The role of root organic acids in the tolerance of Festuca rubra to zinc,lead and cadmium

Abstract

Festuca rubra L. plants are pseudometallophytes colonizing abandoned Pb/Zn mine areas, successfully employed in phytostabilization. To study the contribution of low-molecular weight organic acids to metal tolerance, F. rubra plants were grown for three months in hydroponics with Cd (1.8, 18 and 36 µmol?L^?1), Pb (50, 250 and 500?µmol?L^?1) and Zn (0.3, 3 and 6?mmol?L^?1), separately, and in ternary combination (18?µmol?L^?1 Cd + 250?µmol?L^?1 Pb + 0.3?mmol?L^?1 Zn). The roots retained most of the metals but their distribution from shoot to root was altered when the plants were treated with the ternary combination. The main organic acids in roots were citrate and malate. At the lowest concentrations, the metals caused small reductions in biomass, had no effects on photosynthetic pigments nor on malondialdehyde, but led to increases in root organic acids. At higher concentrations, phytotoxic responses were observed, associated with a decline of citrate and malate in the roots.     

Mineralogical variables that control the antibacterial effectiveness of a natural clay deposit

As antibiotic-resistant bacterial strains emerge and pose increased global health risks, new antibacterial agents are needed as alternatives to conventional antimicrobials. Naturally occurring antibacterial clays have been identified which are effective in killing antibiotic-resistant bacteria. This study examines a hydrothermally formed antibacterial clay deposit near Crater Lake, OR (USA). Our hypothesis is that antibacterial clays buffer pH and Eh conditions to dissolve unstable mineral phases containing transition metals (primarily Fe²⁺), while smectite interlayers serve as reservoirs for time release of bactericidal components. Model pathogens (Escherichia coli ATCC 25922 and Staphylococcus epidermidis ATCC 14990) were incubated with clays from different alteration zones of the hydrothermal deposit. In vitro antibacterial susceptibility testing showed that reduced mineral zones were bactericidal, while more oxidized zones had variable antibacterial effect. TEM images showed no indication of cell lysis. Cytoplasmic condensation and cell wall accumulations of <100 nm particles were seen within both bacterial populations. Electron energy loss analysis indicates precipitation of intracellular Fe³⁺-oxide nanoparticles (<10 nm) in E. coli after 24 h. Clay minerals and pyrite buffer aqueous solutions to pH 2.5–3.1, Eh > 630 mV and contain elevated level (mM) of soluble Fe (Fe²⁺ and Fe³⁺) and Al³⁺. Our interpretation is that rapid uptake of Fe²⁺ impairs bacterial metabolism by flooding the cell with excess Fe²⁺ and overwhelming iron storage proteins. As the intracellular Fe²⁺ oxidizes, it produces reactive oxygen species that damage biomolecules and precipitates Fe-oxides. The ability of antibacterial clays to buffer pH and Eh in chronic non-healing wounds to conditions of healthy skin appears key to their healing potential and viability as an alternative to conventional antibiotics.     

Effects of lead and selected pyrethroids/piperonyl butoxide alone and in combination on Na,K‐ATPase

In vitro effects of Pb²⁺, the pyrethroid insecticides cypermethrin, fenvalerate and the syner‐gist piperonyl butoxide on sodium‐potassium‐activated adenosine triphosphatase (Na,K‐ATPase) from dog kidney were determined. Pb²⁺ with an estimated IC50 value of 5.2 μM was found to be a potent inhibitor of Na,K‐ATPase activity, whereas Na,K‐ATPase was less sensitive to the pyrethroids tested and piperonyl butoxide. Investigation with circular dichroism (CD) spec‐troscopy showed that inhibition occurs through conformational changes of the α‐subunit of the enzyme. The kinetic characteristics of inhibition of Na,K‐ATPase with varying substrate (ATP) concentrations as well as with varying Na⁺ concentrations exhibited a competitive type of inhibition with Pb²⁺ in the μM range. With Pb²⁺ alone in the enzyme assay no conformational changes of the protein could be observed which confirmed the assumption that Pb²⁺ can bind to the Na⁺ binding site of the α‐subunit. Uncompetitive type of inhibition occurred with varied K⁺ concentrations demonstrating that this cation binding site is not affected directly by Pb²⁺.

Complete reversal of Pb²⁺ by DTT confirms that a possible target for interaction of this heavy metal ion with Na, K‐ATPase are specific SH groups.

