TY - JOUR
T1 - Inhibition is a prevalent mode of activity in the neocortex around awake hippocampal ripples in mice
AU - Abadchi, Javad Karimi
AU - Rezaei, Zahra
AU - Knöpfel, Thomas
AU - McNaughton, Bruce L.
AU - Mohajerani, Majid H.
N1 - Publisher Copyright:
© Karimi Abadchi et al.
PY - 2023/1/25
Y1 - 2023/1/25
N2 - Coordinated peri-ripple activity in the hippocampal-neocortical network is essential for mnemonic information processing in the brain. Hippocampal ripples likely serve different functions in sleep and awake states. Thus, the corresponding neocortical activity patterns may differ in important ways. We addressed this possibility by conducting voltage and glutamate wide-field imaging of the neocortex with concurrent hippocampal electrophysiology in awake mice. Contrary to our previously published sleep results, deactivation and activation were dominant in post-ripple neocortical voltage and glutamate activity, respectively, especially in the agranular retrosplenial cortex (aRSC). Addi-tionally, the spiking activity of aRSC neurons, estimated by two-photon calcium imaging, revealed the existence of two subpopulations of excitatory neurons with opposite peri-ripple modulation patterns: one increases and the other decreases firing rate. These differences in peri-ripple spatio-temporal patterns of neocortical activity in sleep versus awake states might underlie the reported differences in the function of sleep versus awake ripples.
AB - Coordinated peri-ripple activity in the hippocampal-neocortical network is essential for mnemonic information processing in the brain. Hippocampal ripples likely serve different functions in sleep and awake states. Thus, the corresponding neocortical activity patterns may differ in important ways. We addressed this possibility by conducting voltage and glutamate wide-field imaging of the neocortex with concurrent hippocampal electrophysiology in awake mice. Contrary to our previously published sleep results, deactivation and activation were dominant in post-ripple neocortical voltage and glutamate activity, respectively, especially in the agranular retrosplenial cortex (aRSC). Addi-tionally, the spiking activity of aRSC neurons, estimated by two-photon calcium imaging, revealed the existence of two subpopulations of excitatory neurons with opposite peri-ripple modulation patterns: one increases and the other decreases firing rate. These differences in peri-ripple spatio-temporal patterns of neocortical activity in sleep versus awake states might underlie the reported differences in the function of sleep versus awake ripples.
UR - http://www.scopus.com/inward/record.url?scp=85146858037&partnerID=8YFLogxK
U2 - 10.7554/eLife.79513
DO - 10.7554/eLife.79513
M3 - Journal article
C2 - 36645126
AN - SCOPUS:85146858037
SN - 2050-084X
VL - 12
JO - eLife
JF - eLife
M1 - e79513
ER -