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1.
Cell Physiol Biochem ; 55(6): 704-725, 2021 Nov 18.
Article in English | MEDLINE | ID: mdl-34791862

ABSTRACT

BACKGROUND/AIMS: Pulmonary fibrosis can be caused by genetic abnormalities, autoimmune disorders or exposure to environmental pollutants. All these causes have in common the excessive production of oxidative stress species that initiate a cascade of molecular mechanism underlying fibrosis in a variety of organs, including lungs. The chemical name of Atrazine (ATR) is 6-chloro-N-ethyl-N'-(1-methylethyl)-1,3,5-triazine-2,4-diamine, and it is the most commonly used broad-spectrum herbicide in agricultural crops. Additionally, Bleomycin is a chemotherapeutic agent often used for different lymphoma with a seriously pulmonary complication. The most accredited hypothesis that may explain the mechanism of toxicity induced by ATR or bleomycin is exactly the production of reactive oxygen species (ROS) that leads to an unbalance in the physiological anti-oxidant system. However, until today, nobody has investigated the effect of ATR exposure during pulmonary fibrosis. METHODS: Mice were subject to ATR exposure, to bleomycin injection or to both. At the end of experiment, the lungs and blood were collected. Additionally, we analyzed by different test such as open field, pole and rotarod test or other we investigated the effects of ATR or bleomycin exposure on behavior. RESULTS: Following ATR or bleomycin induction, we found a significant increase in lung damage, fibrosis, and oxidative stress. This condition was significantly worsened when the animals injected with bleomycin were also exposed to ATR. Additionally, we observed significant motor and non-motor impairment in animals exposed to ATR. CONCLUSION: Our study demonstrates that ATR exposure, decrease nuclear factor-erythroid 2-related factor (Nrf2) pathways in both lung and brain.


Subject(s)
Atrazine/adverse effects , Brain Diseases/metabolism , Brain/metabolism , NF-E2-Related Factor 2/metabolism , Administration, Inhalation , Animals , Atrazine/pharmacology , Bleomycin/adverse effects , Bleomycin/pharmacology , Brain/pathology , Brain Diseases/etiology , Brain Diseases/pathology , Male , Mice , Pulmonary Fibrosis/chemically induced , Pulmonary Fibrosis/complications , Pulmonary Fibrosis/metabolism , Pulmonary Fibrosis/pathology
2.
Biol Reprod ; 104(5): 1162-1180, 2021 05 07.
Article in English | MEDLINE | ID: mdl-33624745

ABSTRACT

Atrazine (ATZ) is an extensively used herbicide and ubiquitous environmental contaminant. ATZ and its metabolite, diaminochlorotriazine (DACT), cause several cellular and functional alterations in spermatozoa. We aimed to examine the effect of ATZ/DACT on spermatozoon DNA integrity, fertilization competence, embryonic development, and transcriptome profile of in vitro-produced embryos derived from fertilization with pre-exposed sperm. Bovine spermatozoa exposed to ATZ (0.1 or 1 µM) or DACT (1 or 10 µM) during in vitro capacitation were used for in vitro fertilization of untreated oocytes. Cleavage and blastocyst-formation rates were evaluated 42 h and 7 days postfertilization, respectively. The association between DNA fragmentation and apoptosis (annexin V kit) was determined. Fertilization competence of annexin-positive (AV+) and annexin-negative (AV-) spermatozoa was examined. Microarray analysis was performed for 7-day blastocysts. Intracytoplasmic sperm injection was performed with control (AV+, AV-) and DACT (AV+, AV-) spermatozoa. Cleavage rates did not differ between groups and blastocyst formation tended to be higher for AV- vs. AV+ in both control and DACT groups, suggesting that acrosome reaction, rather than DNA fragmentation, underlies the reduced cleavage. Transcriptomic analysis revealed 139 and 230 differentially expressed genes in blastocysts derived from ATZ- and DACT-exposed spermatozoa, respectively, relative to controls. Proteomic analysis shown differential expression of proteins in ATZ- or DACT-treated spermatozoa, in particular proteins related to cellular processes and biological pathways. Therefore, we assume that factors delivered by the spermatozoa, regardless of DNA fragmentation, are also involved. Overall, the current study reveals a deleterious carryover effect of ATZ/DACT from the spermatozoa to the developing embryo.


Subject(s)
Atrazine/adverse effects , Cattle/physiology , Herbicides/adverse effects , Spermatozoa/drug effects , Transcriptome/drug effects , Animals , Embryo, Mammalian/drug effects , Embryo, Mammalian/metabolism , Male , Spermatozoa/metabolism
3.
Cell Biol Toxicol ; 37(3): 421-439, 2021 06.
Article in English | MEDLINE | ID: mdl-32737625

