Noxious heat threshold temperature and pronociceptive effects of allyl isothiocyanate (mustard oil) in TRPV1 or TRPA1 gene-deleted mice

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• 作者：Valé ; ria Té ; kus^a ; ^c ; Á ; dá ; m Horvá ; th^a ; ^c ; Zsó ; fia Hajna^a ; ^c ; É ; va Borbé ; ly^a ; ^c ; Kata Bö ; lcskei^a ; ^c ; Melinda Boros^a ; ^c ; Erika Pinté ; r^a ; ^d ; Zsuzsanna Helyes^a ; ^b ; ^c ; ^d ; Gá ; bor Pethő^a ; ¹ ; ^{gabor.petho@aok.pte.hu" class="auth_mail" title="E-mail the corresponding author} ; Já ; nos Szolcsá ; nyi^a ; ^d ; ¹
• 关键词：TRPV1 ; TRPA1 ; Noxious heat threshold ; Mustard oil ; Allodynia
• 刊名：Life Sciences
• 出版年：2016
• 出版时间：1 June 2016
• 年：2016
• 卷：154
• 期：Complete
• 页码：66-74
• 全文大小：1107 K

文摘

To investigate the roles of TRPV1 and TRPA1 channels in baseline and allyl isothiocyanate (AITC)-evoked nociceptive responses by comparing wild-type and gene-deficient mice.

Main methods

In contrast to conventional methods of thermonociception measuring reflex latencies, we used our novel methods to determine the noxious heat threshold.

Key findings

It was revealed that the heat threshold of the tail measured by an increasing-temperature water bath is significantly higher in TRPV1^−/−, but not TRPA1^−/−, mice compared to respective wild-types. There was no difference between the noxious heat thresholds of the hind paw as measured by an increasing-temperature hot plate in TRPV1^−/−, TRPA1^−/− and the corresponding wild-type mice. The withdrawal latency of the tail from 0 °C water was prolonged in TRPA1^−/−, but not TRPV1^−/−, mice compared to respective wild-types. In wild-type animals, dipping the tail or paw into 1% AITC induced an 8–14 °C drop of the noxious heat threshold (heat allodynia) of both the tail and paw, and 40–50% drop of the mechanonociceptive threshold (mechanical allodynia) of the paw measured by dynamic plantar esthesiometry. These AITC-evoked responses were diminished in TRPV1^−/−, but not TRPA1^−/−, mice. Tail withdrawal latency to 1% AITC was significantly prolonged in both gene-deleted strains.

Significance

Different heat sensors determine the noxious heat threshold in distinct areas: a pivotal role for TRPV1 on the tail is contrasted with no involvement of either TRPV1 or TRPA1 on the hind paw. Noxious heat threshold measurement appears appropriate for preclinical screening of TRP channel ligands as novel analgesics.