Attenuation of Paraquat-Induced Nephrotoxicity and Dysfunction in Male Wistar Albino Rats

Authors

  • Cosmas O. Ujowundu Federal University of Technology, Nigeria
  • Peter-Oscar I. Anaba Federal University of Technology, Nigeria
  • Ngozi B. Ulinasombu Federal University of Technology, Nigeria
  • Favour N. Ujowundu Federal University of Technology, Nigeria
  • Kalu O. Igwe Federal University of Technology, Nigeria
  • Henry D. Ogbuagu Federal University of Technology, Nigeria

DOI:

https://doi.org/10.20535/ibb.2020.4.1.191259

Keywords:

Paraquat, Herbicide, Nephrotoxicity, Xenobiotics, Antioxidants

Abstract

Background. Paraquat (PQ) is a pesticide commonly used in the control of weed in agricultural practices worldwide. Exposure to PQ has adverse biochemical and physiological consequences to humans and animals. The mechanism of toxicity is linked to the generation of reactive oxygen species and subsequent lipid peroxidation. Presently, no single effective antidote to PQ toxicity has been established. Therefore, the need to continually investigate different treatment approaches is of paramount importance.

Objective. This study evaluated the capacity of selected dietary supplements to attenuate paraquat-induced kidney dysfunction and damages by determining some kidney function biomarkers and oxidative parameters.

Methods. Thirty-six Wistar albino rats were randomly separated into six groups. Each group (except Normal control) was intoxicated every other day with 1.5 mg/kg body weight of PQ and four groups (except PQ and Normal control groups) were treated daily with 40 mg/kg of garlic, glutathione and vitamin C for two weeks.

Results. The results showed significant (p < 0.05) increases in concentration of kidney malondialdehyde, urea, creatinine, and blood lipid profiles. Also, significant decrease in concentrations of high-density lipoprotein cholesterol, kidney glutathione and total antioxidant capacity were presented by PQ control group compared to other PQ exposed groups treated with the antioxidant compounds.

Conclusions. PQ-induced changes indicated kidney dysfunction and damage. However, the administration of antioxidant supplements attenuated the PQ-induced biochemical and physiological dysfunction in the rats.

Author Biographies

Cosmas O. Ujowundu, Federal University of Technology

Department of Biochemistry

Peter-Oscar I. Anaba, Federal University of Technology

Department of Biochemistry

Ngozi B. Ulinasombu, Federal University of Technology

Department of Biochemistry

Favour N. Ujowundu, Federal University of Technology

Department of Biochemistry

Kalu O. Igwe, Federal University of Technology

Department of Biochemistry

Henry D. Ogbuagu, Federal University of Technology

Department of Biology

References

Raghu K, Mahesh V, Sasidhar P, Reddy PR, Venkataramaniah V, Agrawal A. Paraquat poisoning: A case report and review of literature. Journal of Family and Community Medicine. 2013;20(3):198-200. DOI: 10.4103/2230-8229.122023

Lalruatfela PL, Saminathan M, Ingole RS, Dhama K, Joshi MV. Toxicopathology of Paraquat Herbicide in Female Wistar Rats. Asian Journal of Animal and Veterinary Advances. 2014;9(9):523-42. DOI: 10.3923/ajava.2014.523.542

Dawson AH, Eddleston M, Senarathna L, Mohamed F, Gawarammana I, Bowe SJ, et al. Acute Human Lethal Toxicity of Agricultural Pesticides: A Prospective Cohort Study. PLoS Medicine. 2010;7(10):e1000357. DOI: 10.1371/journal.pmed.1000357

Akinloye OA, Abioye OA, Olaojoyetan OE, Awosika OT, Akinloye DI. Dose-Dependent Effects of Paraquat on C-reactive protein, Some Lipid Profile Parameters and Histology of Tissues in Male Albino Rats. Biochemistry & Physiology: Open Access. 2013;2(1):106. DOI: 10.4172/2168-9652.1000106

The WHO recommended classification of pesticides by hazard and guidelines to classification. Geneva: World Health Organization; 2009, 78 p.