ABSTRACT

Atrazine (ATZ), a commonly used pesticide linked to endocrine disruption, cancer, and altered neurochemistry, frequently contaminates water sources at levels above the US Environmental Protection Agency's 3 parts per billion (ppb; µg/L) maximum contaminant level. Adult male zebrafish behavior, brain transcriptome, brain methylation status, and neuropathology were examined to test the hypothesis that embryonic ATZ exposure causes delayed neurotoxicity, according to the developmental origins of health and disease paradigm. Zebrafish (Danio rerio) embryos were exposed to 0 ppb, 0.3 ppb, 3 ppb, or 30 ppb ATZ during embryogenesis (1-72 h post fertilization (hpf)), then rinsed and raised to maturity. At 9 months post fertilization (mpf), males had decreased locomotor parameters during a battery of behavioral tests. Transcriptomic analysis identified altered gene expression in organismal development, cancer, and nervous and reproductive system development and function pathways and networks. The brain was evaluated histopathologically for morphometric differences, and decreased numbers of cells were identified in raphe populations. Global methylation levels were evaluated at 12 mpf, and the body length, body weight, and brain weight were measured at 14 mpf to evaluate effects of ATZ on mature brain size. No significant difference in genome methylation or brain size was observed. The results demonstrate that developmental exposure to ATZ does affect neurodevelopment and neural function in adult male zebrafish and raises concern for possible health effects in humans due to ATZ's environmental presence and persistence. Graphical abstract.


Subject(s)
Atrazine/adverse effects , Brain/drug effects , Pesticides/adverse effects , Transcriptome/genetics , Animals , Brain/pathology , Embryonic Development/drug effects , Endocrine Disruptors/adverse effects , Epigenesis, Genetic/drug effects , Gene Expression Regulation/drug effects , Gene Expression Regulation, Developmental/drug effects , Humans , Larva/drug effects , Larva/genetics , Larva/growth & development , Transcriptome/drug effects , Water Pollutants, Chemical/adverse effects , Zebrafish/embryology , Zebrafish/genetics , Zebrafish/growth & development
4.
Int J Mol Sci ; 22(15)2021 Jul 26.
Article in English | MEDLINE | ID: mdl-34360708

ABSTRACT

BACKGROUND: exposure to environmental contaminants has been linked to an increased risk of neurological diseases and poor outcomes. Chemical name of Atrazine (ATR) is 6-chloro-N-ethyl-N'-(1-methylethyl)-1,3,5-triazine-2,4-diamine, and it is the most commonly used broad-spectrum herbicide in agricultural crops. Several studies have demonstrated that ATR has the potential to be harmful to the brain's neuronal circuits. Until today nobody has explored the effect of ATR inhalation on young and aged mice. METHODS: young and aged mice were subject to 25 mg of ATR in a vehicle made with saline and 10% of Dimethyl sulfoxide (DMSO) every day for 28 days. At the end of experiment different behavioral test were made and brain was collected. RESULTS: exposure to ATR induced the same response in terms of behavioral alterations and motor and memory impairment in mice but in aged group was more marked. Additionally, in both young and aged mice ATR inhalations induced oxidative stress with impairment in physiological antioxidant response, lipid peroxidation, nuclear factor kappa-light-chain-enhancer of activated B cells (nf-κb) pathways activation with consequences of pro-inflammatory cytokines release and apoptosis. However, the older group was shown to be more sensitive to ATR inhalation. CONCLUSIONS: our results showed that aged mice were more susceptible compared to young mice to air pollutants exposure, put in place a minor physiologically response was seen when exposed to it.


Subject(s)
Aging/drug effects , Apoptosis/drug effects , Atrazine/adverse effects , Brain/metabolism , Administration, Inhalation , Aging/metabolism , Aging/pathology , Animals , Atrazine/pharmacology , Brain/pathology , Inflammation/chemically induced , Inflammation/metabolism , Inflammation/pathology , Male , Mice
5.
Ecotoxicology ; 28(5): 499-506, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30969405

ABSTRACT

The behavior of many animals relies upon the input of chemical signals throughout the environment. Those animals that live in close proximity to humans may then be at risk, as the input of anthropogenic chemicals can have significant sublethal effects by masking or altering these naturally occurring signals. While the herbicide atrazine has been found to have the potential to alter such chemical information, research is lacking on how it may impact agrobiont arthropods which are the first and most direct line of exposure. Here we investigated the sublethal effects atrazine may be playing on an agrobiont wolf spider that makes up a major component of agricultural spider communities in the Eastern United States. We exposed spiders to ecologically relevant doses of atrazine and monitored general activity patterns as well as mating behaviors. We found that while sex determined a large portion of activity variation in these predators, both males and females spent more time mobile but at lower speeds in the presence of atrazine. We did not find any evidence for info-disruption based on male courtship rate and mating success, but with increasing dosage of atrazine came shortened bouts of courtship leading to copulation. These results suggest that atrazine changed activity patterns of a wolf spider, which may result in altered foraging, survival, and reproduction.


Subject(s)
Atrazine/adverse effects , Herbicides/adverse effects , Predatory Behavior/drug effects , Sexual Behavior, Animal/drug effects , Spiders/drug effects , Animals , Female , Male , Spiders/physiology
6.
J Oral Pathol Med ; 47(7): 641-651, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29489035

ABSTRACT

Humans may be exposed to pesticides such as fungicides, herbicides, and insecticides, during occupational and non-occupational activities. Pesticides could be related to cancer development mainly because of their effects on the endocrine and immune systems and their cumulative effect. The present review evaluated in current literature evidence of an association between exposure to pesticides and the occurrence of head and neck cancer (HNC). A literature search for cohort studies was conducted in the PubMed, Web of science, and Cochrane databases. Methodological quality of each study was rated with the Scottish Intercollegiate Guidelines Network (SIGN) checklist. One thousand one hundred and thirty-two studies were identified. Thirty-two were included. Most of the studies found addressed occupational exposure to pesticides and were conducted in Europe and North America. Eleven high-quality studies were found. Most of them found no association between exposure to pesticides and increased risk of HNC. Two studies found some evidence of a positive association between pesticide (malathion and atrazine) exposure and thyroid cancer. The literature review does not support a clear evidence for association between pesticides exposure and HNC. Only limited evidence points to a positive association between exposure to some pesticides and thyroid cancer. Further standardized studies based on appropriate designs are required to clarify the effect of pesticides on the genesis of HNC, considering dose, length of exposure, and type of pesticide.


