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العنوان
The Relationship Between Some Adipokines, Pro-inflammatory Molecules and Diabetes Type II /
الناشر
Amira Abdulrahim Eldosokky Elfayoumy،
المؤلف
Amira Abdulrahim Eldosokky Elfayoumy
هيئة الاعداد
باحث / Amira Abdulrahim Eldosokky Elfayoumy
مشرف / Entsar Ali Ali Saad
مشرف / Wael Abdel-Hamid Refai
مناقش / Amal Kamel Reda Elsaied
الموضوع
Diabetes Type.
تاريخ النشر
2017.
عدد الصفحات
112 ص. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
Biophysics
تاريخ الإجازة
4/2/2018
مكان الإجازة
جامعة دمياط - كلية العلوم - الكيمياء
الفهرس
Only 14 pages are availabe for public view

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from 145

Abstract

Great interest is directed to inflammation and oxidative stress involvement in type 2 diabetes pathogenesis. Many researchers suggest they play roles but exactly how is still not clear enough. This encouraged us to investigate relations and potential inter-relationships between them and insulin resistance in type 2 diabetes in its early stage. Whether metformin drug alone, as frequently prescribed, is enough for type 2 diabetes management in this early stage was also an objective.
Blood sugar indices, adiponectin (ADIPOQ), tumor necrosis factor-α (TNF-α), malondialdehyde (MDA), nitric oxide (NO), C-reactive protein (CRP), liver and kidney function tests and lipid profile were monitored in non-diabetic volunteers, pre-diabetic and newly diagnosed type 2 diabetic patients before and after metformin drug utilization for 5 mo.
MDA, inflammation markers and alanine aminotransferase (ALT) were elevated, and blood sugar indices and lipid profile showed pathological alterations in diabetics compared to non-diabetics; changes were worse in type 2 cases. They were improved to different degrees by metformin treatment except for pancreatic β-cells function and ADIPOQ level showed no significant improvements and it couldn’t normalize ALT.
Results reflected significant relations and inter-relationships between oxidative stress and inflammation markers in type 2 diabetes in its early stage and indicated that metformin may need to be combined with another drug.