ABSTRACT
Background: Chloramine-T (CL-T) is a synthetic sodium salt used as a disinfectant in fish farms to combat bacterial infections in fish gills and skin. While its efficacy in pathogen control is well-established, its reactivity with various functional groups has raised concerns. However, limited research exists on the toxicity of disinfection by-products to aquatic organisms. Therefore, this study aims to assess the sublethal effects of CL-T on adult zebrafish by examining biomarkers of nucleus cytotoxicity and genotoxicity, acetylcholinesterase (AChE) inhibition, and histopathological changes. Methods: Male and female adult zebrafish (wildtype AB lineage) specimens were exposed to 70, 140, and 200 mg/L of CL-T and evaluated after 96 h. Cytotoxic and genotoxic effects were evaluated by estimating the frequencies of nuclear abnormalities (NA), micronuclei (MN), and integrated optical density (IOD) of nuclear erythrocytes. Histopathological changes in the gills and liver were assessed using the degree of tissue changes (DTC). AChE activity was measured in brain samples. Results and conclusions: At a concentration of 200 mg/L, NA increased, indicating the cytogenotoxic potential of CL-T in adult zebrafish. Morphological alterations in the nuclei were observed at both 70 and 200 mg/L concentrations. Distinct IOD profiles were identified across the three concentrations. There were no changes in AChE activity in adult zebrafish. The DTC scores were high in all concentrations, and histological alterations suggested low to moderate toxicity of CL-T for adult zebrafish.
Subject(s)
Perciformes , Zebrafish , Animals , Male , Female , Acetylcholinesterase , Chloramines/toxicity , Tosyl CompoundsABSTRACT
Inorganic chloramines are not commercially available, but monochloramine is produced in situ for disinfection or for use in chemical synthesis. Inorganic chloramines are also formed when free chlorine reacts with nitrogen containing substances, e.g. ammonia and urea, present in chlorinated water sources. Occupational exposure may, therefore, occur in e.g. swimming pool facilities and the food processing industry. Monochloramine is soluble and stable in water and the dominating inorganic chloramine in chlorinated water sources. No clinical effects were seen in healthy volunteers given monochloramine in drinking water during 4 or 12 weeks in doses of 0.043 or 0.034 mg/kg bw/day, respectively. Limited data indicate that monochloramine is weakly mutagenic in vitro but not genotoxic in vivo. One drinking water study indicated equivocal evidence of carcinogenicity in female rats but not in male rats and mice. No reproductive or developmental effects were shown in rodents in the few studies located. Dichloramine is soluble but unstable in water. In the only study located, mild histological effects in kidneys, thyroid and gastric cardia were observed in rats administered dichloramine in drinking water for 13 weeks. Trichloramine is immiscible with water and evaporates easily from water into air. Therefore, the primary exposure route of concern in the occupational setting is inhalation. Occupational exposure to trichloramine has been demonstrated in indoor swimming pool facilities and in the food processing industry where chlorinated water is used for disinfection. Exposure-response relationships between airborne levels and self-reported ocular and upper airway irritation have been shown in several studies. Exposure to trichloramine may aggravate asthma symptoms in individuals with existing asthma. The risk of developing asthma following long-term exposure to trichloramine cannot be evaluated at present. No data on genotoxic, carcinogenic, reproductive or developmental effects were located. The toxicological data for mono- and dichloramine are insufficient to recommend health-based occupational exposure limits (OELs).As regard trichloramine, the critical effect is judged to be irritation observed in several studies on pool workers, starting at approximately 0.4 mg/m3 (stationary sampling). Based on these data, a health-based OEL of 0.1 mg/m3 (8-h time-weighted average) is recommended. This corresponds to 0.2 mg/m3 for stationary measurements in swimming pool facilities. No short-term exposure limit (STEL) is recommended.
