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Do the effects of prenatal exposure and acute treatment of methamphetamine on anxiety vary depending on the animal model used
R. Šlamberová, M. Pometlová, E. Macúchová, K. Nohejlová, A. Stuchlík, K. Valeš,
Language English Country Netherlands
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NT14484
MZ0
CEP Register
- MeSH
- Interpersonal Relations MeSH
- Rats MeSH
- Methamphetamine administration & dosage MeSH
- Disease Models, Animal * MeSH
- Motor Activity drug effects MeSH
- Rats, Wistar MeSH
- Pregnancy MeSH
- Anxiety chemically induced MeSH
- Vocalization, Animal drug effects MeSH
- Prenatal Exposure Delayed Effects chemically induced psychology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Pregnancy MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The aim of the present study was an evaluation of prenatal exposure to acute methamphetamine (MA) treatment on manifestations of anxiety. Anxiety was evaluated in adult animals in three different experimental models: the Elevated plus-maze (EPM), Social interaction test (SIT) and Ultrasound vocalization (USV). Female rats were administered saline (S) or MA (5 mg/kg) daily throughout their entire gestation period. The male progeny, in adulthood, were administered with challenge dose of S or MA (1 mg/kg) prior to evaluation of anxiety. The study demonstrated that prenatal MA exposure increased the anxiogenic effect on evaluated behaviour patterns in the USV model and to a lesser degree in the EPM model. In addition, the acute MA challenge in adulthood decreased the time spent during social interaction suggesting an anxiogenic effect in the SIT model as well. On the other hand, some of the evaluated parameters (e.g. the number of head-dipping in the EPM and number of dropped boluses in the SIT) also suggest MA-induced anxiolytic effects. Sensitization to a MA challenge was apparent in several parameters of the EPM (e.g. increased number of entries to the closed arms, increased stretched attend postures and increased approach-avoid conflicts) and SIT (total social interaction and following). The present data demonstrate that prenatal MA exposure and adult challenge of the same drug have diverse effects on animal behaviour that depends on the type of anxiety model used.
References provided by Crossref.org
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