ABSTRACT
This study investigated the effects of 6-gingerol-rich fraction of Zingiber officinale (6-GIRIFZO) on mercury chloride (HgCl2)-induced neurotoxicity in Wistar rats. Thirty -five male Wistar rats weighing between (150-200 g) were divided randomly into five groups (n = 7): group 1: control, received 0.5 mL of normal saline, group 2: received HgCl2 (5 mg/kg), group 3: received N-acetylcysteine (NAC) (50 mg/kg) as well as HgCl2 (5 mg/kg), group 4: received 6-GIRIFZO (100 mg/kg) and HgCl2 (5 mg/kg), group 5: had 6-GIRIFZO (200 mg/kg) and HgCl2 (5 mg/kg), consecutively for 14 days. On the day14, the rats were subjected to behavioural tests using a Morris water maze and novel object recognition tests. The rats were then euthanized to obtain brain samples for the determination of biochemical parameters (acetylcholinesterase (AchE), nitric oxide (NO), malondialdehyde (MDA), superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT), glutathione (GSH), tumor necrosis factor- alpha (TNF-α), nuclear factor kappa-B (NF-κB), interleukin-1ß (IL-1ß) and interleukin-6 (IL-6)) using standard methods. The result revealed a significant increase in escape latency and a significant decrease in recognition ratio in the rats that were exposed to HgCl2 only. However, 6-GIRIFZO produced a significant reduction in the escape latency and (p < 0.05) increase in the recognition ratio. Similarly, HgCl2 exposure caused a significant (p < 0.05) decrease in the brain SOD, GPx, CAT, GSH with increased brain levels of MDA, NO, AchE, TNF-α, NF-κB, IL-1ß and IL-6. Similarly to the standard drug, NAC, 6-GIRIFZO (100 and 200 mg/kg) significantly (p < 0.05) increased brain SOD, GPx, CAT, and GSH levels with decreased concentrations of MDA, NO, AchE, TNF-α, NF-κB, IL-1ß and IL-6. Also, pre-treatment with 6-GIRIFZO prevented the HgCl2-induced morphological aberrations in the rats. This study concludes that 6-GIRIFZO prevents HgCl2-induced cognitive deficit via reduction of brain inflammation as well as oxidative stress in rats.
Subject(s)
Catechols , Cognitive Dysfunction , Fatty Alcohols , Mercury , Zingiber officinale , Rats , Male , Animals , Antioxidants/pharmacology , Antioxidants/metabolism , Rats, Wistar , Chlorides , Neuroinflammatory Diseases , Mercuric Chloride/toxicity , Tumor Necrosis Factor-alpha/metabolism , NF-kappa B/metabolism , Interleukin-6 , Acetylcholinesterase , Oxidative Stress , Glutathione/metabolism , Acetylcysteine/pharmacology , Superoxide Dismutase/metabolism , Mercury/pharmacologyABSTRACT
The pollution of aquatic ecosystems due to the elevated concentration of a variety of contaminants, such as metal ions, poses a threat to humankind, as these ecosystems are in high relevance with human activities and survivability. The exposure in heavy metal ions is responsible for many severe chronic and pathogenic diseases and some types of cancer as well. Metal ions of the groups 11 (Cu, Ag, Au), 12 (Zn, Cd, Hg), 14 (Sn, Pb) and 15 (Sb, Bi) highly interfere with proteins leading to DNA damage and oxidative stress. While, the detection of these contaminants is mainly based on physicochemical analysis, the chemical determination, however, is deemed ineffective in some cases because of their complex nature. The development of biological models for the evaluation of the presence of metal ions is an attractive solution, which provides more insights regarding their effects. The present work critically reviews the reports published regarding the toxicity assessment of heavy metal ions through Allium cepa and Artemia salina assays. The in vivo toxicity of the agents is not only dose depended, but it is also strongly affected by their ligand type. However, there is no comprehensive study which compares the biological effect of chemical agents against Allium cepa and Artemia salina. Reports that include metal ions and complexes interaction with either Allium cepa or Artemia salina bio-indicators are included in the review.
