Comparison of the Hypophosphatasemic Effects of
Erythropoietin and U-74389G on Acid Phosphatase Levels
Volume 2 - Issue 4
C Τsompos1*, C Panoulis, K Τοutouzas3, A Triantafyllou4, CG Ζografos3, K Tsarea5, M Karamperi5 and A Papalois5
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- 1Department of Gynecology, General Hospital of Thessaloniki “St. Dimitrios” Thessaloniki, Hellas, Greece
- 2Department of Obstetrics & Gynecology, Aretaieion Hospital, Athens University, Athens, Attiki, Hellas, Greece
- 3Department of Surgery, Ippokrateion General Hospital, Athens University, Athens, Attiki, Hellas, Greece
- 4Department of Biologic Chemistry, Athens University, Athens, Attiki, Hellas, Greece
- 5Experimental Research Centre ELPEN Pharmaceuticals, S.A. Inc., Co., Pikermi, Attiki, Hellas, Greece
*Corresponding author:
Tsompos Constantinos, Department of Gynecology, General Hospital of Thessaloniki “St. Dimitrios”
Thessaloniki, Hellas, Greece
Received: January 28, 2019; Published: February 05, 2018
DOI: 10.32474/OSMOAJ.2019.02.000142
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Abstract
Aim: This study calculated the effects on acid phosphatase (ACP) levels, after treatment with either of 2 drugs: the erythropoietin
(Epo) and the antioxidant lazaroid (L) drug U-74389G. The calculation was based on the results of 2 preliminary studies, each one of
which estimated the certain influence, after the respective drug usage in an induced ischemia reperfusion (IR) animal experiment.
Materials and Methods: The 2 main experimental endpoints at which the serum ACP levels (ACPl) were evaluated was the
60th reperfusion min (for the groups A, C and E) and the 120th reperfusion 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 the L administration.
Results: The first preliminary study of Epo presented a non-significant hypophosphatasemic effect by 9.29%+6.36%
(p-value=0.1396). The second preliminary study of U-74389G presented a significant hypophosphatasemic effect by 74.46%+9.63%
(p-value=0.0000). These 2 studies were co-evaluated since they came from the same experimental setting. The outcome of the coevaluation
was that L is 8.011334-fold [7.996741 - 8.025953] more hypophosphatasemic than Epo (p-value=0.0000).
Conclusion: The anti-oxidant capacities of U-74389G ascribe 8.011334-fold more hypophosphatasemic effects than Epo
(p-value=0.0000).
Keywords:Ischemia; Erythropoietin; U-74389G; Acid Phosphatase Levels; Reperfusion
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