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Manzanares-Sierra, I.

Publications and source records attributed to Manzanares-Sierra, I..

2 recordsLinked to original sources

Dorsal hippocampus mediates light-tone sensory preconditioning task in mice

Daily choices are often influenced by environmental cues that are not directly associated with reinforcers. This phenomenon, known as higher-order conditioning, can be studied using sensory preconditioning tasks in rodents. This behavioral paradigm involves the repeated pairing of two innocuous stimuli, such as a light and a tone, followed by a devaluation phase in which one stimulus is associated with an unconditioned stimulus, such as a mild foot-shock. The result is a conditioned response (e.g., freezing) to both the conditioned stimulus (direct learning) and the non-conditioned stimulus (mediated learning). In our study, we successfully established a light-tone sensory preconditioning task specifically in male mice, as sex differences were observed in both control experimental groups and in sensory preconditioning responses. We employed in vivo, freely moving fiber photometry to monitor neural activity in the dorsal and ventral subregions of the hippocampus in male mice during the formation of associations between innocuous stimuli and reinforcers. Additionally, we combined our sensory preconditioning task with chemogenetic approaches to investigate the roles of these hippocampal subregions in sensory preconditioning. Our results indicate that dorsal, but not ventral, CaMKII-positive neurons are involved in encoding innocuous stimuli during the preconditioning phase. Overall, we developed a novel light-tone sensory preconditioning protocol in male mice, enabling the detection of sex differences and furthering our understanding of how specific hippocampal subregions and cell types regulate complex cognitive processes.

neuroscience↗

A low repeated dose of Δ9-tetrahydrocannabinol affects memory performance through serotonergic signalling in mice

Cannabis is the most widely used illicit drug worldwide. Its principal psychoactive component, {Delta}9-tetrahydrocannabinol (THC), acts as a partial agonist of the main cannabinoid receptor in the brain, the cannabinoid type-1 receptor (CB1R), that is responsible for the central effects of THC including memory impairment. CB1Rs may form heterodimers with the serotonin 5-HT2A receptor (5-HT2AR) which were found responsible for the memory impairment produced by acute high dose of THC in mice. In this study we investigated whether a repeated low dose of THC (1 mg/kg), with no acute consequence on memory performance, could eventually have deleterious cognitive effects. We found that this dose of THC impaired novel object-recognition memory and fear conditioning memory 24 h after the last of 7 consecutive daily treatments. At that time, a general enhancement of c-Fos expression was also observed in several brain regions of THC-exposed animals, as well as a decreased dendritic spine density on hippocampal CA1 pyramidal neurons that was accompanied by reduced long-term potentiation (LTP) at Schaffer collateral-CA1 synapses. Interestingly, an up-regulation in the expression of CB1R/5-HT2AR heterodimers was observed in the hippocampus after THC exposure and pre-treatment with the 5-HT2AR antagonist MDL 100,907 (0.01 mg/kg) prevented the enhanced heterodimerization and the THC-associated memory impairment. Together, these results reveal the significance of serotonergic signalling through 5-HT2ARs in the memory-impairing effects of repeated low doses of THC.

neuroscience↗