CPT1C is required for synaptic plasticity and oscillatory activity that supports motor, associative and non‐associative learning

Author:

Iborra‐Lázaro Guillermo1ORCID,Djebari Souhail1ORCID,Sánchez‐Rodríguez Irene1,Gratacòs‐Batlle Esther23ORCID,Sánchez‐Fernández Nuria2,Radošević Marija3,Casals Núria4ORCID,Navarro‐López Juan de Dios1ORCID,Soto del Cerro David23ORCID,Jiménez‐Díaz Lydia1ORCID

Affiliation:

1. Neurophysiology & Behaviour Laboratory, Regional Centre for Biomedical Research (CRIB), Faculty of Medicine of Ciudad Real University of Castilla‐La Mancha Ciudad Real Spain

2. Laboratory of Neurophysiology, Department of Biomedicine, Faculty of Medicine and Health Sciences, Institute of Neurosciences University of Barcelona Barcelona Spain

3. August Pi i Sunyer Biomedical Research Institute (IDIBAPS) Barcelona Spain

4. Basic Sciences Department, Faculty of Medicine and Health Sciences Universitat Internacional de Catalunya and Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y la Nutrición (CIBEROBN), Instituto de Salud Carlos III Barcelona Spain

Abstract

AbstractCarnitine palmitoyltransferase 1c (CPT1C) is a neuron‐specific protein widely distributed throughout the CNS and highly expressed in discrete brain areas including the hypothalamus, hippocampus, amygdala and different motor regions. Its deficiency has recently been shown to disrupt dendritic spine maturation and AMPA receptor synthesis and trafficking in the hippocampus, but its contribution to synaptic plasticity and cognitive learning and memory processes remains mostly unknown. Here, we aimed to explore the molecular, synaptic, neural network and behavioural role of CPT1C in cognition‐related functions by using CPT1C knockout (KO) mice. CPT1C‐deficient mice showed extensive learning and memory deficits. The CPT1C KO animals exhibited impaired motor and instrumental learning that seemed to be related, in part, to locomotor deficits and muscle weakness but not to mood alterations. In addition, CPT1C KO mice showed detrimental hippocampus‐dependent spatial and habituation memory, most probably attributable to inefficient dendritic spine maturation, impairments in long‐term plasticity at the CA3–CA1 synapse and aberrant cortical oscillatory activity. In conclusion, our results reveal that CPT1C is not only crucial for motor function, coordination and energy homeostasis, but also has a crucial role in the maintenance of learning and memory cognitive functions. imageKey points CPT1C, a neuron‐specific interactor protein involved in AMPA receptor synthesis and trafficking, was found to be highly expressed in the hippocampus, amygdala and various motor regions. CPT1C‐deficient animals exhibited energy deficits and impaired locomotion, but no mood changes were found. CPT1C deficiency disrupts hippocampal dendritic spine maturation and long‐term synaptic plasticity and reduces cortical γ oscillations. CPT1C was found to be crucial for motor, associative and non‐associative learning and memory.

Funder

Ministerio de Ciencia, Innovación y Universidades

Publisher

Wiley

Subject

Physiology

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