scholarly journals Antimutagenic effect of resveratrol

2011 ◽  
Vol 23 (No. 5) ◽  
pp. 202-208 ◽  
Author(s):  
M. Langová ◽  
Z. Polívková ◽  
P. Šmerák ◽  
J. Bártová ◽  
I. Bárta
Keyword(s):  
Protective Effect ◽  
Ames Test ◽  
Micronucleus Test ◽  
Mutagenic Activity ◽  
Population Based ◽  
Antimutagenic Activity ◽  
Protective Effects ◽  
Laboratory Studies ◽  
Micronucleus Tests ◽  
Aflatoxin B

Evidence exists from population-based and laboratory studies that some phytochemicals have protective effects against tumors or other diseases and reveal antimutagenic activity. We studied the protective effect of the plant phytoallexin resveratrol on the mutagenic activity of three mutagens, i.e. aflatoxin B<sub>1</sub> (AFB<sub>1</sub>), 2-amino-3-methylimidazo[4,5-f]qui-noline (IQ) and N-nitroso-N-methylurea (MNU) using the Ames and the micronucleus tests. In the Ames test, we proved a significant antimutagenic activity only against the indirect mutagens AFB<sub>1</sub> and IQ, not against the direct mutagen MNU. A significant decrease of mutagenicity of all three mutagens was detected by the micronucleus test. &nbsp;

scholarly journals Antimutagenic effect of epigallocatechin gallate and its effect on the immune response in mice

2011 ◽  
Vol 24 (No. 4) ◽  
pp. 180-192 ◽  
Author(s):  
P. Šmerák ◽  
H. Šestáková ◽  
Z. Polívková ◽  
R. Štětina ◽  
M. Langová ◽  
...  
Keyword(s):  
Green Tea ◽  
Ames Test ◽  
Bone Marrow Cells ◽  
Micronucleus Test ◽  
Epigallocatechin Gallate ◽  
Antimutagenic Activity ◽  
Dna Breaks ◽  
Colon Cells ◽  
Antimutagenic Effect ◽  
Aflatoxin B

Green tea is the second-most consumed beverage in the world (water is the first one) and has been used medicinally for centuries in Indiaand China. The active substances in the green tea are polyphenols (catechins) and flavonols which possess a potent antioxidant activity. Epigallocatechin gallate (EGCG) is one of the four major green tea catechins. Using the Ames test, micronucleus test, comet assay, chemiluminescence test, and blastic transformation test, we examined the antimutagenic effects of chemoprotective substance epigallocatechin gallate (EGCG) in the pure form on the mutagenicity induced by three reference mutagens: aflatoxin B<sub>1</sub> (AFB<sub>1</sub>), 2-amino-3-methylimidazo [4,5-f] qui-noline (IQ), and N-nitroso-N-methylurea (MNU), and the effect of EGCG on the immunosuppression caused by these mutagens. Using the Ames test the dose dependent antimutagenic activity of EGCG was proved against indirect mutagens AFB<sub>1</sub> and IQ, but not against the direct mutagen MNU. In the micronucleus test, EGCG had antimutagenic effect upon all three mutagens. EGCG decreased the level of DNA breaks induced by AFB<sub>1</sub> in bone marrow cells and colon epithelium, and the level of DNA breaks induced by MNU in colon cells to the level found in control. The reparatory effect of EGCG on immunosupression induced by all three carcinogenic compounds was proved using chemiluminescence and blastic trasformation tests. &nbsp;

scholarly journals Mutagenic effects of selected trichothecene mycotoxins and their combinations with aflatoxin B1

2013 ◽  
Vol 19 (No. 3) ◽  
pp. 90-96 ◽  
Author(s):  
P. Šmerák ◽  
I. Bárta ◽  
Z. Polívková ◽  
J. Bártová ◽  
M. Sedmíková
Keyword(s):  
Ames Test ◽  
Micronucleus Test ◽  
Mutagenic Activity ◽  
Mutagenic Effect ◽  
Low Doses ◽  
Test Systems ◽  
Strong Mutagen ◽  
The Individual ◽  
Aflatoxin B ◽  
Mutagenic Effects

