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العنوان
Possible antidiabetic and renoprotective effects of aliskiren and spironolactone in STZ-induced diabetes in rats /
الناشر
Amal Mohamed Mahfoz Ahmed ,
المؤلف
Amal Mohamed Mahfoz Ahmed
هيئة الاعداد
باحث / Amal Mohamed Mahfoz Ahmed
مشرف / Afaf Abd El-Monaem Ain Shoka
مشرف / Hekma Abd El-Tawab Abd El-Latif
مشرف / Nahed Mohamed Ahmed Hassanein
مشرف / Nesrin Ahmed Safwat
تاريخ النشر
2017
عدد الصفحات
192 Leaves :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
العلوم الصيدلية
تاريخ الإجازة
19/9/2017
مكان الإجازة
جامعة القاهرة - كلية الصيدلة - Pharmacology and Toxicology
الفهرس
Only 14 pages are availabe for public view

from 222

from 222

Abstract

Diabetic nephropathy (DN) is becoming an ever larger health burden worldwide, more effective therapies are needed. In the present study, the antidiabetic and renoprotective effects of aliskiren a renin inhibitor and spironolactone an aldosterone antagonist were evaluated in streptozotocin (STZ) induced DN in rats. Diabetic nephropathy was induced by a single intraperitoneal injection of STZ (65 mg/kg). After 3 days, rats were divided into 6 groups: normal, diabetic, diabetic rats treated with gliclazide (10 mg/kg/day), diabetic rats treated with aliskiren (50 mg/kg/day), diabetic rats treated with spironolactone (20 mg/kg/day) and diabetic rats treated with combination of aliskiren (25 mg/kg/day) and spironolactone (10 mg/kg/day). After one month of treatment, mean arterial blood pressure and heart rate were recorded. Then rats were euthanized and serum was separated for determination of glucose, insulin, kidney function tests, superoxide dismutase activity (SOD), adiponectin and nitric oxide (NO). Kidneys were isolated, one kidney was used for estimation of malondialdehyde (MDA), reduced glutathione (GSH) and tumor necrosis factor alpha (TNF-Ü), whereas the other kidney was used for histopathological study and immunohistochemical measurement of caspase 3 and transforming growth factor beta (TGF-Ý). In addition, islets of Langerhans were isolated from non-fasting normal rats by collagenase digestion technique. Isolated Ý cells were divided into 11 groups and were treated as follows: normal control, 20 æl (40 omol/L) gliclazide, 20 æl (100 omol/L) aliskiren alone or in combination with gliclazide, 20æl (5æg/L) spironolactone alone or in combination with gliclazide