Histochemical Study on the Atrophy of the Quadriceps Femoris Muscle Caused by Knee Joint Injuries of Rats

アクセス数 : 828
ダウンロード数 : 170

今月のアクセス数 : 3
今月のダウンロード数 : 0
ファイル情報(添付)
HiroshimaJMedSci_38_13.pdf 618 KB 種類 : 全文
タイトル ( eng )
Histochemical Study on the Atrophy of the Quadriceps Femoris Muscle Caused by Knee Joint Injuries of Rats
作成者
Okada Yuji
収録物名
Hiroshima Journal of Medical Sciences
38
1
開始ページ 13
終了ページ 21
収録物識別子
[PISSN] 0018-2052
[EISSN] 2433-7668
[NCID] AA00664312
抄録
Atrophy developing in the quadriceps femoris muscle following knee injury is one of the serious problems not only in the field of orthopedics but also of rehabilitation. However the pathogenesis of this atrophy has not yet been elucidated. The author therefore produced a complex ligament injury model using the knee joints of rats in order to study the pathogenesis of this atrophy. After severing the anterior cruciate ligament, the medial collateral ligament and tibial insertion of the medial meniscus of rats, these animals were sacrificed at 4, 8 and 12 weeks. After removing the vastus lateralis muscle, vastus medialis muscle, and rectus femoris muscle, specimens of these muscles were stained for ATPase. The transection area of the muscle fibers was measured and the fiber type composition was determined. At 4 weeks the vastus medialis muscle and at 12 weeks the vastus lateralis muscle showed marked atrophy. The rectus femoris muscle exhibited the least atrophy throughout the entire observation period. In examining the atrophy of the quadriceps femoris muscle by muscle fiber type, the degree of atrophy was found to differ among the venters and even the same venter showed a different reaction depending on the elapsed time after sustaining the injury. Neither changes in the fiber type composition not neurogenic findings could be observed.
著者キーワード
Muscle atrophy
Knee injury
Histochemistry
ATPase
NDC分類
医学 [ 490 ]
言語
英語
資源タイプ 紀要論文
出版者
Hiroshima University Medical Press
発行日 1989-03
出版タイプ Version of Record(出版社版。早期公開を含む)
アクセス権 オープンアクセス
収録物識別子
[ISSN] 0018-2052
[NCID] AA00664312
[PMID] 2526800