Subject(s)
Head and Neck Neoplasms/chemically induced , Occupational Exposure/adverse effects , Pesticides/adverse effects , Atrazine/adverse effects , Cohort Studies , Databases, Bibliographic , Humans , Malathion/adverse effects , Risk Factors , Thyroid Neoplasms/chemically induced
7.
Nucleic Acids Res ; 44(20): 9784-9802, 2016 Nov 16.
Article in English | MEDLINE | ID: mdl-27655631

ABSTRACT

The epigenetic events imposed during germline reprogramming and affected by harmful exposure can be inherited and transferred to subsequent generations via gametes inheritance. In this study, we examine the transgenerational effects promoted by widely used herbicide atrazine (ATZ). We exposed pregnant outbred CD1 female mice and the male progeny was crossed for three generations with untreated females. We demonstrate here that exposure to ATZ affects meiosis, spermiogenesis and reduces the spermatozoa number in the third generation (F3) male mice. We suggest that changes in testis cell types originate from modified transcriptional network in undifferentiated spermatogonia. Importantly, exposure to ATZ dramatically increases the number of transcripts with novel transcription initiation sites, spliced variants and alternative polyadenylation sites. We found the global decrease in H3K4me3 occupancy in the third generation males. The regions with altered H3K4me3 occupancy in F3 ATZ-derived males correspond to altered H3K4me3 occupancy of F1 generation and 74% of changed peaks in F3 generation are associated with enhancers. The regions with altered H3K4me3 occupancy are enriched in SP family and WT1 transcription factor binding sites. Our data suggest that the embryonic exposure to ATZ affects the development and the changes induced by ATZ are transferred up to three generations.


Subject(s)
Atrazine/adverse effects , Environmental Exposure/adverse effects , Epigenesis, Genetic/drug effects , Herbicides/adverse effects , Histones/metabolism , Prenatal Exposure Delayed Effects , Transcription, Genetic/drug effects , Animals , Binding Sites , Chromatin Immunoprecipitation , Cluster Analysis , Female , Gene Expression Profiling , High-Throughput Nucleotide Sequencing , Male , Maternal Exposure , Meiosis/drug effects , Methylation/drug effects , Mice , Nucleotide Motifs , Organ Specificity/genetics , Position-Specific Scoring Matrices , Pregnancy , Protein Binding , RNA, Long Noncoding/genetics , Spermatogenesis/drug effects , Spermatozoa/drug effects , Spermatozoa/metabolism , Testis/drug effects , Testis/metabolism , Testis/pathology
8.
J Insect Sci ; 18(5)2018 Sep 01.
Article in English | MEDLINE | ID: mdl-30312460

ABSTRACT

Agricultural runoff containing herbicide is known to have adverse effects on freshwater organisms. Aquatic insects are particularly susceptible, and herbicide runoff has the potential to affect immunity in this group. Here we examined the effect of ecologically relevant levels of atrazine, an herbicide commonly used in the United States, on immune function in larvae of the blue dasher dragonfly (Odonata: Libelluludae, Pachydiplax longipennis Burmeister 1839) during a long-term exposure at ecologically relevant concentrations. Larvae were exposed to concentrations of 0, 1, 5, and 10 ppb atrazine for 3 or 6 wk. Hemocyte counts, hemolymph phenyloxidase (PO) activity, cuticular PO, and gut PO were measured at the end of each trial period as indicators of immune system strength. Atrazine concentration had a significant effect on hemocyte counts after controlling for larval size. There was a significant interaction between time and concentration for hemolymph PO, cuticular PO, and a marginal interaction for gut PO. The effect of atrazine on the measured immune parameters was often nonmonotonic, with larger effects observed at intermediate concentrations. Therefore, atrazine affects both hemocyte numbers and PO activity over time in P. longipennis, and the changed immune function demonstrated in this study is likely to modify susceptibility to pathogens, alter wound healing, and may decrease available energy for growth and metamorphosis.