Subject(s)
Chloramines/toxicity , Occupational Exposure/statistics & numerical data , HumansABSTRACT
A model cooling tower system was experimentally seeded with Legionella pneumophila and real industrial cooling tower (CT) water has been run at the closest to full-scale system operating conditions. The water/biofilm samples were taken from the model system monthly, and the effectiveness of the different concentrations of Chloramine T trihydrate biocide was evaluated in terms of its ability to control both planktonic/sessile microbial populations. Although Chloramine T is a recommended commercial formulation for disinfecting CTs, there is a lack of published data on the efficacy of this compound against both planktonic and sessile populations in the cooling tower. Biocide response in both sessile/planktonic bacteria counts varied according to months. Tested biocide concentrations provided the clean tower conditions by reducing the concentration of heterotrophic plate count (HPC) below <104 cfu mL-1, L. pneumophila <10 cfu mL-1 and of adenosine triphosphate (ATP) values <300 relative light units (RLU), after 1, 3 and 24 h of exposure, during a 6-month period. There were no statistically significant differences in efficacy between concentrations in terms of reduction in the number of bacteria, decrease in ATP value and viability. The results revealed that Chloramine T can effectively control biofouling in cooling systems according to the limit values of the successful control program.
Subject(s)
Chloramines/toxicity , Disinfectants/toxicity , Plankton/drug effects , Tosyl Compounds/toxicity , Water Microbiology , Water Purification/methods , Bacteria/drug effects , Disinfection/methods , Legionella , Plankton/physiologyABSTRACT
The variations of disinfection byproduct (DBP) precursors and DBPs-associated toxic potencies were evaluated by ozonation, followed by a up-flow biological activated carbon (O3/UBAC) filter treating two reconstituted water samples, featuring either high bromide (105.3⯵g/L) or dissolved organic nitrogen (0.73â¯mgâ¯N/L) concentration, respectively. Ozonation contributed to â¼20% decrease in dissolved organic carbon (DOC) concentration at a dosage of 0.7â¯mg of O3/mg of DOC, but no further reduction in DOC level was observed with an increased dose of 1.0â¯mg of O3/mg of DOC. When chlorine or preformed monochloramine was used as a disinfectant, UBAC process led to â¼40% reduction in the sum of detected DBP formation potential (FP) due to the removal of precursors at a feasible empty bed contact time of 15â¯min. The integrated effect of ozonation and UBAC biofiltration decreased the sum of DBP FP by â¼50% including halonitromethanes (THNMs), N-nitrosamines (NAs), and bromate, which increased in the effluent of ozonation. Chloramination produced less DBPs by weight as well as DBPs-associated additive toxic potencies than chlorination. The reduction in additive toxic potencies was generally lower than the removal efficiency of DBP FP after chlor(am)ination of treated waters by O3/UBAC, indicating that the removal of DBPs-associated additive toxic potencies should be focused to better understand on the residual risk to public health in controlling DBP precursors.
Subject(s)
Charcoal/chemistry , Chloramines/toxicity , Chlorine/toxicity , Disinfectants/isolation & purification , Disinfection/methods , Ozone/chemistry , Water Purification/methods , Disinfectants/toxicity , Halogenation , Water Pollutants, Chemical/analysisABSTRACT
Amending feed water with biocide is one of the strategy conventionally used to control biofouling in membrane-based water treatment systems. In this study, the impacts of two biocides, monochloramine (MCA) and hydrogen peroxide (H2O2), on the bacterial community in wastewater samples were investigated at equivalent biocidal efficiency levels. Viable bacterial numbers were determined before and after treatment for 10 min and 60 min using both culture-dependent heterotrophic plate count (HPC) and culture-independent propidium monoazide (PMA)-droplet digital PCR (ddPCR). Shifts of the live bacterial diversity were studied using high-throughput sequencing of 16S rRNA genes and followed by bioinformatics analysis. At the genus level, MCA treatment increased the relative abundance of Mycobacterium, Pseudomonas, Sphingomonas, Clostridium, Streptococcus, Undibacterium, Chryseobacterium and Cloacibacterium, while decreasing Arcobacter, Nitrospira and Sphingobium. H2O2 treatment increased the relative abundance of Anaerolinea and Filimonas, and diminished Denitratisoma and Thauera. The findings of this study suggest a combination of different types of biocide may be the most efficient strategy for biofouling mitigation and increasing membrane treatment efficiency.
