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Modulation of TRP channels by resveratrol and other stilbenoids

BACKGROUND: Resveratrol (3,5,4’ - trihydroxy-trans-stilbene), a widely distributed natural stilbenoid, was proposed to account for the unique effects of red wine on life span and health. It has been reported to possess various biological and pharmacological activities, such as anti-oxidant, anti-inf...

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Autores principales: Yu, Lina, Wang, Shenglan, Kogure, Yoko, Yamamoto, Satoshi, Noguchi, Koichi, Dai, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585750/
https://www.ncbi.nlm.nih.gov/pubmed/23413875
http://dx.doi.org/10.1186/1744-8069-9-3
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author Yu, Lina
Wang, Shenglan
Kogure, Yoko
Yamamoto, Satoshi
Noguchi, Koichi
Dai, Yi
author_facet Yu, Lina
Wang, Shenglan
Kogure, Yoko
Yamamoto, Satoshi
Noguchi, Koichi
Dai, Yi
author_sort Yu, Lina
collection PubMed
description BACKGROUND: Resveratrol (3,5,4’ - trihydroxy-trans-stilbene), a widely distributed natural stilbenoid, was proposed to account for the unique effects of red wine on life span and health. It has been reported to possess various biological and pharmacological activities, such as anti-oxidant, anti-inflammatory, and anti-carcinogenic effects. Here, using whole-cell patch-clamp techniques and behavioral analyses, we investigated whether resveratrol and other stilbenoids can modulate TRP channels in sensory neurons in vitro, and have analgesic effects in vivo. RESULTS: We found that resveratrol dose-dependently suppressed the allyl isothiocyanate (AITC)-induced currents (I(AITC)) in HEK293 cells that express TRPA1, as well as in rat dorsal root ganglion (DRG) neurons. Instead, pinosylvin methyl ether (PME), another derivate of stilbene which has a similar structure to resveratrol, dose-dependently blocked the capsaicin-induced currents (I(CAP)) in HEK293 cells that express TRPV1 as well as in DRG neurons. Interestingly, resveratrol had no inhibitory effect on the I(CAP), and PME had no effect on the I(AITC). Otherwise, trans-stilbene showed no any effect on I(AITC) or I(CAP). The concentration response curve of AITC showed that resveratrol inhibited the action of TRPA1 not by changing the EC(50), but by suppressing the AITC-induced maximum response. By contrast, the inhibition of TRPV1 by PME did not change the capsaicin-induced maximum response but did cause a right shift of the EC(50). Moreover, pre-administration of resveratrol suppressed intraplantar injections of AITC-evoked nocifensive behaviors, as well as that PME suppressed capsaicin-evoked one. CONCLUSIONS: These data suggest that resveratrol and other stilbenoids may have an inhibitory effect on TRP channels. In addition, these stilbenoids modulate TRP channel activity in different ways.
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spelling pubmed-35857502013-03-03 Modulation of TRP channels by resveratrol and other stilbenoids Yu, Lina Wang, Shenglan Kogure, Yoko Yamamoto, Satoshi Noguchi, Koichi Dai, Yi Mol Pain Research BACKGROUND: Resveratrol (3,5,4’ - trihydroxy-trans-stilbene), a widely distributed natural stilbenoid, was proposed to account for the unique effects of red wine on life span and health. It has been reported to possess various biological and pharmacological activities, such as anti-oxidant, anti-inflammatory, and anti-carcinogenic effects. Here, using whole-cell patch-clamp techniques and behavioral analyses, we investigated whether resveratrol and other stilbenoids can modulate TRP channels in sensory neurons in vitro, and have analgesic effects in vivo. RESULTS: We found that resveratrol dose-dependently suppressed the allyl isothiocyanate (AITC)-induced currents (I(AITC)) in HEK293 cells that express TRPA1, as well as in rat dorsal root ganglion (DRG) neurons. Instead, pinosylvin methyl ether (PME), another derivate of stilbene which has a similar structure to resveratrol, dose-dependently blocked the capsaicin-induced currents (I(CAP)) in HEK293 cells that express TRPV1 as well as in DRG neurons. Interestingly, resveratrol had no inhibitory effect on the I(CAP), and PME had no effect on the I(AITC). Otherwise, trans-stilbene showed no any effect on I(AITC) or I(CAP). The concentration response curve of AITC showed that resveratrol inhibited the action of TRPA1 not by changing the EC(50), but by suppressing the AITC-induced maximum response. By contrast, the inhibition of TRPV1 by PME did not change the capsaicin-induced maximum response but did cause a right shift of the EC(50). Moreover, pre-administration of resveratrol suppressed intraplantar injections of AITC-evoked nocifensive behaviors, as well as that PME suppressed capsaicin-evoked one. CONCLUSIONS: These data suggest that resveratrol and other stilbenoids may have an inhibitory effect on TRP channels. In addition, these stilbenoids modulate TRP channel activity in different ways. BioMed Central 2013-02-15 /pmc/articles/PMC3585750/ /pubmed/23413875 http://dx.doi.org/10.1186/1744-8069-9-3 Text en Copyright ©2013 Yu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Yu, Lina
Wang, Shenglan
Kogure, Yoko
Yamamoto, Satoshi
Noguchi, Koichi
Dai, Yi
Modulation of TRP channels by resveratrol and other stilbenoids
title Modulation of TRP channels by resveratrol and other stilbenoids
title_full Modulation of TRP channels by resveratrol and other stilbenoids
title_fullStr Modulation of TRP channels by resveratrol and other stilbenoids
title_full_unstemmed Modulation of TRP channels by resveratrol and other stilbenoids
title_short Modulation of TRP channels by resveratrol and other stilbenoids
title_sort modulation of trp channels by resveratrol and other stilbenoids
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585750/
https://www.ncbi.nlm.nih.gov/pubmed/23413875
http://dx.doi.org/10.1186/1744-8069-9-3
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