Activation and desensitization of TRPV1 channels in sensory neurons by the PPAR alpha agonist palmitoylethanolamide

作者：Ambrosino Paolo; Soldovieri Maria Virginia; Russo Claudio; Taglialatela Maurizio^*

来源：British Journal of Pharmacology, 2013, 168(6): 1430-1444.

DOI：10.1111/bph.12029

• palmitoylethanolamide
• transient receptor potential vanilloid type-1 channels
• PPAR transcription factor
• bradykinin
• capsaicin
• intracellular calcium concentrations
• pain

Background and Purpose Palmitoylethanolamide (PEA) is an endogenous fatty acid amide displaying anti-inflammatory and analgesic actions. To investigate the molecular mechanism responsible for these effects, the ability of PEA and of pain-inducing stimuli such as capsaicin (CAP) or bradykinin (BK) to influence intracellular calcium concentrations ([Ca2+]i) in peripheral sensory neurons, has been assessed in the present study. The potential involvement of the transcription factor PPAR and of TRPV1 channels in PEA-induced effects was also studied. Experimental Approach [Ca2+]i was evaluated by single-cell microfluorimetry in differentiated F11 cells. Activation of TRPV1 channels was assessed by imaging and patch-clamp techniques in CHO cells transiently-transfected with rat TRPV1 cDNA. Key Results In F11 cells, PEA (130M) dose-dependently increased [Ca2+]i. The TRPV1 antagonists capsazepine (1M) and SB-366791 (1M), as well as the PPAR antagonist GW-6471 (10M), inhibited PEA-induced [Ca2+]i increase; blockers of cannabinoid receptors were ineffective. PEA activated TRPV1 channels heterologously expressed in CHO cells; this effect appeared to be mediated at least in part by PPAR. When compared with CAP, PEA showed similar potency and lower efficacy, and caused stronger TRPV1 currents desensitization. Sub-effective PEA concentrations, closer to those found in vivo, counteracted CAP- and BK-induced [Ca2+]i transients, as well as CAP-induced TRPV1 activation. Conclusions and Implications Activation of PPAR and TRPV1 channels, rather than of cannabinoid receptors, largely mediate PEA-induced [Ca2+]i transients in sensory neurons. Differential TRPV1 activation and desensitization by CAP and PEA might contribute to their distinct pharmacological profile, possibly translating into potentially relevant clinical differences.

• 出版日期2013-3