Subject(s)
Bacteria/drug effects , Chloramines/toxicity , Hydrogen Peroxide/toxicity , Waste Disposal, Fluid/methods , Wastewater/microbiology , Azides , Biofouling/prevention & control , Disinfectants/pharmacology , High-Throughput Nucleotide Sequencing , Polymerase Chain Reaction , Propidium/analogs & derivatives , RNA, Ribosomal, 16S/genetics , Wastewater/chemistryABSTRACT
We evaluated the antifungal and anti-biofilm activity, mechanism of action and cytotoxicity of chloramine T trihydrate (CAT) against Candida spp. The Minimum Inhibitory and Fungicidal Concentrations (MIC/MFC) of CAT were determined. Changes in CAT-treated C. albicans growth kinetics and micromorphology were evaluated, as well as the mechanism of action, and its effects on biofilm. Cytotoxicity was assessed by the hemolysis method. The data were analyzed by inferential statistics (p ≤ 0.05). CAT showed antifungal activity against all strains, with MIC values ranging between 1.38 and 5.54 mmol/L (MIC75%: 2.77 mmol/L). CAT demonstrated an immediate and sustained action on C. albicans growth kinetics, particularly at 2 × MIC. This compound likely acts on the cell wall and membrane permeability simultaneously and was found to cause changes in C. albicans micromorphology. Tha antibiofilm activity of CAT was similar to that of sodium hypochlorite (p > 0.05) against mature biofilms. CAT was more effective than NaOCl in reducing mature biofilm upon 1-min exposure at 2 × MIC (24 h) and 4 × MIC (48 h) (p < 0.05). Toxicological analysis revealed that CAT had hemolytic activity between 61 and 67.7% as compared to 100% by NaOCl. CAT has antifungal and anti-biofilm properties, probably acting on both cell wall and membrane permeability, and showed low toxicity in vitro.
Subject(s)
Antifungal Agents/pharmacology , Biofilms/drug effects , Candida albicans/drug effects , Chloramines/pharmacology , Disinfectants/pharmacology , Tosyl Compounds/pharmacology , Antifungal Agents/toxicity , Candida albicans/growth & development , Cell Line , Cell Survival/drug effects , Chloramines/toxicity , Disinfectants/toxicity , Hemolysis , Humans , Kinetics , Permeability , Tosyl Compounds/toxicityABSTRACT
Recycling wastewater is becoming more common as communities around the world try to better control their water resources against an increased frequency of either prolonged droughts or intense flooding. For communities in coastal areas, wastewaters may contain elevated levels of bromide (Br-) and iodide (I-) from seawater intrusion or high mineral content of source waters. Disinfection of such wastewater is mandatory to prevent the spread of pathogens, however little is known about the toxicity of wastewater after disinfection in the presence of Br- and I-. In this study we compared the induction of chronic cytotoxicity in mammalian cells in samples of municipal secondary wastewater effluent amended with elevated levels of Br-/I- after disinfection by chlorine, chloramines or ozone to identify which disinfection process generated wastewater with the lowest level of adverse biological response. Chlorination increased mammalian cell cytotoxicity by 5 times as compared to non-disinfected controls. Chloramination produced disinfected wastewater that expressed 6.3 times more cytotoxicity than the non-disinfected controls and was 1.3 times more cytotoxic than the chlorinated samples. Ozonation produced wastewater with cytotoxicity comparable to the non-disinfected controls and was at least 4 times less cytotoxic than the chlorine disinfected wastewaters. These results indicate that compared to chlorination and chloramination, ozonation of wastewater with high Br-/I- levels yielded the lowest mammalian cell cytotoxicity, suggesting its potential as a more favorable method to disinfect wastewater with minimizing the biological toxicity in mind.
Subject(s)
Wastewater/toxicity , Water Pollutants, Chemical/toxicity , Animals , Bromides/toxicity , Chloramines/toxicity , Disinfectants/toxicity , Disinfection/methods , Halogenation , Iodides/toxicity , Ozone/toxicity , Water Purification/methodsABSTRACT
Haemolysis in haemodialysis, although rare in current times, is associated with significant mortality and morbidity. As such prompt recognition, treatment, analysis of root cause and correction of underlying causative factors is crucial. Dialysate, extracorporeal circuit and patient related factors all contribute to haemolysis risk. Haemolysis can manifest with non-specific signs and symptoms including but not restricted to hypertension, nausea, pain (abdominal, chest, back) and dyspnoea. It may present acutely during the dialysis session or may take a protracted course. Potential life threating consequences include; hyperkalaemia induced cardiac arrhythmias, profound anaemia and associated acute coronary events and respiratory distress, and severe necrotizing pancreatitis. Chronic haemolysis results in impaired endothelial function thus contributing to the long-term cardiovascular risk profile in haemodialysis patients. Stringent national and international standards, technological advancements in membrane and dialysis equipment design, dialyser purification methods and water treatment systems have greatly reduced the incidence of haemolysis. Despite these improvements recognition of haemolysis risk and ongoing clinical vigilance is important.
