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1.
Biol Res ; 47: 13, 2014 Apr 01.
Article in English | MEDLINE | ID: mdl-25027256

ABSTRACT

BACKGROUND: Acute toxicity testing were carried out the freshwater swamp shrimp, Macrobrachium nipponense, as the model animal for the semiconductor applied metals (gallium, antimony, indium, cadmium, and copper) to evaluate if the species is an suitable experimental animal of pollution in aquatic ecosystem. RESULTS: The static renewal test method of acute lethal concentrations determination was used, and water temperature was maintained at 24.0 ± 0.5°C. Data of individual metal obtained from acute toxicity tests were determined using probit analysis method. The median lethal concentration (96-h LC50) of gallium, antimony, indium, cadmium, and copper for M. nipponense were estimated as 2.7742, 1.9626, 6.8938, 0.0539, and 0.0313 mg/L, respectively. CONCLUSIONS: Comparing the toxicity tolerance of M. nipponense with other species which exposed to these metals, it is obviously that the M. nipponense is more sensitive than that of various other aquatic animals.


Subject(s)
Antimony/toxicity , Cadmium/toxicity , Copper/toxicity , Gallium/toxicity , Indium/toxicity , Palaemonidae/drug effects , Animals , Ecosystem , Fresh Water , Lethal Dose 50 , Toxicity Tests, Acute , Water Pollution , Water Quality
2.
Biol. Res ; 47: 1-4, 2014. graf, tab
Article in English | LILACS | ID: lil-710936

ABSTRACT

BACKGROUND: Acute toxicity testing were carried out the freshwater swamp shrimp, Macrobrachium nipponense, as the model animal for the semiconductor applied metals (gallium, antimony, indium, cadmium, and copper) to evaluate if the species is an suitable experimental animal of pollution in aquatic ecosystem. RESULTS: The static renewal test method of acute lethal concentrations determination was used, and water temperature was maintained at 24.0 ± 0.5°C. Data of individual metal obtained from acute toxicity tests were determined using probit analysis method. The median lethal concentration (96-h LC50) of gallium, antimony, indium, cadmium, and copper for M. nipponense were estimated as 2.7742, 1.9626, 6.8938, 0.0539, and 0.0313 mg/L, respectively. CONCLUSIONS: Comparing the toxicity tolerance of M. nipponense with other species which exposed to these metals, it is obviously that the M. nipponense is more sensitive than that of various other aquatic animals.


Subject(s)
Animals , Antimony/toxicity , Cadmium/toxicity , Copper/toxicity , Gallium/toxicity , Indium/toxicity , Palaemonidae/drug effects , Ecosystem , Fresh Water , Toxicity Tests, Acute , Water Pollution , Water Quality
3.
Toxicology ; 118(2-3): 129-36, 1997 Mar 28.
Article in English | MEDLINE | ID: mdl-9129167

ABSTRACT

Indium arsenide and gallium arsenide are important new materials in the semiconductor industry due to their superior electronic properties in comparison with the older silicon-based materials. Animal experiments have shown that exposure to these compounds induces marked alterations in gene expression and immune response. Toxicity to the immune system has frequently been related to T and B cell apoptosis. In the present study we show that the semiconductor elements indium (In) and arsenic (As) are able to induce apoptosis in rat thymocytes in vitro. The results show that exposure to InCl3 (1, 10, or 100 microM) or Na AsO2 (0.01, 0.1, or 1 microM) induced DNA laddering after 6 h of incubation without compromising cell viability. These results were corroborated by flow cytometry analysis of propidium iodide-loaded cells, showing a typical high hypodiploid DNA peak in apoptotic thymocytes. Higher doses of In (1 mM) or As (10-100 microM) induced cell death by necrosis. These data indicate that In and As can induce apoptosis and necrosis in T lymphocytes in a dose-dependent manner, which may be of relevance for their immunotoxicity.


Subject(s)
Apoptosis/drug effects , Arsenic Poisoning , Indium/toxicity , Thymus Gland/drug effects , Animals , Cell Death/drug effects , Cell Survival/drug effects , Cells, Cultured , DNA Fragmentation/drug effects , Dose-Response Relationship, Drug , Electrophoresis, Agar Gel , Flow Cytometry , Male , Necrosis , Propidium/chemistry , Rats , Rats, Sprague-Dawley , Semiconductors , T-Lymphocytes/cytology , T-Lymphocytes/drug effects , Thymus Gland/cytology
4.
Arch Biochem Biophys ; 338(1): 121-7, 1997 Feb 01.
Article in English | MEDLINE | ID: mdl-9015396

ABSTRACT

The capacity of Al3+-related cations (Sc3+, Ga3+, In3+, Be2+, Y3+, and La3+) to promote membrane rigidification and lateral phase separation was evaluated in liposomes containing zwitterionic (phosphatidylcholine, PC) and negatively charged (phosphatidylserine, PS) phospholipids. These effects were correlated with the capacity of the ions to stimulate Fe2+-supported lipid peroxidation. A13+, Sc3+, Ga3+, In3+, Be2+, Y3+, and La3+ (50-200 microM) increased the order parameter of the fluorescent probe 1,3-diphenylhexatriene incorporated in PC:PS membranes. In addition, the electron paramagnetic resonance spectra of spin-labeled fatty acids indicated a reduction in lipid motion induced by Sc3+, Y3+, and La3+. The effect was found to extend down to carbon 16 on the acyl chain. The ions (10-200 microM) were also able to induce lateral phase separation, as evaluated from the increase in fluorescence quenching of the probe 2-(6-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)amino)dodecanoyl-1-hexadec anoyl-sn-glycero-3-phosphocholine. The ability of the ions to alter membrane lipid packing and induce lateral phase separation correlated in a positive manner (r2 = 0.91 and 0.90, respectively) with their capacity to stimulate the production of Fe2+-initiated 2-thiobarbituric-reactive species, a measure of lipid peroxidation. These results show that Al3+-related metal ions cause membrane rigidification and phase separation, which could affect membrane-related processes. The results support the hypothesis that ions without redox capacity can stimulate Fe2+-initiated lipid peroxidation by increasing lipid packing and by promoting the formation of rigid clusters. Both processes will bring phospholipid acyl chains closer together, thus favoring the propagation step of lipid peroxidation.


Subject(s)
Lipid Peroxidation/drug effects , Membrane Lipids/chemistry , Metals/toxicity , Aluminum/toxicity , Animals , Beryllium/toxicity , Cations/chemistry , Cations/toxicity , Electron Spin Resonance Spectroscopy , Gallium/toxicity , In Vitro Techniques , Indium/toxicity , Liposomes , Membrane Fluidity/drug effects , Metals/chemistry , Molecular Structure , Scandium/toxicity , Thermodynamics , Yttrium/toxicity
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