Plasticity in inhibitory networks improves pattern separation in early olfactory processing

Distinguishing between nectar and non-nectar odors is challenging for animals due to shared compounds and varying ratios in complex mixtures. Changes in nectar production throughout the day and over the animal's lifetime add to the complexity. The honeybee olfactory system, containing fewer than 1000 principal neurons in the early olfactory relay, the antennal lobe (AL), must learn to associate diverse volatile blends with rewards. Previous studies identified plasticity in the AL circuits, but its role in odor learning remains poorly understood. Using a biophysical computational model, tuned by in vivo electrophysiological data, and live imaging of the honeybee's AL, we explored the neural mechanisms of plasticity in the AL. Our findings revealed that when trained with a set of rewarded and unrewarded odors, the AL inhibitory network suppresses responses to shared chemical compounds while enhancing responses to distinct compounds. This results in improved pattern separation and a more concise neural code. Our calcium imaging data support these predictions. Analysis of a graph convolutional neural network performing an odor categorization task revealed a similar mechanism for contrast enhancement. Our study provides insights into how inhibitory plasticity in the early olfactory network reshapes the coding for efficient learning of complex odors.

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Publication Details

Journal
Communications Biology
Published
2025-04-09
DOI
https://doi.org/10.1038/s42003-025-07879-2
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Plasticity in inhibitory networks improves pattern separation in early olfactory processing

Shruti Joshi, Seth Haney, Maxim Bazhenov, Hong Lei et al.
Communications Biology
Neurobiology and Insect Physiology Research
article

Plasticity in inhibitory networks improves pattern separation in early olfactory processing

Shruti Joshi, Seth Haney, Maxim Bazhenov, Hong Lei, Brian H. Smith, Fernando Locatelli, Zhenyu Wang, Yu Cao
article en

Abstract

Distinguishing between nectar and non-nectar odors is challenging for animals due to shared compounds and varying ratios in complex mixtures. Changes in nectar production throughout the day and over the animal's lifetime add to the complexity. The honeybee olfactory system, containing fewer than 1000 principal neurons in the early olfactory relay, the antennal lobe (AL), must learn to associate diverse volatile blends with rewards. Previous studies identified plasticity in the AL circuits, but its role in odor learning remains poorly understood. Using a biophysical computational model, tuned by in vivo electrophysiological data, and live imaging of the honeybee's AL, we explored the neural mechanisms of plasticity in the AL. Our findings revealed that when trained with a set of rewarded and unrewarded odors, the AL inhibitory network suppresses responses to shared chemical compounds while enhancing responses to distinct compounds. This results in improved pattern separation and a more concise neural code. Our calcium imaging data support these predictions. Analysis of a graph convolutional neural network performing an odor categorization task revealed a similar mechanism for contrast enhancement. Our study provides insights into how inhibitory plasticity in the early olfactory network reshapes the coding for efficient learning of complex odors.

Communications BiologyVol. 8(1)
University of Minnesota (US), Consejo Nacional de Investigaciones Científicas y Técnicas (AR), Universidad de Buenos Aires (AR), UC San Diego Health System (US), University of California San Diego (US), Fundación Ciencias Exactas y Naturales (AR), Arizona State University (US)
National Science Foundation, Foundation for the National Institutes of Health, UK Research and Innovation, Deutsche Forschungsgemeinschaft, National Institutes of Health, Canadian Institutes of Health Research, Medical Research Council
Openalex Percentile: Top 91%
Neurobiology and Insect Physiology Research
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