پديد آورندگان :
صدري، آزاده نويسنده سازمان انتقال خون ايران,; Sadri, A , قره باغيان، احمد نويسنده مركز تحقيقات سازمان انتقال خون ايران,; Gharehbaghian, A , وائلي، شهرام نويسنده سازمان انتقال خون ايران,; Vaeli, Sh , عسگري پور، فريبا نويسنده مركز تحقيقات سازمان انتقال خون ايران,; Asgari Pour, F , كرباسي زاده، مهدي نويسنده مركز تحقيقات سازمان انتقال خون ايران,; Karbasizadeh, M , قالدي، ژوليت نويسنده مركز تحقيقات سازمان انتقال خون ايران,; , , آقايي پور، مهناز نويسنده سازمان انتقال خون ايران,; , , شعشعاني، طاهره نويسنده سازمان انتقال خون تهران,; , , طباطباييان، اعظم السادات نويسنده مركز تحقيقات سازمان انتقال خون ايران,; , , كامي، فاطمه نويسنده مركز تحقيقات سازمان انتقال خون ايران,; , , احمدي نژاد، مينو نويسنده مركز تحقيقات سازمان انتقال خون ايران,; ,
كليدواژه :
فلوسيتومتري , پلاكت , p-Selectin , تجمع پلاكتي
چكيده لاتين :
Background and Objectives
Platelets have a major role in haemostasis. Platelet concentrates are used in thrombocytopeny and platelet dysfunction disorders. Due to recent studies reporting loss of in vivo function of platelets in platelet concentrate units, we determined the level of surface expression of P-Selectin, conducted platelet aggregation tests and pH measurment to evaluate platelet activation during storage.
Materials and Methods
In a cross-sectional study, 100 platelet concentrate units prepared by PRP method were evaluated. 34, 33 and 33 units were taken from the first, second, and third day of storage respectively. For each platelet concentrate unit, pH, CD62P-Selectin and platelet aggregation tests with Arashidonic acid and Ristocetin agonists were conducted.
Results
Expression of P-Selectin in third day was significantly higher than first day (p<0.05). Platelet aggregation tests showed significant decrease in third day compared to first day (p<0.05). pH in third day was significantly higher than first day (p<0.05).
Conclusions
The present study shows that activated platelets during 3 days of storage have increased P-Selectin on their surface. Therefore, the P-Selectin expression can be used as an in vivo marker for platelet activation function.