ROLE OF OXIDATIVE STRESS IN POTASSIUM BROMATE-INDUCED    NEPHROTOXICITY AND REPRODUCTIVE TOXICITY

Authors

  • Km Priyanka Department of Zoology, agra college agra Affiliated to Dr. bhimrao ambedkar university, agra ,uttar Pradesh , India
  • Amita sarkar Department of Zoology, agra college agra Affiliated to Dr. bhimrao ambedkar university, agra ,uttar Pradesh , India

DOI:

https://doi.org/10.59436/551hbx75

Keywords:

Potassium bromate, nephrotoxicity, reproductive toxicity, oxidative stress, antioxidant enzymes, reactive oxygen species, rodent model

Abstract

This study investigates the nephrotoxic and reproductive toxic effects of potassium bromate (KBrO3), a compound with widespread industrial applications but concerning toxicological profiles. Employing male and female rodent models, the research aims to elucidate the role of oxidative stress in KBrO3-induced toxicity. Animals were divided into control and treatment groups, receiving varying doses of KBrO3. Key parameters assessed included serum creatinine and blood urea nitrogen for renal function; reactive oxygen species (ROS) and malondialdehyde (MDA) levels for oxidative stress; and activities of antioxidant enzymes like superoxide dismutase (SOD) and catalase (CAT). Histological analyses of kidney, testes, and ovaries, alongside gene expression studies of oxidative stress markers, provided insights into the cellular impact of KBrO3 exposure. The findings indicate a significant dose-dependent increase in oxidative stress markers, alongside notable renal and reproductive tissue damage, underscoring the critical role of oxidative stress in KBrO3 toxicity. These results highlight the urgent need for regulatory measures to mitigate exposure risks and protect public health.

References

Potara M, Maniu D, Astilean S. The synthesis of biocompatible and SERS-active gold nanoparticles using chitosan. Nanotechnology 2009; 20(31): 315602.

Aldea M, Florian IS, Potara M, et al. Metformin delivery using chitosan-capped gold nanoparticles in glioblastoma cell lines. Rom Neurosurg 2018; 32(2): 230–239.

Doumas B, Watson W, Biggs H. Colorimetric determination of total protein in serum or plasma. Clin Chem 1975; 21(8): 1159–1166.

Doumas BT, Watson WA, Biggs HG. Albumin standards and the measurement of serum albumin with bromcresol green. Clin Chim Acta 1997; 258(1): 21–30.

Abd Elhalem S, EL-Atrash A, Osman A, et al. Short term toxicity of food additive azo dye, sunset yellow (E110), at low doses, in male Sprague-Dawley rats. Egypt J Exp Biol Zool 2016; 12: 13–21.

Schumann G, Klauke R. New IFCC reference procedures for the determination of catalytic activity concentrations of five enzymes in serum: preliminary upper reference limits obtained in hospitalized subjects. Clin Chim Acta 2003; 327(1–2): 69–79.

Belfield A, Goldberg D. Hydrolysis of adenosine monophosphates by acid phosphatases as measured by a continuous spectrophotometric assay. Biochem Med 1970; 4(2): 135–148.

Mohamed NE, Ashour SE. Influence of ethanolic extract of strawberry leaves for abrogating bromate hazards in male rats. J Basic Appl Zool 2019; 80(1): 19.

Slot C. Plasma creatinine determination a new and specific Jaffe reaction method. Scand J Clin Lab Invest 1965; 17(4): 381–387.

Iwata K, Inayama T, Kato T. Effects of Spirulina platensis on plasma lipoprotein lipase activity in fructose-induced hyperlipidemic rats. J Nutr Sci Vitaminol 1990; 36(2): 165–171.

Rojkin M, Olguin de Mariani MC, Drappo G, et al. Proteínas totales del suero. Bioquímica del Atlántico 1974; 63: 1931–1954.

Misra HP, Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Biol Chem 1972; 247(10): 3170–3175.

