Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Feedback Inhibition00:46

Feedback Inhibition

Biochemical reactions are occurring constantly in cells, converting starting substances to different products, usually with the help of enzymes that speed the reactions. Without enzymes, it would take far too long for most reactions to occur to be useful to the cell!
The Cochlea01:13

The Cochlea

The cochlea is a coiled structure in the inner ear that contains hair cells—the sensory receptors of the auditory system. Sound waves are transmitted to the cochlea by small bones attached to the eardrum called the ossicles, which vibrate the oval window that leads to the inner ear. This causes fluid in the chambers of the cochlea to move, vibrating the basilar membrane.
Ligand-Gated Ion Channel Receptor: Gating Mechanism01:30

Ligand-Gated Ion Channel Receptor: Gating Mechanism

Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow the influx of ions across the membrane once the neurotransmitter binds, allowing the subsequent transmission of electrical excitation across the neurons. Other ligand-gated ion channels, like the γ-aminobutyric acid (GABA) receptor, permit anions like chloride into the cells on the binding of the GABA molecule. Their entry into the cell...
Dose-Response Relationship: Selectivity and Specificity01:25

Dose-Response Relationship: Selectivity and Specificity

Drugs exert their therapeutic effects by interacting with receptors, enzymes, or ion channels that are present throughout the human body. The strength and duration of the interaction between a drug and its target receptor are characterized by the selectivity and specificity of the drug. Selectivity refers to a drug's strong preference for its intended target over other targets. For instance, isoprenaline, a non-selective β-adrenergic agonist, interacts with both β1- and β2-adrenergic receptors...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Trap Depth Engineering of SrSi<sub>2</sub>O<sub>2</sub>N<sub>2</sub>:Ln<sup>2+</sup>,Ln<sup>3+</sup> (Ln<sup>2+</sup> = Yb, Eu; Ln<sup>3+</sup> = Dy, Ho, Er) Persistent Luminescence Materials for Information Storage Applications.

ACS applied materials & interfaces·2017
Same author

Assessing robustness of hazard ratio estimates to outcome misclassification in longitudinal panel studies with application to Alzheimer's disease.

PloS one·2017
Same author

Reverse Reconstruction and Bioprinting of Bacterial Cellulose-Based Functional Total Intervertebral Disc for Therapeutic Implantation.

Small (Weinheim an der Bergstrasse, Germany)·2017
Same author

Achieving Multicolor Long-Lived Luminescence in Dye-Encapsulated Metal-Organic Frameworks and Its Application to Anticounterfeiting Stamps.

ACS applied materials & interfaces·2017
Same author

Association between tea consumption and osteoporosis: A meta-analysis.

Medicine·2017
Same author

[Efficacy and safety of Kuhuang injection in treating viral hepatitis: systematic review and Meta-analysis of randomized controlled trials].

Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica·2017

Related Experiment Video

Updated: May 18, 2026

Manufacturing and Using Piggy-back Multibarrel Electrodes for In vivo Pharmacological Manipulations of Neural Responses
06:52

Manufacturing and Using Piggy-back Multibarrel Electrodes for In vivo Pharmacological Manipulations of Neural Responses

Published on: January 18, 2013

Inhibition shapes response selectivity in the inferior colliculus by gain modulation.

Joshua X Gittelman1, Le Wang, H S Colburn

  • 1Section of Neurobiology, Institute for Neuroscience, Center for Perceptual Systems, The University of Texas Austin, TX, USA.

Frontiers in Neural Circuits
|October 2, 2012
PubMed
Summary

Pharmacological block of inhibition reveals its role in spike selectivity. Inhibition enhances selectivity by modulating neural gain, not just by differences in evoked inhibition.

Keywords:
directional selectivitygain controlinhibitionmodelingresponse selectivityspike threshold

More Related Videos

Long-range Channelrhodopsin-assisted Circuit Mapping of Inferior Colliculus Neurons with Blue and Red-shifted Channelrhodopsins
07:04

Long-range Channelrhodopsin-assisted Circuit Mapping of Inferior Colliculus Neurons with Blue and Red-shifted Channelrhodopsins

Published on: February 7, 2020

Implementing Dynamic Clamp with Synaptic and Artificial Conductances in Mouse Retinal Ganglion Cells
11:46

Implementing Dynamic Clamp with Synaptic and Artificial Conductances in Mouse Retinal Ganglion Cells

Published on: May 16, 2013

Related Experiment Videos

Last Updated: May 18, 2026

Manufacturing and Using Piggy-back Multibarrel Electrodes for In vivo Pharmacological Manipulations of Neural Responses
06:52

Manufacturing and Using Piggy-back Multibarrel Electrodes for In vivo Pharmacological Manipulations of Neural Responses

Published on: January 18, 2013

Long-range Channelrhodopsin-assisted Circuit Mapping of Inferior Colliculus Neurons with Blue and Red-shifted Channelrhodopsins
07:04

Long-range Channelrhodopsin-assisted Circuit Mapping of Inferior Colliculus Neurons with Blue and Red-shifted Channelrhodopsins

Published on: February 7, 2020

Implementing Dynamic Clamp with Synaptic and Artificial Conductances in Mouse Retinal Ganglion Cells
11:46

Implementing Dynamic Clamp with Synaptic and Artificial Conductances in Mouse Retinal Ganglion Cells

Published on: May 16, 2013

Area of Science:

  • Computational Neuroscience
  • Auditory Neuroscience
  • Neural Coding

Background:

  • Spike selectivity, where preferred stimuli evoke more neural spikes than null stimuli, is crucial for sensory processing.
  • Pharmacological block of inhibition is a common method to investigate its contribution to spike selectivity.
  • A prevailing interpretation suggests that differences in evoked inhibition create selectivity from less selective excitatory inputs.

Purpose of the Study:

  • To investigate whether differences in inhibition are necessary for enhancing spike selectivity.
  • To explore the mechanisms by which inhibition influences spike selectivity in computational models.
  • To determine if inhibitory block can distinguish between excitatory and inhibitory sources of synaptic selectivity.

Main Methods:

  • Development of computational models based on empirical properties of inferior colliculus (IC) cells from awake bats.
  • Simulation of five distinct synaptic mechanisms to create preferred stimuli evoking more spikes than null stimuli.
  • Modeling experiments using empirical synaptic conductances derived from responses to preferred and null sounds.

Main Results:

  • Inhibitory differences are not required for enhancing spike selectivity; inhibition can improve selectivity by altering neural gain.
  • Blocking inhibition did not differentiate between purely excitatory or purely inhibitory synaptic selectivity.
  • Inhibition primarily enhanced spike selectivity through gain modulation and firing rate reduction, sometimes eliminating null-evoked spikes.

Conclusions:

  • Inhibition shapes spike selectivity mainly by gain control, rather than solely through differences in evoked inhibition.
  • The study challenges the common interpretation that inhibitory differences are essential for selectivity.
  • Findings highlight the multifaceted role of inhibition in neural processing and sensory coding.