Related Experiment Video
Updated: Aug 16, 2026

Investigations on Alterations of Hippocampal Circuit Function Following Mild Traumatic Brain Injury
Published on: November 18, 2012
L-type Ca2+ channel blocker attenuates impairment induced by acidosis in hippocampal neurons
Xianghui Zeng1, Yanli Zhang2, Chen Qing2
1Key Laboratory of Medicinal Chemistry for Natural Resources, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming, China. zeng-89@hotmail.com
Abstract:
Accumulation of acid in the brain during ischemia may contribute to the activation of voltage-gated Ca2+ channels and subsequent neuronal injury. However, information regarding the role of L-type Ca2+ channel under acidosis remains unclear. In the present study, we examined the role of L-type Ca2+ channel in acidosis induced neuronal death and subsequent pathogenesis events responsible for neuron degeneration. Here we report that preincubation of cells with nifedipine (5 microM, 10 microM), an inhibitor of L-type Ca2+ channel markedly reduced neuronal death induced by moderate extracellular acidosis (pH 6.5) on cultured hippocampus neurons. Furthermore, nifedipine decreased the hippocampus neuronal swelling, as well as the accumulation of Ca2+ and collapse of mitochondrial membrane potential induced by acidosis. These findings demonstrate that pharmacological inhibition of L-type Ca2+ channel would attenuate neuronal degeneration caused by toxic low pH exposure in rat hippocampus neuron.
More Related Videos
Related Concept Videos
The Role of Ion Channels in Neuronal Computation
Sometimes a single EPSP is strong enough to induce an action potential in the postsynaptic neuron. However, multiple presynaptic inputs must often create EPSPs around the same time for the postsynaptic neuron to be sufficiently depolarized to fire an action potential.
Ligand-Gated Ion Channel Receptor: Gating Mechanism
Local Anesthetics: Mechanism of Action
Local anesthetics are amphiphilic molecules consisting of a hydrophobic aromatic part linked to a hydrophilic group by an ester or amide linkage. They are weak bases and are usually available as salts, which increases their solubility and stability. Once administered, LAs exist in the body either...

