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العنوان
Study of the possible protective effects of apigenin and plumbagin in hepatic ischemia-reperfusion injury in rats /
الناشر
Aya Mohamed Zaki Eid ,
المؤلف
Aya Mohamed Zaki Eid
هيئة الاعداد
باحث / Aya Mohamed Zaki Eid
مشرف / Hala Fahmy Zaki
مشرف / Rania Mohsen Abdelsalam
مشرف / Dalia Moustafa Eltanbouly
مناقش / Mostafa Adel Mohamed
تاريخ النشر
2018
عدد الصفحات
168 P. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الصيدلة ، علم السموم والصيدلانيات (المتنوعة)
تاريخ الإجازة
18/2/2018
مكان الإجازة
جامعة القاهرة - كلية الصيدلة - Pharmacology and Toxicology
الفهرس
Only 14 pages are availabe for public view

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from 185

Abstract

Ischemia-reperfusion (I/R) injury is a pathological process which magnifies with the ensuing inflammatory response and endures with the increase of oxidants especially during reperfusion. The present study was conducted to assess the possible modulatory effects of two biologically active constituents of plant origin named apigenin and plumbagin, where the former is the active constituent extracted from the roots of traditional medicinal plant Plumbago zeylanica L and the latter is a flavonoid that exists abundantly in numerous herbs and vegetables, including chamomile, thyme, parsley and broccoli., on the dire role of high mobility group box (HMGB1) as well as the associated inflammation, oxidative stress and apoptotic cell death following hepatic I/R. Six groups of rats were included: sham operated, sham operated treated with apigenin, sham operated treated with plumbagin, I/R (30 min ischemia and 1 h reperfusion) , I/R treated with apigenin and I/R treated with plumbagin. Pretreatment with apigenin and plumbagin markedly improved hepatic function and histology, as indicated by reduced transaminase levels, lactate dehydrogenase activity and ameliorated tissue pathological changes. They significantly reduced high mobility group box 1 (HMGB1) expression and subsequently suppressed inflammatory cascades, as liver NF-mB and TNF-Ü as well as MPO activity. Both were capable of interrupting ROS-HMGB1loop as evident by restored liver GSH, decreased liver lipoperoxidation, and enhanced glutathione peroxidase (GPx) activity. Simultaneously, apoptosis was significantly ameliorated by increasing the Bcl-2/Bax ratio