Subject(s)
Hemolysis , Renal Dialysis/adverse effects , Cannula , Chloramines/toxicity , Humans , Membranes, Artificial , Oxidative Stress , Shear Strength , Sterilization , Temperature , Water Pollutants, Chemical/toxicityABSTRACT
Exposure to chlorination disinfection by-products (CxDBPs) is prevalent in populations using chlorination-based methods to disinfect public water supplies. Multifaceted research has been directed for decades to identify, characterize, and understand the toxicology of these compounds, control and minimize their formation, and conduct epidemiologic studies related to exposure. Urinary bladder cancer has been the health risk most consistently associated with CxDBPs in epidemiologic studies. An international workshop was held to (1) discuss the qualitative strengths and limitations that inform the association between bladder cancer and CxDBPs in the context of possible causation, (2) identify knowledge gaps for this topic in relation to chlorine/chloramine-based disinfection practice(s) in the United States, and (3) assess the evidence for informing risk management. Epidemiological evidence linking exposures to CxDBPs in drinking water to human bladder cancer risk provides insight into causality. However, because of imprecise, inaccurate, or incomplete estimation of CxDBPs levels in epidemiologic studies, translation from hazard identification directly to risk management and regulatory policy for CxDBPs can be challenging. Quantitative risk estimates derived from toxicological risk assessment for CxDBPs currently cannot be reconciled with those from epidemiologic studies, notwithstanding the complexities involved, making regulatory interpretation difficult. Evidence presented here has both strengths and limitations that require additional studies to resolve and improve the understanding of exposure response relationships. Replication of epidemiologic findings in independent populations with further elaboration of exposure assessment is needed to strengthen the knowledge base needed to better inform effective regulatory approaches.
Subject(s)
Disinfectants/toxicity , Disinfection , Environmental Exposure , Halogenation , Urinary Bladder Neoplasms/epidemiology , Water Pollutants, Chemical/toxicity , Chloramines/toxicity , Chlorine/toxicity , Drinking Water/analysis , Humans , Risk Assessment , United States , Urinary Bladder Neoplasms/chemically induced , Water PurificationABSTRACT
Continuous and batch laboratory experiments were used to evaluate the combined effects of copper and chloramine on ammonia oxidizing microbes present in otherwise high nitrifying water samples. The experimental data were analyzed using a biostability concept and quantified with the biostable residual concentratrion (BRC) of monochloramine, or the concentration that prevents the onset of nitrification. In the batch experiments, copper dosing ≥0.25 mg-Cu L(-1) resulted in complete inhibition of nitrification, and a lower copper dosing (0.1 mg-Cu L(-1)) delayed nitrification. The BRC was systematically lowered with the addition of copper. For example, a free-ammonium concentration of 0.1 mg-N L(-1) had a BRC of 0.73 mg-Cl2 L(-1) with no Cu, but addition of 0.1 mg-Cu L(-1) lowered the BRC to 0.16 mg-Cl2 L(-1), while addition of 0.25 mg-Cu L(-1) eliminated the need to add chloramine (BRC = 0). A non-competitive inhibition model fit the experimental data well with a copper threshold of 0.044 mg-Cu L(-1) and can be used to estimate Cu doses needed to prevent nitrification based on the chloramine concentration. Full scale systems applications need further study.
