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    •   صفحهٔ اصلی
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    • Journal of Basic and Clinical Pathophysiology
    • Volume 1, Issue 2
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Journal of Basic and Clinical Pathophysiology
    • Volume 1, Issue 2
    • مشاهده مورد
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    Copper sulfate inhibits seizure activity induced by pentylenetetrazole in mice

    (ندگان)پدیدآور
    Palizvan, Mohammad RezaJand, AbolfazlTaherinejad, Mohammad Reza
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    نوع مدرک
    Text
    Research Paper
    زبان مدرک
    English
    نمایش کامل رکورد
    چکیده
    Background and Objective: Copper is one of the main micronutrients of body which plays a key role as a cofactor in the function of metabolic enzymes. Previous studies have shown that copper sulfate () inhibits long-term potentiation (LTP) in slices of hippocampal CA1 region. Whereas LTP is involved in learning and epilepsy, it seems that copper effects on LTP could be associated with its effects on epilepsy and seizure. Therefore, the aim of this study was to evaluate the effect of  on seizure induced by pentylenetetrazole (PTZ).     Materials and Methods: The effect of various doses of CuSO4 (10, 50 and 100 mg/kg, i.p.), saline (as a control group) or sodium valproate (50, 150 and 100 mg/kg, i.p.) on seizure parameters induced by PTZ (100 mg/kg i.p.) was evaluated in NMRI mice. Twenty minutes after injection of saline or , PTZ (100 mg/kg) was injected to induce seizures in animals and seizure parameters were recorded. Results: Comparison of the effect of , saline or sodium valproate on seizure parameters such as stage 2 latency, stage 5 latency and stage 5 duration showed that  dose-dependently reduced seizure. Conclusion: This study showed that  significantly inhibits seizure parameters compared with the saline and sodium valproate.
    کلید واژگان
    Copper sulfate Seizure Pentylenetetrazole Valproic acid

    شماره نشریه
    2
    تاریخ نشر
    2013-12-01
    1392-09-10
    ناشر
    Shahed University
    سازمان پدید آورنده
    Department of Physiology, Faculty of Medicine, Arak University of Medical Sciences.
    Department of Physiology, Faculty of Medicine, Arak University of medical Sciences.
    Department of Physiology, Faculty of Medicine, Arak University of medical Sciences.

    شاپا
    2322-1895
    2345-4334
    URI
    http://jbcp.shahed.ac.ir/article_37.html
    https://iranjournals.nlai.ir/handle/123456789/286290

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