Suntres ZE. Role of antioxidants in paraquat toxicity. Toxicology. 2002;180(1):65-77. DOI: 10.1016/s0300-483x(02)00382-7

Coats GE, Funderburk HH, Lawrence JM, Davis DE. Factors affecting persistence and inactivation of diquat and paraquat. Weed Research. 1966;6(1):58-66. DOI: 10.1111/j.1365-3180.1966.tb00867.x

Huggins DR, Reganold JP. No-Till: The Quiet Revolution. Scientific American. 2008;299(1):70-7. DOI: 10.1038/scientificamerican0708-70

Kamel F. Paths from Pesticides to Parkinson's. Science. 2013;341(6147):722-3. DOI: 10.1126/science.1243619

Padayatty SJ, Katz A, Wang Y, Eck P, Kwon O, Lee J-H, et al. Vitamin C as an Antioxidant: Evaluation of Its Role in Disease Prevention. Journal of the American College of Nutrition. 2003;22(1):18-35. DOI: 10.1080/07315724.2003.10719272

Pompella A, Visvikis A, Paolicchi A, De Tata V, Casini AF. The changing faces of glutathione, a cellular protagonist. Biochemical Pharmacology. 2003;66(8):1499-503. DOI: 10.1016/s0006-2952(03)00504-5

Maldonado PD, Alvarez-Idaboy JR, Aguilar-González A, Lira-Rocha A, Jung-Cook H, Medina-Campos ON, et al. Role of Allyl Group in the Hydroxyl and Peroxyl Radical Scavenging Activity of S-Allylcysteine. The Journal of Physical Chemistry B. 2011;115(45):13408-17. DOI: 10.1021/jp208233f

Borlinghaus J, Albrecht F, Gruhlke MCH, Nwachukwu ID, Slusarenko AJ. Allicin: Chemistry and Biological Properties. Molecules. 2014;19(8):12591-618. DOI: 10.3390/molecules190812591

Guide for the Care and Use of Laboratory Animals. National Institute of Health (NIH); 1985.

Wallin B, Rosengren B, Shertzer HG, Camejo G. Lipoprotein Oxidation and Measurement of Thiobarbituric Acid Reacting Substances Formation in a Single Microtiter Plate: Its Use for Evaluation of Antioxidants. Analytical Biochemistry. 1993;208(1):10-5. DOI: 10.1006/abio.1993.1002

Raja S, Nazeer Ahamed KFH, Kumar V, Mukherjee K, Bandyopadhyay A, Mukherjee PK. Antioxidant effect of Cytisus scoparius against carbon tetrachloride treated liver injury in rats. Journal of Ethnopharmacology. 2007;109(1):41-7. DOI: 10.1016/j.jep.2006.06.012

Benzie IFF, Strain JJ. The Ferric Reducing Ability of Plasma (FRAP) as a Measure of “Antioxidant Power”: The FRAP Assay. Analytical Biochemistry. 1996;239(1):70-6. DOI: 10.1006/abio.1996.0292

Okoro I. Manual of practical histology. 2nd ed. Owerri: Peace Publishers; 2002.

Conn HJ, Darrow MA, Emmel VM. Staining procedure used by the biological stain commission. 2nd ed. Baltimore, MD: Williams & Wilkins; 1960, 289 p.

Spitz DR, Azzam EI, Li JJ, Gius D. Metabolic oxidation/reduction reactions and cellular responses to ionizing radiation: A unifying concept in stress response biology. Cancer and Metastasis Reviews. 2004;23(3-4):311-22. DOI: 10.1023/B:CANC.0000031769.14728.bc

Soliman SM. Protective role of oregano oil against histological changes in whole body gamma irradiated albino rats. Journal of the Egyptian-German Society of Zoology. 2007;52C:46-56.

Dudley RWR, Khairallah M, Mohammed S, Lands L, Des Rosiers C, Petrof BJ. Dynamic responses of the glutathione system to acute oxidative stress in dystrophic mouse (mdx) muscles. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 2006;291(3):R704-R710. DOI: 10.1152/ajpregu.00031.2006

Ahmad I, Kumar A, Shukla S, Prasad Pandey H, Singh C. The involvement of nitric oxide in maneb- and paraquat-induced oxidative stress in rat polymorphonuclear leukocytes. Free Radical Research. 2008;42(10):849-62. DOI: 10.1080/10715760802513733

Ujowundu CO, Nnanna CG, Ndubuisi EU, Ngwu PC, Uzoma CW, Ezeji EU. Glyphosate-Based Pesticide-Induced Biochemical Changes in Hepatic and Renal Tissues of Clarias Gariepinus. Futo Journal Series. 2017;3(1):225-35.

Abdel-Mageid SA. Structural changes in the kidney of albino rat in response to the administration of paraquat herbicide. Journal of the Egyptian-German Society of Zoology. 1994;15:153-75.

Mongi S, Mahfoud M, Amel B, Kamel J, Abdelfattah EF. Protective effects of vitamin C against haematological and biochemical toxicity induced by deltamethrin in male Wistar rats. Ecotoxicology and Environmental Safety. 2011;74(6):1765-9. DOI: 10.1016/j.ecoenv.2011.04.003

Wershana KZ. The Influence of Vitamin C or Selenium on Paraquat-induced Toxicity in Guinea Pigs. Pakistan Journal of Biological Sciences. 2001;4(1):81-8. DOI: 10.3923/pjbs.2001.81.88

Valipour P, Heidarian E, Khoshdel A, Gholami-Arjenaki M. Protective Effects of Hydroalcoholic Extract of Ferulago Angulata Against Gentamicin-induced Nephrotoxicity in Rats. Iranian Journal of Kidney Diseases. 2016;10(4):189-96.

