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Erschienen in: Cardiovascular Drugs and Therapy 4/2009

01.08.2009

Myocardial Infarct Size-Limiting and Anti-Arrhythmic Effects of Mildronate Orotate in the Rat Heart

verfasst von: Reinis Vilskersts, Edgars Liepinsh, Janis Kuka, Helena Cirule, Maris Veveris, Ivars Kalvinsh, Maija Dambrova

Erschienen in: Cardiovascular Drugs and Therapy | Ausgabe 4/2009

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Abstract

Purpose

Mildronate and orotic acid act as modulators of energy metabolism and are considered as cardioprotective agents. This study was performed to compare the cardioprotective effects of mildronate, orotic acid and mildronate orotate.

Methods

Male Wistar rats received mildronate, orotic acid or mildronate orotate for 14 days. The isolated rat heart infarction and isoproterenol-induced ischemia models were used to test the cardioprotective effects of compounds studied. Experimental arrhythmias were induced by the ligation of the left anterior descending coronary artery for 10 min with subsequent reperfusion or by administration of calcium chloride or aconitine at arrhythmogenic doses.

Results

The data obtained showed a statistically significant decrease of necrotic area in 25% of infarcted rat hearts after 14 days of treatment with mildronate and orotic acid, whereas mildronate orotate decreased the infarct size by 50%. Moreover, we found that the administration of mildronate and its orotate salt decreased the duration and incidence of arrhythmias in experimental arrhythmia models.

Conclusions

The study provides experimental evidence that the combination of orotic acid and mildronate possesses additive pharmacological effects and that mildronate orotate might be considered as a powerful therapeutic agent facilitating recovery from ischemia-reperfusion injury.
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Metadaten
Titel
Myocardial Infarct Size-Limiting and Anti-Arrhythmic Effects of Mildronate Orotate in the Rat Heart
verfasst von
Reinis Vilskersts
Edgars Liepinsh
Janis Kuka
Helena Cirule
Maris Veveris
Ivars Kalvinsh
Maija Dambrova
Publikationsdatum
01.08.2009
Verlag
Springer US
Erschienen in
Cardiovascular Drugs and Therapy / Ausgabe 4/2009
Print ISSN: 0920-3206
Elektronische ISSN: 1573-7241
DOI
https://doi.org/10.1007/s10557-009-6179-2

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