Do the effects of prenatal exposure and acute treatment of methamphetamine on anxiety vary depending on the animal model used?
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26149414
DOI
10.1016/j.bbr.2015.07.001
PII: S0166-4328(15)30072-3
Knihovny.cz E-zdroje
- Klíčová slova
- Anxiety, Drug abuse, Elevated plus-maze, Methamphetamine, Prenatal exposure, Social interaction text, Ultrasound vocalization,
- MeSH
- interpersonální vztahy MeSH
- krysa rodu Rattus MeSH
- methamfetamin aplikace a dávkování MeSH
- modely nemocí na zvířatech * MeSH
- pohybová aktivita účinky léků MeSH
- potkani Wistar MeSH
- těhotenství MeSH
- úzkost chemicky indukované MeSH
- vokalizace zvířat účinky léků MeSH
- zpožděný efekt prenatální expozice chemicky indukované psychologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- methamfetamin 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.
Citace poskytuje Crossref.org
Prenatal Exposure to Methamphetamine: Up-Regulation of Brain Receptor Genes