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J Neurosci. 2015 Apr 22;35(16):6318-25. doi: 10.1523/JNEUROSCI.4051-14.2015.

Cortical Synaptic Inhibition Declines during Auditory Learning.

Author information

1
Center for Neural Science, New York University, New York, New York 10003 emma.sarro@nyumc.org.
2
Center for Neural Science, New York University, New York, New York 10003.

Abstract

Auditory learning is associated with an enhanced representation of acoustic cues in primary auditory cortex, and modulation of inhibitory strength is causally involved in learning. If this inhibitory plasticity is associated with task learning and improvement, its expression should emerge and persist until task proficiency is achieved. We tested this idea by measuring changes to cortical inhibitory synaptic transmission as adult gerbils progressed through the process of associative learning and perceptual improvement. Using either of two procedures, aversive or appetitive conditioning, animals were trained to detect amplitude-modulated noise and then tested daily. Following each training session, a thalamocortical brain slice was generated, and inhibitory synaptic properties were recorded from layer 2/3 pyramidal neurons. Initial associative learning was accompanied by a profound reduction in the amplitude of spontaneous IPSCs (sIPSCs). However, sIPSC amplitude returned to control levels when animals reached asymptotic behavioral performance. In contrast, paired-pulse ratios decreased in trained animals as well as in control animals that experienced unpaired conditioned and unconditioned stimuli. This latter observation suggests that inhibitory release properties are modified during behavioral conditioning, even when an association between the sound and reinforcement cannot occur. These results suggest that associative learning is accompanied by a reduction of postsynaptic inhibitory strength that persists for several days during learning and perceptual improvement.

KEYWORDS:

associative learning; auditory cortex; inhibition; synaptic plasticity

PMID:
25904785
PMCID:
PMC4405553
DOI:
10.1523/JNEUROSCI.4051-14.2015
[Indexed for MEDLINE]
Free PMC Article

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