptor 4(TLR4)and NOD-like receptor protein 3(NLRP3)in the retina were analyzed by immunohistochemistry.The RGCs were isolated from the retina of 4 rats at 4 d and divided into three groups:blank group,CoCl 2 group,and CoCl 2+galangin group.The RGCs in the CoCl 2 group and the CoCl 2+galangin group were incubated with 200μmol·L-1 CoCl 2 for 48 h,and the CoCl 2+galangin group was additionally administered with 20μmol·L-1 galangin for 48 h.Cells from each group were collected,then the apoptosis rate and expression levels of related proteins of RGCs were detected by flow cytometry and Western blot,and the interleukin(IL)-18 and IL-1βproteins in the blank group,CoCl 2 group and CoCl 2+galangin group were detected by using enzyme-linked immunosorbent assay.Results From 3 d to 28 d after the modeling,compared with the control group,the IOP increased significantly in the high IOP group(all P<0.001),and that in the high IOP+galangin group showed statistically significant differences(all P<0.05).From 0 d to 28 d,there was no significant difference in the IOP between the control group and the control+galangin group(all P>0.05).From 18 d to 28 d,compared with the high IOP group,th
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