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

Olfaction01:25

Olfaction

The sense of smell is achieved through the activities of the olfactory system. It starts when an airborne odorant enters the nasal cavity and reaches olfactory epithelium (OE). The OE is protected by a thin layer of mucus, which also serves the purpose of dissolving more complex compounds into simpler chemical odorants. The size of the OE and the density of sensory neurons varies among species; in humans, the OE is only about 9-10 cm2.
The olfactory receptors are embedded in the cilia of the...
Physiology of Smell and Olfactory Pathway01:20

Physiology of Smell and Olfactory Pathway

Humans detect odors with the help of specialized cells located in the upper part of the nasal cavity, called olfactory receptor neurons (ORNs). ORNs possess hair-like structures called cilia, which are receptive to sensations from the inhaled air. When an odorant molecule binds to a specific receptor on the cell of the cilia, it leads to a series of events that ultimately cause the ORN to send electrical signals to the olfactory bulb in the brain through the olfactory nerves.
The olfactory...
Olfactory Receptors: Location and Structure01:03

Olfactory Receptors: Location and Structure

The process of olfaction, also known as the sense of smell, is a sophisticated chemical response system. The specialized sensory neurons that facilitate this process, known as olfactory receptor neurons, are situated in an upper segment of the nasal cavity, known as the olfactory epithelium. Olfactory sensory neurons are bipolar, with their dendrites extending from the epithelium's apex into the mucus that lines the nasal cavity. Airborne molecules, when inhaled, traverse the olfactory...

You might also read

Related Articles

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

Sort by
Same author

Disentangling cephalopod chromatophores motor units with computer vision.

eLife·2026
Same author

Incorporation of multiple diversity genes in the TCRδ chain is highly regulated and evolutionarily conserved.

Journal of immunology (Baltimore, Md. : 1950)·2026
Same author

Chromosome-scale genome assembly of the European common cuttlefish <i>Sepia officinalis</i>.

eLife·2026
Same author

Wavelet-based visual compass.

PloS one·2026
Same author

In vivo modeling of human γδ T cell ontogeny reveals terminal deoxynucleotidyl transferase as a key regulator of type 3 Vδ2 T cell development.

Cell reports·2026
Same author

Introduction to the Proceedings of the CNS*2025 Meeting.

Journal of computational neuroscience·2026

Related Experiment Video

Updated: Jun 2, 2026

Multi-unit Recording Methods to Characterize Neural Activity in the Locust (Schistocerca Americana) Olfactory Circuits
12:13

Multi-unit Recording Methods to Characterize Neural Activity in the Locust (Schistocerca Americana) Olfactory Circuits

Published on: January 25, 2013

Normalization for sparse encoding of odors by a wide-field interneuron.

Maria Papadopoulou1, Stijn Cassenaer, Thomas Nowotny

  • 1Division of Biology, Computation and Neural Systems Program, California Institute of Technology, Pasadena, CA 91125, USA.

Science (New York, N.Y.)
|May 10, 2011
PubMed
Summary
This summary is machine-generated.

Researchers discovered a negative-feedback loop in locust mushroom bodies that creates sparse odor representations. This neural circuit ensures reliable sensory information processing for memory and storage.

More Related Videos

New Methods to Study Gustatory Coding
10:59

New Methods to Study Gustatory Coding

Published on: June 29, 2017

Perforated Patch-clamp Recording of Mouse Olfactory Sensory Neurons in Intact Neuroepithelium: Functional Analysis of Neurons Expressing an Identified Odorant Receptor
10:16

Perforated Patch-clamp Recording of Mouse Olfactory Sensory Neurons in Intact Neuroepithelium: Functional Analysis of Neurons Expressing an Identified Odorant Receptor

Published on: July 13, 2015

Related Experiment Videos

Last Updated: Jun 2, 2026

Multi-unit Recording Methods to Characterize Neural Activity in the Locust (Schistocerca Americana) Olfactory Circuits
12:13

Multi-unit Recording Methods to Characterize Neural Activity in the Locust (Schistocerca Americana) Olfactory Circuits

Published on: January 25, 2013

New Methods to Study Gustatory Coding
10:59

New Methods to Study Gustatory Coding

Published on: June 29, 2017

Perforated Patch-clamp Recording of Mouse Olfactory Sensory Neurons in Intact Neuroepithelium: Functional Analysis of Neurons Expressing an Identified Odorant Receptor
10:16

Perforated Patch-clamp Recording of Mouse Olfactory Sensory Neurons in Intact Neuroepithelium: Functional Analysis of Neurons Expressing an Identified Odorant Receptor

Published on: July 13, 2015

Area of Science:

  • Neuroscience
  • Insect Olfaction
  • Computational Neuroscience

Background:

  • Sparse coding is crucial for efficient sensory representation and memory.
  • In insects, olfactory information transforms from dense in antennal lobes to sparse in mushroom bodies.
  • This transformation in locusts involves oscillatory output, inhibitory circuits, and specific neuron properties.

Purpose of the Study:

  • To investigate the neural mechanisms maintaining sparse odor representation in the locust mushroom body.
  • To identify the components of the negative-feedback loop responsible for sparse coding.

Main Methods:

  • Electrophysiological recordings in locusts.
  • Circuit analysis of the mushroom body.
  • Investigating the role of a specific inhibitory interneuron.

Main Results:

  • A normalizing negative-feedback loop exists within the mushroom body.
  • This loop involves a unique "giant" nonspiking inhibitory interneuron.
  • The interneuron exhibits ubiquitous connectivity and graded release, crucial for maintaining sparse output.

Conclusions:

  • The identified negative-feedback loop is essential for sparse coding in the insect olfactory system.
  • This mechanism ensures robust odor representation across varying input conditions.
  • The "giant" inhibitory interneuron plays a key role in regulating neural sparsity.