Abnormalities in platelet functions including aggregation and the rele
ase reaction have long been recognized to be present in neonatal plate
lets. Because calcium is an important mediator of many platelet functi
ons, we have investigated the mobilization of calcium in neonatal plat
elets. All umbilical cord blood samples were obtained from healthy, fu
ll term gestations. Changes in cytoplasmic calcium levels were monitor
ed using Fura-2 as a fluorescent probe. Fura-2-loaded washed platelets
were stimulated with the agonists collagen (2 mu g/mL) or thrombin (1
.0 U/mL). When compared with adult controls, intracellular calcium rel
ease in the platelets of the neonate was significantly impaired in res
ponse to these agonists. Mean levels for calcium release in adults ver
sus neonates in response to collagen were 168 +/- 120 nM (+/-SD, n = 1
0), and 61 +/- 69 nM (n = 7, p < 0.05). A decrease in response to thro
mbin was also observed [1296 +/- 503 nM (n = 8) in adults versus 603 /- 482 nM (n = 7) in neonates, p < 0.025]. Results similar to those ob
served with unpaired neonatal and adult platelets were also obtained w
hen neonatal platelets (n = 5) were compared with their paired materna
l controls. In further studies, we have documented that the calcium co
ntent of the dense tubular system was normal in the neonatal platelet,
indicating that the observed impairment in calcium mobilization in th
e neonate was not due to a decrease in calcium stores. The previously
documented abnormalities in neonatal platelet function appear to be du
e to the impaired mobilization of this important intracellular mediato
r.