María Ángeles Martínez-Caballero , Claudia Calpe-López , María Pilar García-Pardo , María Carmen Arenas , Carmen Manzanedo , María Asunción Aguilar
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引用次数: 0
Abstract
Several studies have demonstrated that exposure to different protocols of social defeat induces anxiety- and depression-like symptoms in male and female mice. Moreover, male mice exposed to an intermittent social defeat (ISD) show increased vulnerability to the rewarding effects of cocaine, although several behavioural traits have been found to confer resilience against this effect. However, the effects of ISD on the vulnerability to drugs of abuse in female mice have not been studied. Thus, our aim was to evaluate the short-term behavioural effects of ISD and its long-term influence on the rewarding effects of cocaine in female mice. Intruder female mice were exposed to an ISD protocol and performed the elevated plus maze, hole-board, social interaction, splash, object recognition and tail suspension tests 24 or 48 h after the last episode of defeat. Three weeks later, female mice underwent the conditioned place preference procedure with cocaine. ISD exposure induced a slight anxiogenic effect, decreased novelty-seeking behaviour and enhanced sensitivity to the conditioned rewarding effects of cocaine. However, defeated female mice characterized by an active coping response during episodes of defeat and an avoidance of potential dangers in unknown environments did not develop cocaine preference. Our results show that defeat in an inter-female aggression protocol is a useful way to study the long-term consequences of social stress on cocaine reward and the behavioural traits associated with resilience.
期刊介绍:
Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.