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. 2022 Jan 17;27(2):581. doi: 10.3390/molecules27020581

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© 2022 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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The effect of Laurel and Myrtle extract on oxidative stress biomarkers in the liver and kidney tissues homogenates measured by MDA level (a), GSH level (b) CAT activity (c) and carbonyl content (d). Male rats (n = 5) were administered Laurel and Myrtle extracts ig at a dose of 50 and 100 mg/kg once a day for 14 days. The control group was treated with ig saline. The results are expressed as the mean value of each experimental group ± SE of the mean of two different observations. * Significantly different in relation to Control (* p < 0.05). ^■ Significantly different in relation to Myrtle-100 (^■■ p < 0.01); ^♦ Significantly different in relation to Laurel-100 (^♦ p < 0.05) ^□ Significantly different in relation to Myrtle-50 (^□ p < 0.05); ^◊ Significantly different in relation to Laurel-50 (^◊ p < 0.05).

The effect of Laurel and Myrtle extract on oxidative stress biomarkers in the liver and kidney tissues homogenates measured by MDA level (a), GSH level (b) CAT activity (c) and carbonyl content (d). Male rats (n = 5) were administered Laurel and Myrtle extracts ig at a dose of 50 and 100 mg/kg once a day for 14 days. The control group was treated with ig saline. The results are expressed as the mean value of each experimental group ± SE of the mean of two different observations. * Significantly different in relation to Control (* p < 0.05). ^■ Significantly different in relation to Myrtle-100 (^■■ p < 0.01); ^♦ Significantly different in relation to Laurel-100 (^♦ p < 0.05) ^□ Significantly different in relation to Myrtle-50 (^□ p < 0.05); ^◊ Significantly different in relation to Laurel-50 (^◊ p < 0.05).