Experimental study on elucidation of target molecule of joint contracture and development of therapeutic strategy for new physical therapy
| Project/Area Number |
15H03045
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Rehabilitation science/Welfare engineering
|
|---|
| Research Institution | Nagasaki University |
|---|
Principal Investigator |
OKITA Minoru 長崎大学, 医歯薬学総合研究科(保健学科), 教授 (50244091)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
中野 治郎 長崎大学, 医歯薬学総合研究科(保健学科), 准教授 (20380834)
坂本 淳哉 長崎大学, 医歯薬学総合研究科(保健学科), 准教授 (20584080)
本田 祐一郎 長崎大学, 病院(医学系), 技術職員 (40736344)
佐々部 陵 長崎大学, 病院(医学系), 技術職員 (50710985)
|
|---|
| Project Period (FY) |
2015-04-01 – 2018-03-31
|
| Project Status |
Completed (Fiscal Year 2017)
|
| Budget Amount *help |
¥16,770,000 (Direct Cost: ¥12,900,000、Indirect Cost: ¥3,870,000)
Fiscal Year 2017: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Fiscal Year 2016: ¥6,630,000 (Direct Cost: ¥5,100,000、Indirect Cost: ¥1,530,000)
Fiscal Year 2015: ¥7,670,000 (Direct Cost: ¥5,900,000、Indirect Cost: ¥1,770,000)
|
|---|
| Keywords | 拘縮 / 関節包 / 靱帯 / 線維化 / 標的分子 / HIF-1α / 理学療法 / 治療戦略 / 理学療法学 / 機能障害科学 / 責任病巣 / 前十字靱帯 |
|---|
| Outline of Final Research Achievements |
In this study, we used an experimental animal model of joint contracture to investigate the molecular mechanisms of the contracture derived from changes in joint capsule and ligament. As a result, the fibrosis of the joint capsule, which is the main pathology of contracture, is a change caused by the increase of type I collagen, suggesting that the producing cell is myofibroblast. On the other hand, in the ligament, fibrosis was not observed, and collagen production was decreased. Therefore, we guessed that the ligament did not contribute to the responsible lesion of contracture. In addition, intervention experiments were conducted to induce cyclic muscle contraction in the skeletal muscle during the progress of contracture and to promote muscle pumping action. As a result, expression of HIF-1α assumed to be a target molecule of contracture was suppressed, and it became clear that occurrence of fibrosis can also be prevented.
|
Report
(4 results)
Research Products
(34 results)
-
-
-
-
-
-
-
[Journal Article] Association of early physical activity time with pain, activities of daily living, and progression of vertebral body collapse in patients with vertebral compression fractures: an observational study at single institution2017
Author(s)
Kataoka H, Ikemoto T, Yoshimura A, Shibuya M, Goto K, Yamashita J, Morita K, Sakamoto J, Nakano J, Okita M
-
Journal Title
Eur J Phys Rehabil Med
Volume: in press
Related Report
Peer Reviewed
-
[Journal Article] Heat shock transcription factor 1-associated expression of slow myosin heavy chain in mouse soleus muscle in response to unloading with or without reloading2016
Author(s)
Yokoyama S, Ohno Y, Egawa T, Yasuhara K, Nakai A, Sugiura T, Ohira Y, Yoshioka T, Okita M, Origuchi T, Goto K
-
Journal Title
Acta Physiol (Oxf)
Volume: 217
Issue: 4
Pages: 325-337
DOI
Related Report
Peer Reviewed / Open Access
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
[Presentation] 拘縮のメカニズム2015
Author(s)
沖田 実
Organizer
第17回日本褥瘡学会
Place of Presentation
仙台国際センター（宮城県・仙台市）
Year and Date
2015-08-28
Related Report
Invited
-
-
-
-
-
-
-
-
