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Der Einfluss serotonerger Aktivität in der Amygdala bei prosozialem Verhalten von Ratten

Fachliche Zuordnung Allgemeine, Kognitive und Mathematische Psychologie
Förderung Förderung von 2013 bis 2019
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 237274537
 
Erstellungsjahr 2020

Zusammenfassung der Projektergebnisse

Humans are social animals. We accept costs to help others, even if we don’t obtain immediate or future benefits from our altruistic actions, even if we don’t know the recipient of our help, and even if the recipient will never repay the favour. Such social behaviour is a puzzle for economists, psychologists and evolutionary biologists alike: why do people consider the well‐being of others? Why do they voluntarily reduce their own evolutionary fitness to increasing someone else’s? Interestingly, not only human decision‐makers, but also non‐human animals often reveal social preferences. Judging by face validity, humans and some animal species have very similar, maybe even identical social cognitions. Therefore, one promising avenue to understand the cognitive, neural and evolutionary underpinnings of social decision‐making is to investigate animal social behavior. This was the primary goal of the projects conducted during the two funding period. In these two funding periods, we developed a Rodent Prosocial Choice Task (PCT) to investigate a special type of prosocial behavior in rats - mutual‐reward preferences (preference for a reward distribution that benefit the ‘actor’ rat and a conspecific over a distribution that benefits only the actor rat, not the conspecific). Using this task, we provided evidence that rats show advantageous (aversion against being better off than a conspecific and disadvantageous inequity aversion (aversion against being worse off than a conspecific. We argued that mutualreward preferences do not necessarily require empathy, but may be the result of social reinforcement learning where social signals, e.g., ultrasonic vocalizations, emitted by the conspecific receiving reward might reinforce those behaviors in the actor rat that produce rewards to conspecifics. We furthermore found that the integrity of basolateral amygdala (BLA) was necessary for expressing mutual‐reward preferences. This finding has translational value as a potential animal model for studying callousness – a trait characteristic for several psychiatric conditions, including conduct disorder and psychopathy. The role of the amygdala in orchestrating social behavior was corroborated in another study showing that lesions of BLA abolished the behavioral responses to ultrasonic vocalizations - the main candidate for social reinforcement learning in the PCT. We also demonstrated that psychopharmacological microinjections of a serotonin receptor agonist locally into BLA, boosting serotonin action in the amygdala, increased rat mutual‐reward tendencies in the PCT. Finally, we found no evidence for a correlation between mutual‐reward preferences and time preferences (delay discounting), possibly because of power concerns (too small effect size for a manageable sample size). In summary, our set of studies demonstrated that rats reveal two special kinds of social preferences - mutual‐reward preferences and inequity aversion which are likely the result of social reinforcement learning. Mutual‐reward preferences are amygdala‐dependent and can be fostered by increasing serotonin‐action in the amygdala. The two funding period resulted in the completion of two doctorates (Dr. Julen Hernandez‐Lallement, PhD defense in 2016 and Dr. Lina Oberließen, PhD defense in 2019).

Projektbezogene Publikationen (Auswahl)

 
 

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