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العنوان
The possible antigenotoxic potential of ginger
oil on etoposide - treated albino rats /
المؤلف
Ouda, Rania Ibrahim Mohammed.
هيئة الاعداد
باحث / رانيا إبراهيم محمد عوده
مشرف / صبحى السيد حسب الله
مشرف / غسلام محمد جروانى
الموضوع
Etoposide. Cancer - Chemotherapy
تاريخ النشر
2017.
عدد الصفحات
157 p. :
اللغة
الإنجليزية
الدرجة
ماجستير
التخصص
الكيمياء
الناشر
تاريخ الإجازة
1/3/2017
مكان الإجازة
جامعة المنوفية - كلية العلوم - الكيمياء والحيوان
الفهرس
Only 14 pages are availabe for public view

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Abstract

The aim of this work was to study the different side effects
appeared in rats after exposure to etoposide and the protective potential
of ginger (Zingiber officinale) oral administration against toxicity of
etoposide.
: Material used in the work
1- Etoposide (1mg/kg b.wt.): it was used as an anticancer drug and
served as a toxicant.
2- Ginger volatile oil (Zingiber officinale) (75mg/kg b.wt., 150mg/kg
b.wt.): is a medicinal plant material and administered as a
protective agent.
The present study was carried out using 60 adult male albino
rats (Rattus norvegicus) weighting 130±10 g.
In this study, the major experiments are planned as
- : following
1- Choice of etoposide (1mg/kg b.wt.) period of treatment and selection
was carried out according to maximum damage occurred in DNA in liver
and spleen tissues.
2-The protective role of Zingiber officinale volatile oil (75mg/kg b.wt.,
150mg/kg b.wt.) against DNA damage induced by etoposide in liver and
spleen after 21 days.
Summary
109
3- Determination of the protective potential of ginger oil against damage
induced by etoposide in liver and spleen tissue after 21 days of treatment.
4- Determination of DNA damaged cells percentage by alkaline single
cell gel electrophoresis (SCGE)/comet assay and the protective potential
of Zingiber officinale (ginger) volatile oil against damage induced by
etoposide in peripheral blood leukocytes after 72 hours of treatment.
5- Determination of chromosomal aberrations in bone marrow, these
aberrations include chromatid deletion, fragmentation, centromeric
attenuation, end to end association, centric fusion, break, gap and ring
chromosome after 72 hours of treatment.
6- Determination of mitotic index in bone marrow after 72 hours of
treatment.
7-Determination of the oxidative status in liver and spleen tissue as
(SOD, MDA, CAT, NO and GSH) after 21days of treatment.
The findings of this study are summariezed as follows:
Determination of total genomic DNA damage and apoptosis detection
in liver and spleen treated with etoposide to specify the treatment
period which cause the maximum damage.
The results showed that etoposide induced the maximum DNA
damage (apoptosis) after 21 days of treatment.
The protective role of Zingiber officinale volatile oil against genomic
DNA damage induced by etoposide in liver and spleen after 21 day of
treatment.
The obtained results showed that Zingiber officinale can exert
preventive effects on the development of genotoxic potential produced
due to the administration of etoposide at the level of DNA damage
determination by agarose gel electrophoresis.
Summary
110
Alkaline single gel electrophoresis (SCGE)/comet assay for
leukocytes after 72 hours of treatment.
The results of comet assay technique revealed that, administration
of Zingiber officinale oil showed significant improvement by the
reduction in DNA damaged cells when compared with etoposide
treatment groups.
Determination of chromosomal aberrations after 72 hours of
treatment.
The obtained results showed that Zingiber officinale oil can
decrease the percentage of chromosomal aberrations when compared with
etoposide treatment groups.
Determination of mitotic index after 72 hours of treatment.
The results showed that treatment with etoposide decreased the
mitotic index in contrast the treatment with ginger oil which improved
the percentage of mitotic index.
Examination of Biochemical assay after 21 days of treatment.
Animal treated with etoposide alone showed increase in the level
of MDA and NO but decrease in the level of (CAT, SOD and GSH)
while animals protected with ginger oil shows decrease in the level of
MDA and NO but increase in the level of (CAT, SOD and GSH) in liver
and spleen tissue.
Hense, all these results together showed that etoposide treatment
could induce cytotoxicity and genotoxicity but these side effects also can
be reduced or even prevented in some cases by the protective agents of
plant origin such as Zingiber officinale oil which has been used in this
study.