Synergistic effects could only be determined with higher Pb²⁺ concentrations of 3, 5 and 7 μM plus piperonyl butoxide while all other combinations with this heavy metal plus organic substances where of the additive type. With CD spectroscopy also only additive effects were observed. These results demonstrate that higher concentrations of piperonyl butoxide favor the binding of Pb²⁺ to the Na⁺ binding site by conformational changes of the protein.     

In vitro and in vivo inhibition of Ca2+-Mg2+-ATPase activity by cadmium in post larvae of Penaeus monodon

Ca²⁺-Mg²⁺-ATPase is a membrane-bound enzyme and is responsible for regulating cytosolic free calcium. In vitro and in vivo effects of cadmium were studied on Ca²⁺-Mg²⁺-ATPase activity in plasma membrane/mitochondrial fraction of Penaeus monodon post larvae. In vitro studies revealed a concentration-dependent decrease in enzyme activity with an IC₅₀ value of 11.02?µM. In vivo experiments were conducted by exposing the post larvae to 1/10th (0.12?ppm) and 1/5th (0.24?ppm) of LC₅₀ values of cadmium for 30 days. Both ATPase activity and metal accumulation were estimated in post larvae exposed to 0.12 and 0.24?ppm of cadmium at different intervals of 24?h, 48?h, 96?h, 10 days and 30 days. ATPase activity showed a gradual decrease in post larvae on exposure to both the sub-lethal concentrations with respect to their controls and the decrease was significant (p?相似文献   

Effects of benzo[a]pyrene toxicity on morphology and ultrastructure of Hordeum sativum

Many studies have been devoted to investigation of toxic benzo(a)pyrene (BaP) compound, but studies involving changes at the cellular level are insufficient to understand the mechanisms of polycyclic aromatic hydrocarbons (PAHs) effect on plants. To study the toxicity of BaP, a model vegetation experiment was conducted on cultivation of spring barley (Hordeum sativum distichum) on artificially polluted BaP soil at different concentrations. The article discusses the intake of BaP from the soil into the plant and its effect on the organismic and cellular levels of plant organization. The BaP content in the organs of spring barley was determined by the method of saponification. With an increase in the concentration of BaP in the soil, its content in plants also rises, which leads to inhibition of growth processes. The BaP content in the green part of Hordeum sativum increased from 0.3 µg kg^?1 in control soil up to 2.6 µg kg^?1 and 16.8 µg kg^?1 under 20 and 400 ng/g BaP applying in soil, as well as in roots: 0.9 µg kg^?1, 7.7 µg kg^?1, 42.8 µg kg^?1, respectively. Using light and electron microscopy, changes in the tissues and cells of plants were found and it was established that accumulation of BaP in plant tissues caused varying degrees of ultrastructural damage depending on the concentration of pollutant. BaP had the greatest effect on the root, significant changes were found in it both at histological and cytological levels, while changes in the leaves were observed only at the cytological level. The results provide significant information about the mechanism of action of BaP on agricultural plants.

     

Nano-titanium dioxide (TiO2)-induced changes affecting Cu2+-mediated alterations in bacterium Bacillus subtilis and α-amylase

Titanium dioxide (TiO₂) nanoparticles possess the potential to coexist with Copper (Cu²⁺) in soil. The individual and combined toxicity of these two chemicals was evaluated using the bacterium Bacillus subtilis, a known soil model bacterium. Cu²⁺ (6.25–50?µg?mL^?1) alone produced toxicity to bacteria as evidenced by the decreased cell viability and deceased α-amylase production. The addition of TiO₂ (50?mg?mL^?1) enhanced the Cu²⁺-induced decrease in cell viability but elevated amylase activity. TiO₂ did not markedly affect the growth rate and lag period. A primary cause of TiO₂ increasing Cu²⁺ toxicity is presumed to be associated with hydroxyl radical formation, while increased amylase activity is considered to arise from Cu²⁺ facilitating TiO₂ degradation ability.     

