简介:TenfractionatedsamplesofChineselacquerpolysaccharideinaqueous0.1MNaC1solutionwerestudiedbyaqueous-phasegelpermeationchromatography(GPC).Theuniversalcalibration,broadMWDcalibrationandcorrectedcolumndispersionwereadoptedtotheanalysisofGPCchromatogramsofthepolysaccharide.ThemolecularweightsM_w,M_nandpolydispersityindexM_w/M_nobtainedfromGPCareingoodagreementwiththeresultsoflightscatteringandmembraneosmometry.Itisverifiedthattheuniversalcalibrationconceptisapplicabletothelacquerpolysaccharidehavinganumberofsidechains.
简介:H3,ahomogeneousacidicpolysaccharidewasobtainedfromtheseedsofCuscutachinensisLam.Itsstructurewascharacterizedforthefirsttimebychemicalandspectroscopicmethodstobeahighlybranchedheteropolysaccharidewithmeanmolecularweightofmorethanlxl0^6.Itwascomposedof1,6-1inked-β-DGalp,1,4-linked-β-DGalp,1,4-1inked-β-DGalA,1,3,6-1inked-β-DGalpand1,2,4-1inkedRhap,withbranchingpointsatO-2or0-4of1,2,4-1inkedRhapand0-3of1,3,6-1inked-β-DGalp.Itssidechainsincluded1-1inkedAraf,1,5-1inkedArafand1,3,5-1inkedArafatO-3of1,6-1inkedGalpinthemainchain.
简介:Cholesterolmodifieddextran(CHD)havingself-aggrgationorself-assemblypropertywassynthesizedfromcholesteroland1,6-hexyldiisocyanate.Thedegreeofsubstitutionofcholesterylmoietyindextranmainlineis3-5cholesterolsthe100glucoseunits.WehavepreparedwatersolutionofCHDusingprobetypesonifierandN-Phenyl-a-naphthylamine(PNA)asafluorescentprobetostudyCHDself-aggregateprocess.Foreachsolutionoftwosamples,wefoundthatthemaximumemissionofPNAinCHDconcentration.Thischangecorrespondstotheformationofmicelle-likeclustersself-aggregatedbythecholesterolmoietyoncetheCHDconcentration.Thischangecorrespondstotheformationofmicelle-likeclustersself-aggregatedbythecholesterolmoietyoncetheCHDconcentrationexceeds0.01mg/ml.
简介:PolysaccharideextractedfromEnteromorphaproliferapossessedexcellentbiologicalactivities,butitsmolecularweightwasgreatlyhighwhichinfluencedtheactivity.OrganicSehadhigherbiologicalactivitiesandwassaferthaninorganicSespecies.Inthepresentstudy,Enteromorphapolysaccharidewasdegradedtolowmolecularweightbyfree-radicaldegradationmethodofH2O2andascorbicacid.Bysinglefactorandorthogonalexperiments,theoptimaldegradationconditionswerereactiontimeof2h,reactiontemperatureof50℃,H2O2/ascorbicacid(n/n=1:1)concentrationof15mmolL-1,andsolid-liquidratioof1:50(gmL-1).Then,thedegradedpolysaccharidewaschemicallymodifiedtoobtainitsselenidederivativesbynitricacid-sodiumselenitemethod.Theseleniumcontentwas1137.29μgg?1,whilethecontentofsulfateradicalhadnochange.IRspectraindicatedthattheseleniteestergroupwasformed.Degradedpolysaccharideselenidewascharacterizedandevaluatedforantioxidant,antifungalandantibacterialactivities.TheresultsshowedthatdegradedpolysaccharideselenidehadstrongcapacityofscavengingDPPHand·OHfreeradical.IthadsignificantantibacterialpropertiesforEscherichiacoli,BacillussubtilisandSalmonellaspp.,anditalsohadsignificantantifungalpropertiesforAppleanthrax.Theresultascertaineddegradationandselenylationmodificationdidnotchangethemainstructureofpolysaccharides.Itwaspossiblethatfree-radicaldegradationwasaneffectivewayforenhancingantioxidantactivitytodecreasemolecularweightofpolysaccharides.
