1992
DOI: 10.1111/j.1525-1594.1992.tb00533.x
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A Heparin‐Coated Circuit Reduces Complement Activation and the Release of Leukocyte Inflammatory Mediators During Extracorporeal Circulation in a Rabbit

Abstract: Heparin coating modifies complement activation during extracorporeal circulation much more effcclively than systemically administered heparin. This rabbit study was undertaken to address possible mechanisms responsible for this difference. We evaluated the effect of heparin coating on complement activation and subsequently the release of leukocyte inflammatory mediators during extracorporeal circulation through a simplified circuit. We found in the heparin-coated group a significantly reduced complement hemoly… Show more

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Cited by 23 publications
(3 citation statements)
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“…1,19 The inflammatory response to ECC has been investigated by many research groups. 20,21 Additionally, ECC-related anticoagulation might be associated with a higher risk for bleeding in stroke patients. In the past decade, several neurological studies have investigated isovolemic or hypervolemic hemodilution as a treatment option for stroke patients to lower viscosity and increase cerebral blood flow in the penumbra zone.…”
Section: Discussionmentioning
confidence: 99%
“…1,19 The inflammatory response to ECC has been investigated by many research groups. 20,21 Additionally, ECC-related anticoagulation might be associated with a higher risk for bleeding in stroke patients. In the past decade, several neurological studies have investigated isovolemic or hypervolemic hemodilution as a treatment option for stroke patients to lower viscosity and increase cerebral blood flow in the penumbra zone.…”
Section: Discussionmentioning
confidence: 99%
“…Heparin-coated circuits reduce cytokine release, complement activation in vivo and in vitro , kallikrein, and leukocyte activation ( 180 184 ). They have been shown to reduce platelet adhesion and improve platelet function, as well as inhibit the release of pro-inflammatory cytokines TNF-α, IL-6, IL-8 as well as soluble TNF receptors ( 180 , 185 187 ). Significant reduction in mean concentrations of polymorphonuclear (PMN) elastase and soluble C5b-9 ( p < 0.001 and p = 0.006, respectively) at one hour following initiation of CPB have been reported.…”
Section: Strategies To Modulate Cpb-associated Inflammatory Responsementioning
confidence: 99%
“…Its action on the burn probably derives from its anti-inflammatory and angiogenic properties that do not depend on its´ well-known anticoagulant action 8,9 . The anti-inflammatory action results from deactivation of pro-inflammatory cytokines such as TNF-alpha 10 , selectins secreted by leukocytes such as CD11b 11,12 integrins such as ICAM-1 13 and attenuation of complement activation 14 . Angiogenic effect derives from the interaction with vascular endothelium growth factor (VEGF) 15,16 and with fibroblasts' growth factors (FGFs) 17,18 .…”
Section: Introductionmentioning
confidence: 99%