دانلود مقاله ISI انگلیسی شماره 153611
ترجمه فارسی عنوان مقاله

اثرات متقابل وابسته به زمان کافئین، دیازپام و اتانول بر روی رفتار ماهیان زینتی

عنوان انگلیسی
Time-dependent interacting effects of caffeine, diazepam, and ethanol on zebrafish behaviour
کد مقاله سال انتشار تعداد صفحات مقاله انگلیسی
153611 2017 12 صفحه PDF
منبع

Publisher : Elsevier - Science Direct (الزویر - ساینس دایرکت)

Journal : Progress in Neuro-Psychopharmacology and Biological Psychiatry, Volume 75, 3 April 2017, Pages 16-27

ترجمه کلمات کلیدی
کافئین، دیازپام، اتانول، تعاملات دارویی، تغییرات رفتاری وابسته به زمان،
کلمات کلیدی انگلیسی
Caffeine; Diazepam; Ethanol; Drug interaction; Time-dependent behavioural changes;
پیش نمایش مقاله
پیش نمایش مقاله  اثرات متقابل وابسته به زمان کافئین، دیازپام و اتانول بر روی رفتار ماهیان زینتی

چکیده انگلیسی

Zebrafish have become a popular animal model for behavioural pharmacology due to their small size, rapid development, and amenability to high throughput behavioural drug screens. Furthermore, water-soluble compounds can be administered via immersion of the fish in the drug solution, which provides a non-invasive drug delivery method. Numerous studies have demonstrated stimulant effects of alcohol. Diazepam and caffeine, on the other hand have been found to have inhibitory effect on locomotor activity in zebrafish. However, the time-dependent changes induced by these psychoactive drugs are rarely reported, and potential drug interactions have not been examined in zebrafish, despite the translational relevance of this question. In the current study, we examine time- and dose-dependent changes in zebrafish following exposure to caffeine, diazepam, and ethanol quantifying four different behavioural parameters over a 30 min recording session. We subsequently analyze potential drug-drug interactions by co-administering the three drugs in different combinations. Our time-course and dose-response analyses for each of the three drugs represent so far the most detailed studies available serving as a foundation for future psychopharmacology experiments with zebrafish. Furthermore, we report significant interactions between the three drugs corroborating findings obtained with rodent models as well as in humans, providing translational relevance for the zebrafish model.