Cerebellar dysfunction in the mdx mouse model of Duchenne muscular dystrophy: an electrophysiological and behavioural study

Journal article

Patients with Duchenne muscular dystrophy (DMD) commonly show specific cognitive deficits in addition to a severe muscle impairment caused by the absence of dystrophin expression in skeletal muscle. These cognitive deficits have been related to the absence of dystrophin in specific regions of the central nervous system, notably cerebellar Purkinje cells (PCs). Dystrophin has recently been involved in GABA_A receptors clustering at postsynaptic densities, and its absence, by disrupting this clustering, leads to decreased inhibitory input to PC. We performed an in vivo electrophysiological study of the dystrophin-deficient muscular dystrophy X-linked (mdx) mouse model of DMD to compare PC firing and local field potential (LFP) in alert mdx and control C57Bl/10 mice. We found that the absence of dystrophin is associated with altered PC firing and the emergence of fast (~160-200 Hz) LFP oscillations in the cerebellar cortex of alert mdx mice. These abnormalities were not related to the disrupted expression of calcium-binding proteins in cerebellar PC. We also demonstrate that cerebellar long-term depression is altered in alert mdx mice. Finally, mdx mice displayed a force weakness, mild impairment of motor coordination and balance during behavioural tests. These findings demonstrate the existence of cerebellar dysfunction in mdx mice. A similar cerebellar dysfunction may contribute to the cognitive deficits observed in patients with DMD.

Authors: Prigogine, C; Ruiz, JM; Cebolla, AM; Deconinck, N; Servais, L

• Publication status: Published
• Peer review status: Peer reviewed
• Publisher: Wiley
• Journal: European Journal of Neuroscience
• Volume: 60
• Issue: 10
• Pages: 6470-6489
• Place of publication: France
• Publication date: 2024-10-16
• Acceptance date: 2024-09-25
• DOI: 10.1111/ejn.16566
• EISSN: 1460-9568
• ISSN: 0953-816X
• Pmid: 39415418
• Language: English
• Keywords: muscular dystrophy; pediatric; behavioral and social science; duchenne/ becker muscular dystrophy; neurological; neurosciences; musculoskeletal; mental health; rare diseases; basic behavioral and social science; brain disorders