Skip to main navigation Skip to search Skip to main content

An investigation of maternal and neonatal platelet function

  • M. A. Barradas
  • , D. P. Mikhailidis
  • , D. A.G. Imoedemhe
  • , O. Djahanbakhch
  • , I. L. Craft
  • , P. Dandona
  • Royal Free London NHS Foundation Trust

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

The authors have previously shown that the human placenta possesses a potent platelet anti-aggregatory activity which is probably due to an ADPase. This led them to investigate platelet aggregation (in response to: adenosine diphosphate; adrenaline; collagen) in maternal blood samples obtained pre- and post-delivery and in cord blood at the time of delivery. Platelet aggregation in maternal samples did not differ significantly pre- and post-delivery, nor did it differ significantly from platelet aggregation observed in age-matched, non-pregnant women. On the other hand, platelets obtained from cord blood samples were insensitive to adrenaline even when very high concentrations (100 μmol/l) of this agonist were used. This lack of response to adrenaline could be overcome by incubation of cord platelet rich plasma (PRP) with sub-aggregatory doses of collagen or ADP or by standing PRP at room temperature for 2-3 h. ADP-induced aggregation was also diminished in cord PRP samples but this was only significant at the lowest ADP concentrations. The physiological significance of these findings is unclear but it may be of relevance that plasma catecholamine levels are high in neonates. Some adults show a defect of aggregation with absence of response to adrenaline, suggesting that neonatal platelet function patterns may persist in some adults.

Original languageEnglish
Pages (from-to)60-65
Number of pages6
JournalBiological Research in Pregnancy and Perinatology
Volume7
Issue number2
StatePublished - 1986

Fingerprint

Dive into the research topics of 'An investigation of maternal and neonatal platelet function'. Together they form a unique fingerprint.

Cite this