4.4 Article

NEW MOUSE MODEL OF SKELETAL MUSCLE ATROPHY USING SPIRAL WIRE IMMOBILIZATION

期刊

MUSCLE & NERVE
卷 54, 期 4, 页码 788-791

出版社

WILEY
DOI: 10.1002/mus.25202

关键词

disuse; immobilization; MAFbx/atrogin-1; MuRF1; skeletal muscle atrophy

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology of Japan
  2. IBUKA Foundation
  3. Global COE Program of Waseda University
  4. High-Tech Research Center Project for Private Universities
  5. Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  6. Nakatomi Foundation
  7. Japan Society of Acupuncture and Moxibustion
  8. Grants-in-Aid for Scientific Research [15H01820, 15H04966, 16K15184] Funding Source: KAKEN

向作者/读者索取更多资源

Introduction: Disuse-induced skeletal muscle atrophy is a serious concern; however, there is not an effective mouse model to elucidate the molecular mechanisms. We developed a noninvasive atrophy model in mice. Methods: After the ankle joints of mice were bandaged into a bilateral plantar flexed position, either bilateral or unilateral hindlimbs were immobilized by wrapping in bonsai steel wire. Results: After 3, 5, or 10 days of immobilization of the hip, knee, and ankle, the weight of the soleus and plantaris muscles decreased significantly in both bilateral and unilateral immobilization. MAFbx/atrogin-1 and MuRF1 mRNA was found to have significantly increased in both muscles, consistent with disuse-induced atrophy. Notably, the procedure did not result in either edema or necrosis in the fixed hindlimbs. Conclusions: This method allows repeated, direct access to the immobilized muscle, making it a useful procedure for concurrent application and assessment of various therapeutic interventions.

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