Subject(s)
Atrazine/adverse effects , Herbicides/adverse effects , Immunity, Innate/drug effects , Odonata/drug effects , Water Pollutants, Chemical/adverse effects , Animals , Larva/drug effects , Larva/growth & development , Larva/immunology , Metamorphosis, Biological/drug effects , Odonata/growth & development , Odonata/immunology , Time Factors
9.
Wei Sheng Yan Jiu ; 46(1): 103-108, 2017 Jan.
Article in Zh | MEDLINE | ID: mdl-29903161

ABSTRACT

OBJECTIVE: To elucidate the effects of atrazine( ATZ) on apoptosis in cultured rat Sertoli cells. METHODS: The Sertoli cells isolated from male SD rats( 18-21day) were used to set up Sertoli cells primary culture model in vitro, and these cells were treated with 0, 10, 50, 100 and 200 µmol / L ATZ for 24 h. Cell viability was assessed by MTT assay, and the vimentin expression of Sertoli cells was analyzed by immunofluorescence assay, and apoptosis were evaluated by flow cytometry. Real timePCR was used to analyze the mRNA levels of Fas L, caspase-3 and caspase-8, and the protein contents of Fas L, caspase-3 and caspase-8 were determined by ELISA. RESULTS: The viability of Sertoli cells of 50, 100 and 200 µmol / L ATZ groups were 82. 47%, 75. 23% and 53. 76%. Compared with the control group, the viability of Sertoli cells decreased by 17. 53%( P < 0. 05), 24. 77%( P < 0. 05) and 46. 24%( P < 0. 01), respectively. The apoptosis rates of Sertoli cell of 50, 100 and 200 µmol / L ATZ groups were 8. 53%, 13. 07% and 14. 45%. Compared with the control group, the apoptosisrates of Sertoli cells were increased by 86. 86%( P < 0. 01), 186. 13%( P < 0. 01), 216. 06%( P < 0. 01), respectively. the mRNA and protein expressions of Fas L, caspase-3 and caspase-8 were significantly increased at 50, 100 and 200 µmol / L ATZ groups( P < 0. 05, P < 0. 01). The Vimentin expression of Sertoli cells was inhibited in treated groups. CONCLUSION: ATZ can affect the viability of Sertoli cells, and induce apoptosis of Sertoli cells through a Fas L dependent pathway.


Subject(s)
Apoptosis/drug effects , Atrazine/pharmacology , Herbicides/pharmacology , Sertoli Cells/drug effects , Animals , Atrazine/adverse effects , Atrazine/toxicity , Caspase 3 , Caspase 8 , Cell Survival/drug effects , Cells, Cultured , Fas Ligand Protein , Herbicides/adverse effects , Herbicides/toxicity , Male , Rats , Rats, Sprague-Dawley
10.
Occup Environ Med ; 73(9): 582-7, 2016 09.
Article in English | MEDLINE | ID: mdl-27371663

ABSTRACT

BACKGROUND: Few studies have evaluated environmental chemical exposures in relation to ovarian cancer. We previously found an increased risk of ovarian cancer among postmenopausal women in Iowa associated with higher nitrate levels in public water supplies (PWS). However, elevated nitrate levels may reflect the presence of other agricultural chemicals, such as atrazine, one of the most commonly detected pesticides in Iowa PWS. METHODS: We evaluated the association between atrazine in drinking water and incident ovarian cancer (N=145, 1986-2010) among 13 041 postmenopausal women in the Iowa Women's Health Study who used their PWS for ≥11 years as reported in 1989. Average levels of atrazine (1986-1987), nitrate-nitrogen (NO3-N, 1955-1988) and estimated levels of total trihalomethanes (TTHM, 1955-1988) from PWS monitoring data were linked to the participants' cities of residence. We computed HRs and 95% CIs by categories of the average atrazine level (not detected, ≤ or >0.37 parts per billion=median) using Cox proportional hazards regression adjusting for ovarian cancer risk factors. RESULTS: Atrazine was detected in water samples from 69 cities where 4155 women (32%) lived and levels were moderately correlated with NO3-N (ρ=0.35) and TTHM (ρ=0.24). Atrazine levels were not associated with ovarian cancer risk with or without adjusting for NO3-N and TTHM levels (p-trend=0.50 and 0.81, respectively). Further, there was no evidence for effect modification of the atrazine association by NO3-N or TTHM levels. CONCLUSIONS: In our study with low atrazine detection rates, we found no association between atrazine in PWS and postmenopausal ovarian cancer risk.


Subject(s)
Atrazine/adverse effects , Drinking Water/adverse effects , Environmental Exposure/adverse effects , Herbicides/adverse effects , Ovarian Neoplasms/chemically induced , Ovarian Neoplasms/epidemiology , Aged , Atrazine/analysis , Drinking Water/analysis , Female , Humans , Iowa/epidemiology , Middle Aged , Nitrates/adverse effects , Postmenopause , Proportional Hazards Models , Prospective Studies , Risk Factors , Surveys and Questionnaires , Trihalomethanes/adverse effects , Water Pollutants, Chemical/adverse effects , Water Pollutants, Chemical/analysis , Water Supply , Women's Health
11.
J Environ Sci Health B ; 51(7): 465-8, 2016 Jul 02.
Article in English | MEDLINE | ID: mdl-27052932

ABSTRACT

Carrot (Daucus carota L.) is a vegetable crop that is grown throughout the year across various regions of Brazil in rotation or in succession to other cultures. Herbicide residual effect has emerged as a concern, because of the possibility of carryover. Thus, the objective of this study was to evaluate the effect of tembotrione and atrazine residues - in mixture and isolated - on carrot planted in succession to corn. The experiment was designed in randomized blocks with five replications. Treatments consisted of tembotrione (50.4 g ha(-1)), tembotrione (100.8 g ha(-1)), tembotrione + atrazine (50.4 g ha(-1)+ 2 L ha(-1)), tembotrione + atrazine (100.8 g ha(-1)+ 2 L ha(-1)), and atrazine (2.00 L ha(-1)) applied eight months before carrot seeding, plus a control treatment with no herbicide application. Investigated variables were shoot dry mass, productivity, and classification of carrot roots. The presence of atrazine and tembotrione decreased dry mass in the area, and only tembotrione reduced total root productivity. Thus, there is a carryover effect to tembotrione application that reduces the dry matter accumulation of shoot and total productivity, and an atrazine + tembotrione (100.8 g ha(-1)) mixture reduces the total productivity after application of these herbicides to soil.


