Evaluation of the Genotoxicity of Extracts of Houttuynia cordata Thunb.

2012 ◽  
Vol 40 (05) ◽  
pp. 1019-1032 ◽  
Author(s):  
Chang Keun Kang ◽  
Dae Sik Hah ◽  
Chung Hui Kim ◽  
Euikyung Kim ◽  
Jong Shu Kim
Keyword(s):  
Salmonella Typhimurium ◽  
Chromosome Aberration ◽  
Metabolic Activation ◽  
Mouse Bone Marrow ◽  
Houttuynia Cordata ◽  
Reverse Mutation ◽  
Methanol Extracts ◽  
Polychromatic Erythrocytes ◽  
Houttuynia Cordata Thunb ◽  
Mutation Assay

The present study was conducted to evaluate the activity of methanol extracts from Houttuynia cordata Thunb. (HC) in a reverse mutation assay in Salmonella typhimurium, and a chromosome aberration assay in the Chinese hamster ovary (CHO) cell line and to evaluate its effect on the occurrence of polychromatic erythrocytes in mice. In the reverse mutation assay using Salmonella typhimurium TA98, TA100, TA1535, and TA1537 and Escherichia coli WP2urvA-, methanol extracts of HC (5, 2.5, 1.25, 0.62, or 0.312 mg/plate) did not induce reverse mutations in the presence or absence of an S9 metabolic activation mixture. In the chromosome aberration test using CHO cells, methanol extracts (1.25, 2.5 or 5 μg/ml) caused a few incidences of structural and numerical aberrations, in both of absence or presence of an S9 metabolic activation mixture, but in comparison with the positive control group, these incidences were not significantly increased. In the mouse micronucleus test, no significant increases in the occurrence of micronucleated polychromatic erythrocytes were observed in male ICR mice that were orally administered methanol extracts of HC at doses of 2.0, 1.0, or 0.5 g/kg. From these results, we concluded that the methanol extracts of HC did not induce harmful effects on genes in bacteria, a mammalian cell system or in mouse bone marrow cells. Thus, HC's use for health promotion and/or a sick remedy for humans may be safe.

An Evaluation of Genotoxicity Tests With Aquateric® Aqueous Enteric Coating

1999 ◽  
Vol 18 (2) ◽  
pp. 117-122 ◽  
Author(s):  
Kathryn J. Batt ◽  
Lois A. Kotkoskie
Keyword(s):  
Bone Marrow ◽  
Ames Test ◽  
Micronucleus Test ◽  
Micronucleus Assay ◽  
Metabolic Activation ◽  
Mouse Bone Marrow ◽  
Enteric Coating ◽  
Polychromatic Erythrocytes ◽  
Mutation Assay ◽  
Mouse Lymphoma

The genotoxic potential of Aquateric® Aqueous Enteric Coating was evaluated in the Ames test, the mouse lymphoma mutation assay, and the mouse micronucleus test. Aquateric was not mu-tagenic when tested in Salmonella typhimurium cell strains TA98, TA100, TA1535, TA1537, TA1538, with or without metabolic activation. A mouse lymphoma assay was conducted at concentrations ranging from 116 to 2000 μg/ml and 116 to 1250 μg/ml in the absence and presence of metabolic activation, respectively. No increased mutant frequencies were noted for any concentration tested. Aquateric was tested in the mouse micronucleus assay at a single oral dose of 7200 mg/kg Aquateric (equivalent to 5000 mg/kg cellulose acetate phthalate, the major ingredient) and bone marrow was harvested at 24, 48, and 72 hours after treatment. There was no significant increase in the number of mouse bone marrow mi-cronucleated polychromatic erythrocytes in Aquateric-treated animals at any of the harvest times. Based on the negative results in the Ames test, the mouse lymphoma mutation assay, and the mouse micronucleus test, it was concluded that Aquateric is not genotoxic.

scholarly journals In VitroandIn VivoGenotoxicity Assessment ofAristolochia manshuriensisKom.

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Youn-Hwan Hwang ◽  
Taesoo Kim ◽  
Won-Kyung Cho ◽  
Hye Jin Yang ◽  
Dong Hoon Kwak ◽  
...  
Keyword(s):  
Chromosomal Aberration ◽  
Micronucleus Test ◽  
Safety Information ◽  
Chinese Hamster ◽  
Metabolic Activation ◽  
Vehicle Group ◽  
Reverse Mutation ◽  
Significant Difference ◽  
Chromosomal Aberration Test ◽  
Mutation Assay

Arisolochiae speciesplants containing aristolochic acids I and II (AA I and AA II) are well known to cause aristolochic acid nephropathy (AAN). Recently, there are various approaches to use AAs-containing herbs after the removal of their toxic factors. However, there is little information about genotoxicity ofArisolochiae manshuriensisKom. (AMK)per se. To obtain safety information for AMK, its genotoxicity was evaluated in accordance with OECD guideline. To evaluate genotoxicity of AMK, we tested bacterial reverse mutation assay, chromosomal aberration test, and micronucleus test. Here, we also determined the amounts of AA I and II in AMK (2.85 ± 0.08 and 0.50 ± 0.02 mg/g extract, resp.). In bacterial reverse mutation assay, AMK dose-dependently increased revertant colony numbers in TA98, TA100 and TA1537 regardless of metabolic activation. AMK increased the incidence of chromosomal aberration in Chinese hamster ovary-K1 cells, but there was no statistically significant difference. The incidences of micronucleus in bone marrow erythrocyte were significantly increased in mice after oral administration of AMK (5000 mg/kg), comparing with those of vehicle group (P<0.05). The results of three standard tests suggest that the genotoxicity of AMK is directly related to the AAs contents in AMK.

