简介:ObjectivesToinvestigatetheeffectandmechanismofendovaseularbraehytherapywith^192IronexpressionoftypeIcollagen,metalloproteinases-1(MMP-1)andthetissueinhibitor(TIMP-1)afterangioplasty.MethodsRestenotiemodelofdomesticmieroswinewasemployedandtheiliaearterieswererandomizedtoradiationgroup(n=12),whichweretreatedwith20-25Gyof^192Ir,andnon-radiationgroup(n=36)afterangioplasty.Thetargetvesselswereharvestedintheendof3monthsand6monthsafterangioplasty.Im-munohistochemistryandinsituhybridizationwereusedtodetectproteinsoftypeIcollagen,MMP-1andTIMP-1,andmRNAexpressionoftypeIcollagen.ResultsTheproteinandmRNAoftypeIcollagen,theratiosofTIMP-1/MMP-1weresignificantlylowerinradiationgroupthaninnon-radiationgroup(P<0.05or0.01).ThepeakoftranscriptionoftypeIcollagenmRNAwasat6monthsand3monthsinnon-radiationgroupandradiationgrouprespectively.ConclusionsEndovascularbrachytherapywith^192IrmightmodifythemetabolismofextracellularmatrixafterangioplastybyinhibitingthesynthesisoftypeIcollagenandtheactivitiesofMMP-1andTIMP-1.
简介:InfluenceoftheeffectivefermionhexadecapoleforcenewlyincorporatedinamicroscopicsdgIBM-1onspectra,reducedE2andE4transitionmatrixelements(T(E2)sandT(E4)s)intheeven-evenplatinumisotopes(A=192,194,196,198)isinvestigatedintermsofnumericalcalculations.ItisfoundthattheintroducedinteractioncausesonlylimitedmodificationtothespectrumandT(E2)s,apartfromafewexceptions.However,itplaysanessentialroleindescribingE4transitions.Thusinthecasethattheinteractionisincorporatedwithcertainstrength,areasonabledescriptionofalltheE4transitionsintheplatinumisotopesisreachedinthemicroscopicsdgIBM-1incomparingbothtoexperimentaldataandtheresultscalculatedinphenomenologicalbosonmodel.``
简介:目的:探讨中国北方地区I型对氧磷酯酶(paraoxonase,PON1)基因192Gln/Arg遗传多态性及其与冠心病发病的关系。方法:应用PCR-RFLP技术,检测49例老年CHD患者和38例对照者的PON1-192Gln/Arg基因多态性,等位基因以A/B表示。结果:各基因组(AA,AB,BB)分布在冠心病组:18.4%,51%,30.6%;对照组:39.5%,47.3%,13.2%。两组比较各基因型分布具有显著性差异(X^2=6.35,P=0.042);B等位基因在冠心病组明显增高(0.56vs.0.370);B等位基因携得(AB型+B型)与AA型纯合子比较,两组间具有显著性差异(x^2=4.77,P=0.029).B等位基因是中国北方地区冠心病发病的危险因素(OR=2.19,95%CI:1.19-4.05)。结论:PON1基因192Gln/Arg遗传多态性与中国北方地区冠心病发病明显相关。该酶切位点多态性具有明显的种族差异。
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