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A brain mechanism involved in mediated learning is identified

Neurone d’hippocampe Crédits: Inserm/Peris, Leticia

Imagine that you are eating a Granny apple under a red parasol on the terrace of a public garden. The next day you eat another Granny apple at home in your kitchen, but soon afterwards find yourself ill. The next time you go back to the public garden, you avoid sitting under that red parasol. While there may not seem to be a link between the parasol and the fact that you were ill, there actually is! This is an example of the mediated learning process, and researchers from INRA and INSERM have just identified the brain mechanism involved in it. Their results, published online on 30 August 2018 in Neuron, show that cannabinoid receptors in the hippocampus play a key role in establishing these types of associations.

Direct learning, which implies a specific link between information and positive or negative consequences, influences our future choices. However, our behaviour is most often guided by mediated learning, which is based on associations between seemingly insignificant information. This explains why we are often put off or attracted by people, places and things we have never directly associated with aversive (or positive) situations, but which were previously encountered along with other information that acquired an aversive or positive meaning. The apple and red parasol case is an example of this.

Receptors, neurons and the brain structure involved in mediated learning have been identified

While the neurobiological bases of direct learning have been thoroughly studied, understanding of mediated learning mechanisms remains rather limited. Researchers from INRA and INSERM began by establishing mediated learning behaviour models in mice in laboratory experiments. They repeatedly and simultaneously exposed mice to an odour (banana or almond) and a taste (sweet or salty) without a particular effect on the animal. They then associated the taste with a gastric malaise (similar to food poisoning). When the researchers later exposed the mice to the odour initially associated with this taste, they observed that the animals specifically avoided this odour, which showed a transfer of the aversive value between the taste and the odour. The scientists were able to demonstrate similar results with light and sound and the transfer between these sensory inputs of an attractive value (by giving the animals a reward), and thereby generalising the phenomenon.

The scientists were able to pinpoint the mechanism in question: the mediated learning process (between an odour and a taste or a light and a sound) involves the hippocampus and a major neuromodulatory system within this brain structure, called the endocannabinoid system. More specifically, this particular form of learning requires the involvement of type 1 cannabinoid receptors (CB1R) in hippocampal GABAergic neurons.

These unprecedented results will help researchers evaluate whether CB1R are also involved in other brain structures during mediated learning. This could lead to new research to understand certain pathologies (schizophrenia or psychosis) in which mediated learning is altered.

Researcher Contact
Guillaume FERREIRA Directeur de recherche Inra Unité mixte de recherche « Nutrition et Neurobiologie intégrée (NutriNeuro) » Inra, Université de Bordeaux Département scientifique « Alimentation humaine » Centre Inra Nouvelle Aquitaine - Bordeaux 05 57 57 12 32 rf.arni@arierref.emualliug   Giovanni MARSICANO Directeur de recherche Inserm NeuroCentre Magendie U 1215 INSERM - Université de Bordeaux Equipe « Endocannabinoids and Neuroadpatation » 33077 Bordeaux 05 57 57 37 56 rf.mresni@onacisram.innavoig
Press Contact
Service de presse de l'Inserm rf.mresni@esserp Service de presse de l'INRA rf.arni@esserp 01 42 75 91 86
Busquets-Garcia A, Oliveira da Cruz J, Terral G, Pagano Zottola AC, Soria-Gómez E, Contini A, Martin H, Redon B, Varilh M, Ioannidou C, Drago F, Massa F, Fioramonti X, Trifilieff P, Ferreira G*, Marsicano G* (2018). Hippocampal CB1 receptors control incidental associations. * contribution équivalente Neuron,