Identification of polyunsaturated fatty acids as potential biomarkers of osteoarthritis after sodium hyaluronate and mesenchymal stem cell treatment through …

Q Yang, Y Zhao, N Li, JL Wu, X Huang… - Frontiers in …, 2023 - frontiersin.org
Introduction: Osteoarthritis (OA) is a prevalent joint disorder worldwide. Sodium hyaluronate
(SH) and mesenchymal stem cells (MSCs) are promising therapeutic strategies for OA …

Mechanism and therapeutic effectiveness of nerve growth factor in osteoarthritis pain

X Shang, Z Wang, H Tao - Therapeutics and Clinical Risk …, 2017 - Taylor & Francis
Osteoarthritis (OA) is the most common form of articular joint arthritis and a cause of
significant morbidity. In this review, we present the role of nerve growth factor (NGF) in pain …

Computational approach reveals pronociceptive potential of cannabidiol in osteoarthritis: role of transient receptor potential channels

J Mlost, M Kędziora, K Starowicz - Pharmaceuticals, 2021 - mdpi.com
Systems pharmacology employs computational and mathematical methods to study the
network of interactions a drug may have within complex biological pathways. These tools …

Sensitization of transient receptor potential vanilloid 4 and increasing its endogenous ligand 5, 6-epoxyeicosatrienoic acid in rats with monoiodoacetate-induced …

M Hinata, S Imai, T Sanaki, J Tsuchida, T Yoshioka… - Pain, 2018 - journals.lww.com
Transient receptor potential vanilloid 4 (TRPV4) receptor modulates pain, and this has been
noted in several animal models. However, the involvement of TRPV4 in osteoarthritic (OA) …

[HTML][HTML] Osteoarthritis-dependent changes in antinociceptive action of Nav1. 7 and Nav1. 8 sodium channel blockers: An in vivo electrophysiological study in the rat

W Rahman, AH Dickenson - Neuroscience, 2015 - Elsevier
Voltage-gated sodium channel blockers are not traditionally recommended for osteoarthritis
(OA) pain therapy, but given the large peripheral drive that follows OA development there is …

Mechanism of aspirin-induced inhibition on the secondary hyperalgesia in osteoarthritis model rats

M Niibori, Y Kudo, T Hayakawa, K Ikoma-Seki… - Heliyon, 2020 - cell.com
Aims The daily activity of osteoarthritis (OA) patients is limited by chronic pain and central
sensitization. Although non-steroidal anti-inflammatory drugs (NSAIDs) and acetaminophen …

Molecular understanding of the activation of CB1 and blockade of TRPV1 receptors: implications for novel treatment strategies in osteoarthritis

J Mlost, M Kostrzewa, N Malek, K Starowicz - International journal of …, 2018 - mdpi.com
Osteoarthritis (OA) is a joint disease in which cartilage degenerates as a result of
mechanical and biochemical changes. The main OA symptom is chronic pain involving both …

[HTML][HTML] Osteoarthritis is a neurological disease–an hypothesis

JJ McDougall - Osteoarthritis and Cartilage Open, 2019 - Elsevier
Objective This commentary aims to summarise the importance of the joint nervous system in
maintaining joint homeostasis and the role of nerves in contributing to degenerative …

Contribution of salidroside to the relieve of symptom and sign in the early acute stage of osteoarthritis in rat model

L Sa, X Wei, Q Huang, Y Cai, D Lu, R Mei… - Journal of …, 2020 - Elsevier
Abstract Ethnopharmacological relevance The genus Rhodiola has been used to treat
cough, hemoptysis, fever, pain, bruise and other symptoms which are related to injury and …

Targeting the transient receptor potential vanilloid type 1 (TRPV1) assembly domain attenuates inflammation-induced hypersensitivity

R Flynn, K Chapman, M Iftinca, R Aboushousha… - Journal of Biological …, 2014 - ASBMB
The transient receptor potential channel vanilloid type 1 (TRPV1) is a non-selective cation
channel expressed in sensory neurons of the dorsal root and trigeminal ganglia. TRPV1 is a …