Quercetin protects cardiomyoblasts against hypertonic cytotoxicity by abolishing intracellular Ca elevations and mitochondrial depolarisation.

BACKGROUND AND AIM

Osmotic changes represent a burden for the body and their limitation would be beneficial. We hypothesized that ubiquitous natural compounds could guard against cytotoxic effects of osmotic stress. We evaluated the anti-hypertonic mechanism of quercetin and 2,3-dehydrosilybin in H9c2 cells in vitro.

EXPERIMENTAL PROCEDURE

Protective effect of both compounds was determined by neutral red assay, cell apoptosis was estimated by measuring caspase-3 activity and verified by western blot and annexin V assay. Phosphorylation level of selected proteins was also detected. Mitochondrial membrane potential was evaluated using dye JC-1. Ca signals were evaluated using genetically encoded fluorescent Ca biosensor GCaMP7f. Formation of reactive oxygen species was measured using an oxidant-sensing probe dihydrofluorescein diacetate.

KEY RESULTS

Quercetin protected H9c2 cells against hypertonic stress-induced cell death. We observed a significant increase in intracellular Ca levels ([Ca]) when cells originally placed in a hypertonic solution were returned to a normotonic environment. Quercetin was found to prevent this increase in [Ca] and also the depolarization of mitochondrial membrane potential.

CONCLUSIONS AND IMPLICATIONS

Quercetin, but not 2,3-dehydrosilybin, reduced adverse effects of osmotic stress mainly by dampening the elevation of [Ca] and mitochondrial Ca overload. This may consequently prevent MPTP pore opening and activation of apoptosis.

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