Abstract
Objectives:
The herbal compound Allergina has a long history in the clinical treatment of allergic inflammatory diseases in some countries including Korea. However, the direct effect of Allergina on ventricular contractile function has not been defined.
Design:
This study was designed to investigate the impact of Allergina on ventricular contractile function.
Settings:
Ventricular contractile function was examined in single isolated left ventricular cardiomyocytes.
Subjects/interventions:
Isolated cardiomyocytes from adult male Sprague-Dawley rats were electrically stimulated to contract at 0.5 Hz.
Outcome measures:
Mechanical and intracellular Ca2+ transients properties of cardiomyocytes were evaluated using an IonOptix Myocam® (IonOptix Inc., Milton, MA) system and fura-2 fluorescent dye. Contractile properties analyzed included peak shortening (PS), time-to-peak shortening (TPS), time-to-90% relengthening (TR90), and maximal velocity of shortening/relengthening (±dL/dt). Intracellular Ca2+ transients were evaluated as the fura-fluorescence intensity change (ΔFFI) and fluorescence decay time.
Results:
Allergina (10-7–10-3 mg/mL) significantly augmented PS in a dose-dependent manner with a maximal response of 50.4%. Allergina did not elicit any effect on TPS, TR90, and ±dL/dt. Intracellular Ca2+ transients displayed consistent findings in that Allergina enhanced the electrically-stimulated increase in change of intracellular Ca2+ transients (ΔFFI) and slowed intracellular Ca2+ fluorescence decay without affect the resting intracellular Ca2+ levels.
Conclusions:
Collectively, these data demonstrated a direct cardiac stimulatory property of Allergina on cardiac contraction and intracellular Ca2+ transients in isolated left ventricular cardiomyocytes.
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