کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6261594 1613232 2016 10 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Guanosine may increase absence epileptic activity by means of A2A adenosine receptors in Wistar Albino Glaxo Rijswijk rats
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب سلولی و مولکولی
پیش نمایش صفحه اول مقاله
Guanosine may increase absence epileptic activity by means of A2A adenosine receptors in Wistar Albino Glaxo Rijswijk rats
چکیده انگلیسی


- i.p. 50 mg/kg Guo decreased the number of spike-wave discharges (SWDs).
- i.p. 100 mg/kg Guo enhanced the number of SWDs in WAG/Rij rats.
- Effect of 100 mg/kg Guo was inhibited by theophylline, SCH 58261 and indomethacin.
- i.p. 100 mg/kg Guo may increase SWD number by means of adenosinergic system.

The non-adenosine nucleoside guanosine (Guo) was demonstrated to decrease quinolinic acid(QA)-induced seizures, spontaneously emerged absence epileptic seizures and lipopolysaccharide(LPS)-evoked induction of absence epileptic seizures suggesting its antiepileptic potential. It was also described previously that intraperitoneal (i.p.) injection of 20 and 50 mg/kg Guo decreased the number of spike-wave discharges (SWDs) in a well investigated model of human absence epilepsy, the Wistar Albino Glaxo Rijswijk (WAG/Rij) rats during 4th (20 mg/kg Guo) and 3rd as well as 4th (50 mg/kg Guo) measuring hours. Guanosine can potentially decrease SWD number by means of its putative receptors but absence epileptic activity changing effects of Guo by means of increased extracellular adenosine (Ado) cannot be excluded. An increase in the dose of i.p. injected Guo is limited by its low solubility in saline, therefore, we addressed in the present study whether higher doses of Guo, diluted in sodium hydroxide (NaOH) solution, have more potent antiepileptic effect in WAG/Rij rats. We confirmed that i.p. 50 mg/kg Guo decreased but, surprisingly, i.p. 100 mg/kg Guo enhanced the number of SWDs in WAG/Rij rats. Combined i.p. injection of a non-selective Ado receptor antagonist theophylline (5 mg/kg) or a selective Ado A2A receptor (A2AR) antagonist SCH 58261 (7-(2-phenylethyl)-5-amino-2-(2-furyl)-pyrazolo-[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine) (1 mg/kg) and a cyclooxygenase 1 and 2/COX-1 and COX-2 inhibitor indomethacin (10 mg/kg) with 100 mg/kg Guo decreased the SWD number compared to i.p. 100 mg/kg Guo alone. The results suggest that i.p. 100 mg/kg Guo can increase SWD number by means of the adenosinergic system.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research Bulletin - Volume 124, June 2016, Pages 172-181
نویسندگان
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