Scientific Article
previous document  unige:29765  next document
add to browser collection

Diminished thrombus formation and alleviation of myocardial infarction and reperfusion injury through antibody- or small-molecule-mediated inhibition of selectin-dependent platelet functions

Oostingh, Gertie J.
Pozgajova, Miroslava
Ludwig, Ralf J.
Krahn, Thomas
Nieswandt, Bernhard
Schon, Michael P.
Published in Haematologica. 2007, vol. 92, no. 4, p. 502-512
Abstract BACKGROUND AND OBJECTIVES: P-selectin ctin has been implicated in important platelet functions. However, neither its role in thrombus formation and cardiovascular disorders nor its suitability as a therapeutic target structure is entirely clear. DESIGN AND METHODS: Platelet aggregation was assessed in complementary in vitro settings by measurements of static aggregation, standardized aggregometry and dynamic flow chamber assays. Degradation of aggregates was also analyzed under flow conditions using video microscopy. In vivo, platelet rolling in cutaneous venules was assessed by intravital microscopy in wild-type mice treated with selectin-blocking compounds as well as in P-selectin-deficient mice. FeCl3-induced arterial thrombosis was studied by intravital microscopy in untreated mice or mice treated with an inhibitor of selectin functions. Finally, inhibition of selectin functions was studied in an ischemia/reperfusion injury model in rats. RESULTS: Antibody- or small-molecule-mediated inhibition of P-selectin functions significantly diminished platelet aggregation (p<0.03) and platelet-neutrophil adhesion in vitro (p<0.01) as well as platelet aggregate sizes under flow (p<0.03). Established aggregates were degraded, either via detachment of single platelets following addition of efomycine M, or via detachment of multicellular clumps when P-selectin-directed Fab-fragments were used. In vivo, selectin inhibition resulted in a greater than 50% reduction of platelet rolling in cutaneous venules (p<0.01), producing rolling fractions similar to those observed in P-selectin-deficient mice (p<0.05). Moreover, inhibition of selectin functions significantly decreased the thrombus size in FeCl3-induced arterial thrombosis in mice (p<0.05). In an ischemia/reperfusion injury model in rats, small-molecule-mediated selectin inhibition significantly reduced myocardial infarct size from 18.9% to 9.42% (p<0.001) and reperfusion injury (p<0.001). INTERPRETATION AND CONCLUSIONS: Inhibition of P-selectin functions reduces platelet aggregation and can alleviate platelet-related disorders in disease-relevant preclinical settings.
Keywords AnimalsAntibodies, Monoclonal/immunology/pharmacology/*therapeutic useArterial Occlusive Diseases/blood/chemically induced/*prevention & controlChloridesDrug Evaluation, PreclinicalEndothelial Cells/cytologyFerric Compounds/toxicityFibrinolytic Agents/pharmacology/*therapeutic useHemorheologyHumansImmunoglobulin Fab Fragments/pharmacologyMacrolides/pharmacology/*therapeutic useMiceMice, Inbred C57BLMice, KnockoutMolecular WeightMyocardial Infarction/*blood/physiopathologyMyocardial Reperfusion Injury/*prevention & controlNeutrophils/cytologyOligosaccharides/pharmacologyP-Selectin/immunology/*physiologyPlatelet Adhesiveness/drug effectsPlatelet Aggregation/*drug effects/physiologyPlatelet Aggregation Inhibitors/pharmacology/*therapeutic useRatsRats, Inbred LewThrombosis/blood/chemically induced/*prevention & control
PMID: 17488661
Full text
Article - document accessible for UNIGE members only Limited access to UNIGE
Other version:
(ISO format)
OOSTINGH, Gertie J. et al. Diminished thrombus formation and alleviation of myocardial infarction and reperfusion injury through antibody- or small-molecule-mediated inhibition of selectin-dependent platelet functions. In: Haematologica, 2007, vol. 92, n° 4, p. 502-512.

138 hits

0 download


Deposited on : 2013-09-20

Export document
Format :
Citation style :