4.7 Article

Effects of (-) epigallocatechin-3-gallate on Na+ currents in rat dorsal root ganglion neurons

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 604, Issue 1-3, Pages 20-26

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2008.12.015

Keywords

Catechins; Dorsal root ganglion; (-)Epigallocatechin-3-gallate; Green tea; Na+ current; Tetrodotoxin-resistant; Tetrodotoxin-sensitive

Funding

  1. Korean Government (MOEHRD) [KRF-2007-314-C00194]

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The natural product(-) epigallocatechin-3-gallate (EGCG) is the major polyphenolic constituent found in green tea. Dorsal root ganglion neurons are primary sensory neurons, and express tetrodotoxin-sensitive and tetrodotoxin-resistant Na+ currents, which are both actively involved in the generation and propagation of nociceptive signals. Effects of EGCG on tetrodotoxin-sensitive and tetrodotoxin-resistant Na+ currents in rat dorsal root ganglion neurons were investigated using the whole-cell variation of the patch-clamp techniques. EGCG inhibited both types of Na+ currents potently and in a concentration-dependent manner. The apparent dissociation constant, K-d, was estimated to be 0.74 and 0.80 mu M for tetroclotoxin-sensitive and tetrodotoxin-resistant Na+ currents, respectively. (-) Epigallocatechin (EGC) was far less potent to inhibit Na+ currents than EGCG, suggesting that gallate moiety of EGCG is an important functional group to modulate Na+ currents. EGCG had little or no effect on the activation or steady-state inactivation voltage of either type of Na+ current. EGCG simply reduced the availability of Na+ channels for activation. Thus, EGCG appears to bind to resting Na+ channels to inhibit them. EGCG slowed the recovery of tetrodotoxin-sensitive Na+ current from inactivation. The property of EGCG to inhibit sensory Na+ currents can be utilized to develop an analgesic agent. (C) 2008 Elsevier B.V. All rights reserved.

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