Inflammatory mediators convert anandamide into a potent activator of the vanilloid type 1 transient receptor potential receptor in nociceptive primary sensory neurons

Neuroscience

Volumn 136, Issue 2, 2005, Pages 539-548

  Singh Tahim, A ^a   Santha P ^a,b   Nagy, I ^a  

^a CHELSEA AND WESTMINSTER HOSPITAL   (United Kingdom)

^b UNIVERSITY OF SZEGED   (Hungary)

Author keywords

Capsaicin; Heat hyperalgesia; Inflammation; Nociception; Pain; TRPV1

Indexed keywords

ANANDAMIDE; AUTACOID; BRADYKININ; CAPSAICIN; CAPSAZEPINE; COBALT; CYCLIC AMP DEPENDENT PROTEIN KINASE INHIBITOR; PHOSPHOLIPASE C INHIBITOR; PROSTAGLANDIN E2; PROTEIN KINASE C INHIBITOR; UNCLASSIFIED DRUG; VANILLOID RECEPTOR 1; VANILLOID TYPE 1 TRANSIENT RECEPTOR POTENTIAL RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN NERVE CELL; CELL CULTURE; CONTROLLED STUDY; HYPERALGESIA; INFLAMMATION; NOCICEPTION; NONHUMAN; PRIORITY JOURNAL; RAT; SENSORY NERVE CELL;

AMIDOHYDROLASES; ANIMALS; ARACHIDONIC ACIDS; BRADYKININ; CAPSAICIN; CELLS, CULTURED; COBALT; CYCLIC AMP-DEPENDENT PROTEIN KINASES; DINOPROSTONE; ENZYME INHIBITORS; INFLAMMATION MEDIATORS; NEURONS, AFFERENT; NOCICEPTORS; PHOSPHOLIPASE C; POLYUNSATURATED ALKAMIDES; PROTEIN KINASE C; RATS; RATS, SPRAGUE-DAWLEY; TRPV CATION CHANNELS;

EID: 27744472280     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2005.08.005     Document Type: Article

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