Vanilloid Receptor TRPV1 in Drug Discovery 2010
DOI: 10.1002/9780470588284.ch3
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Biochemical Pharmacology of TRPV1: Molecular Integrator of Pain Signals

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Cited by 4 publications
(5 citation statements)
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“…Cough severity as assessed by VAS and LCQ, was not associated with increased airway gene or protein expression of TRPV-1 and TRPA-1 statistically or clinically in terms of minimal important difference (MID) in patients with IPF or CC (data not shown). In addition, there was no association between cough severity and lung function measurements in any group in keeping with previous studies (data not shown) [ 9 ].…”
Section: Resultssupporting
confidence: 90%
See 1 more Smart Citation
“…Cough severity as assessed by VAS and LCQ, was not associated with increased airway gene or protein expression of TRPV-1 and TRPA-1 statistically or clinically in terms of minimal important difference (MID) in patients with IPF or CC (data not shown). In addition, there was no association between cough severity and lung function measurements in any group in keeping with previous studies (data not shown) [ 9 ].…”
Section: Resultssupporting
confidence: 90%
“…The capsaicin receptor is a member of the transient receptor potential (TRP) family of ion channels known as transient receptor potential vanniloid-1 (TRPV-1) [ 10 , 11 ]. TRPV-1 is a poly-modal channel which is predominantly expressed in sensory afferent fibres and is activated by capsaicin, noxious stimuli and heat [ 9 , 10 ]. Immuno-histochemical (IHC) studies comparing bronchial biopsies from patients with and without chronic cough identified a significant increase of TRPV-1 staining nerve profiles, which was positively correlated with capsaicin tussive response [ 11 ].…”
Section: Introductionmentioning
confidence: 99%
“…[24][25][26][27][28][29][30] These mediators may activate TRPV1 directly (bradykinin) or activate protein kinases A and C, which can phosphorylate and thus sensitize the receptor. 12,13,[30][31][32][33][34][35][36] Had the analgesic efficacy of ABT-116 been evaluated by use of an inflammatory model in the present study, efficacy may have been detected in response to thermal threshold testing.…”
Section: Discussionmentioning
confidence: 99%
“…Transient receptor potential vanilloid receptors (TRPVs) are mechanosensitive channels highly associated with nervous system functions including pain, memory, and mechanical sensations. Furthermore, capsaicin receptor TRPV1 is a key regulator of pain and inflammation and is upregulated in microglia in the brain, especially in the anterior cingulate cortex [138][139][140]. The stimulation of microglial TRPV1 induces cortical microglial activation and indirectly enhances glutamatergic neuronal transmission by promoting the shedding of extracellular microglial microvesicles (release of vesicles in the extracellular space [141]).…”
Section: Trpv1 and The P38 Pathwaymentioning
confidence: 99%
“…This signal transduction can be inhibited by the p38 MAPK inhibitor SB203580. Thus, p38 MAPK is a downstream TRPV1 activator whose phosphorylation plays an essential role in microglial microvesicle shedding by activating P2X purinoceptor 7 (P2X7) ATP receptor [138][139][140][141][142][143]. Whereas TRPV1 mediates communication between microglia and neurons, inhibition of the phosphorylation of its downstream p38 MAPK inhibits sphingosine metabolism [140][141][142][143].…”
Section: Trpv1 and The P38 Pathwaymentioning
confidence: 99%