| Literature DB >> 27650754 |
Wanlop Kunanusornchai1, Bhee Witoonpanich2, Tulyapruek Tawonsawatruk2, Rath Pichyangkura3, Varanuj Chatsudthipong1, Chatchai Muanprasat4.
Abstract
Synovial inflammation plays an important role in the early pathogenesis of osteoarthritis (OA). Chitosan oligosaccharide (COS) has been shown to activate AMPK and suppress inflammatory responses in intestinal epithelial cells. This study aimed to investigate the effect of COS on AMPK activation and synovial inflammation using both primary cultures of synoviocytes and a rabbit model of anterior cruciate ligament (ACL) transection-induced OA. COS induced AMPK activation in both rabbit and human synoviocytes. The mechanism of COS-induced AMPK activation involves an increase in the ADP/ATP ratio but not calcium/calmodulin-dependent protein kinase kinase beta (CaMKKβ). Interestingly, COS suppressed the TNFα-induced iNOS and COX-2 expression via an AMPK-dependent mechanism in both rabbit and human synoviocytes. Importantly, oral administration of COS (10mg/kg/day) induced AMPK activation and alleviated signs of inflammation including COX-2 expression in the synovium of a rabbit ACL transection model. Taken together, our results indicate that COS suppresses synovial inflammation in vitro and in vivo via AMPK activation. COS may be useful in the prevention of OA.Entities:
Keywords: AMPK; Chitosan oligosaccharide; NF-κB; Osteoarthritis; Synovial fibroblast
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Year: 2016 PMID: 27650754 DOI: 10.1016/j.phrs.2016.09.016
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658