BLOCKING THE ACQUISITION OF ETHANOL-INDUCED CONDITIONED PLACE PREFERENCE WITH 11, 21-BISPHENYL-19-NORPREGNANE (PT150) IN COTURNIX QUAIL
2022
- 164Usage
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Usage164
- Downloads117
- Abstract Views47
Thesis / Dissertation Description
Alcohol use disorder (AUD) has been associated with a dysregulated stress system. Therefore, regulating stress hormones has been investigated as a potential therapeutic target for AUDs. The purpose of the current study was to investigate whether a stress hormone receptor antagonist, PT150, would block the rewarding properties of ethanol. Quail were used as subjects because a conditioned place preference (CPP) apparatus that utilized visual cues was used, and quail readily attend to visual cues. Visual cues in the environment have been shown to become associated with alcohol effects and later induce craving. Starting on day one, quail were pretreated with vehicle or PT150 (20mg/kg). Thirty minutes later, quail received a treatment of either water or ethanol (0.75g/kg) and were placed in their initially least preferred side as determined by a preference test. On alternate days, all quail received pretreatment and treatment of water. Results revealed pretreatment of PT150 blocked the acquisition of a place preference in quail that were treated with ethanol. This further supports that PT150 is highly selective at blocking CORT without causing peripheral effects associated with ethanol consumption. These preliminary findings suggest that PT150 may reduce the rewarding properties of ethanol by blocking the stress hormone receptor.
Bibliographic Details
University of Kentucky Libraries
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