Rotenone inhibits primary murine myotube formation via Raf-1 and ROCK2

Rotenone (ROT) is a widely used inhibitor of complex I (CI), the first complex of the mitochondrial oxidative phosphorylation (OXPHOS) system. However, particularly at high concentrations ROT was also described to display off-target effects. Here we studied how ROT affected in vitro primary murine myotube formation. We demonstrate that myotube formation is specifically inhibited by ROT (10–100 nM), but not by piericidin A (PA; 100 nM), another CI inhibitor. At 100 nM, both ROT and PA fully blocked myoblast oxygen consumption. Knock-down of Rho-associated, coiled-coil containing protein kinase 2 (ROCK2) and, to a lesser extent ROCK1, prevented the ROT-induced inhibition of myotube formation. Moreover, the latter was reversed by inhibiting Raf-1 activity. In contrast, ROT-induced inhibition of myotube formation was not prevented by knock-down of RhoA. Taken together, our results support a model in which ROT reduces primary myotube formation independent of its inhibitory effect on CI-driven mitochondrial ATP production, but via a mechanism primarily involving the Raf-1/ROCK2 pathway.

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Bibliographic Details
Main Authors: Grefte, Sander, Wagenaars, J.A., Jansen, R., Willems, P.H., Koopman, Werner
Format: Article/Letter to editor biblioteca
Language:English
Subjects:ROCK2, Raf-1, Rotenone, murine myotube formation,
Online Access:https://research.wur.nl/en/publications/rotenone-inhibits-primary-murine-myotube-formation-via-raf-1-and-
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