{"title":"Effects of minocycline on leakage of retinal microvessels induced by glycation end products and its mechanism","authors":"陈永东, 许迅, 吴强, 郑志, 朱冬青, 顾青","doi":"10.3969/J.ISSN.1003-0808.2010.12.001","DOIUrl":"https://doi.org/10.3969/J.ISSN.1003-0808.2010.12.001","url":null,"abstract":"目的 研究基质金属蛋白酶-9(MMP-9)在糖基化终末产物(AGEs)所致血-视网膜屏障损害中的作用,评估米诺环素对AGEs所致血-视网膜屏障损害的治疗作用.方法 36只SD大鼠用随机数字表法分为牛血清白蛋白(BSA)组、AGEs-BSA组和AGEs-BSA+米诺环素组.BSA组和AGEs-BSA组分别自尾静脉注入BSA和AGEs-BSA,每日1次,每次40mg/kg,AGEs-BSA+米诺环素组在每日注射AGEs-BSA的同时隔日腹腔注射米诺环素45mg/kg.14d后,每组取6只大鼠用伊文思蓝(EB)法观察并比较各组视网膜血管的通透性,其余大鼠处死后,采用RT-PCR及Western blot法观察视网膜MMP-9的表达.结果 AGEs-BSA组MMP-9 mRNA和蛋白水平均较BSA组升高,差异有统计学意义(P<0.01),同时,视网膜微血管渗透性也显著升高(P<0.01).而在AGEs-BSA+米诺环素组大鼠视网膜基因和蛋白水平的MMP-9均被抑制(P<0.01),同时视网膜微血管渗漏被部分逆转(P<0.01).视网膜微血管的渗透性与MMP-9蛋白的表达呈正相关(r=0.891,P=0.000).结论 AGEs所致的视网膜微血管渗漏与MMP-9的高表达有密切关系,AGEs的作用至少部分是通过MMP-9实现的.米诺环素能部分逆转AGEs-MMP-9途径所致的血管渗漏。","PeriodicalId":186994,"journal":{"name":"Chinese Ophthalmic Research","volume":"29 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2010-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"121425035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Effects of curcumin on expression of macrophage migration inhibitory factor in retina of diabetic rats","authors":"刘娟, 游志鹏","doi":"10.3969/J.ISSN.1003-0808.2010.12.008","DOIUrl":"https://doi.org/10.3969/J.ISSN.1003-0808.2010.12.008","url":null,"abstract":"目的 检测巨噬细胞游走抑制因子(MIF)在糖尿病大鼠视网膜中的表达,探讨MIF在糖尿病视网膜病变(DR)中的作用及姜黄素早期干预对其表达的影响.方法 对30只清洁级SD大鼠行腹腔注射质量分数1%链脲佐菌素(STZ)诱导建立糖尿病动物模型,选取其中的20只随机分为糖尿病组和姜黄素治疗组,各10只,另取10只正常匹配的大鼠作为正常对照组.姜黄素治疗组自STZ注射后3d起给予含羧甲基纤维素的姜黄素200mg/(kg*d)灌胃,共8周,正常对照组和糖尿病组给予等量的羧甲基纤维素灌胃.动物处死后收集各组大鼠眼球,苏木精-伊红染色观察大鼠视网膜组织的病理变化;采用ELISA法检测各组大鼠视网膜组织中MIF的表达;应用免疫组织化学法观察各实验组大鼠视网膜中MIF的表达及定位;透射电镜下观察大鼠视网膜超微结构的改变.结果 与正常对照组比较,糖尿病组大鼠和姜黄素治疗组大鼠血糖明显升高,差异均有统计学意义(P<0.01);姜黄素治疗组大鼠血糖水平明显低于糖尿病组,差异有统计学意义(P<0.01).与正常对照组比较,糖尿病组和姜黄素治疗组大鼠体重明显下降,差异均有统计学意义(P<0.01);姜黄素治疗组大鼠体重明显大于糖尿病组,差异有统计学意义(P<0.01).糖尿病组大鼠视网膜变薄,但姜黄素治疗组大鼠视网膜接近正常.