Molecular pharmacology of voltage-dependent calcium channels

Yasuo Mori, Gabor Mikala, Gyula Varadi, Tsutomu Kobayashi, Sheryl Koch, Minoru Wakamori, Arnold Schwartz

Research output: Contribution to journalReview article

91 Citations (Scopus)


Voltage-dependent Ca2+ channels serve as the only link to transduce membrane depolarization into cellular Ca2+-dependent reactions. A wide variety of chemical substances that have the ability to modulate Ca2+ channels have been demonstrated both for their clinic utility and for importance in elucidating the molecular basis of various biological responses. Recently, introduction of molecular biology to pharmacology has brought a great deal of information about the molecular basis of drug action in Ca2+ channels. In this review, we attempt to overview recent progress in understanding the interactions between Ca2+ channels and their blockers, namely Ca2+ antagonists, from a molecular and structural point of view.

Original languageEnglish
Pages (from-to)83-109
Number of pages27
JournalJapanese Journal of Pharmacology
Issue number2
Publication statusPublished - Jan 1 1996


  • Ca antagonist
  • Ca channel
  • Inorganic blocker
  • Peptide toxin

ASJC Scopus subject areas

  • Pharmacology

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    Mori, Y., Mikala, G., Varadi, G., Kobayashi, T., Koch, S., Wakamori, M., & Schwartz, A. (1996). Molecular pharmacology of voltage-dependent calcium channels. Japanese Journal of Pharmacology, 72(2), 83-109.