简介:TheantineoplasticactivityofpolysaccharidewasinvestigatedinStichopuschlorontus,Isostichopusbadionotus,StichopushorrensandHolothurialessonimassin.CrudepolysaccharidewaspreparedwithenzymehydrolyzationmethodandpurifiedbyanionexchangechromatographyusingDEAE-sepharosefastflowcolumn.TheeffectofpolysaccharideoncellsapoptosisofSiHaandU87wasexaminedwithcellcountingkit-8colorimetrymethod.Westernblottingwasusedtoanalyzerelatedproteinsofcellularapoptosisincludingp53andBcl-2.Resultsshowedthatthereweretwomaincomponentsineachseacucumberpolysaccharide,whichcouldbeeluteddownby1.0mol/LNaClsolution.ThefourtypesofpolysaccharideinthesecondcomponentwerenamedasSC-2,IB-2,HLM-2andSH-2,respectively.Theywereusedforcomparingtheantineoplasticactivity.ResultsshowedthatSC-2,IB-2,HLM-2andSH-2couldpromoteapoptosisofU87andSiHacells.SH-2andHLM-2wereselectedforthesubsequentexperimenttoexploretheadditionaleffectofU87andSiHacells,TheproteinexpressionsofBcl-2andp53decreasedconsiderablywiththeincreaseofpolysaccharideconcentrationinU87cells.InSiHacells,proteinexpressionsofBcl-2andhighdosagegroupofp53decreasedsignificantly,whereasnoobviousdecreasewasobservedinothergroups.ThepolysaccharidesaremoreeffectiveinpromotingapoptosisofU87andSiHacellsfromS.horrensandH.lessonimassinthanfromtherestspecies.
简介:ToinvestigatethechangesofimmunefunctionsandtheeffectsofAstragaiuspolysaccharide(ASP)onthecell-mediatedimmunityofthetraumaticstressmodelofmousebyamputation,50micewererandomlydividedinto5groupsforstudy,inwhichthegroupAandBservedasthenormalcontrol(byinjectonof0.5mlofsalineintra-peritoneallydaily),andasthestresscontrol(byintra-peritonealinjectonof0.5mlofnormalsalineintomiceafteramputation)respectively,tothegroupC,DandEofmice,1000mg/kg(highdose),300mg/kg(mediandose)and250mg/kg(lowdose).TheCD4^+andCD8^+Tcellsaswellastheexpressionofthec-fosproteinweredeterminedbyimmunohistochemicaltechniques,andtheexpressionsofNF-κBmRNAandIL-10mRNAwereassayedbyhybridizationinsitu.Theexperimentalresultsshowedthatincomparisonwiththenormalcontrolgroupofmice(groupA),theexpressionlevelsofNF-κBmRNA,IL-10mRNAandthec-fosproteininthetissuesofthymusandspleeninthestresscontrolsweresignificantlyelevatedandtheCD4^+TcellsandCD4/CD8ratioweredecreased.However,incomparisonwiththestresscontrolofmice(groupB),theexpressionsofNF-κBmRNAandIL-10mRNAwereinhibitedbyASP,andtheCD4^+TcellsandCD4/CD8ratiowereincreasedingroupsC,DandE,butthelevelofc-fosproteinwasdecreased.TherewasnosignificantdifferenceintheseparametersamonggroupC,DandE.Itiscon-cludedthatthefunctionsofcell-mediatedimmunityofmiceweredisturbedunderthestressconditionofthetraumaticinjuriesafteramputation.AndtheimmunefunctionscanbeeffectivelyrestoredbytheuseofAstraga/uspolysaccharide.
简介:Inthepresentstudy,theeffectsofPleurotusnebrodensispolysaccharide(PN-S)ontheimmunefunctionsofimmunosuppressedmiceweredetermined.Theimmunosuppressedmousemodelwasestablishedbytreatingthemicewithcyclophosphamide(40mg/kg/2d,CY)throughintraperitonealinjection.TheresultsshowedthatPN-SadministrationsignificantlyreversedtheCY-inducedweightloss,increasedthethymicandsplenicindices,andpromotedproliferationofTlymphocyte,Blymphocyte,andmacrophages.PN-SalsoenhancedtheactivityofnaturalkillercellsandincreasedtheimmunoglobulinM(IgM)andimmunoglobulinG(IgG)levelsintheserum.Inaddition,PN-Streatmentsignificantlyincreasedthephagocyticactivityofmouseperitonealmacrophages.PN-Salsoincreasedthelevelsofinterleukin-6(IL-6),tumornecrosisfactor-α(TNF-α),interferon-γ(INF-γ),andnitricoxide(NOS)insplenocytes.qRT-PCRresultsalsoindicatedthatPN-SincreasedthemRNAexpressionofIL-6,TNF-α,INF-γ,andnitricoxidesynthase(iNOS)inthesplenocytes.TheseresultssuggestthatPN-Streatmentenhancestheimmunefunctionofimmunosuppressedmice.Thisstudymayprovideabasisfortheapplicationofthisfungusinadjacentimmunopotentiatingtherapyagainstcancerandinthetreatmentofchemotherapy-inducedimmunosuppression.