scholarly journals Genotoxicity of triiodothyronine: Effects on Salmonella typhimurium TA100 and human lymphocytes in vitro

Genetika ◽  
2017 ◽  
Vol 49 (2) ◽  
pp. 387-397
Author(s):  
Jasna Bosnjak-Neumüller ◽  
Ninoslav Djelic ◽  
Milena Radakovic ◽  
Stoimir Kolarevic ◽  
Dragana Mitic-Culafic ◽  
...  
Keyword(s):  
Salmonella Typhimurium ◽  
Mammalian Cells ◽  
Ames Test ◽  
Human Lymphocytes ◽  
Genetic Material ◽  
Genotoxic Effects ◽  
Reverse Mutation ◽  
Mutagenic Effects ◽  
Mutation Assay

There is increasing evidence that substances which are normally present in human or animal bodies may, under the certain circumstances, exhibit deleterious effects on genetic material, therefore acting as endogenous mutagenic agents. Since hormones represent one of the best studied endogenous mutagens, some research focused on the possible role of thyroid hormone in mutagenesis and carcinogenesis. Indeed, thyroid hormones accelerate aerobic metabolism and production of reactive oxygen species (ROS) and, therefore, may exhibit mutagenic effects in various test systems on mammalian cells. However, possible mutagenic effects on prokaryotic DNA has not been investigated so far. Hence, the aim of this research was to compare the sensitivity of TA 100 Salmonella typhimurium with and without metabolic activation with S9 fraction, and human lymphocytes to possible genotoxic effects of triiodothyronine (T3). Therefore, we used the reverse mutation assay on S. typhimurium (Ames test) and in vitro Comet assay in isolated peripheral blood human lymphocytes. In both tests-systems a broad spectrum of T3 concentrations was applied. The obtained results showed absence of genotoxic effects of T3 in bacterial reverse mutation assay and very profound genotoxic effects in human lymphocytes at concentrations higher than 15 ?M. We only observed cytotoxic effects in bacterial system at very high T3 concentrations (300 and 500 ?M). In conclusion, T3 was unable to increase the level of reverse mutations in Ames test both with and without S9 mix. Therefore, it seems that ROS production in mitochondria may be the primary cause of DNA damage caused by T3 in mammalian cells.

scholarly journals EVALUATION OF CERTAIN PESTICIDE MIXTURES FOR THEIR MUTAGENICITY USING AMES Salmonella typhimurium - REVERSE MUTATION ASSAY

2019 ◽  
Vol 7 (6) ◽  
pp. 606-612
Author(s):  
B. Reddi Bhargavi ◽  
◽  
Ravi Kumar VELLANKI ◽  
Jagadeeswara Kanala Reddy ◽  
◽  
...  
Keyword(s):  
Salmonella Typhimurium ◽  
Reverse Mutation ◽  
Pesticide Mixtures ◽  
Mutation Assay

scholarly journals Effects of Flue-curing on Cigarette Smoke Condensates Mutagenicity

2010 ◽  
Vol 24 (2) ◽  
pp. 72-77
Author(s):  
A Morin ◽  
N Poirier ◽  
D Prefontaine ◽  
M Lacasse
Keyword(s):  
Salmonella Typhimurium ◽  
Cigarette Smoke ◽  
Tobacco Smoke ◽  
Ames Test ◽  
Chemical Properties ◽  
Metabolic Activation ◽  
Leaf Chemistry ◽  
Cigarette Smoke Condensate ◽  
Tobacco Leaves ◽  
Reverse Mutation

AbstractFlue-curing is a post harvest conditioning process which strongly affects the tobacco leaf chemistry, and consequently the chemical properties of tobacco smoke. Several studies identified the major changes in tobacco chemistry occurring during flue-curing. It is not known how flue-curing contributes to changes in bioactivity of cigarette smoke condensate (CSC). In this study, tobacco leaves collected throughout the twelve days of flue-curing were used to prepare cigarettes that were smoked to generate CSC samples. The assessment of mutagenicity was performed using the Bacterial Reverse Mutation / Ames test with Salmonella typhimurium TA98 in the presence of S9 metabolic activation. CSC from cured leaves were significantly more mutagenic than CSC from uncured leaves. The number of revertants was positively influenced by the duration of the curing. The effect of the duration of curing on the number of revertants was more pronounced with increasing CSC concentration.

