scholarly journals Tonic modulation of spinal hyperexcitability by the endocannabinoid receptor system in a rat model of osteoarthritis pain

2010 ◽  
Vol 62 (12) ◽  
pp. 3666-3676 ◽  
Author(s):  
Devi Rani Sagar ◽  
Lydia E. Staniaszek ◽  
Bright N. Okine ◽  
Stephen Woodhams ◽  
Leonie M. Norris ◽  
...  
Pain ◽  
2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Kaylee Townsend ◽  
Ian Imbert ◽  
Victoria Eaton ◽  
Glenn W. Stevenson ◽  
Tamara King

2016 ◽  
Vol 24 (9) ◽  
pp. 1587-1595 ◽  
Author(s):  
L. Xu ◽  
L.N. Nwosu ◽  
J.J. Burston ◽  
P.J. Millns ◽  
D.R. Sagar ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Aihui Li ◽  
Yu Zhang ◽  
Lixing Lao ◽  
Jiajia Xin ◽  
Ke Ren ◽  
...  

Osteoarthritis currently has no cure. Acupuncture can benefit patients with knee osteoarthritis by providing pain relief, improving joint function and serving as an effective complement to standard care. However, the underlying mechanisms of its effects are still not completely understood. The present study, an investigation of the effectiveness and mechanisms of electroacupuncture (EA) in attenuating osteoarthritis pain in a rat model, is focused on the involvement of 5-hydroxytryptamine 2A/C (5-HT2A/C) receptors, which play an important role in pain modulation at the spinal level. Osteoarthritis was induced under isoflurane anesthesia by a single intraarticular injection of monosodium iodoacetate (3 mg/50 μL/rat) into one hind leg of each rat. EA was given at acupoints GB 30 and ST 36 on days 1–4 after the injection. Vehicle or ketanserin, a 5-HT2A/C receptor antagonist, was given intraperitoneally (1 mg kg−1) or intrathecally (5 μg or 10 μg/10 μL), 30 min before each EA treatment. Assessment of weight-bearing difference between injected and uninjected hind legs was done on days 0, 1–4 and 7. Fos /serotonin and serotonin/Fluorogold double labeling were performed to determine EA activation of serotonergic neurons in the nucleus raphe magnus (NRM) that project to spinal cord. The results showed that EA significantly decreases weight-bearing difference compared to sham EA. Ketanserin pretreatment blocked the analgesic effect of EA but did not influence weight bearing in sham EA control rats. EA also activated serotonergic NRM neurons that project to the spinal cord. These data show that EA inhibits osteoarthritis-induced pain by enhancing spinal 5-HT2A/2C receptor activity.


2017 ◽  
Vol 69 (5) ◽  
pp. 996-1008 ◽  
Author(s):  
Junting Huang ◽  
James J. Burston ◽  
Li Li ◽  
Sadaf Ashraf ◽  
Paul I. Mapp ◽  
...  

2012 ◽  
Vol 367 (1607) ◽  
pp. 3300-3311 ◽  
Author(s):  
Devi Rani Sagar ◽  
James J. Burston ◽  
Stephen G. Woodhams ◽  
Victoria Chapman

The analgesic effects of cannabinoid ligands, mediated by CB1 receptors are well established. However, the side-effect profile of CB1 receptor ligands has necessitated the search for alternative cannabinoid-based approaches to analgesia. Herein, we review the current literature describing the impact of chronic pain states on the key components of the endocannabinoid receptor system, in terms of regionally restricted changes in receptor expression and levels of key metabolic enzymes that influence the local levels of the endocannabinoids. The evidence that spinal CB2 receptors have a novel role in the modulation of nociceptive processing in models of neuropathic pain, as well as in models of cancer pain and arthritis is discussed. Recent advances in our understanding of the spinal location of the key enzymes that regulate the levels of the endocannabinoid 2-AG are discussed alongside the outcomes of recent studies of the effects of inhibiting the catabolism of 2-AG in models of pain. The complexities of the enzymes capable of metabolizing both anandamide (AEA) and 2-AG have become increasingly apparent. More recently, it has come to light that some of the metabolites of AEA and 2-AG generated by cyclooxygenase-2, lipoxygenases and cytochrome P450 are biologically active and can either exacerbate or inhibit nociceptive signalling.


Pharmacology ◽  
2015 ◽  
Vol 95 (5-6) ◽  
pp. 251-257 ◽  
Author(s):  
Han Li ◽  
Fei Wang ◽  
Xiaofeng Wang ◽  
Ran Sun ◽  
Jingqing Chen ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document