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Oxidative Stress in Extrahepatic Tissues of Rats Co-Exposed to Aflatoxin B1 and Low Protein Diet
Oluwakemi A Rotimi1, Solomon O Rotimi1, Flora Oluwafemi2
1Department of Biochemistry, Covenant University, Ota, Nigeria.
Insights
Early life exposure to aflatoxin B1 (AFB1) and low protein diets harm developing rats. This combination significantly reduces weight gain, causes anemia, impairs kidney function, and increases oxidative stress, posing a public health risk.
Area of Science:
- Toxicology
- Nutritional Science
- Public Health
Background:
- Early life exposure to aflatoxin B1 (AFB1) and low protein diets is prevalent in parts of Africa and Asia.
- Complementary foods are a common source of co-exposure during weaning.
Purpose of the Study:
- To evaluate the combined effects of AFB1 and low protein diet on extrahepatic tissues in weanling rats.
- To assess the impact on biomarkers of anemia, kidney function, and oxidative stress.
Main Methods:
- Twenty-four male albino rats were divided into four groups: control, low protein diet, normal protein diet + AFB1, and low protein diet + AFB1.
- Diets were administered for eight weeks, followed by analysis of blood and tissue biomarkers.
Main Results:
- Co-exposure significantly decreased body weight gain and packed cell volume (PCV).
- Biomarkers indicated impaired kidney function and increased oxidative stress (reduced glutathione, increased TBARS).
- Additive effects on weight loss and potentiation of kidney dysfunction were observed.
Conclusions:
- Co-exposure to AFB1 and low protein diet has detrimental effects on extrahepatic tissues, including anemia, kidney dysfunction, and oxidative stress.
- This combination poses a significant public health concern, particularly in regions with high AFB1 contamination.
Abstract:
Early life exposure to aflatoxin B1 (AFB1) and low protein diet through complementary foods during weaning is common in parts of Africa and Asia. This study evaluated the effect of co-exposure to AFB1 and low protein diet on the extrahepatic tissues of rats. Twenty-four three-week old weanling male albino rats were used for this study and were randomly assigned into four groups: group 1 served as control and was fed normal protein diet (20% protein), group 2 was fed low protein diet (5% protein), group 3 was fed normal protein diet + 40 ppb AFB1 while group 4 received low protein diet + 40 ppb AFB1, all for eight weeks. Afterward, biomarkers of anemia (packed cell volume (PCV), hemoglobin) and kidney function (urea, uric acid, and creatinine) were determined in the blood while biomarkers of oxidative stress were determined in the tissues spectrophotometrically. Co-exposure to AFB1 and low protein diet significantly (p < 0.05) decreased body weight gain and PCV, increased biomarkers of kidney functions and induced oxidative stress in the tissues studied. There was significant (p < 0.05) reduction in glutathione concentration while TBARS was significantly increased in the tissues. Co-exposure to AFB1 and low protein diet had additive effects on decreasing the weight gain and potentiation effect of kidney dysfunction in the rats. The co-exposure also decreased antioxidant enzymes and increased oxidant status in the tissues. Our results demonstrate that this co-exposure has deleterious health effects on extrahepatic tissues and should be a public health concern especially in developing countries where AFB1 contamination is common.
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