The authors focused on the amplification of data on the mutagenicity of selected trichothecene mycotoxins (T-2 toxin, vomitoxin) and their combination with aflatoxin B<sub>1</sub>,which is known to be a strong mutagen. Mutagenic activity was investigated using the Ames test in a prokaryote model at low doses (close to 0.1 LD<sub>50</sub>). Whereas the individual trichothecene mycotoxins (T-2 toxin, vomitoxin) did not show any mutagenic activity in the test systems mentioned, in combination with AFB<sub>1</sub>, or as a combination of all three mycotoxins, they showed a mutagenic effect significantly greater than AFB<sub>1</sub> alone in the Ames test (in strain TA98 at all concentrations) as well as in the micronucleus test (combination of T-2 toxin with AFB<sub>1</sub>).

scholarly journals Antimutagenic effect of curcumin and its effect on the immune response in mice

2011 ◽  
Vol 24 (No. 2) ◽  
pp. 72-83 ◽  
Author(s):  
P. Šmerák ◽  
Z. Polívková ◽  
H. Šestáková ◽  
R. Štětina ◽  
BártaI ◽  
...  
Keyword(s):  
Immune Response ◽  
Comet Assay ◽  
Ames Test ◽  
Micronucleus Test ◽  
Pure Form ◽  
Edible Plants ◽  
Blastic Transformation ◽  
Antimutagenic Effect ◽  
Aflatoxin B

A wide array of antioxidative and anti-inflammatory substances derived from edible plants have been reported to possess chemopreventive and chemoprotective activities. Among the most extensively investigated and well-defined dietary chemopreventives is curcumin. Using the Ames test and in vivo micronucleus test, chemiluminescence test, blastic transformation test, and comet assay, we examined the antimutagenic effects of the chemically identified chemoprotective substance curcumin (diferuloylmethane) in the pure form on mutagenicity induced by three reference mutagens: aflatoxin B<sub>1</sub> (AFB<sub>1</sub>), 2-amino-3-metylimidazo[4,5-f]quinoline (IQ), and N-nitroso-N-metylurea (MNU), and the effect of curcumin on the immunosuppression caused by these mutagens. Curcumin in the pure form showed a clear antimutagenic and immunomodulatory activities on mutagenicity and immunosuppression induced by reference mutagens. &nbsp;

scholarly journals Potential hazard of simultaneous occurrence of aflatoxin B-1 and ochratoxin A

2001 ◽  
Vol 46 (No. 6) ◽  
pp. 169-171 ◽  
Author(s):  
M. Sedmíková ◽  
H. Reisnerová ◽  
Z. Dufková ◽  
I. Bárta ◽  
F. Jílek
Keyword(s):  
Ochratoxin A ◽  
Aflatoxin B1 ◽  
Ames Test ◽  
Mutagenic Activity ◽  
Simultaneous Occurrence ◽  
Potential Hazard ◽  
Aflatoxin B

Contents of aflatoxin B1&nbsp;(AFB1) and ochratoxin A (OA) in the samples of wheat and barley were detected by RIA method. Average contents of AFB1&nbsp;in the samples of wheat and barley were 2.4 &micro;g/kg and 2.2 &micro;g/kg, respectively. Average contents of OA in the samples of wheat and barley were 3.1 &micro;g/kg and 2.4 &micro;g/kg, respectively. The contents of mycotoxins corresponded to the allowed limits in food. During the studies of mutagenic activity of mycotoxins and their combinations by means of Ames test it was found that OA could increase the mutagenicity of AFB1&nbsp;in the case of their simultaneous occurrence in the same substrate.

scholarly journals The Mutagenicity and Antimutagenicity of Canarium odontophyllum (Dabai) Acetone Leaves Extracts

2017 ◽  
Vol 9 (13) ◽  
pp. 62
Author(s):  
Ahmad Rohi Ghazali ◽  
Farah Mardhiah Khairuddin ◽  
Tava Shelan Nagapan ◽  
Dayang Fredalina Basri
Keyword(s):  
Ames Test ◽  
Mutagenic Activity ◽  
Biological Activities ◽  
Negative Control ◽  
Antimutagenic Activity ◽  
Bacterial Strains ◽  
Mutagenicity Assay ◽  
Control Plate ◽  
Canarium Odontophyllum ◽  
Acetone Extracts

