简介:目的:探讨无囊膜支撑的无晶状体眼植入Artisan人工晶状体的有效性和安全性。方法:前瞻性地分析24例24眼无囊膜支撑的无晶状体眼植入虹膜固定Artisan人工晶状体的手术后结果。纳入病例包括外伤性晶状体脱位、视网膜脱离或球内异物行晶状体玻璃体切除术后及晶状体摘出术后囊膜缺失。手术前后进行完整的眼部检查,包括裸眼视力、眼压、角膜内皮计数、瞳孔形态、人工晶状体固定情况、虹膜玻璃体视网膜情况,记录手术中和手术后出现的并发症。结果:患者随访12~24mo。所有手术眼视力均有提高,手术前裸眼视力为手动~0.2(logMAR1.91±0.89),手术后末次随访裸眼视力为0.2~1.0(logMAR0.46±0.59)。手术后1,3,12mo术眼平均等效球镜度数分别为-1.26,-0.43,-0.35D,±2.0D以内者术后3mo和12mo分别占66.7%和83.3%,±1.0D以内者分别占41.7%和50%。手术前及术后3,12mo眼压分别为16.95±7.85,12.38±4.68,15.96±5.25mmHg。手术前及手术后3,12mo平均角膜内皮计数分别为2493.8,2270.3,2263.7个/mm2,手术后1~3mo,4~12mo内皮细胞丢失率分别为8.96%,0.27%,手术后12mo内皮细胞总丢失率为9.23%。手术后无持续性葡萄膜炎,虹膜无明显手术损伤和萎缩,瞳孔形态无变化,Artisan人工晶状体正位牢固固定,对玻璃体视网膜无影响。玻璃体切除眼手术中使用前房灌注可避免眼球塌陷。结论:无囊膜支撑的无晶状体眼植入虹膜固定Artisan人工晶状体是有效和安全的方法,但仍需要长期的随访观察以进一步对Artisan人工晶状体植入术作出评价。
简介:目的:研究在高糖条件下,从海藻中萃取的新型多糖化合物对高糖诱导的视网膜色素上皮(RPE)细胞异常增殖的保护作用.方法:将体外培养的RPE细胞分为空白组、高糖组和多糖化合物组,空白组为正常RPE细胞培养液,高糖组为含30mmol/L葡萄糖的培养液,多糖化合物组为含30mmol/L葡萄糖和200mg/L多糖化合物的培养液.应用MTT法测量36h内不同时间点(6,12,24和36h)高糖以及多糖化合物对RPE细胞增殖影响.结果:高糖导致RPE细胞异常增殖,多糖化合物组RPE的细胞异常增殖明显得到保护,与高糖组比较差异具有统计学意义(P〈0.01).结论:从海藻中萃取的新型多糖化合物可以明显保护高糖所导致的RPE细胞的异常增殖.
简介:AIM:ToinvestigatethesideeffectsofthecommonlyusedlasertreatmentalongwithtestingtheneuroprotectiveeffectofbFGFonapotentialretinalimpairment.METHODS:Todothis,30chinchillapigmentedadultmalerabbitsweredividedintothecontrolandexperimentalgroups.ThecontrolandexperimentalgroupsunderwentbothlaserapplicationandbFGFtreatment.Theretinaltissueimpairmentanditsrenewalrateweretestedunderthelightandelectronmicroscopicallevels.RESULTS:Thefocallaserapplicationonrabbiteyescausedmorphologicalalterationsbothintheapplicationregionandintheneighbouringareas.Inthedamagedareas,theouternuclearlayeroftheneuralretinawasalmostdisappeared,retinapigmentepitheliumwasinterrupted,theretinapigmentepitheliummigratedintraretinally,andthedamagedregionalongwithneighbouringareasseemedtobenotseparated.bFGFapplicationjustafterthelaserphotocoagulation,revealedbetterresultsinapplicationareas.CONCLUSION:ItcouldbesuggestedthatthebFGFapplicationfollowinglaserphotocoagulationmighthaveprotective,repairingandwoundhealingeffectsontheretina.