Subject(s)
Mercury , Metals, Heavy , Animals , Artemia/metabolism , Cadmium/metabolism , Chemistry, Bioinorganic , Ecosystem , Humans , Ions/metabolism , Lead , Ligands , Mercury/pharmacology , Metals, Heavy/metabolism , Metals, Heavy/toxicity , OnionsABSTRACT
Aureobasidium pullulans is a ubiquitous and widely distributed fungus in the environment, and exhibits substantial tolerance against toxic metals. However, the interactions between metals and metalloids with the copious extracellular polymeric substances (EPS) produced by A. pullulans and possible relationships to tolerance are not well understood. In this study, it was found that mercury (Hg) and selenium (Se), as selenite, not only significantly inhibited growth of A. pullulans but also affected the composition of produced EPS. Lead (Pb) showed little influence on EPS yield or composition. The interactions of EPS from A. pullulans with the tested metals and metalloids depended on the specific element and their concentration. Fluorescence intensity measurements of the EPS showed that the presence of metal(loid)s stimulated the production of extracellular tryptophan-like and aromatic protein-like substances. Examination of fluorescence quenching and calculation of binding constants revealed that the fluorescence quenching process for Hg; arsenic (As), as arsenite; and Pb to EPS were mainly governed by static quenching which resulted in the formation of a stable non-fluorescent complexes between the EPS and metal(loid)s. Se showed no significant interaction with the EPS according to fluorescence quenching. These results provide further understanding of the interactions between metals and metalloids and EPS produced by fungi and their contribution to metal(loid) tolerance. KEY POINTS: ⢠Metal(loid)s enhanced production of tryptophan- and aromatic protein-like substances. ⢠Non-fluorescent complexes formed between the EPS and tested metal(loid)s. ⢠EPS complexation and binding of metal(loid)s was dependent on the tested element. ⢠Metal(loid)-induced changes in EPS composition contributed to metal(loid) tolerance.
Subject(s)
Aureobasidium/drug effects , Fluorescence , Metalloids/pharmacology , Metals/pharmacology , Aureobasidium/growth & development , Extracellular Polymeric Substance Matrix/chemistry , Mercury/pharmacology , Selenium/pharmacologyABSTRACT
Ayurvedic medicines are often used in different formulations, the heavy metals, which are generally referred to as being toxic. In this work, we report on the physicochemical characterization and biological activity of some typical Ayurvedic drugs available in the market that contain arsenic, mercury and lead with the emphasis on their antibacterial performance. Among the formulations studied, some of the drugs with 'amorphous' texture (and higher solubility) were found quite active against some bacterial strains whereas the formulations possessing crystalline texture (and low solubility) were found practically ineffective. The moderate activity of some drugs against Gram-negative bacteria fairly suggested the presence of the small-sized polar molecules which was also supported by the FTIR spectroscopic data.
Subject(s)
Anti-Bacterial Agents/pharmacology , Medicine, Ayurvedic , Metals, Heavy/pharmacology , Anti-Bacterial Agents/analysis , Arsenic/analysis , Arsenic/pharmacology , Bacteria/drug effects , Lead/analysis , Lead/pharmacology , Mercury/analysis , Mercury/pharmacology , Metals, Heavy/analysisABSTRACT
Earlier we showed formulation-specific beneficial effects of dietary supplement of Ayurvedic Amalaki Rasayana (AR, a herbal formulation) and Rasa-Sindoor (RS, a mercury-based organo-metallic formulation) on various biological parameters in Drosophila, parallel to traditional Ayurvedic literature. These formulations also suppressed cell death and pathology in fly models of neurodegeneration. To understand basis of inhibition of apoptosis, we examined effects of AR and RS on induced and developmental apoptosis in Drosophila. Dietary AR or RS significantly reduced apoptosis induced by GMR-GAL4-, sev-GAL4- or hs-GAL4-directed expression of Rpr, Hid or Grim (RHG) proapoptotic proteins or by GMR-GAL4-directed DIAP1-RNAi, resulting in significant restoration of organism's viability and eye morphology. AR or RS supplement enhanced levels of inhibitor of apoptosis proteins, DIAP1 and DIAP2, and of Bancal/Hrb57A, while the levels of RHG proteins and of initiator Dronc and effecter Drice caspases were reduced in non-apoptotic wild type as well as in RHG over-expressing tissues. Levels of Dronc or Drice remained unaffected in cells developmentally destined to die so that developmental apoptosis occurred normally. Elevated levels of DIAPs and reduced levels of RHG proteins and caspases reflect a more robust physiological state of AR or RS fed organisms allowing them to tolerate greater insults without triggering the cell-death response. Such homeostatic effects of these Rasayanas seem to contribute to 'healthy ageing', one of their effects suggested in traditional Ayurvedic practices.