Effects of cadmium on intracellular cation homoeostasis in the yeast Saccharomyces cerevisiae

Previous studies have demonstrated that cadmium can induce biochemical and physiological changes in yeast Saccharomyces cerevisiae. However, studies on the influence of cadmium on the ion balance in the cell and the interaction between cadmium and other ions are still relatively few in number. By using inductively coupled plasma-atomic emission spectrometry, the contents of some cations, including Zn²⁺, Ca²⁺, Fe³⁺, Cu²⁺, Mg²⁺, K⁺, and Na⁺ were measured. The data showed that the levels of Zn²⁺ and Fe³⁺ were increased, while those of Cu²⁺, K⁺, and Na⁺ were decreased after cadmium treatment. Afterwards, using the drop test assay, the interactions between cadmium and the selected ions were investigated. The results suggested that the cytotoxicity of cadmium could be attributable to the interference of cadmium with the intracellular cation homoeostasis. Calcium channel transporter Cch1 participates in the intracellular uptake of cadmium. Additionally, Zn²⁺, Ca²⁺, Fe³⁺, Mg²⁺, and K⁺ can rescue the toxic effect of cadmium in yeast.     

The effects of <Emphasis Type="Italic">Acidithiobacillus ferrooxidans</Emphasis> on the leaching of cobalt and strontium adsorbed onto soil particles

Bioleaching from soil artificially contaminated with analogues of radionuclides, Co and Sr, was carried out using a Fe-oxidizing bacterium, Acidithiobacillus ferrooxidans. Due to bacterial metabolism, the pH and dissolved Fe³⁺ concentration in a biotic slurry decreased and increased respectively, over time, but the concentrations of Co and Sr extracted from the soil showed no significant enhancement compared with those under abiotic control. In both cases, Co and Sr were leached from the soil during the initial period of the experiment, due to the initially low solution pH of 2.0, and the dissolved concentrations remained almost constant for the duration of the experiment (300 h). Since oxidation of Fe²⁺ by A. ferrooxidans led to the production of Fe precipitates and colloidal suspensions, the Co and Sr extracted into solution were most likely re-adsorbed onto the Fe solids. Also, A. ferrooxidans, without an external supply of Fe²⁺, extracted almost equal or greater amounts of Co and Sr from the soil than when Fe²⁺ was supplied. Under the same leaching conditions, the extent of Sr removal was much lower than that of Co. On the contrary to the high efficiency of microbial metal leaching in biohydrometallurgy for low-graded sulfide ores, which has been widely documented, conventional bioleaching techniques with A. ferrooxidans supplied with enough Fe²⁺ showed low efficiency for the removal of radionuclides loosely bound onto soil particle surfaces.     

Response of Lupinus albus to Pb–EDTA indicates relatively high tolerance

White lupin plants were grown in hydroponics with 0, 90 and 180 µmol L^?1 Pb(II) ethylenediaminetetraacetate complex for 30 days. Pb distribution (shoot/root ratio) was 0.34 and 0.46 for both Pb treatments. In the shoots, no decrease in biomass nor in photosynthetic pigment levels and no changes in the concentrations of malondialdehyde and glutathione were detected. In the roots, malondialdehyde increased by 20%, glutathione 2–3.6 times and phytochelatin concentrations 4–5 times. The high tolerance of white lupin makes it a valuable plant for phytoremediation of Pb-contaminated soil.     

Ocean acidification and warming alter photosynthesis and calcification of the symbiont-bearing foraminifera Marginopora vertebralis

The impact of elevated CO₂ and temperature on photosynthesis and calcification in the symbiont-bearing benthic foraminifer Marginopora vertebralis was studied. Individual specimens of M. vertebralis were collected from Heron Island on the southern Great Barrier Reef (Australia). They were maintained for 5 weeks at different temperatures (28, 32 °C) and pCO₂ (400, 1,000 µatm) levels spanning a range of current and future climate-change scenarios. The photosynthetic capacity of M. vertebralis was measured with O₂ microsensors and a pulse-amplitude-modulated chlorophyll (Chl) fluorometer, in combination with estimates of Chl a and Chl c ₂ concentrations and calcification rates. After 5 weeks, control specimens remained unaltered for all parameters. Chlorophyll a concentrations significantly decreased in the specimens at 1,000 µatm CO₂ for both temperatures, while no change in Chl c ₂ concentration was observed. Photoinhibition was observed under elevated CO₂ and temperature, with a 70–80 % decrease in the maximum quantum yield of PSII. There was no net O₂ production at elevated temperatures in both CO₂ treatments as compared to the control temperature, supporting that temperature has more impact on photosynthesis and O₂ flux than changes in ambient CO₂. Photosynthetic pigment loss and a decrease in photochemical efficiency are thus likely to occur with increased temperature. The elevated CO₂ and high temperature treatment also lead to a reduction in calcification rate (from +0.1 to >?0.1 % day^?1). Thus, both calcification and photosynthesis of the major sediment-producing foraminifer M. vertebralis appears highly vulnerable to elevated temperature and ocean acidification scenarios predicted in climate-change models.     

