Amyotrophic lateral sclerosis (ALS) is an adult-onset neurodegenerative disorder that is typically fatal within 3–5 years of diagnosis. While motoneuron death is the defining characteristic of ALS, the events that underlie its pathology are not restricted to the nervous system. In this regard, ALS muscle atrophies and weakens significantly before presentation of neurological symptoms. Since the skeletal muscle L-type Ca²⁺ channel (Ca_V1.1) is a key regulator of both mass and force, we investigated whether Ca_V1.1 function is impaired in the muscle of two distinct mouse models carrying an ALS-linked mutation.

We recorded L-type currents, charge movements, and myoplasmic Ca²⁺ transients from dissociated flexor digitorum brevis (FDB) fibers to assess Ca_V1.1 function in two mouse models expressing a type 1 Cu/Zn superoxide dismutase mutant (SOD1^G93A).

In FDB fibers obtained from “symptomatic” global SOD1^G93A mice, we observed a substantial reduction of SR Ca²⁺ release in response to depolarization relative to fibers harvested from age-matched control mice. L-type current and charge movement were both reduced by ~40 % in symptomatic SOD1^G93A fibers when compared to control fibers. Ca²⁺ transients were not significantly reduced in similar experiments performed with FDB fibers obtained from “early-symptomatic” SOD1^G93A mice, but L-type current and charge movement were decreased (~30 and ~20 %, respectively). Reductions in SR Ca²⁺ release (~35 %), L-type current (~20 %), and charge movement (~15 %) were also observed in fibers obtained from another model where SOD1^G93A expression was restricted to skeletal muscle.

We report reductions in EC coupling, L-type current density, and charge movement in FDB fibers obtained from symptomatic global SOD1^G93A mice. Experiments performed with FDB fibers obtained from early-symptomatic SOD1^G93A and skeletal muscle autonomous MLC/SOD1^G93A mice support the idea that events occurring locally in the skeletal muscle contribute to the impairment of Ca_V1.1 function in ALS muscle independently of innervation status.