Canarium odontophyllum or locally known as Dabai in Sarawak is a fruit largely consumed by the locals. Based on previous studies, the plant possessed various biological activities, such as antimicrobial, antioxidant, antifungal and anticancer. Our aim was to investigate the mutagenicity and antimutagenicity of C. odontophyllum acetone leaves extracts by using the Ames test (Salmonella reverse mutagenicity assay).The Ames test also involved the pre-incubation method against Salmonella typhimurium TA98 and TA100 bacterial strains in the absence and presence of metabolic activator S9 system. C. odontophyllum crude acetone extracts were diluted with 10% DMSO to obtain three different concentrations of 3.125, 12.5 and 50 mg/ml. To determine the mutagenicity effects of the extracts, each concentration of the extract was evaluated based on the two-fold value of the number of revertant’s colony in negative control plate as the cut-of point. No mutagenic activity was observed for the frameshift mutation (TA98) and base-pair substitution mutation (TA100) in all concentrations of C. odontophyllum in the presence and absence of metabolic activator S9 system. Antimutagenicity test was carried out to determine the potential of C. odontophyllum extracts to inhibit the mutation induced by specific mutagens. The highest antimutagenic activity was seen in the presence of metabolic activator S9 system with inhibition percentage greater than 50% in both bacteria strains TA98 (62.38%) and TA100 (58.24%). In conclusion, C. odontophyllum acetone leaves extract was not mutagenic and had significant inhibitory effects on mutagenicity in both bacterial strains with and without the metabolic activator S9 system. Our results could contribute to the safe use of C. odontophyllum. In addition, based on the significant antimutagenic activity demonstrated by the C. odontophyllum acetone leaves extracts, the extract could also be developed as a chemopreventive agent.

scholarly journals Antimutagenic effect of genistein

2011 ◽  
Vol 24 (No. 3) ◽  
pp. 119-126 ◽  
Author(s):  
Z. Polívková ◽  
M. Langová ◽  
P. Šmerák ◽  
B. Bártová ◽  
I. Bárta
Keyword(s):  
Protective Effect ◽  
Salmonella Typhimurium ◽  
Ames Test ◽  
Micronucleus Test ◽  
Health Benefits ◽  
Antimutagenic Effect ◽  
Mutagenicity Test ◽  
Prostate Cancers ◽  
The Individual ◽  
Antigenotoxic Effect

A great variety of health benefits including the protection against breast and prostate cancers has been attributed to the soya consumption, because of the presence of soy beans isoflavones, genistein, and others. We investigated the antigenotoxic effect of genistein on the genotoxicity of three mutagens and carcinogens &ndash; aflatoxine B<sub>1</sub> (AFB<sub>1</sub>), 2-amino-3-methylimidazo [4,5-f]quinoline (IQ), and N-nitroso-N-methylurea (MNU), using the Ames bacterial mutagenicity test and the micronucleus test. In the Ames test on Salmonella typhimurium, a significant antimutagenic effect was determined against the indirect mutagen AFB<sub>1 </sub>in two strains, TA98 and TA100. However, the effect on the IQ indirect mutagenicity was more pronounced in the test with TA98 than with TA100. The mutagenicity of the direct mutagen MNU was suppressed by genistein only at its highest concentration used (300 &micro;g/plate). The protective effect of genistein against all three mutagens was proved in the micronucleus test as the treatment of mice with the combinations of genistein and mutagens resulted in a significant reduction of the number of micronuclei in comparison with the number of micronuclei induced by the individual mutagens alone. &nbsp;

scholarly journals Assessment of the mutagenic, antimutagenic and cytotoxic activities of ethanolic extract of araticum (Annona crassiflora Mart. 1841) by micronucleus test in mice

