1Department of Obstetrics & Gynecology, Mesologi County Hospital, Greece
2Department of Obstetrics & Gynecology, Aretaieion Hospital, Athens University, Greece
3Department of Surgery, Ippokrateion General Hospital, Athens University, Greece
4Department of Biologic Chemistry, Athens University, Greece
5Department of Surgery, Ippokrateion General Hospital, Athens University, Greece
6Experimental Research Centre ELPEN Pharmaceuticals, Greece
Submission: August 09, 2017; Published: August 18, 2017
ISSN: 2576-9170Volume1 Issue1
Aim: This study calculated the opposite capacities of 2 drugs: the erythropoietin (Epo) and the antioxidant drug U-74389G. The calculation was based on the results of 2 preliminary studies, each one of which estimated the platelet crit (PCT) levels alterations, after the respective drug usage in an induced hypoxia reoxygenation animal experiment.
Materials and methods: The 2 main experimental endpoints at which the PCT levels (PCTl) were evaluated were the 60th reoxygenation min (for the groups A, C and E) and the 120th reoxygenation min (for the groups B, D and F). Specially, the groups A and B were processed without drugs, groups C and D after Epo administration; whereas groups E and F after U-74389G administration.
Result: The first preliminary study of Epo non significantly decreased the PCTl by 6.88% ± 3.69% (p-value=0.0615). Also, the second preliminary study of U-74389G non-significantly increased the PCTl by 6.73% ± 37.45% (p-value=0.0712). These 2 studies were co-evaluated since they came from the same experimental setting. The outcome of the co-evaluation was that U-74389G has opposite acute effect than Epo (p-value=0.0000).
Conclusion:The anti-oxidant capacities of U-74389G enhance the acute increasing properties on PCTl than epo (p-value=0.0000).
Keywords: Hypoxia; Erythropoietin; U-74389G; Platelet crit; Reoxygenation