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Effects of analgesics and antidepressants on TREK-2 and TRESK currents
The Korean Journal of Physiology and Pharmacology ; : 379-385, 2016.
Artigo em Inglês | WPRIM | ID: wpr-728434
ABSTRACT
TWIK-related K+ channel-2 (TREK-2) and TWIK-related spinal cord K+ (TRESK) channel are members of two-pore domain K+ channel family. They are well expressed and help to set the resting membrane potential in sensory neurons. Modulation of TREK-2 and TRESK channels are involved in the pathogenesis of pain, and specifi c activators of TREK-2 and TRESK may be benefi cial for the treatment of pain symptoms. However, the effect of commonly used analgesics on TREK-2 and TRESK channels are not known. Here, we investigated the effect of analgesics on TREK-2 and TRESK channels. The effects of analgesics were examined in HEK cells transfected with TREK-2 or TRESK. Amitriptyline, citalopram, escitalopram, and fluoxetine significantly inhibited TREK-2 and TRESK currents in HEK cells (p<0.05, n=10). Acetaminophen, ibuprofen, nabumetone, and bupropion inhibited TRESK, but had no effect on TREK-2. These results show that all analgesics tested in this study inhibit TRESK activity. Further study is needed to identify the mechanisms by which the analgesics modulate TREK-2 and TRESK differently.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Células Receptoras Sensoriais / Medula Espinal / Citalopram / Ibuprofeno / Fluoxetina / Bupropiona / Canais de Potássio de Domínios Poros em Tandem / Amitriptilina / Analgésicos / Acetaminofen Limite: Humanos Idioma: Inglês Revista: The Korean Journal of Physiology and Pharmacology Ano de publicação: 2016 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Células Receptoras Sensoriais / Medula Espinal / Citalopram / Ibuprofeno / Fluoxetina / Bupropiona / Canais de Potássio de Domínios Poros em Tandem / Amitriptilina / Analgésicos / Acetaminofen Limite: Humanos Idioma: Inglês Revista: The Korean Journal of Physiology and Pharmacology Ano de publicação: 2016 Tipo de documento: Artigo