2008 ◽  
Vol 68 (1) ◽  
pp. 141-147 ◽  
Author(s):  
JB. Vilar ◽  
FL. Ferreira ◽  
PH. Ferri ◽  
LA. Guillo ◽  
L. Chen Chen
Keyword(s):  
Micronucleus Test ◽  
Mutagenic Activity ◽  
Ethanolic Extract ◽  
Positive Control ◽  
Control Group ◽  
Cytotoxic Activities ◽  
Antimutagenic Activity ◽  
Polychromatic Erythrocytes ◽  
Significant Difference ◽  
Annona Crassiflora

A typical Brazilian plant, araticum (Annona crassiflora Mart.), is widely used in humans as therapeutic medicine to treat several diseases such as diarrhea, rheumatism and syphilis. It contains acetogenins which present cytotoxic, antitumogenic, and antiparasitic properties. In this study, mutagenic, antimutagenic and cytotoxic effects of araticum leaves ethanolic extract were evaluated by micronucleus test in mice. To evaluate the mutagenic activity, animals were treated with ethanolic extract of araticum (EEA) using 10, 20, 50, 100 and 160 mg.kg-1. For all doses, micronucleated polychromatic erythrocytes (MNPCE) frequency was evaluated at 24, 48 and 72 hours after treatment. To evaluate the antimutagenic activity, animals were treated with 10, 20, 50 and 100 mg.kg-1 of EEA and 4 mg.kg-1 of MMC simultaneously. The frequency of MNPCE was evaluated 36 hours after exposure. Cytotoxicity was evaluated by the polychromatic and normochromatic erythrocytes ratio (PCE/NCE). In the mutagenicity assessment, all doses of EEA resulted in no significant increase of MNPCE (P > 0.05), compared to solvent- control group. Regarding administration time, no significant difference among three evaluation periods was observed (P > 0.05). Such results indicate that EEA did not exert mutagenic activity. Cytotoxicity was evident in doses of 50, 100 and 160 mg.kg-1 at 24 and 48 hours after exposure. Concerning antimutagenicity, except the 10 mg.kg-1 co-administered with 4 mg/kg of MMC, all doses reduced significantly the frequency of MNPCE compared to the positive control group (P < 0.05). These results, therefore, indicate an antimutagenic activity of the EEA. Cytotoxicity was significantly increased (P < 0.01) at 100 mg.kg-1 EEA doses co-administered with 4 mg.kg-1 of MMC.

The Protective Effect of Metformin against Oxandrolone-Induced Infertility in Male Rats

2020 ◽  
Vol 26 ◽  
Author(s):  
Abdulqader Fadhil Abed ◽  
Yazun Bashir Jarrar ◽  
Hamzeh J Al-Ameer ◽  
Wajdy Al-Awaida ◽  
Su-Jun Lee
Keyword(s):  
Gene Expression ◽  
Male Infertility ◽  
Protective Effect ◽  
Histological Examination ◽  
Sperm Count ◽  
Serum Testosterone ◽  
Male Rats ◽  
P Value ◽  
Protective Effects ◽  
Rt Pcr

Background: Oxandrolone is a synthetic testosterone analogue that is widely used among bodybuilders and athletes. However, oxandrolone causes male infertility. Recently, it was found that metformin reduces the risk of infertility associated with diabetes mellitus. Aim: This study aimed to investigate the protective effects of metformin against oxandrolone-induced infertility in male rats. Methods: Rats continuously received one of four treatments (n=7) over 14 days: control DMSO administration, oxandrolone administration, metformin administration, or co-administration of oxandrolone and metformin. Doses were equivalent to those used for human treatment. Subsequently, testicular and blood samples were collected for morphological, biochemical, and histological examination. In addition, gene expression of the testosterone synthesizing enzyme CYP11A1 was analyzed in the testes using RT-PCR. Results: Oxandrolone administration induced male infertility by significantly reducing relative weights of testes by 48%, sperm count by 82%, and serum testosterone levels by 96% (ANOVA, P value < 0.05). In addition, histological examination determined that oxandrolone caused spermatogenic arrest which was associated with 2-fold downregulation of testicular CYP11A1 gene expression. However, co-administration of metformin with oxandrolone significantly ameliorated toxicological alterations induced by oxandrolone exposure (ANOVA, P value < 0.05). Conclusion: Metformin administration protected against oxandrolone-induced infertility in male rats. Further clinical studies are needed to confirm the protective effect of metformin against oxandrolone-induced infertility among athletes.

