bioRxiv Science⌕ Search

Biology subjects

Kayumova, R.

Publications and source records attributed to Kayumova, R..

2 recordsLinked to original sources

Circuit-specific reorganization of hippocampal-entorhinal-prefrontal subnetworks supports memory recall across the lifespan

How memories reorganize across brain circuits as they age remains a central question in systems neuroscience. Systems consolidation is thought to progressively shift memory reliance from the hippocampus to distributed cortical networks, yet the contribution of cortical regions beyond the prefrontal cortex and the nature of this shift remains unclear. Here we define the circuit-level organization of remote memory recall across entorhinal, prefrontal, and hippocampal subregions. Using high-resolution activity mapping combined with causal manipulations that leverage natural memory decay, we adapted a murine object-location paradigm to examine memory recall across the lifespan. We find that recall of early remote memories (1 month) selectively depends on a LEC-hippocampal (CA1/CA3) circuit, whereas recall of older memories (6-12 months) recruits a distinct and broader network involving both LEC and MEC together with ACC and CA1. These findings reveal a temporally ordered, circuit-specific reconfiguration of hippocampo-cortical networks and identify the EC as a dynamic hub in remote memory retrieval. Our results refine prevailing systems consolidation theories by showing that memory consolidation is a circuit-specific and temporally ordered process, rather than a passive gradual phenomenon, and position the EC as a central and dynamic component of remote memory retrieval alongside the PFC. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=123 SRC="FIGDIR/small/743925v1_ufig.gif" ALT="Figure 1"> View larger version (30K): org.highwire.dtl.DTLVardef@11d2922org.highwire.dtl.DTLVardef@177b02borg.highwire.dtl.DTLVardef@cf0a11org.highwire.dtl.DTLVardef@9e0668_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗

A VTA-pontine GABA pathway biases backward locomotion via local and distal inhibition

Locomotor direction in mammals is implemented by descending circuits, yet how midbrain selection systems bias directional motor output remains unclear. Here we define a projection-defined inhibitory pathway from the ventral tegmental area to the oral pontine reticular nucleus (VTAPnO) whose activation is sufficient to drive backward locomotion. These TH- VTA neurons form monosynaptic GABAA synapses locally while projecting to PnO, establishing a dual local-projection inhibitory architecture. Somatic activation reliably induced backward locomotion, and selective stimulation of VTAPnO terminals reproduced the effect. Pathway recruitment produced a rapid transient increase in dopaminergic single-unit activity and frequency-dependent increases in dopaminergic population calcium signals in awake mice. During forced locomotion, chronically recorded VTAPnO neurons were preferentially engaged during reverse compared to forward rotations. Together, these findings reveal a projection-defined midbrain pathway that biases locomotor direction through coordinated local inhibition and distal engagement of a brainstem premotor node.

neuroscience↗