简介：目的：确定黄酮对人角膜内皮细胞（humancornealendothelialcells,HCEC）的影响及其对因氧化损伤所致细胞凋亡的抗氧化保护作用。方法：利用体外培养的HCEC,通过添加不同浓度的黄酮继续培养,或经不同浓度黄酮预处理后再添加过氧化氢（H2O2）继续培养,采用光镜形态观察、吖啶橙/溴化乙锭（AO/EB）双染色和DNA琼脂糖凝胶电泳等技术手段,研究黄酮对HCEC的影响及其抗氧化作用。结果：黄酮浓度高于85μmol/L时可诱导HCEC发生细胞凋亡,而低于70μmol/L时对HCEC没有影响;55和70μmol/L黄酮预处理对600μmol/LH2O2所引起的HCEC细胞凋亡具有显著的抑制作用（60%→22%,8%;P〈0.01）,而85和100μmol/L黄酮预处理对H2O2所引起的HCEC细胞凋亡没有显著的抑制作用。结论：55～70μmol/L黄酮对HCEC具有显著的抗氧化保护作用,而浓度高于85μmol/L的黄酮反而能诱发HCEC发生细胞凋亡。

简介：青光眼是全球第二大致盲眼病,是不可逆性盲最主要原因,而原发性闭角型青光眼（primaryangleclosure[1]glaucoma,PACG）是我国最主要的青光眼类型。原发性闭角型青光眼（PACG）的发病机制复杂。PACG发病的主要危险因素是晶状体位置偏前、前房变浅而导致的瞳孔阻滞。此外,周边虹膜肥厚以及睫状体位置前移也是PACG发病的常见危险因素。

简介：研究内源性大麻素N-花生四氢酸氨基乙醇（anan-damide，AEA）对体外培养的牛眼小梁细胞细胞骨架及PGE2表达的影响。方法：对牛眼小梁细胞进行原代及传代培养，并行鉴定。对传3代的牛眼小梁细胞分别施加AEA浓度分别为0，0．1，1．0，10／μmol／L的无血清培养液，作用24h后提取细胞上清液，并将细胞置于倒置显微镜下摄像，计算机图像分析系统计算细胞面积。用ELISA法检测PGE2浓度的变化。结果：AEA可以产生明显的细胞舒张效应，呈浓度依赖性。而且在一定范围内可以成剂量依赖性的促进PGE2的表达。与对照组均有显著性差异（P〈0．05）。结论：AEA可引起小梁细胞的舒张和促进PGE2的释放。

简介：目的分析常年性变应性鼻炎的狗、猫上皮变应原皮肤点刺试验的阳性结果，对其他气传变应原的反应性，并进一步探讨环境接触与其相关性。方法总结1022例常年性变应性鼻炎患者采用阿罗格叶7种气传变应原标准化试液进行的皮肤点刺试验；分析狗、猫上皮变应原的皮试结果及合并其他气传变应原阳性的比例；并根据是否有环境接触分类，比较各组在阳性率分布上的差异。结果常年性变应性鼻炎中狗上皮变应原皮试阳性占13．80％，猫上皮阳性占6．95％；且98％以上合并其他气传变应原阳性，尤以合并粉尘螨、屋尘螨阳性居多。其中21．93％和26．32％环境接触狗／猫的变应性鼻炎相应狗／猫上皮变应原皮试阳性；无环境接触组的阳性率分别为12．78％和6．58％，差异均有统计学意义（P〈0．01）。结论常年性变应性鼻炎的狗上皮及猫上皮的阳性率位居前列，其中绝大多数合并其他气传变应原阳性。鉴于环境接触对狗、猫上皮过敏的高危险性，变应性鼻炎患者应该尽可能地避免饲养、接触宠物。

简介：AIM:TotrainTibetanmonkey(Macacathibetana)forintraocularpressure(IOP)measurementinconsciousstateandobtainnormalIOPinconsciousTibetanMacaque.·METHODS:Thetrainingwasbasedonaward-conditionedbehavior.Foodstimulationandhuman-animalinteractionwereusedinthistraining.·RESULTS:TrainedTibetanmonkeyscalmlyacceptedIOPmeasurementbytheTonoVet?誖reboundtonometerwithoutsedationoranesthesiaandtheirIOPvaluesweresimilartootherprimates.·CONCLUSION:Human-cultivatedThibetanmonkeysaretamable,andcanbeusedforbiomedicalresearchsuchasophthalmicresearchwithoutanesthesia.

简介：AIM:ToevaluatetheefficacyofSeprafilmtransplantationfollowingadhesiolysisforpreventingpostoperativereadhesionandimprovingsurgicaloutcomes.METHODS:Primaryblepharoplastywascarriedoutonbotheyelidsof18albinorabbits.After2weeks,anewskinincisionwasmade,andadhesiolysiswasperformedonbotheyelids.Therabbitswerecategorizedintotwogroups,onewithadhesiolysisaloneinthelefteyelid(controlgroup),andtheotherwithadhesiolysiswithaSeprafilmgraftintherighteyelid(Seprafilmgroup).Thedegreesofinflammationandfibrosiswereexaminedwithhematoxylin-eosin(HE)andMasson’strichromestains.Expressionofα-smoothmuscleactin(α-SMA)wasalsoimmunohistochemicallyexamined.RESULTS:Eyelidexaminationimmediatelyaftertheoperationrevealedmildswellingandhemorrhageinbothgroups,butthesesymptomsresolvedafter1week-2weeks,andeyelidshapehadrecoveredcompletelyinbothgroups.MicroscopicassessmentsdemonstratedthattheSeprafilmgroupshowedlessinflammationandfibrosisthanthecontrolgroup.TheSeprafilmgroupalsoexhibitedfewerα-SMA-positivecellsthanthecontrolgroup.CONCLUSION:Basedonthesefindings,weconcludethatSeprafilmgraftwithadhesiolysisisaneffectivemethodforpreventingpostoperativereadhesionsaftereyelidsurgery.