Subject(s)
Atrazine/adverse effects , Cyclohexanones/adverse effects , Daucus carota/drug effects , Herbicides/adverse effects , Pesticide Residues/adverse effects , Soil Pollutants/adverse effects , Sulfones/adverse effects , Brazil , Daucus carota/growth & development , Plant Roots/drug effects , Plant Roots/growth & development , Plant Shoots/drug effects , Plant Shoots/growth & development
12.
Int J Cancer ; 137(5): 1167-75, 2015 Sep 01.
Article in English | MEDLINE | ID: mdl-25559664

ABSTRACT

Since its registration in 1994 acetochlor has become a commonly used herbicide in the US, yet no epidemiologic study has evaluated its carcinogenicity in humans. We evaluated the use of acetochlor and cancer incidence among licensed pesticide applicators in the Agricultural Health Study. In telephone interviews administered during 1999-2005, participants provided information on acetochlor use, use of other pesticides and additional potential confounders. We used Poisson regression to estimate relative risks (RR) and 95% confidence intervals (95% CI) for cancers that occurred from the time of interview through 2011 in Iowa and 2010 in North Carolina. Among 33,484 men, there were 4,026 applicators who used acetochlor and 3,234 incident cancers, with 304 acetochlor-exposed cases. Increased risk of lung cancer was observed among acetochlor users (RR = 1.74; 95% CI: 1.07-2.84) compared to nonusers, and among individuals who reported using acetochlor/atrazine product mixtures (RR = 2.33; 95% CI: 1.30-4.17), compared to nonusers of acetochlor. Colorectal cancer risk was significantly elevated among the highest category of acetochlor users (RR = 1.75; 95% CI: 1.08-2.83) compared to never users. Additionally, borderline significantly increased risk of melanoma (RR = 1.61; 95% CI: 0.98-2.66) and pancreatic cancer (RR = 2.36; 95% CI: 0.98-5.65) were observed among acetochlor users. The associations between acetochlor use and lung cancer, colorectal cancer, melanoma and pancreatic cancer are suggestive, however the lack of exposure-response trends, small number of exposed cases and relatively short time between acetochlor use and cancer development prohibit definitive conclusions.


Subject(s)
Agricultural Workers' Diseases/epidemiology , Herbicides/adverse effects , Neoplasms/epidemiology , Occupational Exposure/adverse effects , Toluidines/adverse effects , Agricultural Workers' Diseases/chemically induced , Atrazine/adverse effects , Colorectal Neoplasms/chemically induced , Colorectal Neoplasms/epidemiology , Humans , Incidence , Iowa/epidemiology , Lung Neoplasms/chemically induced , Lung Neoplasms/epidemiology , Male , Melanoma/chemically induced , Melanoma/epidemiology , Neoplasms/chemically induced , Neoplasms/classification , North Carolina/epidemiology , Pancreatic Neoplasms/chemically induced , Pancreatic Neoplasms/epidemiology , Prospective Studies
13.
Genet Mol Res ; 14(4): 16585-93, 2015 Dec 11.
Article in English | MEDLINE | ID: mdl-26681004

ABSTRACT

Corn is a major crop and various herbicides are used to maximize its production, which include a dicamba-atrazine mixture. This has great advantages, but can also induce DNA damage. Genotoxic activity was assessed by comet assay following application of two concentrations of dicamba-atrazine: 1000-2000 and 2000-4000 ppm. Apical meristem leaf nuclei from 119 varieties of sweetcorn plants from Mexico and South America, and from five commercial sweetcorn hybrids were used. Each accession comprised two individuals per concentration and two controls. Significant genotoxic activity (P < 0.001) was observed following treatment with 1000-2000 and 2000-4000 ppm compared to the negative control. There was no difference in the genotoxic activity induced by both 1000-2000 and 2000-4000 ppm concentrations in plants from Mexico and South America (P > 0.05) except (P < 0.05) in the 2000-4000 ppm treated plants from Mexico and the 1000-2000 ppm treated plants from South America. Sweetcorn hybrids showed significant genetic damage (P < 0.01) at all concentrations compared to the negative controls. Thus, the dicamba-atrazine mixture caused genetic damage to corn plants, and it suggested that Mexican sweetcorn is more sensitive to dicamba-atrazine than the maize varieties from South America. Neither hybrid status nor the origin avoids DNA damage caused by Marvel. Thus, maize can be useful as a biomonitor of genetic damage induced by chemicals and to identify possible phenotypes based upon the amount of genetic damage induced by herbicides and selection of resistant genotypes.


