The search for translational pain outcomes to refine analgesic development: Where did we come from and where are we going?

R González-Cano, Á Montilla-García… - Neuroscience & …, 2020 - Elsevier
Pain measures traditionally used in rodents record mere reflexes evoked by sensory stimuli;
the results thus may not fully reflect the human pain phenotype. Alterations in physical and …

Antiepileptic drugs as analgesics/adjuvants in inflammatory pain: current preclinical evidence

M Tomić, U Pecikoza, A Micov, S Vučković… - Pharmacology & …, 2018 - Elsevier
Inflammatory pain is the most common type of pain that is treated clinically. The use of
currently available treatments (classic analgesics-NSAIDs, paracetamol and opioids) is …

Mechanistic insights into the role of the chemokine CCL2/CCR2 axis in dorsal root ganglia to peripheral inflammation and pain hypersensitivity

MA Dansereau, É Midavaine, V Bégin-Lavallée… - Journal of …, 2021 - Springer
Background Pain is reported as the leading cause of disability in the common forms of
inflammatory arthritis conditions. Acting as a key player in nociceptive processing …

Treatment of inflammatory and neuropathic pain by uncoupling Src from the NMDA receptor complex

XJ Liu, JR Gingrich, M Vargas-Caballero, YN Dong… - Nature medicine, 2008 - nature.com
Chronic pain hypersensitivity depends on N-methyl-d-aspartate receptors (NMDARs).
However, clinical use of NMDAR blockers is limited by side effects resulting from …

The plant cannabinoid Δ9‐tetrahydrocannabivarin can decrease signs of inflammation and inflammatory pain in mice

D Bolognini, B Costa, S Maione… - British journal of …, 2010 - Wiley Online Library
Background and purpose: The phytocannabinoid, Δ9‐tetrahydrocannabivarin (THCV), can
block cannabinoid CB1 receptors. This investigation explored its ability to activate CB2 …

Analgesic actions of N‐arachidonoyl‐serotonin, a fatty acid amide hydrolase inhibitor with antagonistic activity at vanilloid TRPV1 receptors

S Maione, L De Petrocellis… - British journal of …, 2007 - Wiley Online Library
Background and purpose: N‐arachidonoyl‐serotonin (AA‐5‐HT) is an inhibitor of fatty acid
amide hydrolase (FAAH)‐catalysed hydrolysis of the endocannabinoid/endovanilloid …

Conjugation of a brain-penetrant peptide with neurotensin provides antinociceptive properties

M Demeule, N Beaudet, A Régina… - The Journal of …, 2014 - Am Soc Clin Investig
Neurotensin (NT) has emerged as an important modulator of nociceptive transmission and
exerts its biological effects through interactions with 2 distinct GPCRs, NTS1 and NTS2. NT …

[HTML][HTML] Anti-hyperalgesic activity of corilagin, a tannin isolated from Phyllanthus niruri L.(Euphorbiaceae)

J Moreira, LC Klein-Júnior, V Cechinel Filho… - Journal of …, 2013 - Elsevier
ETHNOPHARMACOLOGICAL RELEVANCE: Corilagin (β-1-O-galloyl-3, 6-(R)-
hexahydroxydiphenoyl-d-glucose) is a tannin isolated from Phyllanthus niruri …

[HTML][HTML] Antinociceptive activity of transient receptor potential channel TRPV1, TRPA1, and TRPM8 antagonists in neurogenic and neuropathic pain models in mice

K Sałat, B Filipek - Journal of Zhejiang University. Science. B, 2015 - ncbi.nlm.nih.gov
The aim of this research was to assess the antinociceptive activity of the transient receptor
potential (TRP) channel TRPV1, TRPM8, and TRPA1 antagonists in neurogenic, tonic, and …

[HTML][HTML] A refinement to the formalin test in mice

DM Lopes, HL Cater, M Thakur, S Wells… - …, 2019 - ncbi.nlm.nih.gov
The constant refinement of tests used in animal research is crucial for the scientific
community. This is particularly true for the field of pain research, where ethical standards are …