Manubolu M, Goodla L, Ravilla S, et al. Protective effect of Actiniopteris radiata (Sw.) link. Against CCl4 induced oxidative stress in albino rats. J Ethnopharmacol 2014; 153(3): 744–752.

Jollow D, Mitchell JR, Zampaglione N, et al. Bromobenzene-induced liver necrosis. Protective role of glutathione and evidence for 3, 4-bromobenzene oxide as the hepatotoxic metabolite. Pharmacology 1974; 11(3): 151–169.

Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases the first enzymatic step in mercapturic acid formation. J Biol Chem 1974; 249(22): 7130–7139.

⮚ Doğru-Abbasoğlu S, Tamer-Toptani S, Uğurnal B, et al. Lipid peroxidation and antioxidant enzymes in livers and brains of aged rats. Mech Ageing Dev 1997; 98(2): 177–180.

Yalçin E, Çavuşoğlu K. (2022). Toxicity assessment of potassium bromate and the remedial role of grape seed extract. Sci Rep. Nov 28; 12(1):20529. doi: 10.1038/s41598-022-25084-7. PMID: 36443372; PMCID: PMC9705420.

Yousef MI, Hussien HM. Cisplatin-induced renal toxicity via tumor necrosis factor-α, interleukin 6, tumor suppressor P53, DNA damage, xanthine oxidase, histological changes, oxidative stress and nitric oxide in rats: protective effect of ginseng. Food Chem Toxicol 2015; 78: 17–25.

Hamed SS, Al-Yhya NA, El-Khadragy MF, et al. The protective properties of the strawberry (Fragaria ananassa) against carbon tetrachloride-induced hepatotoxicity in rats mediated by anti-apoptotic and upregulation of antioxidant genes expression effects. Front Physiol 2016; 7: 325.

Ono M, Yu B, Hardison EG, et al. Increased susceptibility to liver injury after hemorrhagic shock in rats chronically fed ethanol: role of nuclear factor-κB, interleukin-6, and granulocyte colony-stimulating factor. Shock 2004; 21(6): 519–525.

Singh NP, McCoy MT, Tice RR, et al. A simple technique for quantitation of low levels of DNA damage in individual cells. Exp Cell Res 1988; 175(1): 184–191.

Harris H. After Bruce Casselman WC (1959). In: Histochemical technique. London: Methuen and Co. Ltd, 1900. 37. Mercer EH, Birbeck MS. Electron microscopy: a handbook for biologists. Oxford: Blackwell Scientific Publications, 1972.

Bozzola JJ, Russell LD. Electron microscopy: principles and techniques for biologists. Boston, MA: Jones & Bartlett Learning, 1999

Waller RA, Duncan DB. A Bayes rule for the symmetric multiple comparisons problem. J Am Stat Assoc 1969; 64(328): 1484–1503

Khan RA, Khan MR, Sahreen S, et al. Protective effects of Launaea procumbens against KBrO3-induced hepatic serum marker enzymes. Afr J Pharm Pharmacol 2011; 5(23): 2639–2641.

Maharjan B, Jha JC, Adhikari D, et al. Oxidative stress, antioxidant status and lipid profile in ischemic heart disease patients from western region of Nepal. Nepal Med Coll J 2008; 10(1): 20–24.

Ahmad MK, Mahmood R. Oral administration of potassium bromate, a major water disinfection by-product, induces oxidative stress and impairs the antioxidant power of rat blood. Chemosphere 2012; 87(7): 750–756.

Owolabi O, Omogbai E. Effect of metformin on potassium-adapted and nonadapted diabetic rats. Trop J Pharm Res 2012; 11(5): 747–752

Downloads

Published

2024-06-24

How to Cite

ROLE OF OXIDATIVE STRESS IN POTASSIUM BROMATE-INDUCED    NEPHROTOXICITY AND REPRODUCTIVE TOXICITY. (2024). Journal of Science Innovations and Nature of Earth, 4(2), 30-34. https://doi.org/10.59436/551hbx75

Similar Articles

21-30 of 61

You may also start an advanced similarity search for this article.