Sharifi-Rigi A, Heidarian E. Protective and anti-inflammatory effects of silymarin on paraquat-induced nephrotoxicity in rats. Journal of Herbmed Pharmacology. 2019;8(1):28-34. DOI: 10.15171/jhp.2019.05

Samai M, Samai HH, Hague T, Naughton D, Chatterjee PK. Novel Superoxide Dismutase Mimetics for Protection against Paraquat-induced Acute Renal Injury. Sierra Leone Journal of Biomedical Research. 2010;2(1):54-64. DOI: 10.4314/sljbr.v2i1.56608

Weiner ID, Mitch WE, Sands JM. Urea and Ammonia Metabolism and the Control of Renal Nitrogen Excretion. Clinical Journal of the American Society of Nephrology. 2015;10(8):1444-58. DOI: 10.2215/CJN.10311013

Gao L, Yang S, Liu J, Liu L. [Preventive effects of 5-hydroxy-1-methylhydantoin on paraquat-induced nephrotoxicity in rat]. Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2015;27(4):246-9. DOI: 10.3760/cma.j.issn.2095-4352.2015.04.004

Sener G, Sehirli AO, Altunbas HZ, Ersoy Y, Paskaloglu K, Arbak S, Ayanoglu‐Dulger G. Melatonin protects against gentamicin‐induced nephrotoxicity in rats. Journal of Pineal Research. 2002;32(4):231-6. DOI: 10.1034/j.1600-079x.2002.01858.x

Gu S-Y, Yeh T-Y, Lin S-Y, Peng F-C. Unfractionated bone marrow cells attenuate paraquat-induced glomerular injury and acute renal failure by modulating the inflammatory response. Scientific Reports. 2016;6:23287. DOI: 10.1038/srep23287

Chen YW, Yang CY, Huang CF, Hung DZ, Leung YM, Liu SH. Heavy metals, islet function and diabetes development. Islets. 2009;1(3):169-76. DOI: 10.4161/isl.1.3.9262

Samarghandian S, Azimi-Nezhad M, Shabestari MM, Azad FJ, Farkhondeh T, Bafandeh F. Effect of chronic exposure to cadmium on serum lipid, lipoprotein and oxidative stress indices in male rats. Interdisciplinary Toxicology. 2015;8(3):151-4. DOI: 10.1515/intox-2015-0023

Olisekodiaka MJ, Igbeneghu CA, Onuegbu AJ, Oduru R, Lawal AO. Lipid, Lipoproteins, Total Antioxidant Status and Organ Changes in Rats Administered High Doses of Cadmium Chloride. Medical Principles and Practice. 2012;21(2):156-9. DOI: 10.1159/000333385

Pari L, Murugavel P. Diallyl tetrasulfide improves cadmium induced alterations of acetylcholinesterase, ATPases and oxidative stress in brain of rats. Toxicology. 2007;234(1-2):44-50. DOI: 10.1016/j.tox.2007.01.021

Toth DF, Wonger H. Clinical Chemistry Textbook. 3rd ed. Oxford: Oxford University Press; 2003, p. 423.

Franzen D, Baer F, Heitz W, Mecking H, Eidt S, Käferstein H, et al. Failure of Radiotherapy to Resolve Fatal Lung Damage due to Paraquat Poisoning. Chest. 1991;100(4):1164-5. DOI: 10.1378/chest.100.4.1164

Wunnapuk K, Liu X, Peake P, Gobe G, Endre Z, Grice JE, et al. Renal biomarkers predict nephrotoxicity after paraquat. Toxicology Letters. 2013;222(3):280-8. DOI: 10.1016/j.toxlet.2013.08.003

Mohamed F, Buckley NA, Jayamanne S, Pickering JW, Peake P, Palangasinghe C, et al. Kidney damage biomarkers detect acute kidney injury but only functional markers predict mortality after paraquat ingestion. Toxicology Letters. 2015;237(2):140-50. DOI: 10.1016/j.toxlet.2015.06.008

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Published

2020-03-03

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1.
Ujowundu CO, Anaba P-OI, Ulinasombu NB, Ujowundu FN, Igwe KO, Ogbuagu HD. Attenuation of Paraquat-Induced Nephrotoxicity and Dysfunction in Male Wistar Albino Rats. Innov Biosyst Bioeng [Internet]. 2020Mar.3 [cited 2025Jun.16];4(1):26-35. Available from: https://ibb.kpi.ua/article/view/191259

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