論文

査読有り
2016年12月

Stretching After Heat But Not After Cold Decreases Contractures After Spinal Cord Injury in Rats

CLINICAL ORTHOPAEDICS AND RELATED RESEARCH
  • Hiroyuki Iwasawa
  • ,
  • Masato Nomura
  • ,
  • Naoyoshi Sakitani
  • ,
  • Kosuke Watanabe
  • ,
  • Daichi Watanabe
  • ,
  • Hideki Moriyama

474
12
開始ページ
2692
終了ページ
2701
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1007/s11999-016-5030-x
出版者・発行元
SPRINGER

Contractures are a prevalent and potentially severe complication in patients with neurologic disorders. Although heat, cold, and stretching are commonly used for treatment of contractures and/or spasticity (the cause of many contractures), the sequential effects of these modalities remain unclear.
Using an established rat model with spinal cord injury with knee flexion contracture, we sought to determine what combination of heat or cold before stretching is the most effective for treatment of contractures derived from spastic paralyses and investigated which treatment leads to the best (1) improvement in the loss of ROM; (2) restoration of deterioration in the muscular and articular factors responsible for contractures; and (3) amelioration of histopathologic features such as muscular fibrosis in biceps femoris and shortening of the joint capsule.
Forty-two adolescent male Wistar rats were used. After spasticity developed at 2 weeks postinjury, each animal with spinal cord injury underwent the treatment protocol daily for 1 week. Knee extension ROM was measured with a goniometer by two examiners blinded to each other's scores. The muscular and articular factors contributing to contractures were calculated by measuring ROM before and after the myotomies. We quantitatively measured the muscular fibrosis and the synovial intima length, and observed the distribution of collagen of skeletal muscle. The results were confirmed by a blinded observer.
The ROM of heat alone (34A degrees +/- 1A degrees) and cold alone (34A degrees +/- 2A degrees) rats were not different with the numbers available from that of rats with spinal cord injury (35A degrees +/- 2A degrees) (p = 0.92 and 0.89, respectively). Stretching after heat (24A degrees +/- 1A degrees) was more effective than stretching alone (27A degrees +/- 3A degrees) at increasing ROM (p < 0.001). Contrastingly, there was no difference between stretching after cold (25A degrees +/- 1A degrees) and stretching alone (p = 0.352). Stretching after heat was the most effective for percentage improvement of muscular (29%) and articular (50%) factors of contractures. Although quantification of muscular fibrosis in the rats with spinal cord injury (11% +/- 1%) was higher than that of controls (9% +/- 0.4%) (p = 0.01), no difference was found between spinal cord injury and each treatment protocol. The total synovial intima length of rats with spinal cord injury (5.9 +/- 0.2 mm) became shorter than those of the controls (7.6 +/- 0.2 mm) (p < 0.001), and those of stretching alone (6.9 +/- 0.4 mm), stretching after heat (7.1 +/- 0.3 mm), and stretching after cold (6.7 +/- 0.4 mm) increased compared with rats with spinal cord injury (p = 0.01, p = 0.001, and p = 0.04, respectively). The staining intensity and pattern of collagen showed no difference among the treatment protocols.
This animal study implies that heat or cold alone is ineffective, and that stretching is helpful for the correction of contractures after spinal cord injury. In addition, we provide evidence that heat is more beneficial than cold to increase the effectiveness of stretching.
Our findings tend to support the idea that stretching after heat can improve the loss of ROM and histopathologic features of joint tissues. However, further studies are warranted to determine if our findings are clinically applicable.

リンク情報
DOI
https://doi.org/10.1007/s11999-016-5030-x
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/27530397
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000387229700027&DestApp=WOS_CPL
ID情報
  • DOI : 10.1007/s11999-016-5030-x
  • ISSN : 0009-921X
  • eISSN : 1528-1132
  • PubMed ID : 27530397
  • Web of Science ID : WOS:000387229700027

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