Subject(s)
Aging/drug effects , Apoptosis/drug effects , Drosophila melanogaster/cytology , Mercury/pharmacology , Organometallic Compounds/pharmacology , Plant Extracts/pharmacology , Animals , Caspases/metabolism , Dietary Supplements , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Imaginal Discs/metabolism , Inhibitor of Apoptosis Proteins/metabolism , Neurodegenerative Diseases/drug therapy , Transcription Factors/geneticsABSTRACT
Type IA topoisomerase activities are essential for resolving DNA topological barriers via an enzyme-mediated transient single strand DNA break. Accumulation of topoisomerase DNA cleavage product can lead to cell death or genomic rearrangement. Many antibacterial and anticancer drugs act as topoisomerase poison inhibitors that form stabilized ternary complexes with the topoisomerase covalent intermediate, so it is desirable to identify such inhibitors for type IA topoisomerases. Here we report that organomercury compounds were identified during a fluorescence based screening of the NIH diversity set of small molecules for topoisomerase inhibitors that can increase the DNA cleavage product of Yersinia pestis topoisomerase I. Inhibition of relaxation activity and accumulation of DNA cleavage product were confirmed for these organomercury compounds in gel based assays of Escherichia coli topoisomerase I. Hg(II), but not As(III), could also target the cysteines that form the multiple Zn(II) binding tetra-cysteine motifs found in the C-terminal domains of these bacterial topoisomerase I for relaxation activity inhibition. Mycobacterium tuberculosis topoisomerase I activity is not sensitive to Hg(II) or the organomercury compounds due to the absence of the Zn(II) binding cysteines. It is significant that the type IA topoisomerases with Zn(II) binding domains can still cleave DNA when interfered by Hg(II) or organomercury compounds. The Zn(II) binding domains found in human Top3α and Top3ß may be potential targets of toxic metals and organometallic complexes, with potential consequence on genomic stability and development.
Subject(s)
DNA Topoisomerases, Type I/metabolism , Mercury/pharmacology , Organomercury Compounds/pharmacology , Topoisomerase I Inhibitors/pharmacology , Zinc/metabolism , Cysteine/metabolism , DNA Topoisomerases, Type I/chemistry , Databases, Pharmaceutical , Drug Evaluation, Preclinical , Humans , Protein BindingABSTRACT
Breast milk is regarded as an ideal source of nutrients for the growth and development of neonates, but it can also be a potential source of pollutants. Mothers can be exposed to different contaminants as a result of their lifestyle and environmental pollution. Mercury (Hg) and arsenic (As) could adversely affect the development of fetal and neonatal nervous system. Some fish and shellfish are rich in selenium (Se), an essential trace element that forms part of several enzymes related to the detoxification process, including glutathione S-transferase (GST). The goal of this study was to determine the interaction between Hg, As and Se and analyze its effect on the activity of GST in breast milk. Milk samples were collected from women between day 7 and 10 postpartum. The GST activity was determined spectrophotometrically; total Hg, As and Se concentrations were measured by atomic absorption spectrometry. To explain the possible association of Hg, As and Se concentrations with GST activity in breast milk, generalized linear models were constructed. The model explained 44% of the GST activity measured in breast milk. The GLM suggests that GST activity was positively correlated with Hg, As and Se concentrations. The activity of the enzyme was also explained by the frequency of consumption of marine fish and shellfish in the diet of the breastfeeding women.
La leche materna es considerada como una fuente ideal de nutrientes para el crecimiento y el desarrollo de los recién nacidos, pero también puede ser una fuente potencial de contaminantes. Las madres pueden estar expuestas a diversos contaminantes como resultado de su estilo de vida y de la contaminación ambiental. Mercurio (Hg) y arsénico (As) pueden afectar negativamente el desarrollo del sistema nervioso fetal y neonatal. Algunos peces y mariscos son ricos en selenio (Se), un oligoelemento esencial que forma parte de diversas enzimas relacionadas con el proceso de desintoxicación, incluyendo glutatión S-transferasa (GST). El objetivo de este estudio fue determinar la interacción entre Hg, As y Se, así como analizar su efecto sobre la actividad de GST en la leche materna. Muestras de leche materna fueron obtenidas entre los días 7 y 10 después del parto. La actividad de la GST fue determinada espectrofotométricamente. Las concentraciones totales de Hg, As y Se fueron medidas por espectrometría de absorción atómica. Para explicar la posible asociación de las concentraciones de Hg, As y Se con la actividad de la GST en la leche materna, se construyeron modelos lineales generalizados. El modelo explicó el 44% de la actividad de GST medida en leche materna. El MLG sugiere que la actividad de GST se correlacionó positivamente con las concentraciones de Hg, As y Se. La actividad de la enzima se explica también por la frecuencia de consumo de peces marinos y mariscos en la dieta de las mujeres que se encuentran en periodo de lactancia.
