Inhibitory Postsynaptic Potential

An inhibitory postsynaptic potential (IPSP) is a transient change in a postsynaptic neuron’s membrane potential that reduces the likelihood of generating an action potential. It occurs when inhibitory neurotransmitters such as GABA or glycine activate ligand-gated ion channels, typically promoting chloride influx or potassium efflux, which hyperpolarizes the membrane or produces shunting inhibition. IPSPs interact with excitatory postsynaptic potentials through spatial and temporal summation, allowing neural circuits to regulate signal transmission, timing, and activity. Studying IPSPs helps explain synaptic integration, sensory processing, motor control, and disruptions in inhibition associated with neurological disorders.

Inhibitory Postsynaptic Potential - Related Videos

Education

JoVE Core - Anatomy and Physiology

Postsynaptic Potential (PSP)

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2025

Postsynaptic potential (PSP) refers to a change in the electrical potential of a neuron when neurotransmitters released by presynaptic neurons bind to postsynaptic receptors. This potential can either be excitatory, leading to depolarization and ultimately action potential generation, or inhibitory, leading to hyperpolarization and suppression of the postsynaptic neuron. There are two types of receptors: ionotropic and metabotropic. The ionotropic receptor is the membrane protein that has an...

Research

JoVE EoE - Immunodiagnostics

A Technique to Assess the Inhibitory Effect of Toxin Exposure on Miniature Excitatory Postsynaptic Currents (mEPSCs)

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2025

The video demonstrates the electrophysiological analysis of embryonic stem cell-derived neurons after exposure to neurotoxins. Treating these neurons with botulinum neurotoxins reduces the frequency of spontaneous miniature excitatory post-synaptic currents, confirming inhibition of synaptic transmission.

Recording Neuronal Field Excitatory Postsynaptic Potentials in Acute Hippocampal Slices

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2025

This video demonstrates the procedure for setting up a brain slice in a submersion chamber to record synaptic activity. The process involves securing the slice on lens paper, maintaining a continuous flow of artificial cerebrospinal fluid (aCSF) to ensure neuronal viability, and accurately positioning the stimulation and recording electrodes relative to a specific brain region of interest. This setup allows for precise monitoring of baseline synaptic activity and the effects of electrical...

MicroRNA-Mediated Inhibition of Excitatory Postsynaptic Currents in Mouse Hippocampal Slices

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2025

This video demonstrates microRNA-mediated inhibition of excitatory synaptic currents in mouse hippocampal brain slices. The CA3 neurons were infected with a recombinant viral vector harboring a construct for expressing a fluorescent reporter, a light-activated membrane channel, and a microRNA that downregulates the expression of voltage-gated calcium channels. Upon placing a slice in a recording chamber and patching a CA1 neuron with a recording pipette, light pulses were used to stimulate the...

ATP-Based Luciferase Viability Assay: A Homogenous Method to Evaluate the Growth-Inhibitory Potential of Test Agents on Tumor Organoids

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2025

In this video, we demonstrate a rapid, single-addition assay to assess cell viability in patient-derived organoids upon treatment with a test agent using intracellular ATP levels as a marker for cellular metabolic activity. The intracellular ATP levels are measured using the luciferase/luciferin reaction, where the emitted light intensity indicates the cellular viability and, in turn, the test agent's growth-inhibitory potency.

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