Antigenotoxic Effects of Water Extract from Korean Fermented Soybean Paste (Doen-jang)

2004 ◽  
Vol 67 (1) ◽  
pp. 156-161 ◽  
Author(s):  
JONG-GYU KIM
Keyword(s):  
Salmonella Typhimurium ◽  
Chromosome Aberration ◽  
Aflatoxin B1 ◽  
Chinese Hamster ◽  
Water Extract ◽  
Inhibitory Effects ◽  
Soybean Paste ◽  
Mutation Assay ◽  
Chromosome Aberration Test

Aflatoxin B1 is a major metabolite of the toxigenic molds Aspergillus flavus and Aspergillus parasiticus. In this study, a bacterial reverse mutation assay with Salmonella Typhimurium strains TA1535, TA1537, TA98, TA100, and TA102 and an in vitro chromosome aberration test with Chinese hamster lung (CHL) cells were used to investigate the genotoxicity of water extract from Korean soybean paste (doen-jang [dwen-jahng]) and its antigenotoxic activity against aflatoxin B1. The water extract itself did not exhibit cytotoxicity or mutagenicity. The extract significantly reduced the numbers of revertants when it was added to the assay system with Salmonella Typhimurium TA100 (P &lt; 0.05). The extract also exhibited significant inhibitory effects on chromosome aberration in CHL cells (P &lt; 0.05). Dose-response relationships were observed between the concentration of the water extract and both its antimutagenic effect and its suppression of chromosome aberration. The results of this work indicate that water extract from Korean soybean paste could have potential as an antigenotoxic substance.

scholarly journals Genotoxicity Evaluation of an Ethanol Extract Mixture of Astragali Radix and Salviae miltiorrhizae Radix

2018 ◽  
Vol 2018 ◽  
pp. 1-6 ◽  
Author(s):  
Jin-Seok Lee ◽  
Jung-Hyo Cho ◽  
Dong-Soo Lee ◽  
Chang-Gue Son
Keyword(s):  
Bone Marrow ◽  
Chromosome Aberration ◽  
Chinese Hamster ◽  
Ethanol Extract ◽  
Ovary Cell ◽  
Mouse Bone Marrow ◽  
Astragali Radix ◽  
Icr Mouse ◽  
Polychromatic Erythrocytes ◽  
Chromosome Aberration Test

Myelophil, a combination of Astragali Radix and Salviae Radix, is one of the most commonly used remedies for disorders of Qi and blood in traditional Chinese medicine. Based on the clinical applications of these plants, in particular to pregnant woman, this study aimed to evaluate the genotoxic potential of an ethanol extract mixture of the above two herbs, called Myelophil. Following the Organization for Economic Cooperation and Development (OECD) Guideline methods, a genotoxicity test was conducted using a bacterial reverse mutation test with Salmonella typhimurium (TA98, TA100, TA1535, and TA1537) and Escherichia coli (WP2μvrA), an in vitro mammalian chromosome aberration test using a Chinese hamster ovary cell line (CHO-K1), and an in vivo mammalian erythrocyte micronucleus test using ICR mouse bone marrow. In the Ames test, for both types of mutations (base substitution and frameshift) under conditions with/without an S9 mix up to 5,000 μg/plate, Myelophil did not increase the number of revertant colonies of all S. typhimurium strains as well as E. coli strain. For both short (6 h) and long tests with/without S9 mix, the chromosome aberration test did not show any significant increase in the number of structural or numerical chromosome aberrations by Myelophil. In addition, no significant change in the number of micronucleated polychromatic erythrocytes or polychromatic erythrocytes was observed in the bone marrow of an ICR mouse administered Myelophil orally at 2,000 mg/kg/day for 2 days, respectively. These results are the first to provide experimental evidence that Myelophil, an ethanol extract mixture of Astragali Radix and Salviae Radix, has no risk of genotoxicity.

Toxicology of Diethylene Glycol Butyl Ether 3. Genotoxicity Evaluation in an In Vitro Gene Mutation Assay and an In Vivo Cytogenetic Test

1993 ◽  
Vol 12 (2) ◽  
pp. 155-159 ◽  
Author(s):  
B. Bhaskar Gollapudi ◽  
V. A. Linscombe ◽  
M. L. Mcclintock ◽  
A. K. Sinha ◽  
C. R. Stack
Keyword(s):  
Bone Marrow ◽  
Gene Mutation ◽  
Micronucleus Test ◽  
Mouse Bone Marrow ◽  
Butyl Ether ◽  
Polychromatic Erythrocytes ◽  
Mutation Assay ◽  
Gene Mutation Assay

DGBE was evaluated in a forward gene mutation assay at the HGPRT locus of CHO cells in culture and in an in vivo mouse bone marrow micronucleus test for cytogenetic damage. DGBE did not elicit a positive response in the CHO/HGPRT assay when tested up to a maximum concentration of 5000 μg/ml with and without an external metabolic activation system (S-9). In the micronucleus test employing three post-treatment bone marrow sampling times (24, 48, and 72 hr), DGBE was ineffective in increasing the incidence of micronucleated polychromatic erythrocytes (MN-PCE) when tested in both sexes up to a maximum tolerated dose of 3300 mg/kg body weight. Thus, these data and those of others indicate a general lack of genotoxic potential for DGBE in short-term tests.

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