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  • Georg Thieme Verlag KG  (2)
  • Andrew, M  (2)
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  • Georg Thieme Verlag KG  (2)
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  • 1
    Online-Ressource
    Online-Ressource
    Georg Thieme Verlag KG ; 1986
    In:  Thrombosis and Haemostasis Vol. 55, No. 03 ( 1986), p. 342-346
    In: Thrombosis and Haemostasis, Georg Thieme Verlag KG, Vol. 55, No. 03 ( 1986), p. 342-346
    Kurzfassung: Standard heparin and a LMWH, CY222 do not cross the placenta nor alter fetal coagulation when injected into the pregnant ewe. We found that another LMWH, Pharmuka-10169 (PK-10169) alters fetal coagulation without crossing the placenta in the pregnant sheep. To characterize this anticoagulant we measured the in vitro and in vivo effects of 125I-PK-10169 in maternal and fetal plasmas following administration of PK-10169 to the mother or fetus. The fetal anticoagulant activity was not neutralizable by protamine sulphate and was attributable to the inhibition of thrombin but not factor Xa. In vitro, the fetal anticoagulant activity had properties similar to dermatan sulphate : both catalyzed the inhibition of thrombin but not factor Xa by sheep plasma; and neither was neutralizable by protamine sulphate. These effects were due to the enhanced neutralization of thrombin by heparin cofactor II. We conclude that PK-10169 does not cross the placenta, but does induce the release of an endogenous dermatan sulphate-like substance which alters fetal coagulation.
    Materialart: Online-Ressource
    ISSN: 0340-6245 , 2567-689X
    Sprache: Englisch
    Verlag: Georg Thieme Verlag KG
    Publikationsdatum: 1986
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Online-Ressource
    Online-Ressource
    Georg Thieme Verlag KG ; 1988
    In:  Thrombosis and Haemostasis Vol. 60, No. 02 ( 1988), p. 289-292
    In: Thrombosis and Haemostasis, Georg Thieme Verlag KG, Vol. 60, No. 02 ( 1988), p. 289-292
    Kurzfassung: The relative deficiency of antithrombin III (AT III) in neonatal plasma results in lower recovery of heparin in some assay systems. It is uncertain whether low AT III levels also limit the antithrombotic effects of heparin in this age group. We therefore compared the antithrombotic properties of heparin in mature pigs and newborn piglets, whose coagulation and inhibitor system closely resembles that of the human neonate. Animals were pretreated with saline, 10 or 25 U/kg heparin (n ≥16 per age group and dose). Following an injection of 100 U/kg thrombin, systemic 125I-fibrinogen consumption and local 125I-fibrinogen incorporation into jugular venous stasis thrombi were measured. Significantly more 125I-fibrinogen was consumed in piglets than in pigs systemically (p 〈 0.0001), as well as within the occluded vein segment (p = 0.0112), largely because heparin was less effective in piglets than in pigs. This neonatal resistance to heparin could not be explained by lower heparin levels in the newborn animals. However, pretreatment with AT III concentrate significantly improved the antithrombotic properties of heparin in this age group (p 〈 0.0001). We conclude that physiologically low AT III levels reduce the efficacy of heparin in neutralizing thrombin activity in newborn piglets. We speculate that AT III deficiency may also limit the antithrombotic properties of heparin in newborn infants with thrombotic disease.
    Materialart: Online-Ressource
    ISSN: 0340-6245 , 2567-689X
    Sprache: Englisch
    Verlag: Georg Thieme Verlag KG
    Publikationsdatum: 1988
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
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