4 research outputs found
Upon Exposure to Cu Nanoparticles, Accumulation of Copper in the Isopod <i>Porcellio scaber</i> Is Due to the Dissolved Cu Ions Inside the Digestive Tract
The fate of nanoparticles in organisms is of significant interest.
In the current work, we used a test system with terrestrial isopods
(<i>Porcellio scaber</i>) fed with food spiked with Cu NPs
or soluble Cu salt for 14 days. Two different doses were used for
spiking to yield final concentrations of 2000 and 5000 μg Cu/g
dry food. After the exposure period, part of the exposed group of
animals was transferred to clean food to depurate. Cu content was
analyzed in the digestive glands, gut, and the ‘rest’
of the body. Similar patterns of (i) assimilated and depurated amounts
of Cu, (ii) Cu body distribution, and (iii) effect on isopods feeding
behavior were observed regardless of whether the animals were fed
with Cu NPs or soluble Cu salt spiked food. Thus, Cu ions and not
Cu NPs were assimilated by the digestive gland cells. Solubilization
of the Cu NPs applied to the leaves was also analyzed with chemical
methods and recombinant Cu-sensing bacteria. The comparison of the
in vitro data on solubilization of Cu NPs and in vivo data on Cu accumulation
in the animal tissues showed that about 99% of accumulated copper
ions was dissolved from ingested Cu NPs in the digestive system of
isopods
FTIR microscopy reveals distinct biomolecular profile of crustacean digestive glands upon subtoxic exposure to ZnO nanoparticles
<p>Biomolecular profiling with Fourier-Transform InfraRed Microscopy was performed to distinguish the Zn<sup>2+</sup>-mediated effects on the crustacean (<i>Porcellio scaber</i>) digestive glands from the ones elicited by the ZnO nanoparticles (NPs). The exposure to ZnO NPs or ZnCl<sub>2</sub> (1500 and 4000 µg Zn/g of dry food) activated different types of metabolic pathways: some were found in the case of both substances, some only in the case of ZnCl<sub>2</sub>, and some only upon exposure to ZnO NPs. Both the ZnO NPs and the ZnCl<sub>2</sub> increased the protein (∼1312 cm<sup>−1</sup>; 1720–1485 cm<sup>−1</sup>/3000–2830 cm<sup>−1</sup>) and RNA concentration (∼1115 cm<sup>−1</sup>). At the highest exposure concentration of ZnCl<sub>2</sub>, where the effects occurred also at the organismal level, some additional changes were found that were not detected upon the ZnO NP exposure. These included changed carbohydrate (most likely glycogen) concentrations (∼1043 cm<sup>−1</sup>) and the desaturation of cell membrane lipids (∼3014 cm<sup>−1</sup>). The activation of novel metabolic pathways, as evidenced by changed proteins’ structure (at 1274 cm<sup>−1</sup>), was found only in the case of ZnO NPs. This proves that Zn<sup>2+</sup> are not the only inducers of the response to ZnO NPs. Low bioavailable fraction of Zn<sup>2+</sup> in the digestive glands exposed to ZnO NPs further supports the role of particles in the ZnO NP-generated effects. This study provides the evidence that ZnO NPs induce their own metabolic responses in the subtoxic range.</p
Cellular Internalization of Dissolved Cobalt Ions from Ingested CoFe<sub>2</sub>O<sub>4</sub> Nanoparticles: In Vivo Experimental Evidence
With a model invertebrate animal,
we have assessed the fate of
magnetic nanoparticles in biologically relevant media, i.e., digestive
juices. The toxic potential and the internalization of such nanoparticles
by nontarget cells were also examined. The aim of this study was to
provide experimental evidence on the formation of Co<sup>2+</sup>,
Fe<sup>2+</sup>, and Fe<sup>3+</sup> ions from CoFe<sub>2</sub>O<sub>4</sub> nanoparticles in the digestive juices of a model organism.
Standard toxicological parameters were assessed. Cell membrane stability
was tested with a modified method for measurement of its quality.
Proton-induced X-ray emission and low energy synchrotron radiation
X-ray fluorescence were used to study internalization and distribution
of Co and Fe. Co<sup>2+</sup> ions were found to be more toxic than
nanoparticles. We confirmed that Co<sup>2+</sup> ions accumulate in
the hepatopancreas, but Fe<sup><i>n</i>+</sup> ions or CoFe<sub>2</sub>O<sub>4</sub> nanoparticles are not retained in vivo. A model
biological system with a terrestrial isopod is suited to studies of
the potential dissolution of ions and other products from metal-containing
nanoparticles in biologically complex media
Cellular Internalization of Dissolved Cobalt Ions from Ingested CoFe<sub>2</sub>O<sub>4</sub> Nanoparticles: In Vivo Experimental Evidence
With a model invertebrate animal,
we have assessed the fate of
magnetic nanoparticles in biologically relevant media, i.e., digestive
juices. The toxic potential and the internalization of such nanoparticles
by nontarget cells were also examined. The aim of this study was to
provide experimental evidence on the formation of Co<sup>2+</sup>,
Fe<sup>2+</sup>, and Fe<sup>3+</sup> ions from CoFe<sub>2</sub>O<sub>4</sub> nanoparticles in the digestive juices of a model organism.
Standard toxicological parameters were assessed. Cell membrane stability
was tested with a modified method for measurement of its quality.
Proton-induced X-ray emission and low energy synchrotron radiation
X-ray fluorescence were used to study internalization and distribution
of Co and Fe. Co<sup>2+</sup> ions were found to be more toxic than
nanoparticles. We confirmed that Co<sup>2+</sup> ions accumulate in
the hepatopancreas, but Fe<sup><i>n</i>+</sup> ions or CoFe<sub>2</sub>O<sub>4</sub> nanoparticles are not retained in vivo. A model
biological system with a terrestrial isopod is suited to studies of
the potential dissolution of ions and other products from metal-containing
nanoparticles in biologically complex media