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Mg(2+)-dependent facilitation and inactivation of L-type Ca(2+) channels in guinea pig ventricular myocytes.
Zhao, Meimi; Feng, Rui; Shao, Dongxue; Liu, Shuyuan; Lei, Ming; Wang, Hongmei; Sun, Xuefei; Guo, Feng; Hu, Huiyuan; Kameyama, Masaki; Hao, Liying.
Afiliação
  • Zhao M; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China; Cardiovascular Institute of China Medical University, Shenyang 110001, China.
  • Feng R; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China; Cardiovascular Institute of China Medical University, Shenyang 110001, China.
  • Shao D; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Liu S; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Lei M; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Wang H; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China.
  • Sun X; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China; Cardiovascular Institute of China Medical University, Shenyang 110001, China.
  • Guo F; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China; Cardiovascular Institute of China Medical University, Shenyang 110001, China.
  • Hu H; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China; Cardiovascular Institute of China Medical University, Shenyang 110001, China.
  • Kameyama M; Department of Physiology, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8544, Japan.
  • Hao L; Department of Pharmaceutical Toxicology, School of Pharmacy, China Medical University, Shenyang 110122, China; Cardiovascular Institute of China Medical University, Shenyang 110001, China. Electronic address: lyhao@mail.cmu.edu.cn.
J Pharmacol Sci ; 129(3): 143-9, 2015 Nov.
Article em En | MEDLINE | ID: mdl-26422671
This study aimed to investigate the intracellular Mg(2+) regulation of the L-type Ca(2+) channels in guinea pig ventricular myocytes. By adopting the inside-out configuration of the patch clamp technique, single channel currents of the L-type Ca(2+) channels were recorded at different intracellular Mg(2+) concentrations ([Mg(2+)]i). At free [Mg(2+)]i of 0, 10(-9), 10(-7), 10(-5), 10(-3), and 10(-1) M, 1.4 µM CaM + 3 mM ATP induced channel activities of 44%, 117%, 202%, 181%, 147%, and 20% of the control activity in cell-attached mode, respectively, showing a bell-shaped concentration-response relationship. Moreover, the intracellular Mg(2+) modulated the Ca(2+) channel gating properties, accounting for alterations in channel activities. These results imply that Mg(2+) has a dual effect on the L-type Ca(2+) channels: facilitation and inhibition. Lower [Mg(2+)]i maintains and enhances the basal activity of Ca(2+) channels, whereas higher [Mg(2+)]i inhibits channel activity. Taken together, our data from the application of an [Mg(2+)]i series suggest that the dual effect of Mg(2+) upon the L-type Ca(2+) channels exhibits long open-time dependence.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais de Cálcio Tipo L / Células Musculares / Magnésio Limite: Animals Idioma: En Revista: J Pharmacol Sci Assunto da revista: FARMACOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China País de publicação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Canais de Cálcio Tipo L / Células Musculares / Magnésio Limite: Animals Idioma: En Revista: J Pharmacol Sci Assunto da revista: FARMACOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China País de publicação: Japão