简介:目的探讨O形臂导航辅助经皮椎弓根螺钉内固定的准确性与安全性。方法回顾性分析7例经皮椎弓根螺钉内固定病人的临床及影像学资料。病人均在置钉结束后行O形臂系统3D扫描,按照Gertzbein-Robbins分级评估置钉的准确性。结果7例病人在O形臂导航辅助下共置入29枚椎弓根螺钉,其中Gertzbein-Robbins分级A级23枚(79.31%),B级4枚(13.79%),C级1枚(3.45%),E级1枚(3.45%)。手术共置入29枚克氏针,其中1枚(3.45%)突破椎体前缘。术中无关节突关节受到破坏。1例出现置钉相关神经并发症行再次手术调整椎弓根螺钉。随访(8.29±2.43)个月,无钉棒置入后相关并发症。结论O形臂导航辅助经皮椎弓根螺钉内固定具有较高的准确性及安全性。
简介:BACKGROUND:Mailuoning,aChineseherb,hasbeenwidelyusedinChinatotreatacuteischemicstroke,andthemajorcomponentexhibitsanti-oxidativeeffects.However,thepreciseanti-oxidationpathwayremainsuncertain.OBJECTIVE:TovalidatetheprotectiveeffectsofMailuoningonH2O2-inducedprimarycorticalneuroninjuryinembryonicmice.DESIGN,TIMEANDSETTING:ComparativeobservationandinvitroexperimentswereperformedattheJiangsuKeyLaboratoryforMolecularMedicinefromJanuary2008toSeptember2009.MATERIALS:Mailuoning(NanjingJinlingMedicalCompany,China),reactiveoxygenspecies(ROS)kit(BeyotimeBiotechnology,China),superoxidedismutase(SOD),Cu/ZnSODkit,malondialdehyde(MDA)kits(NanjingJiancheng,China),mitochondrialmembranepotential(GMS10013.1,GENMED,USA)andcatalaseactivityassaykit(BeyotimeBiotechnology,China)wereutilizedforthepresentstudy.METHODS:MouseembryoniccorticalneuronswereisolatedandculturedwithculturemediumcontainingH2O2(80μmol/L)and/orMailuoning(1.25μg/mL)for24hours.MAINOUTCOMEMEASURES:Neuronalviabilityanddeathweredetectedbymethylthiazolyltetrazdiumandflowcytometry;ROSproductionwasdeterminedbyflowcytometry;mitochondrialmembranepotentialwasdetectedusingfluorescentstaining;SODactivitywasdetectedusingamodifiednitrobluetetrazoliummethod;Cu/ZnSODandcatalaseactivitywasdetectedbyspectrophotometry;andMDAwasdeterminedusingthelipidperoxidationmethod.RESULTS:H2O2increasedROSproductionandMDAconcentration(P<0.05),anddecreasedmitochondrialmembranepotential,SOD,Cu/ZnSODandcatalaseactivity(P<0.05);thenumberofsurvivingneurons(P<0.05)wasalsoreduced.Mailuoningreversedthesechanges.CONCLUSION:MailuoningprotectsH2O2-inducedinjuryincorticalcellsbyinhibitingROSandMDA,increasingdepolarizationofmitochondrialmembrane,andenhancingSODandcatalaseactivity.
简介:目的研究刺五加多糖(ASPS)对H2O2诱导的海马神经元凋亡的影响及其机制。方法采用H2O2诱导大鼠海马神经元凋亡。采用末端脱氧核苷酸转移酶介导的dUTP原位切口末端标记法检测细胞凋亡率、免疫组化法检测caspase-3蛋白的表达、逆转录PCR法检测caspase-3mRNA的表达。结果H2O2作用后,海马神经元凋亡率、caspase-3蛋白和mRNA表达水平均显著增高(P〈0.05);给予ASPS干预后,均显著下降(P〈0.05);而且,随ASPS剂量增加,作用效果显著增强(P〈0.05)。结论ASPS具有抑制氧化应激损伤诱导神经细胞凋亡作用,其机制与下调caspase-3mRNA的表达有关。
简介:目的:优选枣仁安神胶囊的制备工艺并建立质量控制方法。方法:以浸膏中酸枣仁皂苷A和B的含量作为指标,采用L9(3^4)正交试验优选提取工艺,采用薄层色谱法对枣仁安神胶囊中酸枣仁皂苷A和B进行定性鉴别,同时单波长薄层扫描法测定酸枣仁中酸枣仁皂苷A、B的含量。结果:1)枣仁安神胶囊的最佳提取工艺为8倍量水,煎煮3次,每次2.0h时有效成分含量最高;2)薄层色谱法检测酸枣仁皂苷A和B的专属性较强,酸枣仁A的线性回归方程为:YA=0.958X+0.921×10^-4(r=0.9998),酸枣仁皂苷B的线性回归方程为:YB=0.652X+0.767×10^-4(r=0.9997),皂苷A点样量在2.1~7.1μg,皂苷B点样量在2.0~6.0μg范围内线性关系良好。结论:优选的枣仁安神胶囊提取工艺提取率高,可行性好,工艺稳定,同时建立的鉴别方法专属性强,定量方面简单、准确,适用于对枣仁安神胶囊的质量控制。