Subject(s)
Atrazine/toxicity , DNA Damage , Dicamba/toxicity , Herbicides/toxicity , Zea mays/drug effects , Atrazine/adverse effects , Dicamba/adverse effects , Herbicides/adverse effects , Zea mays/genetics
14.
Int J Mol Sci ; 16(7): 14353-68, 2015 Jun 24.
Article in English | MEDLINE | ID: mdl-26114388

ABSTRACT

Atrazine, a pre-emergent herbicide in the chloro-s-triazine family, has been widely used in crop lands and often detected in agriculture watersheds, which is considered as a potential threat to human health. Although atrazine and its metabolites showed an elevated incidence of mammary tumors in female Sprague-Dawley (SD) rats, no molecular evidence was found relevant to its carcinogenesis in humans. This study aims to determine whether atrazine could induce the expression of DNA damage response-related proteins in normal human breast epithelial cells (MCF-10A) and to examine the cytotoxicity of atrazine at a molecular level. Our results indicate that a short-term exposure of MCF-10A to an environmentally-detectable concentration of atrazine (0.1 µg/mL) significantly increased the expression of tumor necrosis factor receptor-1 (TNFR1) and phosphorylated Rad17 in the cells. Atrazine treatment increased H2AX phosphorylation (γH2AX) and the formation of γH2AX foci in the nuclei of MCF-10A cells. Atrazine also sequentially elevated DNA damage checkpoint proteins of ATM- and RAD3-related (ATR), ATRIP and phospho-Chk1, suggesting that atrazine could induce DNA double-strand breaks and trigger the DNA damage response ATR-Chk1 pathway in MCF-10A cells. Further investigations are needed to determine whether atrazine-triggered DNA double-strand breaks and DNA damage response ATR-Chk1 pathway occur in vivo.


Subject(s)
Atrazine/pharmacology , DNA Breaks, Double-Stranded , DNA Damage , DNA Repair , Herbicides/pharmacology , Adaptor Proteins, Signal Transducing/genetics , Adaptor Proteins, Signal Transducing/metabolism , Atrazine/adverse effects , Cell Cycle Proteins/metabolism , Checkpoint Kinase 1 , DNA-Binding Proteins/genetics , DNA-Binding Proteins/metabolism , Epithelial Cells/drug effects , Herbicides/adverse effects , Histones/metabolism , Humans , MCF-7 Cells , Protein Kinases/genetics , Protein Kinases/metabolism , Receptors, Tumor Necrosis Factor, Type I/genetics , Receptors, Tumor Necrosis Factor, Type I/metabolism
15.
Int J Mol Sci ; 16(6): 13490-506, 2015 Jun 12.
Article in English | MEDLINE | ID: mdl-26075868

ABSTRACT

Atrazine (2-chloro-4-ethytlamino-6-isopropylamine-1,3,5-triazine; ATR) is widely used as a broad-spectrum herbicide. Animal studies have demonstrated that ATR exposure can cause cell death in dopaminergic neurons. The molecular mechanisms underlying ATR-induced neuronal cell death, however, are unknown. In this study, we investigated the autophagy and apoptosis induced by ATR in dopaminergic neurons in vivo. Wistar rats were administered with ATR at doses of 10, 50 and 100 mg/kg body weight by oral gavage for three months. In terms of histopathology, the expression of autophagy- and apoptosis-related genes as well as proteins related to the Beclin-1/B-cell lymphoma 2 (Bcl-2) autophagy and apoptosis pathways were examined in the rat nigrostriatal dopaminergic system. We observed degenerative micromorphology indicative of neuronal apoptosis and mitochondrial autophagy by electron microscopy in ATR-exposed rat striatum. The rat ventral mesencephalon in the ATR-exposed groups also showed increased expression of Beclin-1, LC3-II, Bax and Caspase-9, and decreased expression of tyrosine hydroxylase (TH), Bcl-xl and Bcl-2. These findings indicate that ATR may induce autophagy- and apoptosis-related changes in doparminergic neurons. Furthermore, this induction may be regulated by the Beclin-1 and Bcl-2 autophagy and apoptosis pathways, and this may help to better understand the mechanism underlying the neurotoxicity of ATR.


Subject(s)
Apoptosis , Atrazine/toxicity , Autophagy , Dopaminergic Neurons/drug effects , Herbicides/toxicity , Animals , Apoptosis Regulatory Proteins/metabolism , Atrazine/adverse effects , Beclin-1 , Caspase 9/metabolism , Dopaminergic Neurons/metabolism , Herbicides/adverse effects , Male , Mesencephalon/cytology , Mesencephalon/drug effects , Mesencephalon/metabolism , Mesencephalon/ultrastructure , Microtubule-Associated Proteins/metabolism , Mitochondria/drug effects , Mitochondria/metabolism , Proto-Oncogene Proteins c-bcl-2/metabolism , Rats , Rats, Wistar , bcl-2-Associated X Protein/metabolism
16.
Wei Sheng Yan Jiu ; 44(6): 949-53, 2015 Nov.
Article in Zh | MEDLINE | ID: mdl-26738389

