» Articles » PMID: 24096837

Ameliorative Effects of Thyme and Calendula Extracts Alone or in Combination Against Aflatoxins-induced Oxidative Stress and Genotoxicity in Rat Liver

Overview
Journal Cytotechnology
Specialties Biotechnology
Genetics
Date 2013 Oct 8
PMID 24096837
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

The aims of the current work were to evaluate the hepatoprotective effect of calendula flowers and/or thyme leave extracts on aflatoxins (AFs)-induced oxidative stress, genotoxicity and alteration of p53 bax and bcl2 gene expressions. Eighty male Sprague-Dawley rats were divided into eight equal groups including: the control group, the group fed AFs-contaminated diet (2.5 mg/kg diet) for 5 weeks, the groups treated orally with thyme and/or calendula extract (0.5 g/kg b.w) for 6 weeks and the groups pretreated orally with thyme and/or calendula extract 1 week before and during AFs treatment for further 5 weeks. Blood, liver and bone marrow samples were collected for biochemical analysis, gene expression, DNA fragmentation and micronucleus assay. The results showed that AFs induced significant alterations in oxidative stress markers, increased serum AFP and inflammatory cytokine, percentage of DNA fragmentation, the expression of pro-apoptotic gene p53 and bax accompanied with a decrease in the expression of bcl2. Animals treated with the extracts 1 week before AFs treatment showed a significant decrease in oxidative damage markers, micronucleated cells, DNA fragmentation and modulation of the expression of pro-apoptotic genes. These results suggested that both calendula and thyme extracts had anti-genotoxic effects due to their higher content of total phenolic compounds.

Citing Articles

Thyme ( Celak) Polyphenol-Rich Extract (TPE) Alleviates HFD-Induced Liver Injury in Mice by Inactivating the TLR4/NF-κB Signaling Pathway through the Gut-Liver Axis.

Sheng X, Wang L, Zhan P, He W, Tian H, Liu J Foods. 2023; 12(16).

PMID: 37628072 PMC: 10453248. DOI: 10.3390/foods12163074.


Thyme Oil and Thymol Counter Doxorubicin-Induced Hepatotoxicity Modulation of Inflammation, Apoptosis, and Oxidative Stress.

Ahmed O, Galaly S, Mostafa M, Eed E, Ali T, Fahmy A Oxid Med Cell Longev. 2022; 2022:6702773.

PMID: 35178158 PMC: 8844103. DOI: 10.1155/2022/6702773.


Hepatoprotective effect of Thymus vulgaris extract on sodium nitrite-induced changes in oxidative stress, antioxidant and inflammatory marker expression.

Soliman M, Aldhahrani A, Metwally M Sci Rep. 2021; 11(1):5747.

PMID: 33707592 PMC: 7952422. DOI: 10.1038/s41598-021-85264-9.


Contamination of Aflatoxins Induces Severe Hepatotoxicity Through Multiple Mechanisms.

Hua Z, Liu R, Chen Y, Liu G, Li C, Song Y Front Pharmacol. 2021; 11:605823.

PMID: 33505311 PMC: 7830880. DOI: 10.3389/fphar.2020.605823.


Critical role of caveolin-1 in aflatoxin B1-induced hepatotoxicity via the regulation of oxidation and autophagy.

Xu Q, Shi W, Lv P, Meng W, Mao G, Gong C Cell Death Dis. 2020; 11(1):6.

PMID: 31919341 PMC: 6952418. DOI: 10.1038/s41419-019-2197-6.


References
1.
Zhou H, Lutterodt H, Cheng Z, Yu L . Anti-Inflammatory and antiproliferative activities of trifolirhizin, a flavonoid from Sophora flavescens roots. J Agric Food Chem. 2009; 57(11):4580-5. PMC: 2704566. DOI: 10.1021/jf900340b. View

2.
Braga P, Dal Sasso M, Culici M, Bianchi T, Bordoni L, Marabini L . Anti-inflammatory activity of thymol: inhibitory effect on the release of human neutrophil elastase. Pharmacology. 2006; 77(3):130-6. DOI: 10.1159/000093790. View

3.
Sharma R, Farmer P . Biological relevance of adduct detection to the chemoprevention of cancer. Clin Cancer Res. 2004; 10(15):4901-12. DOI: 10.1158/1078-0432.CCR-04-0098. View

4.
Baek D, Davis C, Ewing B, Gordon D, Green P . Characterization and predictive discovery of evolutionarily conserved mammalian alternative promoters. Genome Res. 2007; 17(2):145-55. PMC: 1781346. DOI: 10.1101/gr.5872707. View

5.
Gursoy-Yuzugullu O, Yuzugullu H, Yilmaz M, Ozturk M . Aflatoxin genotoxicity is associated with a defective DNA damage response bypassing p53 activation. Liver Int. 2011; 31(4):561-71. DOI: 10.1111/j.1478-3231.2011.02474.x. View