Insect brain plasticity: effects of olfactory input on neuropil size
Insect brains are known to express a high degree of experience-dependent structural plasticity. One brain structure in particular, the mushroom body (MB), has been attended to in numerous studies as it is implicated in complex cognitive processes such as olfactory learning and memory. It is, however...
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2019-08-01
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doaj-cf08cee56b914e13a0c3a81b9a7e83272020-11-25T04:02:57ZengThe Royal SocietyRoyal Society Open Science2054-57032019-08-016810.1098/rsos.190875190875Insect brain plasticity: effects of olfactory input on neuropil sizeMaertha ErikssonSören NylinMikael A. CarlssonInsect brains are known to express a high degree of experience-dependent structural plasticity. One brain structure in particular, the mushroom body (MB), has been attended to in numerous studies as it is implicated in complex cognitive processes such as olfactory learning and memory. It is, however, poorly understood to what extent sensory input per se affects the plasticity of the mushroom bodies. By performing unilateral blocking of olfactory input on immobilized butterflies, we were able to measure the effect of passive sensory input on the volumes of antennal lobes (ALs) and MB calyces. We showed that the primary and secondary olfactory neuropils respond in different ways to olfactory input. ALs show absolute experience-dependency and increase in volume only if receiving direct olfactory input from ipsilateral antennae, while MB calyx volumes were unaffected by the treatment and instead show absolute age-dependency in this regard. We therefore propose that cognitive processes related to behavioural expressions are needed in order for the calyx to show experience-dependent volumetric expansions. Our results indicate that such experience-dependent volumetric expansions of calyces observed in other studies may have been caused by cognitive processes rather than by sensory input, bringing some causative clarity to a complex neural phenomenon.https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.190875antennal lobemushroom bodycalyxbutterflyolfactionplasticity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Maertha Eriksson Sören Nylin Mikael A. Carlsson |
spellingShingle |
Maertha Eriksson Sören Nylin Mikael A. Carlsson Insect brain plasticity: effects of olfactory input on neuropil size Royal Society Open Science antennal lobe mushroom body calyx butterfly olfaction plasticity |
author_facet |
Maertha Eriksson Sören Nylin Mikael A. Carlsson |
author_sort |
Maertha Eriksson |
title |
Insect brain plasticity: effects of olfactory input on neuropil size |
title_short |
Insect brain plasticity: effects of olfactory input on neuropil size |
title_full |
Insect brain plasticity: effects of olfactory input on neuropil size |
title_fullStr |
Insect brain plasticity: effects of olfactory input on neuropil size |
title_full_unstemmed |
Insect brain plasticity: effects of olfactory input on neuropil size |
title_sort |
insect brain plasticity: effects of olfactory input on neuropil size |
publisher |
The Royal Society |
series |
Royal Society Open Science |
issn |
2054-5703 |
publishDate |
2019-08-01 |
description |
Insect brains are known to express a high degree of experience-dependent structural plasticity. One brain structure in particular, the mushroom body (MB), has been attended to in numerous studies as it is implicated in complex cognitive processes such as olfactory learning and memory. It is, however, poorly understood to what extent sensory input per se affects the plasticity of the mushroom bodies. By performing unilateral blocking of olfactory input on immobilized butterflies, we were able to measure the effect of passive sensory input on the volumes of antennal lobes (ALs) and MB calyces. We showed that the primary and secondary olfactory neuropils respond in different ways to olfactory input. ALs show absolute experience-dependency and increase in volume only if receiving direct olfactory input from ipsilateral antennae, while MB calyx volumes were unaffected by the treatment and instead show absolute age-dependency in this regard. We therefore propose that cognitive processes related to behavioural expressions are needed in order for the calyx to show experience-dependent volumetric expansions. Our results indicate that such experience-dependent volumetric expansions of calyces observed in other studies may have been caused by cognitive processes rather than by sensory input, bringing some causative clarity to a complex neural phenomenon. |
topic |
antennal lobe mushroom body calyx butterfly olfaction plasticity |
url |
https://royalsocietypublishing.org/doi/pdf/10.1098/rsos.190875 |
work_keys_str_mv |
AT maerthaeriksson insectbrainplasticityeffectsofolfactoryinputonneuropilsize AT sorennylin insectbrainplasticityeffectsofolfactoryinputonneuropilsize AT mikaelacarlsson insectbrainplasticityeffectsofolfactoryinputonneuropilsize |
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