ABSTRACT

OBJECTIVE: To investigate the effects of atrazine (ATZ) on function of peritoneal macrophages in vitro, and to provide data for its immunotoxicity evaluation. METHODS: The murine peritoneal macrophages were isolated from mice. After treated with ATZ at different doses, cells viability was detected by MTT assay, and phagocytosis was evaluated by neutral red absorption. NO and TNF-α release were detected with nitrate reductase method and ELISA method, respectively. ROS was measured by DCFH-DA and flow cytometry. RESULTS: The IC50 values of the peritoneal macrophages for the MTT assay were (887.4 ± 1.11), (360.2 ± 1.13) and (270.6 ± 1.20) µmol/L after 24, 48 and 72 h. While for the NR absorption were (214.2 ± 1.14), (120.0 ± 1.10) and (42.60 ± 1.12) µmol/L. After dosed for 24 h and 72 h, the NO release of low dose groups were higher than those of the controls, while the NO release of high dose groups showed a downward trend when compared with the control's. After treatment for 72 h, the TNF-α secretion of low dose groups (0.01, 0.1 µmol/L) were significantly higher than that of the control (P < 0.05), and TNF-α secretion in the other groups were lower when compared with that of the control (P < 0.05). After exposure for 24 h or 72 h, the ROS release was promoted in both 0.01 and 1 µmol/L ATZ groups (P < 0.05), however, the ROS release were lowered in the 100 µmol/L ATZ group. CONCLUSION: ATZ can affect the cells viability and phagocytosis of peritoneal macrophages. Meanwhile the TNF-α secretion, NO release as well as ROS release are disturbed in peritoneal macrophages exposed to ATZ.


Subject(s)
Atrazine/pharmacology , Herbicides/pharmacology , Macrophages, Peritoneal/drug effects , Animals , Atrazine/adverse effects , Cell Survival/drug effects , Dose-Response Relationship, Drug , Dose-Response Relationship, Immunologic , Enzyme-Linked Immunosorbent Assay , Flow Cytometry , Fluoresceins , Herbicides/adverse effects , Herbicides/toxicity , Immunotoxins , Macrophages, Peritoneal/immunology , Mice , Phagocytosis/drug effects , Toxicity Tests, Acute/methods , Tumor Necrosis Factor-alpha
17.
J Public Health Manag Pract ; 20(2): 210-9, 2014.
Article in English | MEDLINE | ID: mdl-23715219

ABSTRACT

CONTEXT: Environmental Public Health Tracking (EPHT) tracks the occurrence and magnitude of environmental hazards and associated adverse health effects over time. The EPHT program has formally expanded its scope to include finished drinking water quality. OBJECTIVES: Our objective was to describe the features, strengths, and limitations of using finished drinking water quality data from community water systems (CWSs) for EPHT applications, focusing on atrazine and nitrogen compounds in 8 Midwestern states. METHODS: Water quality data were acquired after meeting with state partners and reviewed and merged for analysis. RESULTS: Data and the coding of variables, particularly with respect to censored results (nondetects), were not standardized between states. Monitoring frequency varied between CWSs and between atrazine and nitrates, but this was in line with regulatory requirements. Cumulative distributions of all contaminants were not the same in all states (Peto-Prentice test P < .001). Atrazine results were highly censored in all states (76.0%-99.3%); higher concentrations were associated with increased measurement frequency and surface water as the CWS source water type. Nitrate results showed substantial state-to-state variability in censoring (20.5%-100%) and in associations between concentrations and the CWS source water type. CONCLUSIONS: Statistical analyses of these data are challenging due to high rates of censoring and uncertainty about the appropriateness of parametric assumptions for time-series data. Although monitoring frequency was consistent with regulations, the magnitude of time gaps coupled with uncertainty about CWS service areas may limit linkage with health outcome data.


Subject(s)
Atrazine/analysis , Drinking Water/standards , Nitrates/analysis , Public Health Practice/standards , Water Quality/standards , Abnormalities, Drug-Induced/etiology , Abnormalities, Drug-Induced/prevention & control , Agrochemicals/adverse effects , Agrochemicals/analysis , Atrazine/adverse effects , Data Interpretation, Statistical , Drinking Water/analysis , Humans , Nitrates/adverse effects , United States , Water Pollutants, Chemical/adverse effects , Water Pollutants, Chemical/analysis
18.
JAMA Netw Open ; 7(5): e2410056, 2024 May 01.
Article in English | MEDLINE | ID: mdl-38709530

