論文

査読有り 国際誌
2020年3月10日

Characterization of Osteoarthritis in a Medial Meniscectomy-Induced Animal Model Using Contrast-Enhanced X-ray Microtomography

Biomedicines
  • Takehito Sugasawa
  • Tomoaki Kuji
  • Kai Aoki
  • Koki Yanazawa
  • Akiko Takenouchi
  • Makoto Watanabe
  • Yoshiya Tome
  • Yoshinori Takeuchi
  • Yuichi Aita
  • Naoya Yahagi
  • Yasuhiro Shishikura
  • Seiko Ono
  • Yasuko Yoshida
  • Yasushi Kawakami
  • Kazuhiro Takekoshi
  • 全て表示

8
3
開始ページ
56
終了ページ
56
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.3390/biomedicines8030056
出版者・発行元
MDPI AG

The aim of this study was to clarify degradation characteristics in each tissue of the knee complex of a medial meniscectomy (MMx)-induced knee osteoarthritis (KOA) animal model using classical methods and an alternative comprehensive evaluation method called contrast-enhanced X-ray micro-computed tomography (CEX-μCT), which was developed in the study. Surgical MMx was performed in the right knee joints of five male Wistar rats to induce KOA. At four weeks post-surgery, the synovitis was evaluated using quantitative polymerase chain reaction (qPCR). Degradations of the articular cartilage of the tibial plateau were evaluated using classical methods and CEX-μCT. Evaluation of the synovitis demonstrated significantly increased expression levels of inflammation-associated marker genes in MMx-treated knees compared with those in sham-treated knees. Evaluation of the articular cartilage using classical methods showed that MMx fully induced degradation of the cartilage. Evaluation using CEX-μCT showed that local areas of the medial cartilage of the tibial plateau were significantly reduced in MMx-treated knees compared with those in sham-treated knees. On the other hand, total cartilage volumes were significantly increased in MMx-treated knees. On the basis of the findings of this study, the method could be relevant to study new treatments in KOA research.

リンク情報
DOI
https://doi.org/10.3390/biomedicines8030056
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32164328
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148528
URL
https://www.mdpi.com/2227-9059/8/3/56/pdf
ID情報
  • DOI : 10.3390/biomedicines8030056
  • eISSN : 2227-9059
  • PubMed ID : 32164328
  • PubMed Central 記事ID : PMC7148528

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