Key result
Mavacamten treatment reduced the proportion of ON myosin heads and shortened thin filament length in relaxed skeletal muscle, demonstrating similar effects to those observed in cardiac muscle.
Why the study?
Mavacamten is not completely specific to cardiac myosin and can affect skeletal muscle myosin, an important consideration given its oral administration.
Mavacamten induces an ON-to-OFF transition of myosin heads and shortens thin filaments in skeletal muscle, demonstrating that its structural effects are not strictly cardiac-specific.
Answers are grounded in this paper and cite their sources.
May warrant skeletal-myopathy monitoring in mavacamten patients; extends cardiac structural data and leaves open human translation.
The first-in-its-class cardiac drug mavacamten reduces the proportion of so-called ON-state myosin heads in relaxed sarcomeres, altering contraction performance. However, mavacamten is not completely specific to cardiac myosin and can also affect skeletal muscle myosin, an important consideration since mavacamten is administered orally and so will also be present in skeletal tissue. Here, we studied the effect of mavacamten on skeletal muscle structure using small-angle X-ray diffraction. Mavacamten treatment reduced the proportion of ON myosin heads but did not eliminate the molecular underpinnings of length-dependent activation, demonstrating similar effects to those observed in cardiac muscle. These findings provide valuable insights for the potential use of mavacamten as a tool to study muscle contraction across striated muscle.
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Engels et al. (2024) studied Healthy skeletal muscle (n=8). Mavacamten vs. Pre-treatment baseline was evaluated on Myosin head ON/OFF level (I1,1/I1,0 ratio and SM3 spacing) and thin filament length (SA6 spacing). Mavacamten treatment reduced the proportion of ON myosin heads and shortened thin filament length in relaxed skeletal muscle, demonstrating similar effects to those observed in cardiac muscle.
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