(2024) Biochemical Studies on Efficiency of Natural Gum in Chronic Kidney Failure and Liver Cirrhosis in Rats. World's Veterinary Journal. pp. 293-310. ISSN 23224568
![]() |
Text
WVJ 14(3) 293-310, 2024.pdf - Published Version Download (1MB) |
Abstract
It is well-established that apoptosis, oxidative stress, and inflammation are associated with several disorders, including chronic renal disease and hepatic disease. Oxidative stress (OS) is a major cause of death from end-stage renal disease which also contributes to atherosclerosis and cardiac issues. The present study aimed to assess the efficacy of Gum Arabic (GA) in mitigating renal damage and hepatotoxicity in rats induced by Chloropyrifosmethyl (CPM). A total of 42 male Wistar rats were divided into seven groups, with four groups (group 2 IC, group 5 GA1+ICa, group 6 GA2+IC, and group 7 GA1+ICb treated with CPM for eight weeks to induce hepatic and renal damage. Two models of GA administration, including the standard oral model in drinking water (15% w/v) and the oral model by gavage at a dose of 1 g/kg body weight were administered. Physiological parameters of kidney and liver functions, including urea, creatinine, AST, and ALT along with anti-oxidant factors (Melaodialdehyde, superoxide dismutase, reduced glutathione, and catalase) were measured in plasma, and homogenates of renal and hepatic tissues on day 57 of the experiment. In addition, histopathological examination was conducted on liver and kidney tissues using hematoxylin and eosin stain to evaluate the efficacy of GA on damaged tissues. Gum Arabic was found to significantly reduce CPM toxic effects in the liver and kidney in groups treated with CPM as liver and kidney parameters were reduced to normal levels. Furthermore, GA reduced histological indicators of inflammation, fibrosis, and apoptosis, as well as renal morphological damage. Additionally, it reduced OS in liver and kidney homogenates. In conclusion, GA effectively reduced the damage that CPM inflicted on liver and kidney tissue by stabilizing physiological parameters to normal levels and repairing cellular structures damaged by OS. Open Access: This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit https://creativecommons.org/licenses/by/4.0/. © The Author(s) 2024
Item Type: | Article |
---|---|
Keywords: | alanine aminotransferase; albumin; aspartate aminotransferase; bilirubin; catalase; chlorpyrifos methyl; cholesterol; creatinine; drinking water; eosin; glutathione; gum arabic; hematoxylin; malonaldehyde; protein; superoxide dismutase; triacylglycerol; urea, animal experiment; animal model; animal tissue; antiapoptotic activity; antifibrotic activity; antiinflammatory activity; Article; blood level; cell regeneration; cell structure; chronic kidney failure; controlled study; drug efficacy; histopathology; kidney function; kidney homogenate; kidney tissue; liver cirrhosis; liver function; liver homogenate; liver tissue; male; nonhuman; oxidative stress; rat |
Subjects: | S Agriculture > SF Animal culture |
Divisions: | World's Veterinary Journal (WVJ) |
Page Range: | pp. 293-310 |
Journal or Publication Title: | World's Veterinary Journal |
Journal Index: | Scopus |
Volume: | 14 |
Number: | 3 |
Publisher: | Scienceline Publication |
Identification Number: | https://doi.org/10.54203/scil.2024.wvj36 |
ISSN: | 23224568 |
Depositing User: | Dr. Alireza Sadeghi |
URI: | http://eprints.science-line.com/id/eprint/1186 |
Actions (login required)
![]() |
View Item |