Subject(s)
Ammonia/metabolism , Chloramines/toxicity , Copper/toxicity , Water Purification/methods , Oxidation-ReductionABSTRACT
BACKGROUND: Exposure to chlorinated water in swimming facilities may aggravate preexisting asthma or cause new onset asthma. This may be a particular problem for individuals who work and therefore spend prolonged time at swimming facilities. Chloramines formed by the interaction of chlorine-based disinfection products with the nitrogen in water from human sweat, urine and skin cells are the suspected causal agents. METHODS: Cases were reviewed from the state surveillance systems in California (CA), Michigan (MI) and New Jersey (NJ) to identify individuals with confirmed work-related asthma (WRA) attributed to exposures in swimming pools, water parks or hydrotherapy spas. A standardized method was used to confirm cases. RESULTS: A total of 44 confirmed cases of WRA were identified; 17 from 1994 to 2011 in CA, 15 from 1991 to 2012 in MI and 12 from 1990 to 2011 in NJ. A majority (52.2%) of the cases were new onset; 31.8% secondary to an acute exposure incident and 20.4% to repeated exposure. These represented 0.3-1.6% of all confirmed cases of WRA received during these time periods. Maintenance workers (34.9%) and lifeguards (31.8%) were the most common occupations. CONCLUSIONS: Swimming pool workers were identified from three states where the pool environment was either a trigger of preexisting asthma or associated with new onset of WRA. Regulations to require air monitoring and improvements in ventilation are recommended to reduce exposure levels of chloramines, the presumed etiologic agents. Clinical assessment of patients with asthma should include consideration of the effect on respiratory symptoms from exposures in a swimming pool environment.
Subject(s)
Air Pollutants, Occupational/toxicity , Asthma/chemically induced , Chloramines/toxicity , Occupational Diseases/chemically induced , Occupational Exposure/adverse effects , Adolescent , Adult , Aged , Asthma/epidemiology , California/epidemiology , Female , Humans , Hydrotherapy , Male , Michigan/epidemiology , Middle Aged , New Jersey/epidemiology , Occupational Diseases/epidemiology , Swimming Pools , Young AdultABSTRACT
Disinfectants inactivate pathogens in source water; however, they also react with organic matter and bromide/iodide to form disinfection byproducts (DBPs). Although only a few DBP classes have been systematically analyzed for toxicity, iodinated and brominated DBPs tend to be the most toxic. The objectives of this research were (1) to determine if monochloramine (NH2Cl) disinfection generated drinking water with less toxicity than water disinfected with free chlorine (HOCl) and (2) to determine the impact of added bromide and iodide in conjunction with HOCl or NH2Cl disinfection on mammalian cell cytotoxicity and genomic DNA damage induction. Water disinfected with chlorine was less cytotoxic but more genotoxic than water disinfected with chloramine. For both disinfectants, the addition of Br(-) and I(-) increased cytotoxicity and genotoxicity with a greater response observed with NH2Cl disinfection. Both cytotoxicity and genotoxicity were highly correlated with TOBr and TOI. However, toxicity was weakly and inversely correlated with TOCl. Thus, the forcing agents for cytotoxicity and genotoxicity were the generation of brominated and iodinated DBPs rather than the formation of chlorinated DBPs. Disinfection practices need careful consideration especially when using source waters containing elevated bromide and iodide.
Subject(s)
Bromides/toxicity , Chloramines/toxicity , Chlorine/toxicity , Iodides/toxicity , Water Purification , Animals , Bromides/chemistry , CHO Cells , Chloramines/chemistry , Chlorine/chemistry , Cricetulus , Disinfectants/chemistry , Disinfectants/toxicity , Disinfection , Drinking Water/chemistry , Halogenation , Iodides/chemistry , Toxicity TestsABSTRACT
As the use of alternative drinking water treatment increases, it is important to understand potential public health implications associated with these processes. The objective of this study was to evaluate the formation of disinfection byproducts (DBPs) and cytotoxicity of natural organic matter (NOM) concentrates treated with chlorine, chloramine, and medium pressure ultraviolet (UV) irradiation followed by chlorine or chloramine, with and without nitrate or iodide spiking. The use of concentrated NOM conserved volatile DBPs and allowed for direct analysis of the treated water. Treatment with UV prior to chlorine in ambient (unspiked) samples did not affect cytotoxicity as measured using an in vitro normal human colon cell (NCM460) assay, compared to chlorination alone when toxicity is expressed on the basis of dissolved organic carbon (DOC). Nitrate-spiked UV+chlorine treatment produced greater cytotoxicity than nitrate-spiked chlorine alone or ambient UV+chlorine samples, on both a DOC and total organic halogen basis. Samples treated with UV+chloramine were more cytotoxic than those treated with only chloramine using either dose metric. This study demonstrated the combination of cytotoxicity and DBP measurements for process evaluation in drinking water treatment. The results highlight the importance of dose metric when considering the relative toxicity of complex DBP mixtures formed under different disinfection scenarios.
