RT Journal Article
SR Electronic
T1 Movement and VIP Interneuron Activation Differentially Modulate Encoding in Mouse Auditory Cortex
JF eneuro
JO eNeuro
FD Society for Neuroscience
SP ENEURO.0164-19.2019
DO 10.1523/ENEURO.0164-19.2019
VO 6
IS 5
A1 James Bigelow
A1 Ryan J. Morrill
A1 Jefferson Dekloe
A1 Andrea R. Hasenstaub
YR 2019
UL http://www.eneuro.org/content/6/5/ENEURO.0164-19.2019.abstract
AB Information processing in sensory cortex is highly sensitive to nonsensory variables such as anesthetic state, arousal, and task engagement. Recent work in mouse visual cortex suggests that evoked firing rates, stimulus–response mutual information, and encoding efficiency increase when animals are engaged in movement. A disinhibitory circuit appears central to this change: inhibitory neurons expressing vasoactive intestinal peptide (VIP) are activated during movement and disinhibit pyramidal cells by suppressing other inhibitory interneurons. Paradoxically, although movement activates a similar disinhibitory circuit in auditory cortex (ACtx), most ACtx studies report reduced spiking during movement. It is unclear whether the resulting changes in spike rates result in corresponding changes in stimulus–response mutual information. We examined ACtx responses evoked by tone cloud stimuli, in awake mice of both sexes, during spontaneous movement and still conditions. VIP+ cells were optogenetically activated on half of trials, permitting independent analysis of the consequences of movement and VIP activation, as well as their intersection. Movement decreased stimulus-related spike rates as well as mutual information and encoding efficiency. VIP interneuron activation tended to increase stimulus-evoked spike rates but not stimulus–response mutual information, thus reducing encoding efficiency. The intersection of movement and VIP activation was largely consistent with a linear combination of these main effects: VIP activation recovered movement-induced reduction in spike rates, but not information transfer.