کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9921343 | 1559214 | 2005 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Allosteric modulation of 5-HT3 serotonin receptors
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موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب سلولی و مولکولی
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چکیده انگلیسی
[3H]Granisetron binding to 5-HT3 type serotonin receptors was examined in homogenates of rat forebrain and NG 108-15 cells. We have applied an allosteric model to 5-HT3 receptor binding for the first time. Slope factors of displacement improved the modelling. Serotonin displaced [3H]granisetron binding with micromolar potency in forebrain and with nanomolar potency in NG 108-15 cells. Racemic and (+)verapamil, ifenprodil and GYKI-46903 were used as representative allosteric inhibitors of 5-HT3 receptors. They displaced [3H]granisetron binding with great negative cooperativity (α > 10) and exerted great negative cooperativity with serotonin binding (β > 10). Great negative cooperativity of these agents with serotonin and [3H]granisetron binding cannot be distinguished from dual competitive displacement. Trichloroethanol (data from literature) had no cooperativity with [3H]granisetron binding (α ~ 1) and exhibit positive cooperativity with serotonin (β < 1) in displacement. The allosteric model can lead to a more quantitative method in vitro to develop allosteric agents for 5-HT3 receptors.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: European Journal of Pharmacology - Volume 514, Issue 1, 2 May 2005, Pages 17-24
Journal: European Journal of Pharmacology - Volume 514, Issue 1, 2 May 2005, Pages 17-24
نویسندگان
Gábor Maksay, TÃmea BÃró, Gyula Bugovics,