I(Cl,vol) inhibitors IAA-94 and DIDS abolished doxorubicin-induced decreases in peak shortening and cell volume, and increases in caspase-3 activity and annexin V labelling in rabbit myocytes.
Do volume-sensitive chloride channel inhibitors prevent doxorubicin-induced contractile dysfunction and apoptosis in adult rabbit ventricular myocytes?
Inhibition of volume-sensitive chloride channels prevents doxorubicin-induced apoptosis and contractile dysfunction in rabbit cardiomyocytes via PI3K/Akt and Erk 1/2 pathways, suggesting a potential cardioprotective strategy.
Contractile dysfunction and cardiomyopathies secondary to apoptotic cell death are limiting factors for treating cancer with doxorubicin. Inhibition of volume-sensitive chloride currents (I(Cl,vol)) has been reported to blunt doxorubicin-induced apoptosis in cardiomyocytes. To investigate cellular contractility during acute induction of apoptosis by doxorubicin and to determine whether I(Cl,vol) inhibitors are able to prevent the subsequent contractile dysfunction, electrically paced ventricular myocytes freshly isolated from adult rabbits were acutely exposed to doxorubicin in the presence and absence of I(Cl,vol) inhibitors IAA-94 or DIDS. Doxorubicin induced increases in both annexin V labelling and caspase-3 activity and decreases in cell volume. Alteration in cardiac contractility was observed after doxorubicin exposure. Both IAA-94 and DIDS abolished the doxorubicin-induced decreases in peak shortening and cell volume as well as the increases in caspase-3 activity and annexin V labelling. These protective effects of I(Cl,vol) inhibitors were abolished by previous inhibition of PI(3)kinase, Akt and Erk 1/2. Thus, I(Cl,vol) inhibitors prevent doxorubicin-induced apoptosis and subsequent contractile dysfunction through PI(3)kinase/Akt and Erk 1/2. Inhibition of I(Cl,vol) may represent a new pharmacological strategy for developing cytoprotective drugs against apoptotic cell death and contractile dysfunction.
Tassigny et al. (2008) studied Doxorubicin-induced apoptosis and contractile dysfunction. I(Cl,vol) inhibitors (IAA-94 or DIDS) vs. Absence of I(Cl,vol) inhibitors (doxorubicin alone) was evaluated on Contractile dysfunction (peak shortening), cell volume, caspase-3 activity, and annexin V labelling. I(Cl,vol) inhibitors IAA-94 and DIDS abolished doxorubicin-induced decreases in peak shortening and cell volume, and increases in caspase-3 activity and annexin V labelling in rabbit myocytes.