Key result
Inhibiting TRPC3 channels, either genetically or pharmacologically with pyrazole-3, abolished doxorubicin-induced myocardial atrophy and left ventricular dysfunction in mice by disrupting the TRPC3-Nox2 complex.
Why the study?
Does inhibition of the TRPC3-Nox2 complex prevent doxorubicin-induced myocardial atrophy and left ventricular dysfunction in preclinical models?
Does inhibition of the TRPC3-Nox2 complex prevent doxorubicin-induced myocardial atrophy and left ventricular dysfunction in preclinical models?
Inhibiting the TRPC3-Nox2 complex prevents doxorubicin-induced myocardial atrophy and dysfunction, offering a potential therapeutic strategy for doxorubicin-induced cardiomyopathy.
Hypothesis-generating for TRPC3 inhibition in doxorubicin cardiomyopathy; does not support clinical use without human trials.
Myocardial atrophy is a wasting of cardiac muscle due to hemodynamic unloading. Doxorubicin is a highly effective anticancer agent but also induces myocardial atrophy through a largely unknown mechanism. Here, we demonstrate that inhibiting transient receptor potential canonical 3 (TRPC3) channels abolishes doxorubicin-induced myocardial atrophy in mice. Doxorubicin increased production of ROS in rodent cardiomyocytes through hypoxic stress-mediated upregulation of NADPH oxidase 2 (Nox2), which formed a stable complex with TRPC3. Cardiomyocyte-specific expression of TRPC3 C-terminal minipeptide inhibited TRPC3-Nox2 coupling and suppressed doxorubicin-induced reduction of myocardial cell size and left ventricular (LV) dysfunction, along with its upregulation of Nox2 and oxidative stress, without reducing hypoxic stress. Voluntary exercise, an effective treatment to prevent doxorubicin-induced cardiotoxicity, also downregulated the TRPC3-Nox2 complex and promoted volume load-induced LV compliance, as demonstrated in TRPC3-deficient hearts. These results illustrate the impact of TRPC3 on LV compliance and flexibility and, focusing on the TRPC3-Nox2 complex, provide a strategy for prevention of doxorubicin-induced cardiomyopathy.
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Shimauchi et al. (2017) studied Doxorubicin-induced myocardial atrophy. TRPC3 inhibition (genetic deletion or pyrazole-3) vs. Vehicle or wild-type control was evaluated on Myocardial atrophy and left ventricular dysfunction. Inhibiting TRPC3 channels, either genetically or pharmacologically with pyrazole-3, abolished doxorubicin-induced myocardial atrophy and left ventricular dysfunction in mice by disrupting the TRPC3-Nox2 complex.
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