Subject(s)
Arsenic/pharmacology , Fishes , Food Contamination , Food , Glutathione Transferase/drug effects , Mercury/pharmacology , Milk, Human/drug effects , Milk, Human/enzymology , Selenium/pharmacology , Shellfish , Animals , Arsenic/analysis , Drug Interactions , Eating , Female , Food Contamination/analysis , Humans , Mercury/analysis , Milk, Human/chemistry , Selenium/analysisABSTRACT
Combined pollution of selenium (Se) and mercury (Hg) has been known in Wanshan district (Guizhou Province, China). A better understanding of how Se and Hg interact in plants and the phytotoxicity thereof will provide clues about how to avoid or mitigate adverse effects of Se/Hg on local agriculture. In this study, the biological activity of Se has been investigated in garlic with or without Hg exposure. Se alone can promote garlic growth at low levels (<0.1 mg L(-1)), whereas it inhibits garlic growth at high levels (>1 mg L(-1)). The promotive effect of Se in garlic can be enhanced by low Hg exposure (<0.1 mg L(-1)). When both Se and Hg are at high levels, there is a general antagonistic effect between these two elements in terms of phytotoxicity. Inductively coupled plasma mass spectrometry (ICP-MS) data suggest that Se is mainly concentrated in garlic roots, compared to the leaves and the bulbs. Se uptake by garlic in low Se medium (<0.1 mg L(-1)) can be significantly enhanced as Hg exposure levels increase (P < 0.05), while it can be inhibited by Hg when Se exposure levels exceed 1 mg L(-1). The synchrotron radiation X-ray fluorescence (SRXRF) mapping further shows that Se is mainly concentrated in the stele of the roots, bulbs and the veins of the leaves, and Se accumulation in garlic can be reduced by Hg. The X-ray absorption near edge structure (XANES) study indicates that Se is mainly formed in C-Se-C form in garlic. Hg can decrease the content of inorganic Se mainly in SeO3(2-) form in garlic while increasing the content of organic Se mainly in C-Se-C form (MeSeCys and its derivatives). Hg-mediated changes in Se species along with reduced Se accumulation in garlic may account for the protective effect of Hg against Se phytotoxicity.
Subject(s)
Garlic/metabolism , Mercury/pharmacology , Selenium/metabolism , Mass Spectrometry , X-Ray Absorption SpectroscopyABSTRACT
Transient receptor potential melastatin 2 (TRPM2) is a Ca(2+)-permeable cationic channel in the TRP channel family. The channel activity can be regulated by reactive oxygen species (ROS) and cellular acidification, which has been implicated to the pathogenesis of diabetes and some neuronal disorders. However, little is known about the effect of redox-active metal ions, such as copper, on TRPM2 channels. Here we investigated the effect of divalent copper on TRPM2. TRPM2 channel was over-expressed in HEK-293 cells and the whole-cell current was recorded by patch clamp. We found the whole-cell current evoked by intracellular ADP-ribose was potently inhibited by Cu(2+) with a half maximal inhibitory concentration (IC(50)) of 2.59 µM. The inhibitory effect was irreversible. The single channel activity was abolished in the outside-out patches, and intracellular application of Cu(2+) did not prevent the channel activation, suggesting that the action site of Cu(2+) is located in the extracellular domains of the channel. TRPM2 current was also blocked by Hg(2+), Pb(2+), Fe(2+) and Se(2+). We concluded that Cu(2+) is a potent TRPM2 channel blocker. The sensitivity of TRPM2 channel to heavy metal ions could be a new mechanism for the pathogenesis of some metal ion-related diseases.
