Linda Maxwell, H Smith University of Auckland, New Zealand Nuclear DNA fragmentation and ultrastructural changes, indicative of myonuclear apoptosis, were examined in adult skeletal muscle in response to short-term immobilisation. Adult rabbits were allocated to two (n = 5) or six (n = 5), days of unilateral casting of the ankle in full plantarflexion, or were used as untreated controls (n = 2). Atrophy of the soleus muscle was apparent by significant reductions in wet mass of 15% and 26% after two and six days of casting (p ≤ 0.05) respectively. Mean fibre cross-sectional area and myonuclear number per section were also lower (17% and 9.1% respectively) after six days of casting, in comparison to contralateral control muscles (p ≤ 0.05). Electron microscopic examination showed condensed chromatin and irregularly shaped myonuclei and capillary endothelial cell nuclei in muscles immobilised for either two or six days. Myofibrillar disruption, and abnormalities of the subsarcolemmal mitochondria were also apparent in casted muscles in the absence of inflammation or plasma membrane alterations. Longitudinal and transverse sections showed abundant in-situ end-labelling of DNA strand breaks (TUNEL) after two days, with less after six days, of immobilisation. Positive labelling corresponded to myonuclear locations within fibres, yet additional TUNEL-positive nuclei indicated DNA fragmentation in capillary endothelial cells and fibroblasts. The data indicate that the immobilisation of slow--twitch skeletal muscle in a shortened position rapidly induces morphological alterations consistent with mitochondrial dysfunction and apoptotic myonuclear elimination. Physiotherapy and Parkinson’s Disease: Evaluating best practice
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