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العنوان
Biochemical studies on rosiglitazone and\or hesperidin in diabetic irradiated
experimental animals/
المؤلف
Abdel-Rafei,Mohamed Khairy Mohamed.
هيئة الاعداد
مشرف / Abdel-Rahman Badr Abdel-Ghaffar
مشرف / Wafaa Ibrahim El-Eraky
مشرف / Mahmoud Sayed Soliman Arbid
مشرف / Soheir Abdel Azeim Osman
مشرف / Nadia Yousef Sadek Morcos
الموضوع
Rosiglitazone. Hesperidin. diabetic irradiated. experimental animals.
تاريخ النشر
2012
عدد الصفحات
p.:275
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
Biochemistry
تاريخ الإجازة
1/1/2012
مكان الإجازة
جامعة عين شمس - كلية العلوم - Biochemistry
الفهرس
Only 14 pages are availabe for public view

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from 275

Abstract

Mohamed Khairy Mohamed (2011): Biochemical studies on rosiglitazone and\or hesperidin in diabetic irradiated experimental animals. Ain Shams University, Biochemistry Department-Faculty of Science, Cairo, Egypt.
The present study was designed to investigate the
biochemical and histopathological effect of rosiglitazone and
hesperidin in diabetic irradiated rats. In addition, anti-inflammatory (acute inflammation) and analgesic effects
(centrally mediated analgesia) were also assessed. Type 2 diabetes mellitus (T2DM) was induced in rats by a single intraperitoneal (i.p) injection of streptozotocin (65 mg/kg b.wt.; STZ) followed by single i.p administration of nicotinamide (110 mg/kg b.wt.;
NIC). Diabetic rats were irradiated with a single low dose γ-ray (0.5 Gy) at the beginning of study. Rosiglitazone (4 mg/kg b.wt.; p.o.) and hesperidin (100 mg/kg b.wt.; p.o.) were administered
daily for 30 days after T2DM induction. At the end of
experimental period, blood and tissue samples were collected and blood glucose, glycosylated hemoglobin (HbA1c), insulin, adiponectin, homeostasis model assessment of insulin resistance
(HOMA-IR), lipid profile, oxidative stress, creatinine kinasemonoenzyme B (CK-MB), lactate dehydrogenase (LDH),Creactive protein (CRP), nitric oxide (NO), body weight, heart weight, heart to body weight ratio, hematocrit %, hyaluronidase activity, liver function, kidney function as well as
histopathological examination of heart, liver and kidney were
determined. STZ injection significantly elevated (p<0.01) all
biochemical parameters except plasma adiponectin, serum SOD and GSH levels were significantly reduced (p<0.01) as compared to their respective control group and produced pathological
alterations in all examined tissues. Treatment of rats with
rosiglitazone, hesperidin and low dose radiation significantly
reduced (p<0.01) blood glucose, HbA1c, insulin, total cholesterol, triglycerides, LDL-C, VLDL-C, MDA, CK-MB, LDH, CRP,
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AST, ALT, ALP, creatinine, urea and significantly elevated
adiponectin, HDL-C, SOD, GSH and ameliorated HOMA-IR and
AI as compared to diabetic control group. It was observed that
rosiglitazone treatment alone showed a significant elevation
(p<0.01) in serum hyaluronidase activity, CK-MB, LDH, final body weight, heart weight and heart to body weight ratio as compared to diabetic irradiated rats, diabetic irradiated rats treated
with hesperidin alone and diabetic irradiated rats treated with
rosiglitazone and hesperidin (combination). Moreover, diabetic irradiated rats treated with rosiglitazone alone revealed pathological alterations in heart and liver sections. However, other diabetic treated groups showed reversal of all pathological lesions.
All diabetic treated groups showed a marked protection of renal tissue and reversal of all pathological changes exhibited by STZ in diabetic control kidney sections. Anti-inflammatory effect of rosiglitazone and hesperidin was verified through carrageenan induced paw edema model and their combination was the most
potent. Hesperidin exerted a potent analgesic activity in hot plate test, on the contrary, rosiglitazone devoided of any analgesic effect. It could be concluded from the obtained results that hesperidin combination with rosiglitazone exhibited a potential beneficial effect in reducing side effects and maximized therapeutic efficacy of rosiglitazone.