Cod liver oil in chemically-induced diabetes mellitus in rats
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SOHA M. HAMDY1, SAID S. MOSELHY2,
ABD-ELMONEIM A. MAKHLOUF3 and AMIRA H. FATHY1
1. Biochemistry Division, Department of Chemistry, Faculty of Science, Fayoum University, Egypt
2. Department of Biochemistry, Faculty of Science, Ain Shams University, Egypt
3. Department of Chemistry, Faculty of Science, Fayoum University, Egypt
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Abstract
Alloxan induces diabetes in experimental animals through the selective
damage of pancreatic â-cells. Cod liver oil (CLO) is an important source
of long-chain ù-3 fatty acids (eicosapentaenoic and docosahexaenoic
acids) and vitamins A, E, and D. In the present study, the possible
protective effect of CLO against alloxan-inducing diabetes was
investigated in rats. Sixty male albino rats were divided into six
groups (ten rats each) as following: Group I (control group), rats fed
on a standard diet; Group II (diabetic group), rats injected
intraperitoneally with alloxan (75 mg kg–1 day–1)
for five consecutive days; Group III (CLO group), rats received orally
100 ìl of CLO for five consecutive days; Group IV (treated group), rats
injected with alloxan for five consecutive days followed by CLO
administration for five consecutive days; Group V (protected group),
rats received CLO for five consecutive days followed by alloxan
injection for five consecutive days, and Group VI (simultaneous group),
rats received CLO and alloxan at the same time for five consecutive
days. After 30 days from starting the injection, plasma glucose,
insulin, tumor necrosis factor-á (TNF-á), interleukine-6 (IL-6), and
nitric oxide (NO) were investigated. Results showed that plasma levels
of glucose, TNF-á, and IL-6 were significantly elevated, while levels of
plasma NO and insulin were significantly decreased in diabetic rats when
compared with the control group. Oral administration of CLO (protected
and simultaneous groups) ameliorated the deleterious effects of alloxan
by lowering glucose, TNF-á, IL-6 and by slightly elevating plasma
insulin and NO levels. It is concluded that CLO might prevent alloxan
action by suppressing the release of inflammatory cytokines (TNF-á and
IL-6) that are involved in â-cell damage and development of diabetes.
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