Subject(s)
Chloramines/toxicity , Chlorine/toxicity , Drinking Water/chemistry , Toxicity Tests , Ultraviolet Rays , Water Purification/methods , Cell Death/drug effects , Cell Death/radiation effects , Cell Line , Disinfection , Halogenation/drug effects , Halogenation/radiation effects , Humans , Inhibitory Concentration 50 , Iodine/analysis , Water Pollutants, Chemical/analysisABSTRACT
The crayfish play an essential role in the biomonitoring and may reflect ambient water quality through the biochemical, behavioural and physiological reactions. To assess whether narrow-clawed crayfish Astacus leptodactylus can respond by heart rate changes to presence in water of such biocide as chloramine-T, adult males were exposed to its low (2 and 5 mg L(-1)), moderate (10 mg L(-1), commonly used in industry and aquaculture) and exceeded (20 and 50 mg L(-1)) concentrations. In addition, a physical stress test evaluated energy expenditure following the chemical trials. Three key reactions (cardiac initial, first-hour and daily prolonged exposure) were discussed with particular focus on crayfish initial reaction as the most meaningful in on-line water quality biomonitoring. After short-term exposure to both chloramine-T concentrations, crayfish were found to respond rapidly, within 2-5 min. According to heart rate changes, the 1-h exposure did not adversely affect crayfish at either concentration, as well as during daily exposure to 10 mg L(-1). As assessed by the heart rate, the 24-h exposure to 50 mg L(-1) of chloramine-T was toxic for crayfish and led to substantial loss of energy that became apparent during subsequently conducted physical stress. The results supported a hypothesis that crayfish vital functions are connected with environment they inhabit closely enough to serve as biological monitors. Crayfish were tolerant to short-term chloramine-T exposure, while rapid crayfish reaction to an increased chemical level indicated their high sensitivity, an essential attribute of real-time environmental assessment.
Subject(s)
Astacoidea/drug effects , Chloramines/toxicity , Tosyl Compounds/toxicity , Animals , Environmental Monitoring/methods , Heart Rate/drug effects , Male , Stress, Physiological , Toxicity Tests , Water QualityABSTRACT
The impact of monochloramine disinfection on the complex bacterial community structure in drinking water systems was investigated using culture-dependent and culture-independent methods. Changes in viable bacterial diversity were monitored using culture-independent methods that distinguish between live and dead cells based on membrane integrity, providing a highly conservative measure of viability. Samples were collected from lab-scale and full-scale drinking water filters exposed to monochloramine for a range of contact times. Culture-independent detection of live cells was based on propidium monoazide (PMA) treatment to selectively remove DNA from membrane-compromised cells. Quantitative PCR (qPCR) and pyrosequencing of 16S rRNA genes was used to quantify the DNA of live bacteria and characterize the bacterial communities, respectively. The inactivation rate determined by the culture-independent PMA-qPCR method (1.5-log removal at 664 mg·min/L) was lower than the inactivation rate measured by the culture-based methods (4-log removal at 66 mg·min/L). Moreover, drastic changes in the live bacterial community structure were detected during monochloramine disinfection using PMA-pyrosequencing, while the community structure appeared to remain stable when pyrosequencing was performed on samples that were not subject to PMA treatment. Genera that increased in relative abundance during monochloramine treatment include Legionella, Escherichia, and Geobacter in the lab-scale system and Mycobacterium, Sphingomonas, and Coxiella in the full-scale system. These results demonstrate that bacterial populations in drinking water exhibit differential resistance to monochloramine, and that the disinfection process selects for resistant bacterial populations.