简介:目的:观察糖尿病视网膜病变(diabeticretinopathy,DR)患者行全视网膜光凝(panretinalphotocoagulation,PRP)后服药前及服药2mo后患眼的全视野视网膜电图(fullfieldelectroretinogram,ERG)变化,探讨递法明片对DR暗适应功能的保护作用。方法:选择在我医院就诊的重度非增殖性糖尿病视网膜病变(nonproliferativediabeticretinopathy,NPDR)患者55例55眼,随机分为治疗组和对照组。两组均行全视网膜光凝,治疗组光凝后口服递法明片,对照组口服维生素B1片2次/d,10mg/次。PRP后服药前及服药2mo后行全视野视网膜电图检查,观察其暗视视杆反应的变化并进行统计学处理。结果:两组患者服药前及服药2mo后,暗视视杆反应bT值组内及组间比较差异均无统计学意义(P〉0.05);治疗组bA值服药2mo后与服药前相比振幅升高,差异有统计学意义(P〈0.05),与对照组相比治疗组振幅升高较大,差异有统计学意义(P〈0.05)。结论:递法明片可减轻PRP治疗对视网膜的损害,改善患者的暗适应功能。
简介:目的:探讨褪黑素对过氧化氢诱导晶状体上皮细胞氧化损伤的保护作用。方法:晶状体上皮细胞传代培养后,分别加入不同浓度褪黑素预处理12h后,加入100μmol/LH2O2继续孵育24h,MTT比色法检测褪黑素对H2O2诱导的晶状体上皮细胞活力的影响,流式细胞仪检测细胞凋亡率,比色法检测凋亡相关因子Caspase-3及Caspase-9的活性。结果:MTT结果显示褪黑素对晶状体上皮细胞活性无影响,该药物可以抑制过氧化氢诱导的细胞活性的下降,流式细胞计数结果显示褪黑素可以抑制过氧化氢诱导的细胞凋亡,此外,褪黑素还可以减少过氧化氢所致晶状体上皮细胞内Caspase-3及Caspase-9的活性,并且,伴随褪黑素作用时间的延长其活性呈下降趋势。结论:褪黑素可以明显抑制过氧化氢诱导的晶状体上皮细胞的凋亡,从而为寻求有效的防治白内障药物提供可靠的实验依据。
简介:AIM:Toexploretheeffectofsaturatedhydrogensalineonbluelight-inducedretinaldamageinrats.·METHODS:Theretinaldamageofratswasinducedbybluelightexposurefor6hoursandexamined8hours,16hoursand24hoursaftertheexposure.OnehundredfemaleSprague-Dawleyratswererandomlydividedintofourgroups.Group1included30ratsreceivedlightexposurewithoutanyothertreatment.Group2included30ratsreceivedlightexposurewithintraperitonealinjectionofnormalsaline.Group3included30ratsreceivedlightexposurewithintraperitonealinjectionofsaturatedhydrogensaline.AndGroup4includedtheother10ratswhichdidnotreceiveanytreatment.Theamountofintraperitonealinjectionofsaturatedhydrogensalineandnormalsalinewascalculatedintheratioof1ml/100gofratweight.SpecimenswerecollectedandprocessedbyH-Estaining,ultrastructureobservation,biochemicalmeasurement.Morphologicalchangeswereobservedbylightmicroscopeandtransmissionelectronmicroscope(TEM)andtheretinalouternuclearlayer(ONL)thicknesswasmeasuredbyIPP6.0,whilethemalondialdehyde(MDA)wasmeasuredbycolorimetricdeterminationat532nm.·RESULTS:AlthoughthestructureofretinainGroup1andGroup2wasinjuredheavily,theinjuryinGroup3wasmild.ThedifferencesbetweenGroup1andGroup2werenotsignificant.ComparedwiththeratsinGroup1andGroup2,theonesinGroup3hadmoreclearlydemarcatedretinastructureandmoreorderedcellsbylightmicroscopeandTEMobservation.TheONLthicknesses(400times)offourgroupsateachtimepointexceptbetweenGroup1andGroup2weresignificantlydifferent(P<0.05).ThethicknessesoftheONLinGroup1atthreetimepointswere30.41±4.04μm,26.11±2.82μmand20.63±1.06μm,inGroup2were31.62±4.54μm,25.08±3.63μmand19.07±3.86μm,inGroup3were29.75±3.62μm,28.83±1.97μmand27.61±1.83μm.InGroup4themeanofthethicknesswas37.35±1.37μm.Astimewentby,thedamageg