Prenatal exposure to modafinil alters behavioural response to methamphetamine in adult male mice
Language English Country United States Media print-electronic
Document type Journal Article
PubMed
29571720
DOI
10.1016/j.ijdevneu.2018.03.005
PII: S0736-5748(18)30012-1
Knihovny.cz E-resources
- Keywords
- Locomotion, Methamphetamine, Mice, Modafinil, Prenatal administration,
- MeSH
- Analysis of Variance MeSH
- Benzhydryl Compounds toxicity MeSH
- Phagocytosis drug effects MeSH
- Gestational Age MeSH
- Leukocytes drug effects MeSH
- Locomotion drug effects MeSH
- Methamphetamine pharmacology MeSH
- Modafinil MeSH
- Mice, Inbred ICR MeSH
- Mice MeSH
- Animals, Newborn MeSH
- Exploratory Behavior drug effects MeSH
- Motor Activity drug effects MeSH
- Wakefulness-Promoting Agents toxicity MeSH
- Central Nervous System Stimulants pharmacology MeSH
- Pregnancy MeSH
- Age Factors MeSH
- Prenatal Exposure Delayed Effects chemically induced physiopathology MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Pregnancy MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Benzhydryl Compounds MeSH
- Methamphetamine MeSH
- Modafinil MeSH
- Wakefulness-Promoting Agents MeSH
- Central Nervous System Stimulants MeSH
Modafinil is a psychostimulant drug prescribed for treatment of narcolepsy. However, it is used as a "smart drug" especially by young adults to increase wakefulness, concentration and mental performance. Therefore, it can also be used by women with childbearing potential and its developmental effects can become a concern. The aim of this study was to assess behavioural and immune effects of prenatal modafinil exposure in mice and to evaluate the reaction to methamphetamine exposure on these animals in adult age. Pregnant female mice were given either saline or modafinil (50 mg/kg orally) from gestation day (GD) 3 to GD 10 and then a challenge dose on GD 17. The male offspring were treated analogously at the age of 10 weeks with methamphetamine (2.5 mg/kg orally). Changes in the spontaneous locomotor/exploratory behaviour and anxiogenic profile in the open field test were assessed in naïve animals, after an acute and 8th modafinil dose and the challenge dose following a 7-day wash-out period. One month after completion of the behavioural study, the leukocyte phagocytosis was examined by zymosan induced and luminol-aided chemiluminiscence assay in vitro. The modafinil prenatally exposed mice showed basal hypolocomotion, increased anxiety, lower locomotor effect of acute methamphetamine and increased vulnerability to behavioural sensitization. The leukocyte activity did not show significant differences. Prenatal modafinil exposure alters basal behavioural profile, decreases acute effect of methamphetamine and enhances vulnerability to development of behavioural sensitization at adulthood. This may lead to higher vulnerability to development of addiction.
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