Efficiency of Zn phytoextraction,biomass yield and formation of low-molecular-weight organic acids in S × rubens – a hydroponic experiment

The aim of the study was to estimate Zn phytoextraction and changes in biomass of S?×?rubens growing in modified Knop's solution with different levels of Zn addition (0.5, 1.0, 2.5 and 5.0?mM). Obtained results were correlated with secretion of selected low-molecular-weight organic acids (LMWOAs) in the rhizosphere, roots and leaves. An increase in Zn concentration in Knop's solution resulted in Zn accumulation in roots, shoots and leaves. The highest accumulation was observed for plants growing in 5?mM Zn, at concentration levels 4741.36?±?98.66, 1227.31?±?16.57 and 2241.65?±?34.90?mg?kg^?1 DW in roots, shoots and leaves, respectively. The bioaccumulation factor and the translocation factor for plants growing in 0.5, 1.0 and 2.5?mM Zn clearly indicate that this Salix taxon is an effective Zn accumulator. The general reduction of Salix biomass with an increase in Zn concentration in the solution was observed. In the rhizosphere, the total LMWOA concentration was almost 0.93?µmol?kg^?1 DM for control (Zn free) plants, while for 5.0?mM of Zn it was 4.9?µmol?kg^?1 DM. Increasing concentrations of acids were observed in roots (1.34 for the control and 5.57?µmol?kg^?1 DM for plants treated with 2.5?mM of Zn).     

The use of δ18O as an indicator of vanadium movement in a dormant stratovolcano region

The oxygen isotope (δ¹⁸O) stable water tracer can be a promising new tool for identifying trace metals in volcanoes and their sources. In the present study, the origin of vanadium in water from a spring at the base of Mt. Fuji is examined using δ¹⁸O, a dormant stratovolcano consisting of lava and basalt rock located on the North Pacific Coast of Japan. A comparison of water from the main springs at the foot of the Mt. Fuji volcano indicates that only V, Cr, Mn and Co enrichment could be related to volcanic events, whereas Ni, Cu, Cd and Pb originate from the dissolution of particles of anthropogenic origin from the industrial areas of Fuji and Fujinomiya. The average V concentrations at the mountain sites ranged from 50 to 110 µg L^?1 and from 18 to 47 µg L^?1 in the coastal areas. The δ¹⁸O became depleted at higher elevations and increased in coastal areas as well as in some NO₃^?-contaminated water. Therefore, variations in the dissolved V/δ¹⁸O ratio in springs of the study area occur due to the elevations of their catchments and the increased concentrations of δ¹⁸O from NO₃^? as a contaminant.     

Oxidized multiwalled carbon nanotubes modified with 2-(2-hydroxy-5-nitrophenyl)-4,5-diphenyl imidazole for solid phase extraction and preconcentration of some metal ions

In this work, a new procedure for the enrichment of the trace amount of Cu²⁺, Ni²⁺, Co²⁺, Pb²⁺, Fe²⁺, and Zn²⁺ ions based on the utilization of multiwalled carbon nanotubes (MWCNT) modified with 2-(2-hydroxy-5-nitrophenyl)-4,5-diphenyl imidazole as chelating agent prior to their determination by flame atomic absorption spectrometry has been described. The influence of effective parameters including pH, amount of ligand and MWCNT, composition of eluent, and coexisting ions on recoveries of understudy metal ions was examined. At the optimum pH of 5.0, all metal ions were quantitatively sorbed onto the proposed solid phase and completely desorbed with 8?mL of 5.0?mol?L^?1 HNO₃. The detection limit of Cu²⁺, Co²⁺, Ni²⁺, Pb²⁺, Fe²⁺, and Zn²⁺ ions was 1.7, 2.4, 2.3, 2.9, 2.8, and 1.4?µg?L^?1, while the preconcentration factor was 63 for Cu²⁺ and 94 for the other metal ions and relative standard deviations between 1.8 less than 3.0%. The proposed procedure was applied for the analysis of various samples.     

