2012
DOI: 10.1016/j.neuroscience.2011.11.027
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Effects of ketamine on response properties of neurons in the superior paraolivary nucleus of the mouse

Abstract: The superior paraolivary nucleus (SPON; alternative abbreviation: SPN for the same nucleus in certain species) is a prominent brainstem structure that provides strong inhibitory input to the auditory midbrain. Previous studies established that SPON neurons encode temporal sound features with high precision. These earlier characterizations of SPON responses were recorded under the influence of ketamine, a dissociative anesthetic agent and known antagonist of NMDA receptors. Because NMDA alters neural responses … Show more

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Cited by 16 publications
(16 citation statements)
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References 77 publications
(117 reference statements)
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“…In relating the results of these previous studies to the present results, one must take into account that the auditory systems of all species studied display unique adaptations, and each study was subject to the effects of its anesthesia protocol and recording methodology. In the present study, the known effects of ketamine anesthesia include increased peak latencies of auditory evoked potentials (Church and Gritzke 1987; Smith and Mills 1989, 1991), increased thresholds of auditory brainstem responses (van Looij et al 2004), decreased sound evoked and spontaneous spiking, and reduced the sharpness of frequency tuning (Felix et al 2012). Therefore comparisons between studies must be approached with caution.…”
Section: Discussionmentioning
confidence: 89%
“…In relating the results of these previous studies to the present results, one must take into account that the auditory systems of all species studied display unique adaptations, and each study was subject to the effects of its anesthesia protocol and recording methodology. In the present study, the known effects of ketamine anesthesia include increased peak latencies of auditory evoked potentials (Church and Gritzke 1987; Smith and Mills 1989, 1991), increased thresholds of auditory brainstem responses (van Looij et al 2004), decreased sound evoked and spontaneous spiking, and reduced the sharpness of frequency tuning (Felix et al 2012). Therefore comparisons between studies must be approached with caution.…”
Section: Discussionmentioning
confidence: 89%
“…Ketamine can potentiate inhibition by acting as a GABA‐A receptor agonist (Irifune et al ., ), and it can therefore lengthen neuronal recovery times. In fact, it has been reported that ketamine reduces the range of modulation frequencies that can be tracked by neurons in the mouse superior paraolivary nucleus (Felix et al ., ). Future studies in the bat cortex need to assess whether recovery times measured in awake bats are shorter than those described here (i.e., 80 ms).…”
Section: Discussionmentioning
confidence: 97%
“…Such effects may be achieved if inhibitory interneurons are considered in the network (Oliver and Morest 1984; Malmierca et al 2009). For example, a timed disinhibition mediated by the SPON would enhance the IC SAM response up to the MF limit of SPON neurons (Kuwada and Batra 1999; Kadner and Berrebi 2008; Felix et al 2012). In this scenario, abolishing the SPON input would unmask a potentially tonic inhibition from interneurons, which would smear the synchronization of the response without substantially affecting the overall spiking activity.…”
Section: Discussionmentioning
confidence: 99%