简介:ToexploretheantiviraleffectandmechanismofpolysaccharidefromSpirulinaplatensis(PSP)onherpessimplexvimstype2(HSV-2),astandardstrainofHSV-2(333strain)wasusedtoinvestigatetheantiviraleffectofPSPinvitro.PSPinvariousconcentrationswasappliedtodifferentstagesofHSV-2replicationcycle.Finally,thevirusinfectivity(TCID50),cytopathiceffect(CPE),andMTTstainingmethodforviablecells(MTTassay)wereusedasmarkerstoevaluatetheeffectofPSPonHSV-2.ThequantityofHSV-DNAwasdetectedbyreal-timefluorescencequantitativePCR(FQ-PCR).TheHSV-2infectedVerocellultrastructureswereobservedbytransmissionelectronmicroscopy(TEM).TheresultsshowedthatPSPhadlittlecytotoxiceffectonVerocells,itcouldnotdirectlyinactivateHSV-2infectivity.PSPnotonlyinterferedinadsorptionofHSV-2toVerocellsbutalsoinllibitedHSV-2biosynthesisinthecells.FQ-PCRresultsshowedthattheinhibitoryrateonHSV-DNAalsoincreasedinadose-dependentandtime-dependentmanner.TEMalsoconfirmedthatPSPexhibitedpronouncedinhibitoryeffectonHSV-2.Inconclusion,theantiviraleffectofPSPonHSV-2maybeattributedtotheinhibitionofvimsadsorption,vimsreplicationandsynthesisincells.
简介:BacteriaofthegenusFlammeovirgacandigestcomplexpolysaccharides(CPs),butnodetailshavebeenreportedregardingtheCPdepolymerasesofthesebacteria.MY04,anagarolyticmarinebacteriumisolatedfromcoastalsediments,hasbeenidentifiedasanewmemberofthegenusFlammeovirga.TheMY04strainisabletoutilizemultipleCPsasasolecarbonsourceandgrowswellonagarose,mannan,orxylan.Thisstrainproduceshighconcentrationsofextracellularproteins(490mgL-1±18.2mgL-1liquidculture)thatexhibitefficientandextensivedegradationactivitiesonvariouspolysaccharides,especiallyagarose.Theseproteinshaveanactivityof310Umg-1±9.6Umg-1proteins.Theextracellularagarasesystem(EAS)inthecrudeextracellularenzymescontainsatleastfouragarosedepolymerases,whicharewithmolecularmassesofapproximately30-70kDa.TheEASisstableatawiderangeofpHvalues(6.0-11.0),temperatures(0-50℃),andsodiumchloride(NaCl)concentrations(0-0.9molL-1).TwomajordegradationproductsgeneratedfromagarosebytheEASareidentifiedtobeneoagarotetraoseandneoagarohexaose,suggestingthatβ-agarasesarethemajorconstituentsoftheMY04EAS.TheseresultssuggestthattheFlammeovirgastrainMY04anditspolysac-charide-degradationsystemholdgreatpromiseinindustrialapplications.
