4.6 Article

Nephroprotective effects of 4-4(hydroxyl-3 methoxyphenyl)-2-butane against sodium tellurite induced acute kidney dysfunction by attenuating oxidative stress and inflammatory cytokines in rats

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ARABIAN JOURNAL OF CHEMISTRY
卷 15, 期 6, 页码 -

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ELSEVIER
DOI: 10.1016/j.arabjc.2022.103857

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Nephrotoxicity; 4(hydroxyl-3 methoxyphenyl)-2-butane; Sodium tellurite; Oxidative stress; Inflammatory cytokines; Histopathology

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The aim of this study was to investigate the protective mechanism of 4-(hydroxyl-3-methoxyphenyl)-2-butane against Sodium tellurite-induced nephrotoxicity in rats. The results showed that 4-(hydroxyl-3-methoxyphenyl)-2-butane effectively attenuated renal damage caused by Sodium tellurite, as evidenced by improvements in biochemical markers, antioxidant activity, inflammatory cytokines, and histopathological changes.
The aim of this study was to elucidate the protective action mechanism of 4-4(hydroxyl3-methoxyphenyl)-2-butane against Sodium tellurite (ST) induced nephrotoxicity in rats. ST is a hazardous substance used in metallurgical and glassware industries, but its renal toxicities have not been well established before. Rats were distributed into four groups, six rats contain in each group. Normal control group given only vehicles only, toxic group given ST 8.5 mg/kg p o, treated groups given ST and 4-(hydroxyl-3-methoxyphenyl)-2-butane(100 mg/kg bwt), and positive control given only treatment drug 4-(hydroxyl-3-methoxyphenyl)-2-butane (100 mg/kg bwt) daily for 14 days. ST administration increases an alteration in biochemical, oxidative stress, cytokines markers, and morphological changes in toxic group. When it was treated with 4-(hydroxyl-3methoxyphenyl)-2-butane significantly (p < 0.5) restores all these changes such as biochemical markers, antioxidant, inflammatory cytokines, and histopathological improvements in treated group as compared to toxic group. No significant (p > 0.05) changes have been seen in positive control as compared to normal control. In conclusion, 4(hydroxyl-3 methoxyphenyl)-2-butane successfully defended the kidney from oxidative stress, inflammatory cytokines and necrosis against ST intoxication. Thus, significant improvements were reflected and confirms with the improvement in histopathological changes. (c) 2022 The Author(s). Published by Elsevier B.V. on behalf of King Saud University. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

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