Chronic N‐acetyl cysteine treatment does not improve respiratory system performance in the mdx mouse model of Duchenne muscular dystrophy

Abstract Duchenne muscular dystrophy (DMD) is characterised by respiratory muscle injury, inflammation, fibrosis and weakness, ultimately culminating in respiratory failure. The dystrophin‐deficient mouse model of DMD (mdx) shows evidence of respiratory muscle remodelling and dysfunction contributin...

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Bibliografske podrobnosti

Principais autores:	Michael N. Maxwell, Anthony L. Marullo, Esther Valverde‐Pérez, Aoife D. Slyne, Ben T. Murphy, Ken D. O'Halloran
Format:	Artigo
Jezik:	Inglês
Izdano:	Wiley 2024-08-01
Serija:	Experimental Physiology
Teme:	antioxidant diaphragm inspiratory pressure muscular dystrophy respiratory EMGs
Online dostop:	https://doi.org/10.1113/EP091862
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