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العنوان
A STUDY OF APOPTOTIC CHANGES AND DNA FRAGMENTATION OF GINGIVA AFTER LCHICINE ADMINISTRATION IN RATS
الناشر
Alexandria University.FACULTY OF DENTISTRY
المؤلف
SHREDAH, MOHAMED TAHA HUSSEIN
هيئة الاعداد
مشرف / سحر شفيق كارم
مشرف / على عبدالعليم
مشرف / محمد سيد سلامه
باحث / محمد طه حسين
تاريخ النشر
2003
عدد الصفحات
94
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
طب الأسنان
تاريخ الإجازة
1/1/2003
مكان الإجازة
جامعة الاسكندريه - كلية طب الاسنان - Oral Biology
الفهرس
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Abstract

Colchicines is an anti-inflammatory and antitumour drug. It is used for the treatment of many diseases and syndromes. Little attention was directed to the oral cavity, particularly the effect of colchicine on the gingiva. So the importance of this work is to discuss the effect of colchicine on rat gingiva and how this drug may affect the integrity of the gingival tissues based on the histological, immunohistochemical and molecular biological science.

Thirty male albino rats weighed 200 gm each, were used in this study.

They were divided into two main groups: The control group and study group. The control group animals were received a daily oral administration of distilled water and subdivided into 3 subgroups (2 animals each), which matched the study group in the time of euthanasia. The study group comprises twenty tour animals. they received a daily oral administration of therapeutic dose of colchicine, dissolved in distilled water, of 135 Jig/kg body weight using gastrointestinal tube and they were subdivided into 3 subgroups (8 animals each) according to the time of euthanasia as follows:

One week group! ( W\ group) :In which animals were euthanized after one

week of the drug administration.

Four weeks group! ( W 4 group) :In which animals were euthanized after

four weeks of the drug administration.

Eight weeks group! ( Wg group) :In which animals were received colchicine

for 4 weeks and then euthanized after 8 weeks to examine the cumulative

effect of the drug.

The gingivae obtained from treated the experimental rats were prepared t

be examined histologically using H & E, and immunohistochemically using DAKO LSAB detection kits for visualization of bcl-? protein and molecular