Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2012545 | Pharmacological Reports | 2009 | 5 Pages |
Abstract
4-Chloro-m-cresol (4CmC) is an extensively used activator of ryanodine receptors (RyRs). Studies have shown that 4CmC, at a concentration of 1 mM, is sufficient to cause Ca2+ release through RyRs. Here, we show that mM concentrations of 4CmC also inhibit the sarcoplasmic-endoplasmic reticulum Ca2+-ATPase (SERCA), (IC50 2–3mM) and cause Ca2+ release. 4CmC also causes increased intracellular [Ca2+] levels in COS-7 cells, which lack functional RyRs. Thus, any increase in [Ca2+] levels associated with use of 4CmC (≥ 1mM) could lead to non-specific Ca2+ changes due to SERCA inhibition rather than RyR activation.
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Authors
Fawaz Al-Mousa, Francesco Michelangeli,