TRPV1 receptor inhibition decreases CCL2-induced hyperalgesia

Neuropharmacology

Volumn 81, Issue , 2014, Pages 75-84

  Spicarova, Diana ^a   Adamek, Pavel ^a   Kalynovska, Nataliia ^a   Mrozkova, Petra ^a   Palecek, Jiri ^a  

^a INSTITUTE OF MATHEMATICS   (Czech Republic)

Author keywords

CCL2; EPSC; Pain; Spinal cord; Synaptic transmission; TRPV1

Indexed keywords

AGENTS ACTING ON THE PERIPHERAL NERVOUS AND NEUROMUSCULAR SYSTEMS; ANILIDE; CAPSAICIN; CINNAMIC ACID DERIVATIVE; MITOGEN ACTIVATED PROTEIN KINASE KINASE KINASE 3; MONOCYTE CHEMOTACTIC PROTEIN 1; N-(3-METHOXYPHENYL)-4-CHLOROCINNAMANILIDE; TRPV1 PROTEIN, RAT; VANILLOID RECEPTOR;

ANIMAL; ANTAGONISTS AND INHIBITORS; CHEMICALLY INDUCED; CYTOLOGY; DISEASE MODEL; DOSE RESPONSE; DRUG EFFECTS; EXCITATORY POSTSYNAPTIC POTENTIAL; HYPERALGESIA; IN VITRO STUDY; MALE; METABOLISM; NEWBORN; PAIN THRESHOLD; PATCH CLAMP TECHNIQUE; PHYSIOLOGY; POSTERIOR HORN CELL; RAT; SPINAL CORD; TIME; TOXICITY; WISTAR RAT;

ANILIDES; ANIMALS; ANIMALS, NEWBORN; CAPSAICIN; CHEMOKINE CCL2; CINNAMATES; DISEASE MODELS, ANIMAL; DOSE-RESPONSE RELATIONSHIP, DRUG; EXCITATORY POSTSYNAPTIC POTENTIALS; HYPERALGESIA; IN VITRO TECHNIQUES; MALE; MAP KINASE KINASE KINASE 3; PAIN THRESHOLD; PATCH-CLAMP TECHNIQUES; POSTERIOR HORN CELLS; RATS; RATS, WISTAR; SENSORY SYSTEM AGENTS; SPINAL CORD; TIME FACTORS; TRPV CATION CHANNELS;

EID: 84894279054     PISSN: 00283908     EISSN: 18737064     Source Type: Journal    
DOI: 10.1016/j.neuropharm.2014.01.041     Document Type: Article

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