
The homomeric acid‐sensing ion channel 1a (ASIC1a) is a H+‐activated ion channel with important physiological functions and pathophysiological impact in the central nervous system. Here we show that homomeric ASIC1a is distinguished from other ASICs by a reduced response to successive acid stimulations. Such a reduced response is called tachyphylaxis. We show that tachyphylaxis depends on H+ permeating through ASIC1a, that tachyphylaxis is attenuated by extracellular Ca2+, and that tachyphylaxis is probably linked to Ca2+ permeability of ASIC1a. Moreover, we provide evidence that tachyphylaxis is probably due to a long‐lived inactive state of ASIC1a. A deeper understanding of ASIC1a tachyphylaxis may lead to pharmacological control of ASIC1a activity that could be of potential benefit for the treatment of stroke.
Patch-Clamp Techniques, Gene Expression, Membrane Proteins, Nerve Tissue Proteins, Hydrogen-Ion Concentration, Endocytosis, Sodium Channels, Rats, Acid Sensing Ion Channels, Xenopus laevis, Oocytes, Animals, Calcium, Female, Protons, Tachyphylaxis, Acids, Ion Channel Gating
Patch-Clamp Techniques, Gene Expression, Membrane Proteins, Nerve Tissue Proteins, Hydrogen-Ion Concentration, Endocytosis, Sodium Channels, Rats, Acid Sensing Ion Channels, Xenopus laevis, Oocytes, Animals, Calcium, Female, Protons, Tachyphylaxis, Acids, Ion Channel Gating
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