Subject(s)
Cations, Divalent/pharmacology , Copper/pharmacology , TRPM Cation Channels/antagonists & inhibitors , Adenosine Diphosphate Ribose/metabolism , Adenosine Diphosphate Ribose/pharmacology , Cations, Divalent/metabolism , Copper/metabolism , HEK293 Cells , Humans , Inhibitory Concentration 50 , Iron/metabolism , Iron/pharmacology , Lead/metabolism , Lead/pharmacology , Mercury/metabolism , Mercury/pharmacology , Patch-Clamp Techniques , Selenium/metabolism , Selenium/pharmacologyABSTRACT
ETHNOPHARMACOLOGICAL RELEVANCE: Arogyavardhini vati, an Ayurvedic polyherbal formulation has been used for liver and skin disorders in the Ayurvedic system of medicine. However, toxicity due to the presence of heavy metals in this traditional medicine is a matter of concern. AIM OF THE STUDY: To evaluate the safety of Arogyavardhini vati on brain, liver and kidney in rats. MATERIALS AND METHODS: Arogyavardhini vati at doses of 50, 250 and 500mg/kg (1, 5 and 10 times of human equivalent dose respectively), mercury chloride (1mg/kg) and normal saline were administered orally to male Wistar rats for 28 days. Behavioral parameters were assessed on day 1, 7th, 14th and 28th using Morris water maze, passive avoidance, elevated plus maze and rota rod. Biochemical parameters (acetyl-cholinesterase activity, malondialdehyde, reduced glutathione), histopathology and mercury level in brain, liver, kidney were assessed at the end of the experiment. RESULTS: There was no significant change in behavioral parameters, acetyl-cholinesterase activity, liver function (ALT, AST, ALP and bilirubin) and kidney (serum urea and creatinine) function tests at all doses of Arogyavardhini vati (50, 250 and 500mg/kg) as compared to normal control. However, significant change was observed in mercury chloride treated group. Mercury chloride treated group as well as Arogyavardhini vati treated groups (50, 250 and 500mg/kg) showed increased levels of mercury in brain, liver and kidney as compared to normal control. Histopathological results showed significant cytoarchitectural changes in brain, liver and kidney architecture in mercury chloride treated group. Whereas, normal cytoarchitecture was observed at all doses of Arogyavardhini vati. CONCLUSION: The finding of the present study suggests that Arogyavardhini vati in the doses equivalent up to 10 times of the human dose administered to rats for 28 days does not have appreciable toxicological effects on brain, liver and kidney.
Subject(s)
Brain/drug effects , Kidney/drug effects , Liver/drug effects , Medicine, Ayurvedic , Mercury/metabolism , Metals/toxicity , Minerals/toxicity , Plant Extracts/toxicity , Acetylcholinesterase/metabolism , Animals , Avoidance Learning , Behavior, Animal/drug effects , Bilirubin/blood , Brain/metabolism , Creatinine/blood , Drug Combinations , Humans , Liver/metabolism , Liver/pathology , Male , Maze Learning , Mercury/pharmacology , Rats , Rats, Wistar , Sodium Chloride/pharmacology , Transaminases/blood , Urea/bloodABSTRACT
The hydrocarbon utilizing haloarchaea, Haloferax (two strains), Halobacterium and Halococcus from a hypersaline coastal area of the Arabian Gulf, had the potential for resistance and volatilization of Hg(2+). Individual haloarchaea resisted up to between 100 and 200 ppm HgCl2 in hydrocarbon free media with salinities between 1 and 4 M NaCl, but only up to between 20 and 30 ppm in a mineral medium containing 3 M NaCl, with 0.5% (w/v) crude oil, as a sole source of carbon and energy. Halococcus and Halobacterium volatilized more mercury than Haloferax. The individual haloarchaea consumed more crude oil in the presence of 3 M NaCl than in the presence of 2 M NaCl. At both salinities, increasing the HgCl2 concentration in the medium from 0 to 20 ppm resulted in decreasing the oil consumption values by the individual haloarchaea. However, satisfactory oil consumption still occurred in the presence of 10 ppm HgCl2. It was concluded that haloarchaea with the combined potential for mercury resistance and volatilization and hydrocarbon consumption could be useful in removing toxic mercury forms effectively from oil free, mercury contaminated, hypersaline environments, and mercury and oil, albeit less effectively, from oily hypersaline environments.
Subject(s)
Drug Resistance, Bacterial/physiology , Halobacterium/growth & development , Halococcus/growth & development , Mercury/pharmacology , Petroleum/microbiology , Biodegradation, Environmental , Drug Resistance, Bacterial/drug effects , Mercury/metabolismABSTRACT
The impacts of elevated aqueous mercury levels (0, 2, and 4 ppm) on the growth status and mercury tissue concentrations of Eleocharis parvula, Saururus cernuus, Juncus effuses, Typha latifolia, and Panicum hemitomon were determined. Both short-term (net CO2 assimilation) and long-term (biomass) indicators of plant growth status suggest that Eleocharis parvula, Saururus cernuus, and Juncus effuses were relatively unimpacted by elevated mercury levels, whereas Typha latifolia and Panicum hemitomon were somewhat impacted at elevated mercury levels. Eleocharis parvula, Panicum hemitomon, and Typha latifolia generally had the greatest overall belowground tissue concentrations of mercury (2 ppm treatment: 7.21, 7.32, and 9.64 ppm respectively; 4 ppm treatment: 16.23, 18.23, and 13.98 ppm, respectively) and aboveground tissue concentrations of mercury (2 ppm treatment: 0.01, 0.04, 0.02; 4 ppm treatment: 0.26; 0.11; 0.17 ppm, respectively). However, the species investigated in this study demonstrated lower levels of mercury accumulation into tissues when compared with similar investigations of other aquatic plants, suggesting that the above species are not optimal for phytoremediation efforts.