免疫组织化学检测表明,糖尿病组视网膜组织中含有大量MIF阳性细胞,姜黄素治疗组视网膜中MIF表达明显少于糖尿病组(P<0.01).ELISA法检测结果显示,糖尿病组MIF的表达较正常对照组显著升高(P<0.01);姜黄素治疗组MIF的表达较糖尿病组明显下降(P<0.01).透射电镜下糖尿病组大鼠视网膜光感受器内外节水肿,毛细血管内皮细胞和周细胞染色体边集;姜黄素治疗组大鼠视网膜超微结构的改变轻微.结论 DR与视网膜的炎性改变有关,视网膜组织中MIF的高表达参与早期DR的发生发展.姜黄素可下调MIF的表达,其早期干预可延缓DR的发病进程。","PeriodicalId":186994,"journal":{"name":"Chinese Ophthalmic Research","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2010-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131294397","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Inhibition of human keratocyte proliferation following the transfection of cyclinD1 antisense gene","authors":"荣蓓, 晏晓明","doi":"10.3969/J.ISSN.1003-0808.2010.11.005","DOIUrl":"https://doi.org/10.3969/J.ISSN.1003-0808.2010.11.005","url":null,"abstract":"目的 探讨反义cyclinD1基因转染后人角膜基质细胞增生的改变.方法 人角膜组织来源于北京大学第一医院眼库体外培养人角膜基质细胞,采用第2代或第3代细胞用于实验.利用阳离子脂质体lipofectamine介导反义cyclinD1基因转染入体外培养的人角膜基质细胞.同时设非转染组(以PBS代替cyclinD1质粒及lipofectamine)及lipofectamine转染组(以PBS代替反义cyclinD1质粒)作为对照.应用免疫细胞化学法观察lipofectamine介导反义cyclinD1基因转染对人角膜基质细胞中cyclinD1蛋白表达的影响,应用四甲基偶氮唑盐(MTT)法观察其对人角膜基质细胞增生的影响,并用质量分数0.5%锥虫蓝染色观察活细胞比率.结果 非转染组和lipofectamine转染组均有大量人角膜基质细胞的细胞核cyclinD1染色呈棕褐色,反义cyclinD1转染组只有少量人角膜基质细胞细胞核cyclinD1染色呈棕褐色.与非转染组和lipofectamine转染组比较,反义cyclinD1转染组在转染后2、6、10d cyclinD1蛋白在培养的人角膜基质细胞中的表达明显降低,差异均有统计学意义(t=6.050、t=5.180、t=5.040,P<0.01;t=6.190、t=5.670、t=5.010,P<0.01),而非转染组与lipofectamine转染组间比较,差异均无统计学意义(t=1.120、t=1.310、t=1.010,P>0.05).转染后2、6、10d,反义cyclinD1转染组人角膜基质细胞的A570值分别低于非转染组和lipofectamine转染组,差异均有统计学意义(t=5.830、t=5.210、t=4.920,P<0.01;t=5.130、t=5.010、t=4.850,P<0.01),说明抑制了基质细胞的增生,而非转染组与lipofectamine转染组间比较,差异均无统计学意义(t=1.110、t=1.230、t=1.120,P>0.05).0.5%锥虫蓝染色显示各组活细胞比率均在90%以上,未见明显的细胞毒性.结论 阳离子脂质体介导的反义cyclinD1基因转染在转染后一定时间内可降低人角膜基质细胞中cyclinD1蛋白的表达,抑制人角膜基质细胞的增生,未见明显细胞毒性,为角膜基质过度愈合反应的基因治疗奠定了基础。","PeriodicalId":186994,"journal":{"name":"Chinese Ophthalmic Research","volume":"17 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2010-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"128339026","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}