Work

Neuronal hyperexcitability in dystrophin-deficient mdx hippocampal neurons: the importance of interleukin-6 and GABAergic regulation

Year: 2025

Type: article

Abstract: Duchenne Muscular Dystrophy (DMD) is a severe neuromuscular disorder arising from loss of the structural protein, dystrophin. It also often presents with cognitive deficits and susceptibility to epilepsy. Expressed in neurons of the hippocampus, dystrophin plays an important role in synapse formation, specifically the post-synaptic organisation of γ-aminobutyric acid A receptors (GABA A Rs). This study explored possible interactions between interleukin (IL)-6, which is elevated in DMD, and GABA A R signalling in cultured hippocampal neurons of dystrophic mdx mice. Immunofluorescent imaging revealed altered development of network connectivity that displayed similar characteristics to dystrophin-expressing neurons cultured in elevated levels of IL-6. Mdx neurons dependably exhibited spontaneous oscillations. Calcium (Ca 2+ ) signalling was further modulated by exposure to agonists and antagonists of GABA A and GABA B Rs. IL-6-evoked Ca 2+ responses were enhanced by muscimol, a GABA A R agonist, in wildtype (WT) and mdx neurons, whilst bicuculline, a GABA A R antagonist, only suppressed IL-6-evoked Ca 2+ activity in WT neurons. The GABA B R agonist, baclofen, enhanced IL-6-evoked Ca 2+ responses only in mdx neurons. Our findings support dysfunctional GABAergic signalling in hippocampal neurons that lack dystrophin, resulting in aberrant neuronal network excitability. The contribution of elevated levels of IL-6 further impact upon Ca 2+ dyshomeostasis in dystrophic neurons and may underpin cognitive changes reported in dystrophinopathies.

Source: Scientific Reports

DOI: 10.1038/s41598-025-00880-z