Erasing sensorimotor memories via PKMzeta inhibition.
Sensorimotor cortex has a role in procedural learning. Previous studies suggested that this learning is subserved by long-term potentiation (LTP), which is in turn maintained by the persistently active kinase, protein kinase Mzeta (PKMzeta). Whereas the role of PKMzeta in animal models of declarativ...
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doaj-e133a00200744021a73777da889b9bad2020-11-24T20:49:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-06-0156e1112510.1371/journal.pone.0011125Erasing sensorimotor memories via PKMzeta inhibition.Lee Michael von KrausTodd Charlton SacktorJoseph Thachil FrancisSensorimotor cortex has a role in procedural learning. Previous studies suggested that this learning is subserved by long-term potentiation (LTP), which is in turn maintained by the persistently active kinase, protein kinase Mzeta (PKMzeta). Whereas the role of PKMzeta in animal models of declarative knowledge is established, its effect on procedural knowledge is not well understood. Here we show that PKMzeta inhibition, via injection of zeta inhibitory peptide (ZIP) into the rat sensorimotor cortex, disrupts sensorimotor memories for a skilled reaching task even after several weeks of training. The rate of relearning the task after the memory disruption by ZIP was indistinguishable from the rate of initial learning, suggesting no significant savings after the memory loss. These results indicate a shared molecular mechanism of storage for declarative and procedural forms of memory.http://europepmc.org/articles/PMC2886075?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lee Michael von Kraus Todd Charlton Sacktor Joseph Thachil Francis |
spellingShingle |
Lee Michael von Kraus Todd Charlton Sacktor Joseph Thachil Francis Erasing sensorimotor memories via PKMzeta inhibition. PLoS ONE |
author_facet |
Lee Michael von Kraus Todd Charlton Sacktor Joseph Thachil Francis |
author_sort |
Lee Michael von Kraus |
title |
Erasing sensorimotor memories via PKMzeta inhibition. |
title_short |
Erasing sensorimotor memories via PKMzeta inhibition. |
title_full |
Erasing sensorimotor memories via PKMzeta inhibition. |
title_fullStr |
Erasing sensorimotor memories via PKMzeta inhibition. |
title_full_unstemmed |
Erasing sensorimotor memories via PKMzeta inhibition. |
title_sort |
erasing sensorimotor memories via pkmzeta inhibition. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2010-06-01 |
description |
Sensorimotor cortex has a role in procedural learning. Previous studies suggested that this learning is subserved by long-term potentiation (LTP), which is in turn maintained by the persistently active kinase, protein kinase Mzeta (PKMzeta). Whereas the role of PKMzeta in animal models of declarative knowledge is established, its effect on procedural knowledge is not well understood. Here we show that PKMzeta inhibition, via injection of zeta inhibitory peptide (ZIP) into the rat sensorimotor cortex, disrupts sensorimotor memories for a skilled reaching task even after several weeks of training. The rate of relearning the task after the memory disruption by ZIP was indistinguishable from the rate of initial learning, suggesting no significant savings after the memory loss. These results indicate a shared molecular mechanism of storage for declarative and procedural forms of memory. |
url |
http://europepmc.org/articles/PMC2886075?pdf=render |
work_keys_str_mv |
AT leemichaelvonkraus erasingsensorimotormemoriesviapkmzetainhibition AT toddcharltonsacktor erasingsensorimotormemoriesviapkmzetainhibition AT josephthachilfrancis erasingsensorimotormemoriesviapkmzetainhibition |
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1716805444481056768 |