Ashma Khatun, Mukti Mondal, Sanghamitra Pal, Suraiya Parvin and Goutam Paul*
Molecular Neurotoxicology Laboratory, Department of Physiology,
University of Kalyani, Kalyani, West Bengal-741235, India
*Corresponding author: goutampaul.ku@gmail.com
Received: May 24, 2021 / Revised: June 25, 2021/ Accepted: June 27, 2021
Abstract
Chocolate Brown HT, the bis-azo dye which is extensively used to color different types of foods. We aimed to evaluate the role of Chocolate Brown HT on the functions of the uterus. Studies were carried out on adult female albino rats of the Charles Foster strain. For this study rats were randomly separated into four groups: one was the control group, and the other three groups were exposed to three different effective dosages (100mg/kg body weight/day, 200mg/kg body weight /day, and 400mg/kg body weight /day) of Chocolate Brown HT for 30 days. After the termination of this period, alterations to body weight, the weight of uterus, activities of different antioxidant enzymes, and histomorphology of uterine wall structure were measured. We have observed a significant decrease in mean body weight and weight of uterus in exposed rats. The activities of different antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR), glutathione-s-transferase (GST), and glutathione peroxidase (GPx) were decreased and the level of malondialdehyde (MDA), a biomarker of lipid peroxidation was increased significantly in Chocolate Brown HT exposed rats compared to control group of rats in a dose-dependent manner. From the histomorphological study, significant degeneration and lesions in the wall structure of the uterus have also been detected in Chocolate Brown HT exposed rats. From our study, it may be concluded that Chocolate Brown HT impairs the function of the uterus probably by producing oxidative stress-induced damages of uterine tissues.
Keywords Chocolate Brown HT, uterus, oxidative stress, lipid peroxidation, histopathological study of uterus
How to cite this article:
Khatun, A., Mondal, M., Pal, S., Parvin, S., Paul, G. (2021) Impairment of uterine wall structure by Chocolate Brown HT in Rats. Science Archives, Vol. 2 (2), 93-98. http://dx.doi.org/10.47587/SA.2021.2206
References
Abbas, J. R., & Al-Hamadawi, H. A. (2019). Effect of chocolate brown HT E155 on some hormones in male albino rats. EurAsian Journal of BioSciences, 13(1), 485-489.
Bancroft, J.D., & Gamble, M. (2002). Theory and practice of histological techniques, 5th ed. Edinburgh/New York/London/Philadelphia: Edinburgh Churchill livingstone Pub.
Bawazir, A. E. (2012). Effect of chocolate brown HT with olive oil on some neurotransmitters in different brain regions, physiologicaland histological structure of liver and kidney of male albino rats. Journal of Evolutionary Biology Research, 4(1), 13-23.
Bedard, K., & Krause, K. H. (2007). The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiological Reviews, 87(1), 245-313.
Chambers, P. L., Hunter, C. G., & Stevenson, D. E. (1966). Short-term study of Chocolate Brown HT in rats. Food and Cosmetics Toxicology, 4(2), 151-155.
Devasagayam, T. P., & Tarachand, U. (1987). Decreased lipid peroxidation in the rat kidney during gestation. Biochemical and Biophysical Research Communications, 145(1), 134-138.
Drake, J. J., Butterworth, K. R., Gaunt, I. F., & Hardy, J. (1978). Long-term toxicity studies of Chocolate Brown HT in mice. Toxicology, 10(1), 17-27.
EFSA Panel on Food Additives and Nutrient Sources (ANS). (2010). Scientific Opinion on the re‐evaluation of Brown HT (E 155) as a food additive. EFSA Journal, 8(4), 1536.
El-Tohamy, M. M., (2012). The mechanisms by which oxidative stress and free radical damage produces male infertility. Life Science Journal, 9(1), 674-688.
Habig, W. H., Pabst, M. J., & Jakoby, W. B. (1973). Glutathione S-Transferase: The first enzyme step in mercapturic acid formation. Journal of Biological Chemistry, 249(22), 7130-7139.
Hall, D. E., Lee, F. S., & Fairweather, F. A. (1966). Acute (mouse and rat) and short-term (rat) toxicity studies on Chocolate Brown HT. Food and Cosmetics Toxicology, 4(2), 143-149.
Hong, M. N., Suh, H. J., Lee, O. H., Chun, H. S., & Lee, C. (2014). Improved analytical method of synthetic food colour additive, Brown HT by high-performance liquid chromatography. Journal of International Scientific Publications: Agriculture & Food, 2, 68-75.
Inetianbor, J. E., Yakubu, J. M., & Ezeonu, S. C. (2015). Effects of food additives and preservatives on man-a review. Asian Journal of Science and Technology, 6(2), 1118-1135.
Khatun, A., Sarkar, K., Nath, P. P., Mondal, M., Pal, S., & Paul, G. (2017). Chocolate brown ht impairs the function of the ovary bydepressing the hypothalamic-hypophyseal-ovarian servomechanism inalbino rat. International Journal of Pharma and Bio Sciences, 8(3), 344-350.
Lowry, O. H., Rosebrough, N. J., Farr, A. L., & Randall, R. J. (1951). Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry, 193(1), 265-275.
Marklund, S., & Marklund, G. (1974). Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. European Journal of Biochemistry, 47(3), 469-474.
Mondal, M., Tarafder, P., Sarkar, K., Nath, P. P., & Paul, G. (2014). Monosodium glutamate induces physiological stress by promotingoxygen deficiency, cell mediated immunosuppression and production of cardiovascular risk metabolites in rat. International Journal of Pharmaceutical Sciences Review and Research, 27(1), 328-31.
Orient, A., Donko, A., Szabo, A., Leto, T. L., & Geiszt, M. (2007). Novel sources of reactive oxygen species in the human body. Nephrology Dialysis Transplantation, 22(5), 1281-1288.
PFAA (1954): Prevention of Food Adulteration Act, Rule 55, Lucknow: Indian Eastern Book Company.
Rotruck, J. T., Pope, A. L., Ganther, H. E., Swanson, A. B., Hafeman, D. G., & Hoekstra, W. (1973). Selenium: biochemical role as a component of glutathione peroxidase. Science, 179(4073), 588-590.
SCF (Scientific Committee for Food). (1984). Reports of the Scientific Committee for Food (14th series).
Shubik, P. (1975). Potential carcinogenicity of food additives and contaminants. Cancer Research, 35(11 Part 2), 3475-3480.
Silveira, A. S., Aydos, R. D., Ramalho, R. T., Silva, I. S., Caldas, R. D. A., Santos Neto, A. T. D., & Rodrigues, C. T. (2018). Oxidative stress effects in the uterus, placenta and fetus of pregnant rats submitted to acute and chronic stress. Acta Cirurgica Brasileira, 33(9), 806-815.
Sinha, A. K. (1972). Colorimetric assay of catalase. Analytical Biochemistry, 47(2), 389-394.
Staal, G. E., Visser, J., & Veeger, C. (1969). Purification and properties of glutathione reductase of human erythrocytes. Biochimica et Biophysica Acta (BBA)-Enzymology, 185(1), 39-48.
U.S. Food & Drug Administration. (1999). Summary of color additives listed for use in the United States in food, drugs, cosmetics and medical devices, Washington. DC.
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