| Literature DB >> 30093011 |
Xintian Shao1, Qixin Chen1, Xixi Dou2, Lei Chen3, Jixu Wu1, Wei Zhang3, Huarong Shao3, Peixue Ling4, Fei Liu5, Fengshan Wang6.
Abstract
We have previously reported an application of lower range of molecular weight of xanthan gum (LRWXG) for inhibiting cartilage matrix destruction and preventing mitochondrial damage in rabbit osteoarthritis (OA) model. However, whether LRWXG exerts its anti-OA activity through intrinsic bax-mitochondria cytochrome c-caspase signaling pathway in OA still requires further study. To address this problem, the OA model was induced by anterior cruciate ligament transection (ACLT) in rabbit and then treated with LRWXG. The results showed that LRWXG could inhibit the loss of collagen in cartilage matrix, protect trabecular bone in subchondral, decrease the apoptosis of chondrocytes, down-regulate the expressions of active caspase-9, active caspase-3 and bax, and up-regulate the expression of bcl-2. In addition, LRWXG could up-regulate the expression of cyt-c in mitochondria, while down-regulate the expression of cyt-c in cytoplasm. These findings show that LRWXG inhibits cartilage degradation via an intrinsic bax-mitochondria cytochrome c-caspase pathway in OA.Entities:
Keywords: Cartilage matrix destruction.; Intrinsic bax-mitochondrion cytochrome c-caspase pathway; Lower range of molecular weight of xanthan gum
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Year: 2018 PMID: 30093011 DOI: 10.1016/j.carbpol.2018.06.108
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381