• Arsenic exposure significantly impairs myocardial perfusion and induces cardiac dysfunction in rats, as evidenced by reduced WIS and WIS × PI on myocardial contrast echocardiography.
• Dantrolene treatment, particularly at high dose, effectively mitigates arsenic-induced myocardial injury and improves cardiac perfusion parameters.
• The cardioprotective mechanism of dantrolene is attributed to its stabilization of RyR2, preventing pathological calcium leakage in cardiac myocytes.
• These findings suggest dantrolene as a potential therapeutic agent for arsenic cardiotoxicity, warranting further clinical investigation.
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