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Figure 5 | Molecular Brain

Figure 5

From: The modulation of TRPM7 currents by nafamostat mesilate depends directly upon extracellular concentrations of divalent cations

Figure 5

NM-activated TRPM7 in hippocampal neurons depends on extracellular Ca2+ concentration. A, right, 10 mM Ca2+ blocks NM (200 μM)-induced TRPM7 current, n = 7. Left, high Ca2+ (10 mM) but not 2 mM Ca2+ occlude the TRPM7 activation by NM (200 μM), n = 6. B, left, NM elicited almost no current at 10 mM Ca2+ (with 1 mM Mg2+), small TRPM7 current at 2 mM Ca2+ (with 1 mM Mg2+) and large TRPM7 current at 0.1 Ca2+ (with 0.1 Mg2+) (n = 8). Right, bar graph shows statistics of NM-induced current at various Ca2+ conditions. The current amplitudes were 147 ± 20 pA at 10 mM Ca2+; 291 ± 52 pA at 2 mM Ca2+ and 1018 ± 120 pA at 0.1 mM Ca2+. C, TRPM7 current activated by NM was inhibited 97 ± 2% by Gd3+ (10 μM), n = 5. Left, current-trace example; right, bar graph showing statistics of current amplitude. D, NM-induced Ca2+ entry in hippocampal neurons is attenuated by high extracellular Ca2+. NM (200 μM)-induced Ca2+ entry monitored by Ca2+ imaging and high extracellular Ca2+ (5 mM) attenuated the Ca2+ entry. **, p < 0.01, 2 mM versus 5 mM Ca2+, n = 22. Bath solution contain no Mg2+ and MK801 (10 μM), CNQX (20 μM) and nimodipine (5 μM) was supplemented.

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