Does prenatal methamphetamine exposure affect the drug-seeking behavior of adult male rats?
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21645557
DOI
10.1016/j.bbr.2011.05.021
PII: S0166-4328(11)00410-4
Knihovny.cz E-zdroje
- MeSH
- amfetamin škodlivé účinky MeSH
- analýza rozptylu MeSH
- dopaminové látky škodlivé účinky MeSH
- kokain škodlivé účinky MeSH
- krysa rodu Rattus MeSH
- methamfetamin škodlivé účinky MeSH
- modely nemocí na zvířatech MeSH
- operantní podmiňování účinky léků MeSH
- poruchy spojené s užíváním psychoaktivních látek etiologie patofyziologie psychologie MeSH
- potkani Wistar MeSH
- těhotenství MeSH
- tělesná hmotnost účinky léků MeSH
- zpožděný efekt prenatální expozice chemicky indukované patofyziologie 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
- amfetamin MeSH
- dopaminové látky MeSH
- kokain MeSH
- methamfetamin MeSH
Methamphetamine (MA) is one of the most frequently used illicit drugs worldwide and also one of the most common drugs abused by pregnant women. Repeated administration of psychostimulants induces behavioral sensitization in response to treatment of the same or related drugs in rodents. The effect of prenatal MA exposure on sensitivity to drugs in adulthood is not yet fully determined. Because our most recent studies demonstrated that prenatal MA (5mg/kg) exposure makes adult rats more sensitive to acute injection of the same drug, we were interested whether the increased sensitivity corresponds with the increased drug-seeking behavior. The aim of the present study was to examine the effect of prenatal MA exposure on drug-seeking behavior of adult male rats tested in the conditioned place preference (CPP). The following psychostimulant drugs were used as a challenge in adulthood: MA (5mg/kg), amphetamine (5mg/kg) and cocaine (10mg/kg). All psychostimulant drugs induced increased drug-seeking behavior in adult male rats. However, while MA and amphetamine-induced increase in drug-seeking behavior did not differ based on the prenatal drug exposure, prenatally MA-exposed rats displayed tolerance effect to cocaine in adulthood. In addition, prenatally MA-exposed rats had decreased weight gain after administration of MA or amphetamine, while the weight of prenatally MA-exposed rats stayed unchanged after cocaine administration. Defecation was increased by all the drugs (MA, amphetamine and cocaine), while only amphetamine increased the tail temperature. In conclusion, our results did not confirm our hypothesis that prenatal MA exposure increases drug-seeking behavior in adulthood in the CPP test.
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