Subject(s)
Mercury/pharmacology , Plant Development , Plants, Medicinal/growth & development , Biomass , Eleocharis/drug effects , Eleocharis/growth & development , Environmental Exposure , Panicum/drug effects , Panicum/growth & development , Plants/drug effects , Plants, Medicinal/drug effects , Saururaceae/drug effects , Saururaceae/growth & development , Typhaceae/drug effects , Typhaceae/growth & development , WetlandsABSTRACT
Mercury, an occupational and environmental contaminant, is a well-recognized health hazard. The thymus is a target for inorganic mercury (Hg2+); thymic function is impaired in Hg2+ intoxication and is partially restored by simultaneous L-arginine supplementation. The nitric oxide (NO)-nitric oxide synthase (NOS) pathway and metallothioneins (MTs) were studied to investigate the role of L-arginine in thymic function restoration after mercury exposure. Mice received a higher and a lower dose of inorganic mercury, with and without L-arginine supplementation. Saline-treated mice were used as controls. Thymus weight and thymulin were measured as indices of thymic function. Mice treated with Hg2+ alone displayed an accumulation of metal in the thymus, reduced NOS activity, a lower plasma nitrite plus nitrate concentration and an increased MTs expression compared with control mice. L-arginine supplementation was associated with lower Hg2+ concentrations in the organ and partial preservation of other measures. Reduced accumulation of Hg2+ in mice dosed with L-arginine was probably related to greater NO production and NO-MTs interactions.
Subject(s)
Arginine/pharmacology , Mercury Poisoning/physiopathology , Mercury/administration & dosage , Metallothionein/drug effects , Nitric Oxide Synthase/drug effects , Thymus Gland/drug effects , Animals , Arginine/administration & dosage , Male , Mercury/analysis , Mercury/pharmacology , Mercury Poisoning/drug therapy , Mice , Mice, Inbred BALB C , Reverse Transcriptase Polymerase Chain Reaction , Thymus Gland/physiopathologyABSTRACT
The synthesis and degradation of (1-->3)-beta-glycosidic bonds between glucose moieties are essential metabolic processes in plant cell architecture and function. We have found that a unique, conserved cysteine residue, positioned outside the catalytic centre of potato endo-(1-->3)-beta-glucanase - product of the gluB20-2 gene, participates in determining the substrate specificity of the enzyme. The same residue is largely responsible for endo-(1-->3)-beta-glucanase inhibition by mercury ions. Our results confirm that the spatial adjustment between an enzyme and its substrate is one of the essential factors contributing to the specificity and accuracy of enzymatic reactions.
Subject(s)
Cysteine/metabolism , Glucan 1,3-beta-Glucosidase/metabolism , Solanum tuberosum/enzymology , Amino Acid Sequence , Catalysis , Cysteine/chemistry , Glucan 1,3-beta-Glucosidase/antagonists & inhibitors , Glucan 1,3-beta-Glucosidase/chemistry , Mercury/pharmacology , Molecular Sequence Data , Substrate SpecificityABSTRACT
OBJECTIVES: Human blood levels of mercury are commonly 10nM, but may transiently reach 50-75nM after dental amalgam placement or removal. Controversy persists about the use of mercury because the effects of these 'trace' levels of mercury are not clear. Concentrations of mercury > or =5000nM unequivocally alter redox balance in blood cells including monocytes. In the current study, we tested a hypothesis that concentrations of mercury <100nM altered levels and activities of key proteins that maintain monocytic redox balance. METHODS: Human THP1 monocytes were exposed to 10-75nM of Hg(II) for 6-72h, with or without activation by lipopolysaccharide (LPS). The redox management proteins Nrf2 and thioredoxin-1 (Trx1) were separated by electrophoresis, then quantified by immunoblotting. The activity of the seleno-enzyme thioredoxin reductase (TrxR1), important in maintaining Trx1 redox balance, was measured by cell-free and cell-dependent assays. RESULTS: Concentrations of Hg(II) between 10-75nM increased Nrf2 levels (3.5-4.5 fold) and decreased Trx1 levels (2-3 fold), but these changes persisted <24h. Hg(II) potently inhibited (at concentrations of 5-50nM) TrxR1 activity in both cell-free and intracellular assays. Furthermore, Hg(II) transiently amplified LPS-induced Nrf2 levels by 2-3 fold and limited LPS-induced decreases in Trx1. All effects of Hg(II) were mitigated by pre-adding N-acetyl-cysteine (NAC) or sodium selenide (Na2SeO3), supplements of cellular thiols and selenols, respectively. SIGNIFICANCE: Our results suggest that nanomolar concentrations of Hg(II) transiently alter cellular redox balance in monocytes that trigger changes in Nrf2 and Trx1 levels. These changes indicate that monocytes have a capacity to adapt to trace concentrations of Hg(II) that are introduced into the bloodstream after dental amalgam procedures or fish consumption. The ability of monocytes to adapt suggests that low levels of mercury exposure from dental amalgam may not overtly compromise monocyte function.