ABSTRACT

Importance: The incidence of gastroschisis, a birth defect involving the herniation of the small bowel through the abdominal wall, has increased in the US since the 1960s. The pesticide atrazine is a hypothesized cause of gastroschisis; however, examination of the association between atrazine and gastroschisis has been limited. Objective: To evaluate national trends in gastroschisis incidence, maternal and infant characteristics associated with gastroschisis, and whether county-level atrazine use is associated with gastroschisis. Design, Setting, and Participants: This retrospective, repeated cross-sectional study examined birth certificate data of all live births in the US and data on atrazine use from the US Geological Survey from January 1, 2009, through December 31, 2019. The data analysis was performed between August 5, 2021, and May 26, 2023. Exposures: County-level atrazine use. Main Outcomes and Measures: The primary outcome was gastroschisis incidence. Covariates included maternal age, race and ethnicity, body mass index (measured by weight in kilograms divided by height in meters squared), parity, insurance type, Chlamydia infection during pregnancy, smoking, and rurality. Mixed-effects logistic regression models (year fixed effects and county random effects) were constructed using different county-level atrazine exposure variables (1-, 5-, and 10-year means). Results: Between 2009 and 2019, 39 282 566 live births were identified, with 10 527 infant diagnoses of gastroschisis. Infants with gastroschisis were more likely to have mothers who identified as non-Hispanic White (61% vs 54%; P < .001), had a lower body mass index (median [IQR], 23.4 [20.8-27.2] vs 25.4 [22.0-30.8]; P < .001), were more likely to be nulliparous (median [IQR], 0 [0-1] vs 1 [0-2]; P < .001), and were more commonly covered by Medicaid (63% vs 43%; P < .001). During the study period, the rate (per 1000 live births) of gastroschisis decreased from 0.31 (95% CI, 0.29-0.33) to 0.22 (95% CI, 0.21-0.24). The median (IQR) county-level atrazine use estimates were higher among infants with gastroschisis (1 year, 1389 [IQR, 198-10 162] vs 1023 [IQR, 167-6960] kg; 5 years, 1425 [IQR, 273-9895] vs 1057 [IQR, 199-6926] kg; 10 years, 1508 [IQR, 286-10 271] vs 1113 [IQR, 200-6650] kg; P < .001). In adjusted models, higher county levels of atrazine (each 100 000-kg increase) were associated with a higher incidence of gastroschisis (1 year: adjusted odds ratio [AOR], 1.12 [95% CI, 1.01-1.24]; 5 years: AOR, 1.15 [95% CI, 1.02-1.30]; 10 years: AOR, 1.21 [95% CI, 1.07-1.38]). Conclusions and Relevance: In this cross-sectional study, higher county levels of atrazine were associated with infant diagnoses of gastroschisis. While atrazine is the second-most used herbicide in the US, numerous countries around the world have banned it out of concern for adverse effects on human health. These findings suggest that exploring alternatives to atrazine in the US may be warranted.


Subject(s)
Atrazine , Gastroschisis , Gastroschisis/epidemiology , Gastroschisis/chemically induced , Humans , Atrazine/adverse effects , Female , Cross-Sectional Studies , Retrospective Studies , Adult , Pregnancy , Incidence , United States/epidemiology , Infant, Newborn , Herbicides/adverse effects , Male , Young Adult
19.
J Pediatr ; 162(3): 581-6, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23036484

ABSTRACT

OBJECTIVE: To assess the relationship between estimated residential maternal exposure to atrazine during pregnancy and the risk for choanal atresia or stenosis in offspring. STUDY DESIGN: Data for 280 nonsyndromic cases and randomly selected, population-based controls delivered between 1999 and 2008 were obtained from the Texas Birth Defects Registry. County-level estimates of atrazine levels obtained from the US Geological Survey were assigned to cases and controls based on maternal county of residence at delivery. Unconditional logistic regression was used to assess the relationship between maternal residential atrazine exposure and the risk for choanal atresia or stenosis in offspring. RESULTS: Compared with offspring of mothers with low levels of estimated residential atrazine exposure, those with high levels had nearly a 2-fold increase in risk for choanal atresia or stenosis (aOR, 1.79; 95% CI, 1.17-2.74). A significant linear trend was also observed with increasing levels of atrazine exposure (adjusted P = .002). CONCLUSION: A link between maternal exposure to endocrine disruptors, such as atrazine, and the risk of choanal atresia is plausible based on previous findings. Our results lend further support to this hypothesis.


Subject(s)
Atrazine/adverse effects , Choanal Atresia/epidemiology , Herbicides/adverse effects , Maternal Exposure/statistics & numerical data , Adult , Choanal Atresia/chemically induced , Constriction, Pathologic/chemically induced , Constriction, Pathologic/epidemiology , Female , Humans , Infant , Logistic Models , Male , Pregnancy , Risk Factors
20.
Am J Med Genet A ; 161A(5): 977-82, 2013 May.
Article in English | MEDLINE | ID: mdl-23494929

ABSTRACT

Exposure to endocrine disrupting chemicals has been associated with risk for male genital malformations. However, residential prenatal exposure to atrazine, an endocrine disrupting pesticide, has not been evaluated. We obtained data from the Texas Birth Defects Registry for 16,433 cases with isolated male genital malformations and randomly selected, population-based controls delivered during 1999-2008. County-level estimates of atrazine exposure from the United States Geological Survey were linked to all subjects. We evaluated the relationship between estimated maternal residential atrazine exposure and risk for male genital malformations in offspring. Separate unconditional logistic regression analyses were conducted for hypospadias, cryptorchidism, and small penis. We observed modest, but consistent, associations between medium-low and/or medium levels of estimated periconceptional maternal residential atrazine exposure and every male genital malformation category evaluated (e.g., adjusted odds ratio for medium compared to low atrazine levels and all male genital malformations: 1.2, 95% confidence interval: 1.1-1.3). Previous literature from animal and epidemiological studies supports our findings. Our results provide further evidence of a suspected teratogenic role of atrazine.


Subject(s)
Atrazine/adverse effects , Disorders of Sex Development/epidemiology , Endocrine Disruptors/adverse effects , Herbicides/adverse effects , Maternal Exposure/adverse effects , Case-Control Studies , Disorders of Sex Development/etiology , Female , Humans , Male , Pregnancy , Prenatal Exposure Delayed Effects , Risk Assessment , Risk Factors , Texas
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