First by using conditional mutagenesis we found that mice lacking CB1 receptors in D1-positive cells (D1-CB1-KO) displayed impairment in long-term, but not short-term, novel object recognition memory (NOR). (2/n)
Then we observed that cre-dependent re-expression of CB1 receptors in hippocampal, but not striatal, D1-positive cells rescued the NOR memory deficit. (3/n)
In addition we found that exposure to the NOR task could lead to a learning induced facilitation of in vivo hippocampal long-term potentiation ( #LTP) and we also observed that this phenomenon was absent in our mouse model. (4/n)
Finally we used #chemogenetic and #pharmacological approaches to show that both CB1 receptor-mediated NOR and associated LTP facilitation involved the local control of GABAergic inhibition in a D1-dependent manner. (5/n)
Altogether our study provides new evidence about the
CB1 receptor signaling and its functional link between hippocampal #dopaminergic and #GABAergic control of #synaptic #plasticity and #memory #consolidation. (6/n)
Happy to be part of this collaborative effort with @BGarcialab , @soria_edgar, all the remaining members of @MarsicanoLab and staff of the @NCMagendie !

And this closes my "PhD life chapter" at the @MarsicanoLab. Great lab, great mentorship and great people!
Last but not least mention to all the funding entities involved:
@Inserm
@Neuro_Bordeaux
@NCMagendie
@univbordeaux
@ERC_Research
@FRM_officiel
@AgenceRecherche
@Ikerbasque
You can follow @jfo_cruz.
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