author_facet Levitan, David
Saada-Madar, Ravit
Teplinsky, Anastasiya
Susswein, Abraham J.
Levitan, David
Saada-Madar, Ravit
Teplinsky, Anastasiya
Susswein, Abraham J.
author Levitan, David
Saada-Madar, Ravit
Teplinsky, Anastasiya
Susswein, Abraham J.
spellingShingle Levitan, David
Saada-Madar, Ravit
Teplinsky, Anastasiya
Susswein, Abraham J.
Learning & Memory
Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
Cellular and Molecular Neuroscience
Cognitive Neuroscience
Neuropsychology and Physiological Psychology
author_sort levitan, david
spelling Levitan, David Saada-Madar, Ravit Teplinsky, Anastasiya Susswein, Abraham J. 1549-5485 Cold Spring Harbor Laboratory Cellular and Molecular Neuroscience Cognitive Neuroscience Neuropsychology and Physiological Psychology http://dx.doi.org/10.1101/lm.026393.112 <jats:p>Training paradigms affecting <jats:italic>Aplysia</jats:italic> withdrawal reflexes cause changes in gene expression leading to long-term memory formation in primary mechanoafferents that initiate withdrawal. Similar mechanoafferents are also found in the buccal ganglia that control feeding behavior, raising the possibility that these mechanoafferents are a locus of memory formation after a training paradigm affecting feeding. Buccal ganglia mechanoafferent neurons expressed increases in mRNA expression for the transcription factor <jats:italic>Ap</jats:italic>C/EBP, and for the growth factor sensorin-A, within the first 2 h after training with an inedible food. No increases in expression were detected in the rest of the buccal ganglia. Increased <jats:italic>Ap</jats:italic>C/EBP expression was not elicited by food and feeding responses not causing long-term memory. Increased <jats:italic>Ap</jats:italic>C/EBP expression was directly related to a measure of the efficacy of training in causing long-term memory, suggesting that <jats:italic>Ap</jats:italic>C/EBP expression is necessary for the expression of aspects of long-term memory. In behaving animals, memory is expressed as a decrease in the likelihood to respond to food, and a decrease in the amplitude of protraction, the first phase of consummatory feeding behaviors. To determine how changes in the properties of mechanoafferents could cause learned changes in feeding behavior, synaptic contacts were mapped from the mechanoafferents to the B31/B32 neurons, which have a key role in initiating consummatory behaviors and also control protractions. Many mechanoafferents monosynaptically and polysynaptically connect with B31/B32. Monosynaptic connections were complex combinations of fast and slow excitation and/or inhibition. Changes in the response of B31/B32 to stimuli sensed by the mechanoafferent could underlie aspects of long-term memory expression.</jats:p> Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in <i>Aplysia</i> Learning & Memory
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title Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_unstemmed Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_full Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_fullStr Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_full_unstemmed Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_short Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_sort localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in <i>aplysia</i>
topic Cellular and Molecular Neuroscience
Cognitive Neuroscience
Neuropsychology and Physiological Psychology
url http://dx.doi.org/10.1101/lm.026393.112
publishDate 2012
physical 503-512
description <jats:p>Training paradigms affecting <jats:italic>Aplysia</jats:italic> withdrawal reflexes cause changes in gene expression leading to long-term memory formation in primary mechanoafferents that initiate withdrawal. Similar mechanoafferents are also found in the buccal ganglia that control feeding behavior, raising the possibility that these mechanoafferents are a locus of memory formation after a training paradigm affecting feeding. Buccal ganglia mechanoafferent neurons expressed increases in mRNA expression for the transcription factor <jats:italic>Ap</jats:italic>C/EBP, and for the growth factor sensorin-A, within the first 2 h after training with an inedible food. No increases in expression were detected in the rest of the buccal ganglia. Increased <jats:italic>Ap</jats:italic>C/EBP expression was not elicited by food and feeding responses not causing long-term memory. Increased <jats:italic>Ap</jats:italic>C/EBP expression was directly related to a measure of the efficacy of training in causing long-term memory, suggesting that <jats:italic>Ap</jats:italic>C/EBP expression is necessary for the expression of aspects of long-term memory. In behaving animals, memory is expressed as a decrease in the likelihood to respond to food, and a decrease in the amplitude of protraction, the first phase of consummatory feeding behaviors. To determine how changes in the properties of mechanoafferents could cause learned changes in feeding behavior, synaptic contacts were mapped from the mechanoafferents to the B31/B32 neurons, which have a key role in initiating consummatory behaviors and also control protractions. Many mechanoafferents monosynaptically and polysynaptically connect with B31/B32. Monosynaptic connections were complex combinations of fast and slow excitation and/or inhibition. Changes in the response of B31/B32 to stimuli sensed by the mechanoafferent could underlie aspects of long-term memory expression.</jats:p>
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author Levitan, David, Saada-Madar, Ravit, Teplinsky, Anastasiya, Susswein, Abraham J.
