Author:
Shinohara Issei,Kataoka Takeshi,Mifune Yutaka,Inui Atsuyuki,Sakata Ryosuke,Nishimoto Hanako,Yamaura Kohei,Mukohara Shintaro,Yoshikawa Tomoya,Kato Tatsuo,Furukawa Takahiro,Matsushita Takehiko,Kuroda Ryosuke
Abstract
AbstractTendon rupture and nerve injury cause fatty infiltration of the skeletal muscle, and the adipokines secreted from the infiltrated adipocytes are known to contribute to chronic inflammation. Therefore, in this study, we evaluated the effects of the adipokines on chronic inflammation using a rat sciatic nerve-crushed injury model. In vitro and in vivo experiments showed that the expression of adiponectin was decreased (0.3-fold) and the expression of Il6 (~ 3.8-fold) and Tnf (~ 6.2-fold) was increased in the nerve-crushed group compared to that in the control group. It was also observed that the administration of an adiponectin receptor agonist decreased the levels of Il6 (0.38-fold) and Tnf (0.28-fold) and improved cellular viability (~ 1.9-fold) in vitro. Additionally, in the fatty infiltrated skeletal muscle, low adiponectin levels were found to be associated with chronic inflammation. Therefore, the local administration of adiponectin receptor agonists would prevent chronic inflammation.
Publisher
Springer Science and Business Media LLC
Cited by
7 articles.
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