کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
8529635 1558861 2018 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Effects of the new psychoactive substances diclofensine, diphenidine, and methoxphenidine on monoaminergic systems
ترجمه فارسی عنوان
اثرات داروهای جدید روانگردان، دیکلوفسین، دیفنیدین و متکسافنیدین بر سیستم های مونو آمینیریک
کلمات کلیدی
دیکلوفنسین، دیفنیدین، متوقفنیدین، ماده روانگردان جدید، مونوآمین،
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب سلولی و مولکولی
چکیده انگلیسی
Diclofensine, diphenidine, and methoxphenidine are new psychoactive substances (NPSs) that recently appeared on the illicit drug market. Pharmacological profiling of such newly emerged drugs is crucial for a better understanding of their psychotropic effects and toxicity. We therefore investigated the potential of these NPSs to inhibit the norepinephrine, dopamine, and serotonin transporters in human embryonic kidney cells stably transfected with the respective transporters. In addition, we determined monoamine transporter and receptor affinities for the substances. Diclofensine potently bound to the monoamine transporters in the submicromolar range and had similar inhibition potential for all three transporters in the range of 2.5-4.8 μM. Moreover, diclofensine bound to adrenergic, dopamine, serotonin, and trace amine-associated receptors. Diphenidine was an equipotent inhibitor of the norepinephrine and dopamine transporters in the low micromolar range and a very weak inhibitor of the serotonin transporter. Besides binding to transporters, diphenidine bound to adrenergic α1A and α2A receptors and serotonin 5-hydroxytryptamine 1A (5-HT1A) and 5-HT2A receptors in the range of 4-11 μM. Methoxphenidine bound to all transporters, but considerable inhibition (IC50 < 10 μM) was observed only for the norepinephrine transporter. Moreover, methoxphenidine bound to adrenergic α2A and serotonin 5-HT2A and 5-HT2C receptors in the range of 2.5-8.2 μM. None of the test drugs mediated substrate-type efflux of monoamines. These data demonstrate that the monoamine transporter inhibition and receptor interactions most likely mediate the psychoactive effects of diclofensine and possibly play a contributory role for diphenidine and methoxphenidine.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Pharmacology - Volume 819, 15 January 2018, Pages 242-247
نویسندگان
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