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Modulation of acid-sensing ion channel currents, acid-induced increase of intracellular Ca2+, and acidosis-mediated neuronal injury by intracellular pH.

Abstract
Acid-sensing ion channels (ASICs), activated by lowering extracellular pH (pH(o)), play an important role in normal synaptic transmission in brain and in the pathology of brain ischemia. Like pH(o), intracellular pH (pH(i)) changes dramatically in both physiological and pathological conditions. Although it is known that a drop in pH(o) activates the ASICs, it is not clear whether alterations of pH(i) have an effect on these channels. Here we demonstrate that the overall activities of ASICs, including channel activation, inactivation, and recovery from desensitization, are tightly regulated by pH(i). In cultured mouse cortical neurons, bath perfusion of the intracellular alkalizing agent quinine increased the amplitude of the ASIC current by approximately 50%. In contrast, intracellular acidification by withdrawal of NH(4)Cl or perfusion of propionate inhibited the current. Increasing pH buffering capacity in the pipette solution with 40 mm HEPES attenuated the effects of quinine and NH(4)Cl. The effects of intracellular alkalizing/acidifying agents were mimicked by using intracellular solutions with pH directly buffered at high/low values. Increasing pH(i) induced a shift in H(+) dose-response curve toward less acidic pH but a shift in the steady state inactivation curve toward more acidic pH. In addition, alkalizing pH(i) induced an increase in the recovery rate of ASICs from desensitization. Consistent with its effect on the ASIC current, changing pH(i) has a significant influence on the acid-induced increase of intracellular Ca(2+), membrane depolarization, and acidosis-mediated neuronal injury. Our findings suggest that changes in pH(i) may play an important role in determining the overall function of ASICs in both physiological and pathological conditions.
AuthorsWei-Zhen Wang, Xiang-Ping Chu, Ming-Hua Li, Joshua Seeds, Roger P Simon, Zhi-Gang Xiong
JournalThe Journal of biological chemistry (J Biol Chem) Vol. 281 Issue 39 Pg. 29369-78 (Sep 29 2006) ISSN: 0021-9258 [Print] United States
PMID16882660 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Acid Sensing Ion Channels
  • Ions
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Protons
  • Sodium Channels
  • Calcium
Topics
  • Acid Sensing Ion Channels
  • Acidosis
  • Animals
  • Calcium (metabolism)
  • Cerebral Cortex (embryology)
  • Dose-Response Relationship, Drug
  • Electrophysiology
  • Hydrogen-Ion Concentration
  • Ions (metabolism)
  • Membrane Proteins (metabolism, physiology)
  • Mice
  • Models, Biological
  • Nerve Tissue Proteins (metabolism, physiology)
  • Neurons (metabolism, pathology)
  • Protons
  • Sodium Channels (metabolism, physiology)

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