Abstract

While abnormal muscle tone has been observed in people with stroke, how these changes in muscle tension affect sarcomere morphology remains unclear. The purpose of this study was to examine time-course changes in passive muscle fiber tension and sarcomeric adaptation to these changes post-ischemic stroke in a mouse model by using a novel in-vivo force microscope. Twenty-one mice were evenly divided into three groups based on the time point of testing: 3 days (D3), 10 days (D10), and 20 days (D20) following right middle cerebral artery ligation. At each testing time, the muscle length, width, and estimated volume of the isolated soleus muscle were recorded, subsequently followed by in-vivo muscle tension and sarcomere length measurement. The mass of the soleus muscle was measured at the end of testing to calculate muscle density. Two-way ANOVA with repeated measures was used to examine the differences in each of the dependent variable among the three time-point groups and between the two legs. The passive muscle stress of the impaired limbs in the D3 group (27.65 ± 8.37 kPa) was significantly lower than the less involved limbs (42.03 ± 18.61 kPa; p = 0.05) and the impaired limbs of the D10 (48.92 ± 14.73; p = 0.03) and D20 (53.28 ± 20.54 kPa; p = 0.01) groups. The soleus muscle density of the impaired limbs in the D3 group (0.69 ± 0.12 g/cm3) was significantly lower than the less involved limbs (0.80 ± 0.09 g/cm3; p = 0.04) and the impaired limbs of the D10 (0.87 ± 0.12 g/cm3; p = 0.02) and D20 (1.00 ± 0.14 g/cm3; p < 0.01) groups. The D3 group had a shorter sarcomere length (2.55 ± 0.26 μm) than the D10 (2.83 ± 0.20 μm; p = 0.03) and D20 group (2.81 ± 0.15 μm; p = 0.04). These results suggest that, while ischemic stroke may cause considerable changes in muscle tension and stress, sarcomere additions under increased mechanical loadings may be absent or disrupted post-stroke, which may contribute to muscle spasticity and/or joint contracture commonly observed in patients following stroke.

Highlights

  • Alteration in muscle properties due to motor dysfunction negatively impacts stroke survivors’ mobility and self-care and has been a major clinical concern when treating stroke patients

  • Post-hoc simple main effects analyses indicated that the initial muscle stress of the impaired limbs in the D3 group (27.65 ± 8.37 kPa) was significantly smaller than muscle stress of the impaired limbs in the D10 group (48.92 ± 14.73; p = 0.03) and in the D20 group (53.28 ± 20.54 kPa; p = 0.01)

  • It should be noted that the present study investigated the changes in muscles poststroke under a passive condition, and future work that involves neural component as well as measures examining physiological and molecular mechanism is warranted to further understand the underlying mechanisms regarding the interactions between altered muscle tension and muscle morphological adaptation following neurological pathologies

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Summary

Introduction

Alteration in muscle properties due to motor dysfunction negatively impacts stroke survivors’ mobility and self-care and has been a major clinical concern when treating stroke patients. Aforementioned research investigated muscle functions from a system level at a particular time (i.e., a crosssectional study design); a better understanding through in vivo investigations of the changes in sarcomere morphology and muscle tension at several consequential time points may help advance clinical guidance (Smeulders and Kreulen, 2006). The process of muscle cell adaptation is activated in response to the demand of workload as observed in previous studies involving immobilization and lengthening (Goldspink et al, 1974; Williams and Goldspink, 1978; Williams et al, 1999; Gajdosik, 2001; Caiozzo et al, 2002; Lindsey et al, 2002; Coutinho et al, 2004), hind-limb unloading (Kasper and Xun, 2000; Wang et al, 2006), and tenotomy (Baker and Hall-Craggs, 1978). Little is known regarding changes in the intrinsic properties of muscle cells following stroke

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