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Bepridil inhibition of sodium current in rat hippocampal CA1 neurons.
Hu, H J; Yang, D M; Dai, D Z; Wu, C H; Zhou, P A.
Afiliação
  • Hu HJ; Department of Pharmacology of Chinese Materia Medica, China Pharmaceutical University, Nanjing 210009, China.
Zhongguo Yao Li Xue Bao ; 20(9): 819-23, 1999 Sep.
Article em En | MEDLINE | ID: mdl-11245090
ABSTRACT

AIM:

To study the effects of bepridil on sodium current in rat hippocampal neurons.

METHODS:

All experiments were performed on acutely isolated hippocampal pyramidal neurons by means of whole-cell patch-clamp techniques. Recording media contained ion channel blockers to allow the selective activation of voltage-dependent sodium currents.

RESULTS:

Bepridil reduced the amplitudes of sodium current in time- and concentration-dependent manners. The half-blocking time was about 10 min in bepridil 10 micromol.L-1, and IC50 was 2.6 (2.3-2.9) micromol.L-1. Bepridil 10 micromol.L-1 shifted the maximal activation of sodium current from -50 mV to -40 mV, and the characteristic voltage of inactivation from -71 mV to -89 mV without changing the slope factor.

CONCLUSION:

Bepridil blocked voltage-dependent sodium current of hippocampal CA1 neurons and might have therapeutic actions for ischemia-induced brain damage.
Assuntos
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Base de dados: MEDLINE Assunto principal: Canais de Sódio / Bepridil / Células Piramidais Idioma: En Ano de publicação: 1999 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Canais de Sódio / Bepridil / Células Piramidais Idioma: En Ano de publicação: 1999 Tipo de documento: Article