Potent inhibition by trivalent cations of ATP-gated channels

Ken Nakazawa, Min Liu, Kazuhide Inoue, Yasuo Ohno

Research output: Contribution to journalArticlepeer-review

34 Citations (Scopus)


The effects of La3+ and other trivalent cations on ATP-gated channels (P(2X) purinoceptor/channels) were investigated using rat pheochromocytoma PC12 cells and Xenopus oocytes expressing these channels. La3+, Gd3+, Ce3+ and Nd3+ (30-300 μM) inhibited an inward current activated by 30 μM ATP in PC12 cells. The concentration-response curve for the ATP-activated current was shifted by La3+ or Gd3+ toward a higher concentration range, and the slope of the curve became steeper, suggesting the inhibition is non-competitive. La3+ or Gd3+ did not affect the current component that was slowly activated upon hyperpolarization, and selectively inhibited the remaining 'voltage-independent' component. La3+ and Gd3+ also inhibited currents mediated through P(2X1) and P(2X2) purinoceptors expressed in Xenopus oocytes. The results suggest that La3+ and other trivalent cations inhibit P(2X) purinoceptors at low concentrations. The inhibition may at least partly be attributed to an allosteric inhibition.

Original languageEnglish
Pages (from-to)237-243
Number of pages7
JournalEuropean Journal of Pharmacology
Issue number2-3
Publication statusPublished - May 1 1997
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Pharmacology


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