简介:BACKGROUND:Themostprominentcharacteristicofbrainagingisdecreasedlearningandmemoryability.Thefunctionsoflearningandmemoryarecloselyrelatedtointracerebralacetylcholinesterase(AChE)andmonoamineneurotransmitteractivity.PreviousstudieshaveshownthatSchisandrachinensispolysaccharidehasananti-agingeffect.OBJECTIVE:ToexploretheeffectsofSchisandrachinensispolysaccharideonAChEactivityandmonoamineneurotransmittercontent,aswellaslearningandmemoryabilityinaD-galactose-inducedagingmousebrainmodelcomparedwiththepositivecontroldrugKangnaoling.DESIGN,TIMEANDSETTING:Completelyrandomized,controlledexperimentbasedonneurobiochemistrywasperformedatthePharmacologicalLaboratory,HenanUniversityofTraditionalChineseMedicinefromSeptembertoDecember2003.MATERIALS:SchisandrachinensiswaspurchasedfromHenanProvincialMedicinalCompany.Schisandrachinensispolysaccharidewasobtainedbywaterextractionandalcoholprecipitation.KangnaolingpelletswereprovidedbyLiaoningTianlongPharmaceutical(batchNo.20030804;statedrugpermitNo.H21023095).Atotalof50six-week-oldKunmingmicewererandomlydividedintofivegroups:blankcontrol,model,Kangnaoling,highandlowdosageSchisandrachinensispolysaccharidegroups,with10micepergroup.METHODS:Miceintheblankcontrolgroupweresubcutaneouslyinjectedwith0.5mL/20gnormalsalineintothenapeoftheneckeachday,whiletheremainingmiceweresubcutaneouslyinjectedwith5%D-galactosesalinesolution(0.5mL/20g)inthenapefor40daystoinduceabrainagingmodel.Onday11,miceinthehighandlowdosageSchisandrachinensispolysaccharidegroupswereintragastricallyinfusedwith20mg/mLand10mg/mLSchisandrachinensispolysaccharidesolution(0.2mL/10g),respectively.MicefromtheKangnaolinggroupwereintragastricallyinfusedwith35mg/mLKangnaolingsuspension(0.2ml/10g),andthemiceinthemodelgroupwereintragastricallyinfusedwiththesamevolumeofnormalsal
简介:Houttuyniacordatapolysaccharide(HCP)isextractedfromHouttuyniacordata,akeytraditionalChinesemedicine.ThestudywastoinvestigatetheeffectsofHCPonintestinalbarrierandmicrobiotainH1N1virusinfectedmice.MicewereinfectedwithH1N1virusandorallyadministratedHCPatadosageof40mg(kg^-1(d^-1.H1N1infectioncausedpulmonaryandintestinalinjuryandgutmicrobiotaimbalance.HCPsignificantlysuppressedtheexpressionofhypoxiainduciblefactor-1αanddecreasedmucosubstancesingobletcells,butrestoredthelevelofzonulaoccludens-1inintestine.HCPalsoreversedthecompositionchangeofintestinalmicrobiotacausedbyH1N1infection,withsignificantlyreducedrelativeabundancesofVibrioandBacillus,thepathogenicbacterialgenera.Furthermore,HCPrebalancedthegutmicrobiotaandrestoredtheintestinalhomeostasistosomedegree.TheinhibitionofinflammationwasassociatedwiththereducedlevelofToll-likereceptorsandinterleukin-1βinintestine,aswellastheincreasedproductionofinterleukin-10.OraladministrationofHCPalleviatedlunginjuryandintestinaldysfunctioncausedbyH1N1infection.HCPmaygainsystemictreatmentbylocalactingonintestineandmicrobiota.Thisstudyprovedthehigh-valueapplicationofHCP.
简介:AnovelPleurotusnebrodensispolysaccharide(PN-S)waspurifiedandcharacterized,anditsimmune-stimulatingactivitywasevaluatedinRAW264.7macrophages.PN-SinducedtheproliferationofRAW264.7cellsinadose-dependentmanner,asdeterminedbytheMTTassay.AfterexposuretoPN-S,thephagocytosisofthemacrophageswassignificantlyimproved,withremarkablechangesinmorphologybeingobserved.FlowcytometricanalysisdemonstratedthatPN-SpromotedRAW264.7cellstoprogressthroughSandG2/Mphases.PN-Streatmentenhancedtheproductionsofinterleukin-6(IL-6),nitricoxide(NO),interferongamma(INF-γ),andtumornecrosisfactor-α(TNF-α)inthemacrophages,withup-regulationofmRNAexpressionsofinterleukin-6(IL-6),induciblenitricoxidesynthase(iNOS),interferongamma(INF-γ)andtumornecrosisfactor-α(TNF-α)beingobservedinadose-dependentmanner,asmeasuredbyqRT-PCR.Inconclusion,theseresultssuggestthatthepurifiedPN-Scanimproveimmunitybyactivatingmacrophages.