LSD degrades hippocampal spatial representations and suppresses hippocampal-visual cortical interactions
Carli Domenico, Daniel Haggerty, Xiang Mou, Daoyun Ji
Cell Reports September 17, 2021 DOI: 10.1016/j.celrep.2021.109714 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Observational study Peer reviewed |
|---|---|
| Population | Rats |
| Intervention | Lysergic acid diethylamide (LSD) |
| Topics | LSD |
| Keywords | Place cells Lysergic acid deithylamide Visual cortex Hippocampus Spatial navigation Hallucination |
| Citations | 16 |
| Key findings | LSD suppresses hippocampal-cortical interactions during active behavior and immobility, leading to degraded and isolated internal hippocampal representations that may contribute to abnormal perceptions. |
Abstract
Summary: Lysergic acid diethylamide (LSD) produces hallucinations, which are perceptions uncoupled from the external environment. How LSD alters neuronal activities in vivo that underlie abnormal perceptions is unknown. Here, we show that when rats run along a familiar track, hippocampal place cells under LSD reduce their firing rates, their directionality, and their interaction with visual cortical neurons. However, both hippocampal and visual cortical neurons temporarily increase firing rates during head-twitching, a behavioral signature of a hallucination-like state in rodents. When rats are immobile on the track, LSD enhances cortical firing synchrony in a state similar to the wakefulness-to-sleep transition, during which the hippocampal-cortical interaction remains dampened while hippocampal awake reactivation is maintained. Our results suggest that LSD suppresses hippocampal-cortical interactions during active behavior and during immobility, leading to internal hippocampal representations that are degraded and isolated from external sensory input. These effects may contribute to LSD-produced abnormal perceptions.