کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5555395 1559742 2017 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Suppression of pro-inflammatory cytokine expression and lack of anti-depressant-like effect of fluoxetine in lipopolysaccharide-treated old female mice
ترجمه فارسی عنوان
سرکوب بیان سیتوکین پروتئین التهابی و عدم اثرات ضد افسردگی فلوکستین در موش های صحرایی زن مبتلا به لیپوپلی ساکارید
کلمات کلیدی
فلوکستین، لیپوپلی ساکارید، سیتوکین، موش های قدیمی زن
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی ایمونولوژی
چکیده انگلیسی


- Fluoxetine did not reduce depressive behavior induced in senescent females by LPS injection.
- Fluoxetine attenuated LPS-induced expression of pro-inflammatory cytokines in the periphery and in the brain.
- Fluoxetine inhibited of proliferative activity of Con A-stimulated splenocytes.

Some antidepressants show a significantly lower efficacy in elderly patients, particularly in women. Previous studies have shown that antidepressants administered to young animals reduced depression-like symptoms induced by lipopolysaccharide (LPS). The aim of this study was to find out whether the antidepressant and anti-inflammatory properties of fluoxetine (FLU) can be observed also in old female C57BL/6J mice. A depression-like state was evoked by the administration of LPS (100 μg/kg for 4 consecutive days) which was followed by reduction of sucrose preference (anhedonia) and enhancement of immobility-time in the forced swim test (FST). Animals, which received FLU (10 mg/kg, 11 days) exhibited a decreased LPS-induced expression of some inflammatory cytokines in the hippocampus and spleen but this effect was not accompanied by beneficial changes in animals' behavior. Despite the lack of antidepressant-properties of FLU in this model, our studies have proven significant profound anti-inflammatory properties of chronic FLU treatment which may suggest its suitability for fending off inflammatory processes in the elderly.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Immunopharmacology - Volume 48, July 2017, Pages 35-42
نویسندگان
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