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Original Article

Exp Neurobiol 2013; 22(1): 51-57

Published online March 30, 2013

https://doi.org/10.5607/en.2013.22.1.51

© The Korean Society for Brain and Neural Sciences

TRPV1 Activation in Primary Cortical Neurons Induces Calcium-Dependent Programmed Cell Death

Juhyun Song1, Jun Hong Lee1, Sung Ho Lee1, Kyung Ah Park1, Won Taek Lee1* and Jong Eun Lee1,2*

1Department of Anatomy, 2BK21 Project for Medical Sciences, Yonsei University College of Medicine, Seoul 120-752, Korea

Correspondence to: *To whom correspondence should be addressed.
Jong Eun Lee
TEL: 82-2-2228-1646, 1659, FAX: 82-2-365-0700
e-mail: jelee@yuhs.ac
Won Taek Lee
TEL: 82-2-2228-1644, 1659, FAX: 82-2-365-0700
e-mail: INSKULL@yuhs.ac

Abstract

Transient receptor potential cation channel, subfamily V, member 1 (TRPV1, also known as vanilloid receptor 1) is a receptor that detects capsaicin, a pungent component of chili peppers, and noxious heat. Although its function in the primary nociceptor as a pain receptor is well established, whether TRPV1 is expressed in the brain is still under debate. In this study, the responses of primary cortical neurons were investigated. Here, we report that 1) capsaicin induces caspase-3-dependent programmed cell death, which coincides with increased production of nitric oxide and peroxynitrite ; that 2) the prolonged capsaicin treatment induces a steady increase in the degree of capase-3 activation, which is prevented by the removal of capsaicin; 3) and that blocking calcium entry and calcium-mediated signaling prevents capsaicin-induced cell death. These results indicate that cortical neurons express TRPV1 whose prolonged activation causes cell death.

Keywords: capsaicin, primary neuron, apoptosis, Ca2+, NOS, caspase-3