TY - JOUR
T1 - Potassium bromate-induced kidney damage in rats and the effect of gum acacia thereon
AU - Ali, Badreldin H.
AU - Al Za’abi, Mohammed
AU - Karaca, Turan
AU - Al Suleimani, Yousuf
AU - Al Balushi, Khalid A.
AU - Manoj, Priyadarsini
AU - Ashique, Mohammed
AU - Nemmar, Abderrahim
N1 - Funding Information:
This work was supported by an internal grant from Sultan Qaboos University (IG/MED/PHAR/
Funding Information:
This work was supported by an internal grant from Sultan Qaboos University (IG/MED/PHAR/ 15/01). Thanks to Professor Gerald Blunden for reading the manuscript, and to the Sultan Qaboos University Animal House staff for looking after the animals used in this work.
Publisher Copyright:
© 2018, E-Century Publishing Corporation. All rights reserved.
PY - 2018
Y1 - 2018
N2 - Potassium bromate (KBrO3) is used in many countries in cosmetic and food industries. In this work, we investigated in male Sprague-Dawley rats, the effect of four graded oral doses of KBrO3 (5, 15, 45 and 135 mg/kg/ day for 28 days) on renal function tests, inflammation, oxidative damage, and apoptosis, as well as on histopathology, using several traditional and novel renal injury biomarkers in plasma, urine and renal tissues. We also tested the possible ameliorative action of the renoprotective prebiotic agent gum acacia (GA) on the actions of KBrO3 when given concomitantly with it in the drinking water at a concentration of 15%w/v. Taken together, the results indicated that treatment with KBrO3 at the 45 and 135 mg/kg doses caused a significant dose-dependent nephrotoxicity, as evident by the measured renal structural and functional indices and biomarkers of toxicity. GA co-treatment significantly abated most of the indices and biomarkers of the renal toxicity caused by KBrO3, suggesting a beneficial effect and its possible inclusion in edible products where KBrO3 is still used.
AB - Potassium bromate (KBrO3) is used in many countries in cosmetic and food industries. In this work, we investigated in male Sprague-Dawley rats, the effect of four graded oral doses of KBrO3 (5, 15, 45 and 135 mg/kg/ day for 28 days) on renal function tests, inflammation, oxidative damage, and apoptosis, as well as on histopathology, using several traditional and novel renal injury biomarkers in plasma, urine and renal tissues. We also tested the possible ameliorative action of the renoprotective prebiotic agent gum acacia (GA) on the actions of KBrO3 when given concomitantly with it in the drinking water at a concentration of 15%w/v. Taken together, the results indicated that treatment with KBrO3 at the 45 and 135 mg/kg doses caused a significant dose-dependent nephrotoxicity, as evident by the measured renal structural and functional indices and biomarkers of toxicity. GA co-treatment significantly abated most of the indices and biomarkers of the renal toxicity caused by KBrO3, suggesting a beneficial effect and its possible inclusion in edible products where KBrO3 is still used.
KW - Gum acacia
KW - Kidneys
KW - Potassium bromate
KW - Sprague-Dawley rats
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M3 - Article
AN - SCOPUS:85041130086
SN - 1943-8141
VL - 10
SP - 126
EP - 137
JO - American Journal of Translational Research
JF - American Journal of Translational Research
IS - 1
M1 - AJTR0060604
ER -