Subject(s)
Dental Materials/pharmacology , Mercury/pharmacology , Monocytes/drug effects , NF-E2-Related Factor 2/drug effects , Thioredoxin Reductase 1/drug effects , Thioredoxins/drug effects , Acetylcysteine/pharmacology , Antioxidants/pharmacology , Cells, Cultured , Electrophoresis , Enzyme Inhibitors/pharmacology , Free Radical Scavengers/pharmacology , Humans , Immunoblotting , Lipopolysaccharides/pharmacology , Materials Testing , Monocytes/enzymology , Monocytes/metabolism , Oxidation-Reduction , Selenium Compounds/pharmacology , Thioredoxin Reductase 1/antagonists & inhibitorsABSTRACT
Gap junctional intercellular communication (GJIC) is used to control cell proliferation. It is not surprising then that a lack of GJIC (i.e., during loss of contact inhibition among adjacent cells) is associated with cancer promotion/progression. There also seems to be a link between ineffective GJIC and increases in inflammatory events. Interestingly, many cytokines released during an inflammatory response also have critical roles in cancer cell survival. Specifically, TNFalpha and IL-1beta are important for initiating/augmenting CD8(+)- and NK-cell mediated killing; however, in what appears counterintuitive, each--at times--can act to protect cancer cells against apoptosis, a major mechanism for cell killing from within. It is thus plausible to assume that certain toxicants might act as cancer promoters in manners distinct from/augmentive of direct effects on DNA, i.e., by concurrently altering GJIC and cytokine formation in host or microenvironment of a cancer cell. Our research has evaluated effects of many toxicants upon keratinocytes; in particular, we have examined effects of mercury on GJIC and on TNFalpha and IL-1beta levels in (and secretion by) these cells. In the studies here, a tomato preparation (i.e., an oleoresin) bearing the antioxidant carotenoid lycopene was examined for its effects on GJIC and cytokine formation by keratinocytes in general, and its potential ability to mitigate/reverse the toxic effects of mercury in the cells in particular. It was shown that a 4-hr treatment with the oleoresin (containing 56, 6 nM lycopene) re-established GJIC among--and increased the formation of IL-1beta and TNFalpha that had been significantly reduced within--keratinocytes that had been pre-treated for 24 hr with 10 nM HgCl(2). These results show that effects of mercury likely depend on some level of oxidative stress and that its potential effects on keratinocyte GJIC and cytokine concentrations could, in an exposed host, be mitigated/reversed by increased dietary intake of carotenoids like lycopene.
Subject(s)
Carotenoids/pharmacology , Cell Communication/drug effects , Gap Junctions/drug effects , Interleukin-1beta/metabolism , Keratinocytes/drug effects , Mercury/pharmacology , Tumor Necrosis Factor-alpha/metabolism , Anticarcinogenic Agents/pharmacology , Cells, Cultured , Gap Junctions/metabolism , Humans , Keratinocytes/metabolism , Lipopolysaccharides/pharmacology , Lycopene , Solanum lycopersicum/chemistry , Mercuric Chloride/pharmacology , Plant Extracts/pharmacologyABSTRACT
An attempt was made to study selenium (Se) and mercury (Hg) interactions in plants, specifically soybean (Glycine max), by inductively coupled plasma mass spectrometric detection. Greenhouse-cultivated plants were subjected to treatment with different regimens of Se and Hg and analyzed for their metabolized species in roots, stems, leaves, pods and beans. Most of the water-soluble Hg was found to be localized in the roots in association with Se in a high molecular weight entity, as identified by size exclusion chromatography. This entity was also extracted in protein specific isolate, but it resisted enzymatic breakdown. Complete breakdown of this high molecular weight species was accomplished by acid hydrolysis. Optimization of the conditions for acid hydrolysis is discussed. Hg and Se species found in root extract were studied by ion-pairing chromatography. In a sub-study, the Se distribution pattern was found to be unaffected by the presence of Hg, but the amount of Se assimilated was found to be higher in plants coexposed to Hg.
