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Force–frequency and force–length properties in skeletal muscle following unilateral focal ischaemic insult in a rat model

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Abstract Aim: 

Our purpose was to quantify skeletal muscle properties following unilateral focal ischaemic insult (stroke) in a rat model. Methods: 

Male rats were divided into two groups: stroke and 2 weeks recovery (n = 8) and control group (n = 7). Stroke was induced in the area of the motor neocortex containing hind limb corticospinal neurones. Contractile properties of the medial gastrocnemius muscle were measured in situ in both limbs. Force–length and force–frequency properties were measured before and 35 min after 5 min fatiguing stimulation. Results: 

Stroke resulted in bilateral tetanic fade during 200 Hz stimulation. When normalized to 100 Hz contractions, force at 200 Hz was 95.4 ± 0.9% for the paretic muscles, 96.7 ± 1.7% for non-paretic muscles and 102.2 ± 1.0% for muscles of control rats (P = 0.006). Prior to fatiguing contractions, there was no difference in the length dependence of force. During repetitive contractions, active force fell significantly to 19 ± 4 and 25 ± 5% of initial force in paretic and non-paretic muscles of animals with a stroke respectively. In control animals active force fell to 37 ± 5%. During repetitive contractions, fusion index increased in muscles of stroke animals to 1.0 ± 0 but in control animals it was 0.95 ± 0.02. There was selective force depression at short lengths for fatigued paretic muscle (significant difference at muscle lengths less than reference length −2 mm). Conclusion: 

The tetanic fade at high stimulation frequencies indicates that there may be activation failure following focal ischaemic insult. The greater magnitude of fatigue and selective depression at short lengths following repetitive contractions should be investigated further.
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Keywords: cerebrovascular attack; disuse; length dependence of force; muscular fatigue; stroke; tetanic fade

Document Type: Research Article

Affiliations: 1:  Faculty of Kinesiology, University of Calgary, Calgary, AB, Canada 2:  Department of Cell Biology and Anatomy, University of Calgary, Calgary, AB, Canada

Publication date: 2009-11-01

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