DocumentCode
3342799
Title
Notice of Retraction
Toxic Effects of Nano-Fe2O3 on Liver and Kidney Cells of Rats
Author
Jingyun Zhao ; Huihui You ; Yaran Zhang ; Junlin Yuan
Author_Institution
Hubei Key Lab. of Genetic Regul. & Integrative Biol., Huazhong Normal Univ., Wuhan, China
fYear
2011
fDate
10-12 May 2011
Firstpage
1
Lastpage
4
Abstract
Notice of Retraction
After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.
We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.
The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.
In order to assess the toxic effects of nano-Fe2O3 on organisms, in the present study, the liver and kidney cells of rats were exposed to different concentrations (0.05, 0.50, 5.00, 50.00 μg/mL) of nano-Fe2O3 at 37°C for one hour. Then reactive oxygen species (ROS) levels, glutathione (GSH) contents and DNA protein crosslinks (DPC) coefficients were detected. The results showed that nano-Fe2O3 exposure significantly decreased GSH contents, increased the levels of ROS, as well as DPC coefficients. Compared with control group, under 0.05 μg/mL and 0.50 μg/mL nano-Fe2O3 exposure, the increase levels of ROS and decrease contents of GSH were not significant difference (p>;0.05). With the exposure concentration increased, 5.00 μg/mL and 50.00 μg/mL nano-Fe2O3 concentration groups, the increase levels of ROS and decrease contents of GSH showed significant difference (p<;0.05 or p<;0.01), and demonstrated a certain degree of dose dependent relationship. The increase of DPC coefficients showed significant difference (p<;0.05 or p<;0.01) at 0.50 μg/mL and 5.00 μg/mL concentration group while no significant difference (p>;0.05) was found at 0.05 μg/mL concentration group. This study demonstrates that nano-Fe2O3 exposure can produce oxidative stress in the liver and kidney cells of rats.
After careful and considered review of the content of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE´s Publication Principles.
We hereby retract the content of this paper. Reasonable effort should be made to remove all past references to this paper.
The presenting author of this paper has the option to appeal this decision by contacting TPII@ieee.org.
In order to assess the toxic effects of nano-Fe2O3 on organisms, in the present study, the liver and kidney cells of rats were exposed to different concentrations (0.05, 0.50, 5.00, 50.00 μg/mL) of nano-Fe2O3 at 37°C for one hour. Then reactive oxygen species (ROS) levels, glutathione (GSH) contents and DNA protein crosslinks (DPC) coefficients were detected. The results showed that nano-Fe2O3 exposure significantly decreased GSH contents, increased the levels of ROS, as well as DPC coefficients. Compared with control group, under 0.05 μg/mL and 0.50 μg/mL nano-Fe2O3 exposure, the increase levels of ROS and decrease contents of GSH were not significant difference (p>;0.05). With the exposure concentration increased, 5.00 μg/mL and 50.00 μg/mL nano-Fe2O3 concentration groups, the increase levels of ROS and decrease contents of GSH showed significant difference (p<;0.05 or p<;0.01), and demonstrated a certain degree of dose dependent relationship. The increase of DPC coefficients showed significant difference (p<;0.05 or p<;0.01) at 0.50 μg/mL and 5.00 μg/mL concentration group while no significant difference (p>;0.05) was found at 0.05 μg/mL concentration group. This study demonstrates that nano-Fe2O3 exposure can produce oxidative stress in the liver and kidney cells of rats.
Keywords
DNA; biochemistry; biomedical materials; cellular biophysics; iron compounds; kidney; liver; molecular biophysics; nanomedicine; nanostructured materials; proteins; toxicology; DNA-protein crosslinks; Fe2O3; dose dependent relationship; glutathione contents; kidney cells; liver cells; oxidative stress; reactive oxygen species levels; temperature 37 degC; time 1 hour; toxic effects; DNA; Fluorescence; Kidney; Liver; Nanobioscience; Nanomaterials; Proteins;
fLanguage
English
Publisher
ieee
Conference_Titel
Bioinformatics and Biomedical Engineering, (iCBBE) 2011 5th International Conference on
Conference_Location
Wuhan
ISSN
2151-7614
Print_ISBN
978-1-4244-5088-6
Type
conf
DOI
10.1109/icbbe.2011.5781371
Filename
5781371
Link To Document