Subject(s)
Chromatography, High Pressure Liquid/methods , Glycine max/chemistry , Mercury/antagonists & inhibitors , Plant Roots/chemistry , Selenium/antagonists & inhibitors , Mass Spectrometry/methods , Mercury/analysis , Mercury/pharmacology , Plant Extracts/analysis , Plant Extracts/chemistry , Selenium/analysis , Selenium/pharmacology , Solubility , Water/chemistryABSTRACT
The genome of the plant-colonizing bacterium Pseudomonas fluorescens SBW25 possesses a putative copper-transporting P1-type ATPase (CueA) that is induced on the plant surfaces. Using a chromosomally-integrated cueA-lacZ fusion, we show that transcription of cueA can be induced (in vitro) by ions of copper, silver, gold, and mercury. To investigate the biological significance of cueA, a nonpolar cueA deletion mutant (SBW25 delta cueA) was constructed. This mutant strain displayed a twofold reduction in its tolerance to copper compared with the wild-type strain; however, no change was observed in the sensitivity of the mutant strain to silver, gold, or mercury ions. To obtain insight into the ecological significance of cueA, the competitive ability of SBW25 delta cueA was determined relative to wild-type SBW25 in three environments (none contained added copper): minimal M9 medium, the root of sugar beet (Beta vulgaris), and the root of pea (Pisum sativum). Results showed that the fitness of SBW25 delta cueA was not different from the wild type in laboratory medium but was compromised in the two plant environments. Taken together, these data demonstrate a functional role for CueA in copper homeostasis and reveal an ecologically significant contribution to bacterial fitness in the plant rhizosphere. They also suggest that copper ions accumulate on plant surfaces.
Subject(s)
Adenosine Triphosphatases/metabolism , Cation Transport Proteins/metabolism , Copper/pharmacology , Plants/microbiology , Pseudomonas fluorescens/metabolism , Adenosine Triphosphatases/genetics , Beta vulgaris/microbiology , Cation Transport Proteins/genetics , Copper/metabolism , Copper-Transporting ATPases , Gene Deletion , Gene Expression Regulation, Bacterial/drug effects , Gold/pharmacology , Homeostasis , Mercury/pharmacology , Mutation , Pisum sativum/microbiology , Plant Roots/microbiology , Pseudomonas fluorescens/genetics , Pseudomonas fluorescens/pathogenicity , Silver/pharmacology , Virulence/geneticsABSTRACT
The mercury (Hg) accumulation mechanism was studied in rape (Brassica napus) plants grown under a Hg concentration gradient (0 microm-1,000 microm). Hg mainly accumulated in roots. Therefore, the presence of phytochelatins (PCs) was studied in the roots of the plants. The high stability of the PC-Hg multicomplexes (mPC-nHg) seems to be the main reason for the lack of previous Hg-PC characterization studies. We propose a modification of the method to detect and quantify unbound PC of Hg in plant extracts via high-performance liquid chromatography coupled to electrospray tandem mass spectrometry and inductively coupled plasma mass spectrometry in parallel. We separated the PC from the Hg by adding the chelating agent sodium 2,3-dimercaptopropanesulfonate monohydrate. We only detected the presence of PC after the addition of the chelating agent. Some multicomplexes mPC-nHg could be formed but, due to their large sizes, could not be detected. In this study, only PC(2) was observed in plant samples. Hg accumulation was correlated with PC(2) concentration (r(2) = 0.98).
Subject(s)
Brassica napus/drug effects , Brassica napus/metabolism , Glutathione/metabolism , Mercury/pharmacology , Plant Extracts/chemistry , Dose-Response Relationship, Drug , Glutathione/analysis , Phytochelatins , Plant Roots/metabolismABSTRACT
Pseudomonas fluorescens strains PRS9 and GRS1 (wild type) were made mercury resistant PRS9Hg(r) (147 microM HgCl2) and GRS1Hg(r) (55 microM HgCl2), respectively, in King's medium by enrichment selection and their in situ root colonization studies were carried out. Mercury resistant mutant of PRS9 was stable and resulted in significant increase in root and shoot fresh weight (P < 0.05). Both the mutants are positive for indoleacetic acid (IAA), 'P' solubilization and siderophore production. PRS9, potent 'P' solubilizer, exhibited higher 'P' solubilization as compared to GRS1. After 2 weeks of inoculation, the population level of wild type PRS9 and its mercury resistant mutants has increased (50 fold). Mercury resistance has no adverse effect on the growth promoting properties of mutants besides being comparable in its morphological and physiological properties with their wild type counterpart. Furthermore, mercury resistant character facilitates rhizospheric competition and thus helpful for establishment of growth promoting strains where metal ions are either limiting and/or present at toxic level.