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Cordycepin Inhibits LPS-induced Inflammatory and Matrix Degradation in the Intervertebral Disc

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Journal PeerJ
Date 2016 May 19
PMID 27190710
Citations 25
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Abstract

Cordycepin is a component of the extract obtained from Cordyceps militaris and has many biological activities, including anti-cancer, anti-metastatic and anti-inflammatory effects. Intervertebral disc degeneration (IDD) is a degenerative disease that is closely related to the inflammation of nucleus pulposus (NP) cells. The effect of cordycepin on NP cells in relation to inflammation and degeneration has not yet been studied. In our study, we used a rat NP cell culture and an intervertebral disc (IVD) organ culture model to examine the inhibitory effects of cordycepin on lipopolysaccharide (LPS)-induced gene expression and the production of matrix degradation enzymes (MMP-3, MMP-13, ADAMTS-4, and ADAMTS-5) and oxidative stress-associated factors (nitric oxide and PGE2). We found a protective effect of cordycepin on NP cells and IVDs against LPS-induced matrix degradation and macrophage infiltration. In addition, western blot and luciferase assay results demonstrated that pretreatment with cordycepin significantly suppressed the LPS-induced activation of the NF-κB pathway. Taken together, the results of our research suggest that cordycepin could exert anti-inflammatory and anti-degenerative effects on NP cells and IVDs by inhibiting the activation of the NF-κB pathway. Therefore, cordycepin may be a potential treatment for IDD in the future.

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References
1.
Berenbaum F . Signaling transduction: target in osteoarthritis. Curr Opin Rheumatol. 2004; 16(5):616-22. DOI: 10.1097/01.bor.0000133663.37352.4a. View

2.
England S, Bevan S, Docherty R . PGE2 modulates the tetrodotoxin-resistant sodium current in neonatal rat dorsal root ganglion neurones via the cyclic AMP-protein kinase A cascade. J Physiol. 1996; 495 ( Pt 2):429-40. PMC: 1160802. DOI: 10.1113/jphysiol.1996.sp021604. View

3.
Kim H, Naura A, Errami Y, Ju J, Boulares A . Cordycepin blocks lung injury-associated inflammation and promotes BRCA1-deficient breast cancer cell killing by effectively inhibiting PARP. Mol Med. 2011; 17(9-10):893-900. PMC: 3188885. DOI: 10.2119/molmed.2011.00032. View

4.
Nakamura K, Shinozuka K, Yoshikawa N . Anticancer and antimetastatic effects of cordycepin, an active component of Cordyceps sinensis. J Pharmacol Sci. 2015; 127(1):53-6. DOI: 10.1016/j.jphs.2014.09.001. View

5.
Wang J, Tian Y, Phillips K, Chiverton N, Haddock G, Bunning R . Tumor necrosis factor α- and interleukin-1β-dependent induction of CCL3 expression by nucleus pulposus cells promotes macrophage migration through CCR1. Arthritis Rheum. 2012; 65(3):832-42. PMC: 3582738. DOI: 10.1002/art.37819. View