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Transplantation ; 76(1): 37-43, 2003 Jul 15.
Article in English | MEDLINE | ID: mdl-12865783

ABSTRACT

BACKGROUND: The standard preservation solution used during organ procurement and preservation of most organs is the University of Wisconsin (UW) solution. Despite its superiority over other cold storage solutions, the inclusion of hydroxyethyl starch (HES) as one of the components of the UW solution has been both advocated and denied. This study determined whether HES had any effect on red blood cell (RBC) aggregability and correlated aggregation parameters with HES molecular weight. METHODS: Human RBC aggregability and deformability were investigated in vitro, at 4 degrees C, with a laser-assisted optical rotation cell analyzer. The study of RBC aggregation in a binary HES-HES system gave an indication about the nature of HES-RBCs interactions. Bright field microscopy and atomic force microscopy were used to morphologically characterize the aggregates size and form. RESULTS: High molecular weight HES and UW solution had a potent hyperaggregating effect; low molecular weight HES had a hypoaggregating effect on RBC. RBC aggregates were of large size and their resistance to dissociation by flow-induced shear stress was high. CONCLUSION: The authors' in vitro experiments conclusively showed that the physiologic function of RBCs to form aggregates is significantly affected in the presence of HES. The use of high molecular weight HES in UW solution accounts for extended and accelerated aggregation of erythrocytes that may result in stasis of blood and incomplete washout of donor organs before transplantation.


Subject(s)
Adenosine/pharmacology , Allopurinol/pharmacology , Erythrocyte Aggregation/drug effects , Erythrocyte Deformability/drug effects , Glutathione/pharmacology , Hydroxyethyl Starch Derivatives/pharmacology , Insulin/pharmacology , Raffinose/pharmacology , Dose-Response Relationship, Drug , Erythrocyte Aggregation/physiology , Erythrocytes/cytology , Erythrocytes/drug effects , Humans , In Vitro Techniques , Organ Preservation Solutions/pharmacology
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