Iodo-resiniferatoxin, a new potent vanilloid receptor antagonist

P Wahl, C Foged, S Tullin, C Thomsen - Molecular pharmacology, 2001 - ASPET
The highly potent vanilloid receptor (VR) agonist resiniferatoxin has been radiolabeled with
125I, and the pharmacology to the cloned rodent VR, VR1, and the endogenous VR in rat …

TRPV1 activation and induction of nociceptive response by a non-pungent capsaicin-like compound, capsiate

T Iida, T Moriyama, K Kobata, A Morita, N Murayama… - …, 2003 - Elsevier
Capsiate is a capsaicin-like ingredient of a non-pungent cultivar of red pepper, CH-19
sweet. To elucidate the mechanisms underlying the non-pungency of capsiate, we …

Administration of capsiate, a non-pungent capsaicin analog, promotes energy metabolism and suppresses body fat accumulation in mice

K Ohnuki, S Haramizu, K Oki, T Watanabe… - Bioscience …, 2001 - jstage.jst.go.jp
We investigated the effects of a single oral administra-tion of capsiate, which is found in the
fruits of a non-pungent cultivar of pepper, CH-19 Sweet, and has the same structure as …

TRPV1 receptors and signal transduction

T Rosenbaum, SA Simon - TRP ion channel function in sensory …, 2007 - books.google.com
The perception of pain throughout the body arises when neural signals originating from the
terminals of nociceptors are propagated to second-order neurons in the spinal cord or …

The cannabinoid WIN 55,212-2 inhibits transient receptor potential vanilloid 1 (TRPV1) and evokes peripheral antihyperalgesia via calcineurin

AM Patwardhan, NA Jeske, TJ Price… - Proceedings of the …, 2006 - National Acad Sciences
Cannabinoids can evoke antihyperalgesia and antinociception at a peripheral site of action.
However, the signaling pathways mediating these effects are not clearly understood. We …

TRPV1 is a novel target for omega‐3 polyunsaturated fatty acids

JA Matta, RL Miyares, GP Ahern - The Journal of physiology, 2007 - Wiley Online Library
Omega‐3 (n‐3) fatty acids are essential for proper neuronal function, and they possess
prominent analgesic properties, yet their underlying signalling mechanisms are unclear …

Unsaturated long-chain N-acyl-vanillyl-amides (N-AVAMs): vanilloid receptor ligands that inhibit anandamide-facilitated transport and bind to CB1 cannabinoid …

D Melck, T Bisogno, L De Petrocellis, H Chuang… - Biochemical and …, 1999 - Elsevier
We investigated the effect of changing the length and degree of unsaturation of the fatty acyl
chain of N-(3-methoxy-4-hydroxy)-benzyl-cis-9-octadecenoamide (olvanil), a ligand of …

Cannabinoids desensitize capsaicin and mustard oil responses in sensory neurons via TRPA1 activation

AN Akopian, NB Ruparel, A Patwardhan… - Journal of …, 2008 - Soc Neuroscience
Although the cannabinoid agonists R-(+)-(2, 3-dihydro-5-methyl-3-[(4-morpholinyl) methyl]
pyrol [1, 2, 3-de]-1, 4-benzoxazin-6-yl)-(1-naphthalenyl) methanone mesylate [WIN 55,212-2 …

[HTML][HTML] Interactions between synthetic vanilloids and the endogenous cannabinoid system

V Di Marzo, T Bisogno, D Melck, R Ross, H Brockie… - FEBS letters, 1998 - Elsevier
The chemical similarity between some synthetic agonists of vanilloid receptors, such as
olvanil (N-vanillyl-cis-9-octadecenoamide), and theendocannabinoid'anandamide …

Activation of neurons in rat trigeminal subnucleus caudalis by different irritant chemicals applied to oral or ocular mucosa

E Carstens, N Kuenzler… - Journal of …, 1998 - journals.physiology.org
Carstens, E., Nicole Kuenzler, and HO Handwerker. Activation of neurons in rat trigeminal
subnucleus caudalis by different irritant chemicals applied to oral or ocular mucosa. J …