Gas–liquid chromatography for fenvalerate residue analysis: alterations in the ionic concentration and associated adinosine triphosphatases in fish,Cirrhinus mrigala (hamilton)

In the present study, an attempt has been made to quantify the fenvalerate accumulated in different tissues (gill, muscle and liver) and observe changes involved in the levels of sodium, potassium and calcium ions and Na⁺–K⁺, Mg²⁺ and Ca²⁺ adenosine triphosphatase (ATPase) activities in the freshwater fish, Cirrhinus mrigala on short-term and long-term exposure to the median lethal and sublethal concentration of fenvalerate. Residue analysis using gas–liquid chromatography (GLC) technique revealed that fenvalerate accumulated in highest quantity in gill followed by liver and muscle under median lethal concentration (6?µg?L^?1). Whereas in sublethal concentration (0.6?µg?L^?1), muscle accumulated highest quantity followed by gill and liver, which might be due to the fact that fenvalerate is highly lyphophilic. The ion concentration and ATPase activity were found effected in fish exposed to lethal and sublethal concentrations of fenvalerate. Concentration of Na⁺, K⁺ and Ca²⁺ ions decreased in gill, muscle and liver on being exposed to median lethal concentration to a significant level. Whereas the changes were not highly pronounced at sub lethal level indicating low concentration of fenvalerate and its non-toxic effect at chronic exposure. Na⁺–K⁺, Mg²⁺ and Ca²⁺ ATPases activity were also found decreased in correspondence to the ionic change under median lethal and sub lethal concentrations in target tissues. This might have lead to behavioural changes and create wide-spread disturbance in the normal physiology, ultimately causing the death of the fish. The results suggest that in biomonitoring programmes, ions and associated ATPases can be a good diagnostic tool for fenvalerate toxicity.     

Variable impact of rice (Oryza sativa) on soil metal reduction and availability of pore water Fe2+ and Mn2+ throughout the growth period

Flooding of wetland or agricultural soils can result in substantial alteration of the pore water trace metal profiles and potentially also influence the bioavailability of other trace elements adsorbed to the insoluble oxides. Experimental microcosms were used to quantify the impact of rice (Oryza sativa) plants across an entire growing cycle on the concentrations of Mn²⁺ and Fe²⁺ in two soil types (red sodosol and grey vertosol). Two water management treatments were included: a standard flooded treatment and a saturated treatment (?3?kPa). Soil pore water profiles were established from samples collected at four sampling depths (2.5, 7.5, 15 and 25?cm) on 50 occasions. Fe²⁺ and Mn²⁺ concentrations were higher in flooded soil than in saturated soil and greatest at a depth of 7.5?cm. The presence of rice plants increased Mn²⁺ concentrations in flooded soils, but tended to decrease Mn²⁺ concentrations in saturated soils. The influence of rice plants on Fe²⁺ concentrations was greatest at a depth of 7.5?cm. Changes in soil pore water Fe²⁺ and Mn²⁺ concentrations due to the presence of rice plants were correlated with flowering and reproduction.     

Molecular dynamics of stability and structures in phytochelatin complexes with Zn,Cu, Fe,Mg, and Ca: Implications for metal detoxification

Phytochelatins, or (γ-glutamyl-cysteine) _n -glycine, are specialized peptides produced by plants and algae to mitigate toxic metal exposure, for instance in response to high levels of metals such as Cu, Cd, and Zn. Stability constants and structural characterization of metal–phytochelatin complexes are lacking. This information is required to gain mechanistic insights on the metal selectivity of phytochelatins. Here, we studied structural coordination and thermodynamic stability by performing molecular dynamics simulations of a fully hydrated phytochelatin molecule complexed with Ca²⁺, Mg²⁺, Fe²⁺, Zn²⁺, and Cu²⁺. Our results predict the following decreasing order for the thermodynamic stability of the phytochelatin complexes: Zn²⁺ ≥ Cu²⁺ ≥ Fe²⁺ > Mg²⁺ > Ca²⁺. The favorable binding energies with Zn²⁺ and Cu²⁺ over the other metal cations can be explained by shorter binding distances and greater coordination from carboxylate and keto O atoms. Conformational rearrangement of phytochelatin following metal chelation was captured by monitoring changes in the solvent-accessible volume. Accessibility of solvent molecules to the phytochelatin structure was inversely proportional to the distance between the coordinated ligands and the chelated metal. These new findings demonstrate the influence of the metal–phytochelatin structure on the metal-binding thermodynamics and the phytochelatin conformation, both of which are important to evaluate the intracellular role of phytochelatin in mediating algal response to toxic heavy metal exposure.     