In vitro Cytotoxicity and Genotoxicity Analysis of Ten Tannery Chemicals Using SOS/umu Tests and High-content In vitro Micronucleus Tests

2018 ◽  
Vol 21 (4) ◽  
pp. 262-270 ◽  
Author(s):  
Zehao Huang ◽  
Na Li ◽  
Kaifeng Rao ◽  
Cuiting Liu ◽  
Zijian Wang ◽  
...  
Keyword(s):  
Micronucleus Test ◽  
A549 Cells ◽  
Quantitative Structure Activity Relationship ◽  
In Vitro Cytotoxicity ◽  
Cytotoxic Effects ◽  
Qsar Analysis ◽  
Cell Assays ◽  
Micronucleus Tests ◽  
Damaging Effects

Background: More than 2,000 chemicals have been used in the tannery industry. Although some tannery chemicals have been reported to have harmful effects on both human health and the environment, only a few have been subjected to genotoxicity and cytotoxicity evaluations. Objective: This study focused on cytotoxicity and genotoxicity of ten tannery chemicals widely used in China. Materials and Methods: DNA-damaging effects were measured using the SOS/umu test with Salmonella typhimurium TA1535/pSK1002. Chromosome-damaging and cytotoxic effects were determined with the high-content in vitro Micronucleus test (MN test) using the human-derived cell lines MGC-803 and A549. Conclusion: The cytotoxicity of the ten tannery chemicals differed somewhat between the two cell assays, with A549 cells being more sensitive than MGC-803 cells. None of the chemicals induced DNA damage before metabolism, but one was found to have DNA-damaging effects on metabolism. Four of the chemicals, DY64, SB1, DB71 and RR120, were found to have chromosome-damaging effects. A Quantitative Structure-Activity Relationship (QSAR) analysis indicated that one structural feature favouring chemical genotoxicity, Hacceptor-path3-Hacceptor, may contribute to the chromosome-damaging effects of the four MN-test-positive chemicals.

Antiproliferative and Genotoxic Action of an Underexploited Organoteluran Derivative on Sarcoma 180 Cells

2020 ◽  
Vol 20 ◽  
Author(s):  
Maria L.L. Barreto do Nascimento ◽  
Antonielly Campinho dos Reis ◽  
José V.O. Santos ◽  
Helber A. Negreiros ◽  
Felipe C. Carneiro da Silva ◽  
...  
Keyword(s):  
Flow Cytometry ◽  
Nuclear Division ◽  
Micronucleus Test ◽  
Mutagenic Activity ◽  
Chemical Compounds ◽  
Negative Control ◽  
Nuclear Division Index ◽  
Apoptosis And Necrosis ◽  
Genotoxicity Tests ◽  
Genotoxic Action

Background: The search for novel metallic chemical compounds with toxicogenic effects have been of great importance for more efficient cancer treatment. Objective: The study evaluated the cytotoxic, genotoxic and mutagenic activity of organoteluran RF07 in S-180 cell line. Methods: The bioassays used were cell viability with 3-(4,5-dimethyl-2-thiazole)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) test, evaluation of apoptosis and necrosis using fluorescence and flow cytometry, cytokinesis-block micronucleus test and comet assay. The compound was tested at 1; 2.5 and 5 µM. Results: The results showed the cytotoxicity of RF07 at concentrations of 2.5, 5, 10 and 20 µM when compared to the negative control. For genotoxicity tests, RF07 showed effects in all concentrations assessed by increased index and frequencies of damage and mutagenic alterations. The compound was also cytotoxic due to the significant decrease in nuclear division index, with significant values of apoptosis and necrosis. The results of fluorescence and flow cytometry showed apoptosis as the main type of cell death caused by RF07 at 5 µM, which is thought to avoid an aggressive immune response of the organism. Conclusion: In addition to cytotoxic and genotoxic effects, RF07 creates good perspectives for future antitumor formulations.

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