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. 2022 Jul;37(3):303-310.
doi: 10.1007/s12291-021-01001-z. Epub 2021 Sep 1.

Assessment of Role and Efficacy of Curcumin and Quercetin in Preventing Lead-Induced Oxidative Stress in Rats

Affiliations

Assessment of Role and Efficacy of Curcumin and Quercetin in Preventing Lead-Induced Oxidative Stress in Rats

Mohd Zahid et al. Indian J Clin Biochem. 2022 Jul.

Abstract

Lead (Pb) is found in almost all phases in environment and biological systems. Pb stimulated oxidative stress is a state that involves the generation of free radicals beyond the permissible limits, which can deplete the antioxidant reserves and can result in oxidative stress, thus hampering the ability of the biological system to reverse the result. Exposure of rats to Pb (25 mg/kg body weight) for 8 weeks caused an increase in Pb levels in blood and brain. Activity of delta-aminolevulinic acid dehydratase (δ-ALAD) and antioxidant enzymes such as Superoxide dismutase (SOD) and Catalase (CAT) decreased in the blood of Pb-treated group with a concomitant increase in the level of lipid peroxidation (LPO) and no significant change in the level of reduced glutathione (GSH) level was found. Interestingly, co-treatment of Pb-treated rats with curcumin (30 mg/kg body weight) and quercetin (30 mg/kg body weight) for 8 weeks caused a significant decrease in Pb levels of blood and all brain regions versus those treated with Pb alone. A significant improvement in levels of MDA, δ-ALAD, SOD and CAT activities was observed in rats simultaneously treated with curcumin or Quercetin or both with lead. Therefore, the ameliorative impact of curcumin and Quercetin might be due to their antioxidant property hence were able to counter the oxidative stress generated by Pb. These results suggest that combination of curcumin and Quercetin could be utilized as a possible supplement with the relevant therapeutics in the suitable management of Pb toxicity.

Keywords: Curcumin; Lead; Oxidative stress; Quercetin; Rat model.

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Conflict of interest statement

Conflicts of interestThe authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
Effect of Pb, CUR and QUE and their co-treatment on Pb concentration in blood of rats. Values are mean ± SE (n = 8). Significant change at P < 0.001 in B with respect to values in control group A. Significant change at P < 0.001 in E, F, G with respect to values in group B. Group A-Control; Group B-Lead acetate (Pb) only; Group C-Curcumin (CUR) only; Group D-Quercetin (QUE) only; Group E-Pb + CUR; Group F-Pb + QUE; Group G- Pb + CUR + QUE
Fig. 2
Fig. 2
Effect of Pb, CUR and QUE and their co-treatment on Pb concentration in brain regions a -Hippocampus, b-Prefrontal Cortex and c-Cerebellum of rats. Values are mean ± SE (n = 8). Significant change at P < 0.001 in B with respect to values in control group A. Significant change at P < 0.001 in E, F, G with respect to values in group B
Fig. 3
Fig. 3
Effect of Pb, Curcumin and Quercetin and their co-treatment on the activity of δ -aminolevulinic acid dehydratase (δ-ALAD) in blood of rats. Values are mean ± SE (n = 8). Significant change at P < 0.001 in B with respect to values incontrol group A. Significant change at P < 0.001 in E, F, G with respect to values in group B
Fig. 4
Fig. 4
Effect of Pb, CUR and QUE and their co-treatment on the activity of a- SOD and b- CAT in blood of rats. Values are mean ± SE (n = 8). Significant change at P < 0.001 in B with respect to values in control group A. Significant change at P < 0.001 in E, F, G with respect to values in group B
Fig. 5
Fig. 5
Effect of Pb, CUR and QUE and their co-treatment on the levels of reduced glutathione in blood of rats. All values are expressed as means ± SE (n = 8). Significant change at P < 0.001 in B with respect to the control group A. Not Significant change in E,F,G groups with respect to group B
Fig. 6
Fig. 6
Effect of Pb, CUR and QUE and their co-treatment on the levels of LPO in blood of rats. Values are mean ± SE (n = 8). Significant change at P < 0.001 in B with respect to values in control group A. Significant change at P < 0.001 in E,F,G with respect to values in group B

References

    1. Khodamoradi N, Komaki A, Salehi I, Shahidi S, Sarihi A. Effect of vitamin E on lead exposure- induced learning and memory impairment in rats. Physiol Behav. 2015;144:90–94. doi: 10.1016/j.physbeh.2015.03.015. - DOI - PubMed
    1. Singh N, Kumar A, Gupta VK, Sharma B. Biochemical and Molecular Bases of Lead induced toxicity in mammalian systems and possible mitigations. Chem Res toxicol. 2018 doi: 10.1021/acs.chemrestox.8b00193. - DOI - PubMed
    1. Sharma B, Singh S, Siddiqui NJ. Biomedical implications of heavy metals induced imbalances in redox systems. Biomed Res Int. 2014;2014:640–654. doi: 10.1155/10.1155/2014/640754. - DOI - PMC - PubMed
    1. Links JM, Schwartz BS, Simon D, Roche KB, Stewart WF. Characterization of toxicokinetics and toxicodynamics with linear systems theory: application to lead-associated cognitive decline. Environ Health Perspect. 2001;109:361–368. doi: 10.1289/ehp.01109361. - DOI - PMC - PubMed
    1. Lidsky TI, Schneider JS. Lead neurotoxicity in children: basic mechanisms and clinical correlates. Brain. 2003;126:5–19. doi: 10.1093/brain/awg014. - DOI - PubMed

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