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Marah Salim Hameed

Abstract

Background: The liver is the major organ responsible for metabolism, detoxification, and secretory functions in the body. Vitamin C is an essential co-factor, acting as a reducing agent and may have heaptoprotective property. Vitamin E is an antioxidant factor. Sodium nitrate is a salt and an anti-oxidant that is used as a preservative.  


Objective: To evaluate the effect of sodium nitrate, vitamin E and vitamin C administration on  liver enzymes, alanine transaminase, aspartate transaminase  and alkaline phosphatase.


Materials and Methods: Sixty healthy adult male mice divided randomly into six groups, group 1, received vitamin E solution 0.5 ml / liter distal water daily for 2 weeks. group2, received vitamin C solution 0.5 gm / liter distal water daily for 2 weeks. Group 3, received sodium nitrate solution 0.5gm/liter distal water daily for 2week. Group 4, received sodium nitrate solution orally in dose170 mg/kg body weight and received vitamin E solution 0.5 ml / liter distal water daily for 2 weeks. Group 5, received sodium nitrate solution orally in dose170 mg/kg body weight and received vitamin C solution 0.5 gm / liter distal water daily for 2 weeks. Group 6 (Control), receive distal water daily for 2 weeks. After the last day of administration, the animals were euthanized and blood samples were drawn from the heart    by cardiac puncture into plain tubes, and then subjected to biochemical assays. 


Results: A significant difference in alanine transaminase level was reported between control group and group of mice   received vitamin E (P-value = 0.001), vitamin E+ NaNO3 (P value =0.015). No significant difference in alanine transaminase level was reported between control and other groups. Significant difference in aspartate transaminase level reported between control group and group of mice received vitamin E (P-value = 0.000202573), vitamin C (P value = 0.00143), NaNO3 (p value=0.008076). No significant difference in aspartate transaminase level was reported between control and group of mice received (vitamin E+ NANO3) (vitamin C+NANO3) groups. Significant difference in alkaline phosphatase level reported between control group and group of mice received vitamin E (P-value = 4.5E-13), vitamin C (P value = 4.45E-18), (p value=6.17E-06), vitamin E+ NANO3 (p-value=3.68E-15). No significant difference in aspartate transaminase level was reported between control and group received (Vitamin C+ NANO3), p-value = (0.091718).


Conclusion: Vitamin E and C have the ability to ameliorate the effect of sodium nitrate in exposed groups although the effect of vitamin E more obvious due to pharmaceutical formulation, finally antioxidant effects of vitamins leads to modulation the nitrate toxicity and hepatoprotective effect.

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