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Abloodclotthatblocksanarterytothebraincancauseastroke
Factor I: Fibrinogen
Fibrinogenisglobulininnaturebuthasmuchbiggermoleculethanserumglobulin.The
molecularweightisabout3,30,000.Itiscoagulatedataround56 0C.Itisdistinguished
fromotherplasmaproteinsbyitspropertyofclotting.
Byloweringtemperature,Coagulationcanbeprevented.
Byavoidingcontactwithwaterweltablesurfaceandinjuredtissues.ThispreventsThrombokinaseaction.
Removalofcalciumion.
Precipitationoffibrinogen.
Byaddingthesubstancesofbiologicalorigin.Theseare
Protaminessimpleproteinfoundinfish.
PeptoneWhenitisinjectedinvein
HeparinMucoitinPolysulphuricacidproducedbymastcells.
HirudinLeechextractandvenomofcertainsnakes.
Heparin,Hirudinandvenomofcertainsnakespreventbloodclottingbyinhibitingactionofprothrombin
andthrombinfibrinogenreaction.
Coagulationprocesscanpaceupwithfollowingfactors:
Warmth.
Contactwithwaterwettablesurfaceandroughsurfaces.
Additionsofforeignbodiesintoasampleofblood.
Additionofthrombin.
Additionofthromboplastin.
The most immediate biochemical change that occurred post-mortem is a fall in the
concentrationofoxygenduetoabsenceofcirculation,resultinginaswitchtoanaerobic
metabolismwiththeabsenceofthecitricacidcycle.Anaerobicglycolysisresultedinthe
accumulationoflacticacidandanincreaseintheconcentrationofNADH.Formicacid
also increased post-mortem but because the production of this metabolite requires
enzymesthatfunctionatphysiologicalpHaswellasNAD +asaco-factor,theincreasein
formic acid is most probably attributed to bacterial putrefaction rather than anaerobic
metabolism. It is unclear why the pigs and the rats had such large differences in the
concentrationofformicacidpost-mortem.Itmaybebecausetheypossiblyhavedifferent
bacterialmicroflora.Theaccumulationoflacticacidandformicacidinitiatesthefallin
pHpost-mortem.Furthermore,becausethecirculatorysystemisstasis,thebloodbuffer
systemsfailresultinginarapidpHdeclineasmoreacidicmetabolitesareproduced.The
speedoftheplasmapHdecreasewasillustratedinFigure1Awherepost-mortemblood
pHfellfrom7.45to6.0withinthefirst24hoursafterdeath.TheplasmapHdecreaseis
significant because it is thought to activate fibrinolysin enzymes which prevent blood
clotting resulting in an increase in fluidity (non-coagulation) of the blood [28-31].
Although fibrinolysis was not examined in this study, the post-mortem blood remained
fluidinsidetheratandpigcorpsesoverthe96hourexaminationperiod,consistentwith
fibrinolysinenzymesbeingactive.
Thetimeintervalmaybeshortorextendeddependinguponthedegreeofclotting,source
andquantityofblood,andenvironmentalconditionsexistingatthetime.
Anaveragetimeof3to15minutesforbloodtocommenceclottingoutsidethebodymay
beusedasaguidelineforaminimalinterval
Redbloodcellsaredeliveringoxygentotissues,buttheycannotdothisanymoreinthe
lackofbloodflow.
White blood cells degenerate and after about 84 hours are no longer existing as cells (
BabapulleCJ,JayasunderaNP,1993). Neutrophiles degenerate first and lymphocytes
last.