简介：·AIM:Toinvestigatethetherapeuticeffectsofnanophtha-locyaninephotosensitizersonanexperimentalratchoroidalneovescularization(CNV)model,aswellastoevaluatethecytotoxicityofwhichonhumanretinalpigmentepithelia(HRPE)andhumanretinalendothelialcells(HRECs).·METHODS:Twotypesofphotosensitizers,G1-ZnPc(COOH)8andG1-ZnPc(COOH)8/mrespectively,wereadministratedforphotodynamictherapy(PDT)afterasuccessfulestablishmentofCNVmodelonBrown-Norway(BN)ratsviafundusphotocoagulation.Thetherapeuticeffectsofthetwodrugswereassessedthroughopticalcoherencetomography(OCT),fluoresceinfundusangiography(FFA)andtransmissionelectronmicroscopy(TEM).Forcytotoxicitytests,cellcountingkit-8(CCK-8)assaysandchangesofmitochondrialtransmembranepotential(△Ψm)wereconductedonHRPEandHRECsafterinitialuptakeofthetwodrugs.·RESULTS:Bothphotosensitizersdemonstratedanimprove-mentofvascularleakageandclosureofCNV1weekafterPDTasconfirmedbyfundusimage,OCT,FFAandTEM.TwoweeksafterPDT,G1-ZnPc(COOH)8/mshowedabetterCNVclosureeffectversusG1-ZnPc(COOH)8(P<0.05).Asignificantdifference(P<0.01)wasfoundinuptakeofthetwodrugsinHRPEandHRECs,withnodifferencebetweenthedrugs(P>0.05).BothphotosensitizersshowedcytotoxicityonHRPE,butG1-ZnPc(COOH)8/minducedalowercellviability.·CONCLUSION:G1-ZnPc(COOH)8/mmediatedPDTisbetterthanG1-ZnPc(COOH)8inCNVclosureandalsohavetheadvantageoffastmetabolismleadingtolesssideeffect.·

简介：AIM:ToevaluatetheeffectofCollagencross-linkingonthepreventionofmeltinginrabbitcorneasafteralkaliburn.·METHODS:TwentyNewZealandwhiterabbitswererandomlydividedintomodelcontrolgroupandcollagencross-linkingtreatmentgroup.Thesecondgroupofrabbitsreceivedcollagencrosslinkedtreatment.Bothgroupswereappliedwithantibioticeyedropstopreventinfection.Thecorneaswereevaluatedformelting,opacity,pathologicalandimmunohistochemistry,recordthechangeswhen28daysaftertheanimalswerekilled.·RESULTS:Inthecontrolgroup,6outof8rabbitsshowedcornealmeltingafterinjury(14±4)days,whiletwocornealperforated.Incollagencross-linkingtreatmentgroup,onerabbitshowedcornealmeltingafterinjury23days,withoutcornealperforation;cornealdissolutionratebetweenthetwogroupswassignificantlydifferent(P<0.05).Pathologicalexaminationsuggestedthatinthetreatmentgroup,mildcornealedema,milddamagetocollagenfibers,inflammatorycellinfiltrationwassignificantlylessthanthecontrolgroup.Immunohistochemistryshowedthatcornealcollagenfibersarrangedinneatrowsinthecontrolgroup.·CONCLUSION:Collagencross-linkingtreatmentnotonlycanpreventanddelaythecornealmeltingafteralkaliburn,butalsocanreducethedestructionofcornealcollagenfibersandinfiltrationofinflammatorycellsinthecornealtissue.

简介：·AIM:Toexploretheeffectofimmunizationwithcopolymer-1(COP-1)andretinalstemcells(RSCs)transplantationoninterferon-gamma(IFN-γ)levelsinaratexperimentalglaucomamodel.·METHODS:Anexperimentalglaucomawasinducedbyargonlaserphotocoagulationoftheepiscleralveinsandlimbalplexusintherighteyeofrats.Immediatelyfollowingglaucomainduction,ratswereimmunizedwithCOP-1.RSCswereculturedandtransplantedintravitreallyintotheeyesofglaucomamodelanimals1weekpost-lasertreatment.Sixexperimentalgroupswereused:COP-1/RSC,PBS/RSC,COP-1/PBS,PBS/PBS,glaucomamodelgroup,andanormalcontrolgroup.TheconcentrationofIFN-γinaqueoushumor(AH)andserumwasmeasuredbyenzyme-linkedimmunosorbentassay(ELISA)ineachofthesixgroups.Retinalganglioncell(RGC)survivalwasassessedbyquantifyingapoptosisusingHoechststaining.·RESULTS:ConcentrationsofIFN-γinAHandserumofratsthathadundergoneglaucomainductionwerehigherthanthoseofnon-inducedcontrolrats.TheconcentrationsofIFN-γinAHandserumoftheCOP-1/RSCstreatedgroupweredeterminedtobe2371.9ng/Land710.9ng/L,respectively,whichweresignificantlylowerthanthoseintheothertreatedgroups(P<0.05).Infact,IFN-γlevelsinthedualtreatedgroupwerereducedtobackgroundlevels.TheCOP-1/RSCgrouphadlowernumberofapoptoticRGCsthantheotherthreeexperimentalgroups(P<0.05).·CONCLUSION:ThereducedlevelsofIFN-γinAHandserumoftheCOP-1/RSCgroupmayberelatedtosynergisticeffectsbetweenRSCstransplantationandCOP-1immunemodulation.ItislikelythatthelowerlevelsofIFN-γpreventedRGCsglaucomatousapoptosis.·