author_facet Levitan, David, Saada-Madar, Ravit, Teplinsky, Anastasiya, Susswein, Abraham J., Levitan, David, Saada-Madar, Ravit, Teplinsky, Anastasiya, Susswein, Abraham J.
author_sort levitan, david
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description <jats:p>Training paradigms affecting <jats:italic>Aplysia</jats:italic> withdrawal reflexes cause changes in gene expression leading to long-term memory formation in primary mechanoafferents that initiate withdrawal. Similar mechanoafferents are also found in the buccal ganglia that control feeding behavior, raising the possibility that these mechanoafferents are a locus of memory formation after a training paradigm affecting feeding. Buccal ganglia mechanoafferent neurons expressed increases in mRNA expression for the transcription factor <jats:italic>Ap</jats:italic>C/EBP, and for the growth factor sensorin-A, within the first 2 h after training with an inedible food. No increases in expression were detected in the rest of the buccal ganglia. Increased <jats:italic>Ap</jats:italic>C/EBP expression was not elicited by food and feeding responses not causing long-term memory. Increased <jats:italic>Ap</jats:italic>C/EBP expression was directly related to a measure of the efficacy of training in causing long-term memory, suggesting that <jats:italic>Ap</jats:italic>C/EBP expression is necessary for the expression of aspects of long-term memory. In behaving animals, memory is expressed as a decrease in the likelihood to respond to food, and a decrease in the amplitude of protraction, the first phase of consummatory feeding behaviors. To determine how changes in the properties of mechanoafferents could cause learned changes in feeding behavior, synaptic contacts were mapped from the mechanoafferents to the B31/B32 neurons, which have a key role in initiating consummatory behaviors and also control protractions. Many mechanoafferents monosynaptically and polysynaptically connect with B31/B32. Monosynaptic connections were complex combinations of fast and slow excitation and/or inhibition. Changes in the response of B31/B32 to stimuli sensed by the mechanoafferent could underlie aspects of long-term memory expression.</jats:p>
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spelling Levitan, David Saada-Madar, Ravit Teplinsky, Anastasiya Susswein, Abraham J. 1549-5485 Cold Spring Harbor Laboratory Cellular and Molecular Neuroscience Cognitive Neuroscience Neuropsychology and Physiological Psychology http://dx.doi.org/10.1101/lm.026393.112 <jats:p>Training paradigms affecting <jats:italic>Aplysia</jats:italic> withdrawal reflexes cause changes in gene expression leading to long-term memory formation in primary mechanoafferents that initiate withdrawal. Similar mechanoafferents are also found in the buccal ganglia that control feeding behavior, raising the possibility that these mechanoafferents are a locus of memory formation after a training paradigm affecting feeding. Buccal ganglia mechanoafferent neurons expressed increases in mRNA expression for the transcription factor <jats:italic>Ap</jats:italic>C/EBP, and for the growth factor sensorin-A, within the first 2 h after training with an inedible food. No increases in expression were detected in the rest of the buccal ganglia. Increased <jats:italic>Ap</jats:italic>C/EBP expression was not elicited by food and feeding responses not causing long-term memory. Increased <jats:italic>Ap</jats:italic>C/EBP expression was directly related to a measure of the efficacy of training in causing long-term memory, suggesting that <jats:italic>Ap</jats:italic>C/EBP expression is necessary for the expression of aspects of long-term memory. In behaving animals, memory is expressed as a decrease in the likelihood to respond to food, and a decrease in the amplitude of protraction, the first phase of consummatory feeding behaviors. To determine how changes in the properties of mechanoafferents could cause learned changes in feeding behavior, synaptic contacts were mapped from the mechanoafferents to the B31/B32 neurons, which have a key role in initiating consummatory behaviors and also control protractions. Many mechanoafferents monosynaptically and polysynaptically connect with B31/B32. Monosynaptic connections were complex combinations of fast and slow excitation and/or inhibition. Changes in the response of B31/B32 to stimuli sensed by the mechanoafferent could underlie aspects of long-term memory expression.</jats:p> Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in <i>Aplysia</i> Learning & Memory
spellingShingle Levitan, David, Saada-Madar, Ravit, Teplinsky, Anastasiya, Susswein, Abraham J., Learning & Memory, Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia, Cellular and Molecular Neuroscience, Cognitive Neuroscience, Neuropsychology and Physiological Psychology
title Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_full Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_fullStr Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_full_unstemmed Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_short Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
title_sort localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in <i>aplysia</i>
title_unstemmed Localization of molecular correlates of memory consolidation to buccal ganglia mechanoafferent neurons after learning that food is inedible in Aplysia
topic Cellular and Molecular Neuroscience, Cognitive Neuroscience, Neuropsychology and Physiological Psychology
url http://dx.doi.org/10.1101/lm.026393.112