Subject(s)
Bacteria/drug effects , Chloramines/toxicity , Disinfection/methods , Drinking Water/microbiology , Drug Resistance, Bacterial/drug effects , Azides/toxicity , Bacteria/genetics , Kinetics , Microbial Viability/drug effects , Microbiota/drug effects , Microbiota/genetics , Phylogeny , Principal Component Analysis , Propidium/analogs & derivatives , Propidium/toxicity , RNA, Ribosomal, 16S/geneticsABSTRACT
Juvenile rainbow trout Oncorhynchus mykiss (Walbaum) were exposed to therapeutic, and higher concentrations of chloramine-T (Cl-T) to assess the effects of this chemical on the antioxidant enzyme system and genetic structure. Red blood cells acetylcholinesterase, ∆-aminolevulinic acid dehydratase, paraoxonase and liver glutathione S-transferase activity were increased at 10 and 20 mg L(-1) Cl-T-exposed fish, while they were decreased at 30 mg L(-1) Cl-T-exposed fish. On the other hand, liver catalase activity and liver protein levels increased at 10 mg L(-1) and decreased at 20 and 30 mg L(-1) concentrations of Cl-T. Liver super-oxide dismutase activity decreased at 10 mg L(-1) and 20 mg L(-1) Cl-T and increased at 30 mg L(-1) of Cl-T. Compared to control, comet assay indicated that Cl-T did not cause significant DNA damage to red blood cells of the fish. Results indicate that 10 or 20 mg L(-1) Cl-T can be safely used to prevent or treat external parasitic and bacterial infection of rainbow trout.
Subject(s)
Anti-Bacterial Agents/toxicity , Chloramines/toxicity , DNA Damage , Erythrocytes/drug effects , Erythrocytes/enzymology , Fish Proteins/genetics , Oncorhynchus mykiss/physiology , Tosyl Compounds/toxicity , Animals , Comet Assay/veterinary , Enzyme Activation/drug effects , Fish Proteins/metabolism , Oncorhynchus mykiss/genetics , Oncorhynchus mykiss/metabolism , Oxidoreductases/metabolismABSTRACT
Chloramine T has been widely used as a disinfectant in many areas such as kitchens, laboratories and hospitals. It has been also used as a biocide in air fresheners and deodorants which are consumer products; however, little is known about its toxic effects by inhalation route. This study was performed to identify the subacute inhalation toxicity of chloramine T under whole-body inhalation exposure conditions. Male and female groups of rats were exposed to chloramine T at concentrations of 0.2, 0.9 and 4.0 mg/m³ for 6 hr/day, 5 days/week during 4 weeks. After 28-day repeated inhalation of chloramine T, there were dose-dependently significant DNA damage in the rat tissues evaluated and inflammation was histopathologically noted around the terminal airways of the lung in both genders. As a result of the expression of three types of antioxidant enzymes (SOD-2, GPx-1, PRX-1) in rat's lung after exposure, there was no significant change of all antioxidant enzymes in the male and female rats. The results showed that no observed adverse effect level (NOAEL) was 0.2 mg/m³ in male rats and 0.9 mg/m³ in female rats under the present experimental condition.
Subject(s)
Chloramines/toxicity , DNA Damage/drug effects , Disinfectants/toxicity , Inhalation Exposure/adverse effects , Pneumonia/chemically induced , Tosyl Compounds/toxicity , Administration, Inhalation , Animals , Chloramines/administration & dosage , Chloramines/adverse effects , Disinfectants/administration & dosage , Disinfectants/adverse effects , Dose-Response Relationship, Drug , Female , Glutathione Peroxidase/metabolism , Homeodomain Proteins/metabolism , Lung/enzymology , Male , No-Observed-Adverse-Effect Level , Pneumonia/enzymology , Rats , Rats, Sprague-Dawley , Superoxide Dismutase/metabolism , Time Factors , Tosyl Compounds/administration & dosage , Tosyl Compounds/adverse effects , Glutathione Peroxidase GPX1ABSTRACT
BACKGROUND: Drugs not commonly considered to be cardioactive agents may cause prolongation of the QT interval with resultant torsades de pointes and ventricular fibrillation. This form of drug toxicity often causes cardiac arrest or sudden death. CASE PRESENTATION: After accidental ingestion of tosylchloramide a caucasian 77-year-old woman, with a family history of cardiovascular disease and hypertension, was admitted to the intensive care unit following episodes of torsades de pointes with a prolonged QT/QTc interval (640/542 ms). The patient received an implantable cardioverter-defibrillator, was discharged from the hospital with normal QT/QTc interval and did not experience additional ventricular arrhythmias during one year of follow-up. CONCLUSION: This is the first report concerning an unusual case of torsades de pointes after accidental intoxication by ingestion of tosylchloramide. The pronounced impact of the oxidyzing agent tosylchloramide on the activity of some of the ion channels regulating the QT interval was identified as a probable cause of the arrhythmia.
