New Challenges Resulting From the Loss of Function of Na1.4 in Neuromuscular Diseases

The voltage-gated sodium channel Na1.4 is a major actor in the excitability of skeletal myofibers, driving the muscle force in response to nerve stimulation. Supporting further this key role, mutations in , the gene encoding the pore-forming α subunit of Na1.4, are responsible for a clinical spectrum of human diseases ranging from muscle stiffness (sodium channel myotonia, SCM) to muscle weakness. For years, only dominantly-inherited diseases resulting from Na1.4 gain of function (GoF) were known, , non-dystrophic myotonia (delayed muscle relaxation due to myofiber hyperexcitability), and hyperkalemic or hypokalemic periodic paralyses (episodic flaccid muscle weakness due to transient myofiber hypoexcitability). These last 5 years, mutations inducing Na1.4 loss of function (LoF) were identified as the cause of dominantly and recessively-inherited disorders with muscle weakness: periodic paralyses with hypokalemic attacks, congenital myasthenic syndromes and congenital myopathies. We propose to name this clinical spectrum sodium channel weakness (SCW) as the mirror of SCM. Na1.4 LoF as a cause of permanent muscle weakness was quite unexpected as the Na current density in the sarcolemma is large, securing the ability to generate and propagate muscle action potentials. The properties of LoF mutations are well documented at the channel level in cellular electrophysiological studies However, much less is known about the functional consequences of Na1.4 LoF in skeletal myofibers with no available pertinent cell or animal models. Regarding the therapeutic issues for Na1.4 channelopathies, former efforts were aimed at developing subtype-selective Na channel antagonists to block myofiber hyperexcitability. Non-selective, Na channel blockers are clinically efficient in SCM and , whereas patient education and carbonic anhydrase inhibitors are helpful to prevent attacks in periodic paralyses. Developing therapeutic tools able to counteract Na1.4 LoF in skeletal muscles is then a new challenge in the field of Na channelopathies. Here, we review the current knowledge regarding Na1.4 LoF and discuss the possible therapeutic strategies to be developed in order to improve muscle force in SCW.