Effects of lead on calmodulin content,proliferation and interleukin-2 in lymphocytes of mice

The mechanism inderlying lead (Pb)-induced toxicity was presumed to involve interaction between Pb²⁺ and calcium (Ca²⁺) associated with calmodulin-dependent systems. The aim of this study was to (1) examine the hypothesis that Pb alters calmodulin content and (2) assess the effects of Pb on proliferation and interleukin-2 (IL-2) levels in lymphocytes. The influence of Pb on calmodulin content in mouse lymphocytes was assessed by western blot, while the proliferation of lymphocytes was studied using MTT test, and IL-2 level by ELISA assay. The results showed that 100?µM PbCl₂ decreased calmodulin content, phytohemagglutinin (PHA)-induced proliferation, and IL-2 levels, but a lower concentration (1?µM PbCl₂) did not appear to be effective. Evidence indicates that IL-2 levels and lymphocyte proliferation might not be calmodulin content dependent. Our data suggested that Pb²⁺-induced toxicity was likely to be complex with multiple factors involved, including calmodulin, IL-2, and proliferation of lymphocytes.     

Environmental human silver exposure

Environmental exposure to silver (Ag) was assessed in occupationally non-exposed adult human population by analyzing Ag in the hair (H?·?Ag) and whole blood (WB?·?Ag). H?·?Ag was analyzed in 311 (123 men, M; 188 women, W); while WB?·?Ag was determined in 235 of these individuals (90 M, 145 W). Women had more H?·?Ag than men (M 0.05 vs. W 0.076), whereas WB?·?Ag concentrations in men and women were not significantly different. A natural distribution of the median derivatives was utilized to generate the dataset to fit the logistic sigmoid curve to assess the current human body burden of environmental Ag population exposure for M and W separately. The H?·?Ag (µg?g^?1) below 0.0105 for M and 0.0145 for W, reflects low level of environmental Ag exposure. The adaptive physiological saturation phase followed where H?·?Ag rose rapidly, first for M and then for W in parallel with biological assay. Both parallel saturation curves converged and plateaued at 0.215 for M and 0.965 for W (µg?g^?1). The current level of human environmental Ag exposure is low, but cases of high Ag exposure occurred sporadically. In conjunction with the medical histories overt clinical neural toxicity may be expected for H?·?Ag at 4?µg?g^?1and higher. There were no significant correlation between the H?·?Ag and WB?·?Ag.     

Effects of daily nickel intake on the bio-accumulation,body weight and length in tilapia (Oreochromis niloticus)

Nickel pollution is a serious environmental problem, and its effects may provoke alterations in the ecosystem and in organism of animals and humans. Dermatitis, eczema, and asthma are some illnesses caused by Ni²⁺ poisoning. In this work, fish fed either Ni²⁺-enriched pellets or commercial pellets were studied. The amount of Ni²⁺ in fish were measurements by adsorptive stripping voltammetry (AdSV) with dimethylglyoxime as a complexing agent. The analysis of Ni²⁺ in fish by AdSV established that its accumulation occurs principally in viscera (670.86 ± 5.82 µg g^?1), in the head (697.12 ± 2.77 µg g^?1) and in the muscle (405.82 ± 3.26 µg g^?1), both after 12 months of experiments. Ni²⁺ adsorbs preferentially in organs such as the stomach, the intestine, and the kidneys and acts in the central nervous system as well. Tilapia growth and mass were significantly affected by Ni²⁺ poisoning. From statistical analysis, observed that the results for lengths, weights and metal concentration were different for each sampling at significance level of p < 0.05. The Ni²⁺ concentration in tilapia was enough to cause the death of tilapias; however, it did not occur because the presence of Zn²⁺ might act as protective agent of heavy metals.     

Tissue-specific stress and hepatic DNA damage in Pelteobagrus fulvidraco caused by low concentrations of cadmium

Physiological stress and DNA damage in Pelteobagrus fulvidraco induced by continuous exposure to cadmium at concentrations of 170 and 1700 µg/L for up to 28 days was evaluated. The activities of acetylcholinesterase and monoamine oxidase in brain tissue, Na⁺-K⁺-ATPase and glutathione in gill tissue, and superoxide dismutase and catalase in liver tissue were measured. In studying random amplified polymorphic DNA to evaluate cadmium-induced hepatic genotoxicity, both the appearance of new bands and the disappearance of existing bands were observed, as well as increased levels of monoamine oxidase and Na⁺-K⁺-ATPase and decreased activities of antioxidant enzymes. The results suggest that continuous exposure to cadmium at the studied levels can induce biochemical and physiological changes and DNA damage in P. fulvidraco.