Subject(s)
Chloramines/toxicity , Disinfectants/toxicity , Long QT Syndrome/chemically induced , Torsades de Pointes/chemically induced , Tosyl Compounds/toxicity , Accidents , Aged , Electrocardiography , Female , HumansABSTRACT
Methionine sulfoxide reductases A (MsrA) has been postulated to act as a catalytic antioxidant system involved in the protection of oxidative stress-induced cell injury. Recently, attention has turned to MsrA in coupling with the pathology of Parkinson's disease, which is closely related to neurotoxins that cause dopaminergic neuron degeneration. Here, we firstly provided evidence that pretreatment with a natural polyphenol resveratrol (RSV) up-regulated the expression of MsrA in human neuroblastoma SH-SY5Y cells. It was also observed that the expression and nuclear translocation of forkhead box group O 3a (FOXO3a), a transcription factor that activates the human MsrA promoter, increased after RSV pretreatment. Nicotinamide , an inhibitor of silent information regulator 1 (SIRT1), prevented RSV-induced elevation of FOXO3a and MsrA expression, indicating that the effect of RSV was mediated by a SIRT1-dependent pathway. RSV preconditioning increased methionine sulfoxide(MetO)-reducing activity in SH-SY5Y cells and enhanced their resistance to neurotoxins, including chloramine-T and 1-methyl-4-phenyl-pyridinium. In addition, the enhancement of cell resistance to neurotoxins caused by RSV preconditioning can be largely prevented by MsrA inhibitor dimethyl sulfoxide. Our findings suggest that treatment with polyphenols such as RSV can be used as a potential regulatory strategy for MsrA expression and function.
Subject(s)
1-Methyl-4-phenylpyridinium/toxicity , Antioxidants/pharmacology , Chloramines/toxicity , Methionine Sulfoxide Reductases/genetics , Stilbenes/pharmacology , Tosyl Compounds/toxicity , Cell Line, Tumor , Forkhead Box Protein O3 , Forkhead Transcription Factors/genetics , Forkhead Transcription Factors/metabolism , Humans , Methionine/analogs & derivatives , Methionine/pharmacology , Methionine Sulfoxide Reductases/metabolism , Models, Biological , Neuroblastoma , Neurotoxins/pharmacology , Oxidative Stress , Resveratrol , Sirtuin 1/genetics , Sirtuin 1/metabolism , Up-RegulationABSTRACT
UNLABELLED: Amino acid chloramines (AACLs) are reactive secondary products of activated neutrophils. To understand AACL damage in cell nuclei, we exploited proliferating cell nuclear antigen (PCNA) as a nuclear protein damage reporter, using western blotting and mass spectrometry. Chloramines of proline, arginine, and glycine caused significant damage to PCNA in cells. Chloramines of taurine and histidine caused slight damage to PCNA in cells. Other AACLs caused no PCNA damage in intact cells. Evidence supports a sulfonamide, sulfinamide, or sulfenamide crosslinking mechanism involving cysteine 148 at the PCNA subunit interface, methionine sulfoxide formation as the basis of electrophoretic mobility shifting, and tyrosine and/or methionine residues as the likely targets of AACL damage to the PCNA antibody epitope. An interstitial fluid model experiment showed that physiological amino acids can mediate HOCl damage to PCNA in the presence of proteins that would otherwise completely quench the HOCl. CONCLUSION: PCNA is a sensitive biomarker of AACL damage in cell nuclei. Arginine chloramine and proline chloramine, or reactive species derived from them, were shown to enter cells and damage PCNA. Amino acids were shown to have at least two different mechanisms for suppressing PCNA damage in cells by their corresponding AACLs. Cysteine 148 was shown to be essential for PCNA subunit crosslinking by AACLs, and a crosslinking mechanism was proposed.