Evaluation of Methanol Induced Free Radicals in Mice Liver

2017 ◽  
Vol 70 (5) ◽  
pp. 499 ◽  
Author(s):  
Lifang Zhou ◽  
Hongli Zhao ◽  
Tieying Pan ◽  
Adrian Trinchi ◽  
Minbo Lan ◽  
...  

Methanol induced oxidative stress (OS) models in mice were successfully established and evaluated by the electron paramagnetic resonance (EPR) spin trapping technique. The capacity for removal of reactive oxygen species (ROS) free radicals by rhubarb and vitamin C (Vc) as candidate materials was also investigated. EPR was employed to determine the free radicals generated from a spin trapping agent, α-phenyl-N-tert-butylnitrone (PBN), that reacted with the ROS. The activities of superoxide dismutase (SOD) and glutathione peroxidase (GSH-PX), and the level of malondialdehyde (MDA) were also evaluated by enzyme assays. The results indicated that methanol clearly promoted the generation of ROS free radicals in the liver of mice. The activity of SOD and GSH-PX was reduced significantly, although the level of MDA was increased as a result of the harmful effect of methanol. In addition, rhubarb and Vc exhibited a protective effect on the mice liver under acute OS.

2011 ◽  
Vol 64 (7) ◽  
pp. 1466-1472 ◽  
Author(s):  
Miaomiao Ye ◽  
Tuqiao Zhang ◽  
Zhiwei Zhu ◽  
Yan Zhang ◽  
Yiping Zhang

The photocatalytic degradation of 4-chloronitrobenzene (4-CNB) was carried out using Degussa P25 TiO2 as photocatalyst in three different gas atmospheres: nitrogen, oxygen, and ozone. The total organic carbon (TOC) and inorganic anions including chloride, nitrite, and nitrate anions were measured to monitor the mineralization processes, while the degradation of 4-CNB and the formation of intermediates were followed by liquid chromatography–mass spectrometry (LC/MS). Results showed that the photocatalytic efficiency followed the order of TiO2/UV/N2 < TiO2/UV/O2 < TiO2/UV/O3, which was further proved by evaluating the reaction activities using electron paramagnetic resonance (EPR) spin trapping technique. Chlorine atom, nitro group and hydrogen atom of the benzene ring could be displaced by hydroxyl radical (•OH) leading to the formation of chloride, nitrite (III) anions and a variety of phenols, then the nitrite (III) anions were further oxidized to nitrate (V) anions. 4-Nitrophenol and 5-chloro-2-nitrophenol were identified and quantified in both of the TiO2/UV/N2 and TiO2/UV/O2 processes while no aromatic intermediates were monitored in the process of TiO2/UV/O3.


2001 ◽  
Vol 55 (10) ◽  
pp. 1375-1381 ◽  
Author(s):  
Richard L. Blakley ◽  
Dwight D. Henry ◽  
Walter T. Morgan ◽  
William L. Clapp ◽  
Carr J. Smith ◽  
...  

Electron paramagnetic resonance (EPR) quantification of free radicals from different samples facilitates comparison of free radical concentrations. Stable free radicals, such as 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO), in a suitable solvent (e.g., benzene) can be used as a quantification standard. Free radicals found in samples can be shorter lived than radicals in prepared standards and require stabilizing spin-trapping agents such as N-tert-butyl-α-phenylnitrone (PBN) in an appropriate solvent (e.g., benzene). Analysis in our laboratory showed that free radicals from spin-trapped samples quantified against a standard of TEMPO in benzene displayed large differences among identical samples measured on either a Micro-Now 8300, Micro-Now 8400, or Bruker EMX EPR instrument. The Bruker instrument reported that the typical TEMPO in benzene standard had a Q-factor of ∼4400 while the Q-factor of our PBN-containing samples was ∼2500. (The Q-factor is inversely proportional to the amount of dissipated microwave energy in an EPR cavity.) By placing the TEMPO standard in a PBN/benzene solvent matrix we were able to match the Q-factor of our standards and samples, resulting in each of the three EPR instruments giving the same quantified free radical yields for the samples. This result points out the importance of matching the Q-factor between samples and standards for any quantitative EPR measurement.


1996 ◽  
Vol 51 (1) ◽  
pp. 139-143 ◽  
Author(s):  
Yong-Kang Zhang

As compared to normal PBN, about fifty percent increase of electron paramagnetic resonance (EPR) spin trapping sensitivity has been gained by using a new 100% 15N-enriched spin trap, C-phenyl N-tert-butyl[15N]nitrone (PBN-15N). PBN-15N has been prepared by a convenient four-step route using ammonium-15N chloride as the starting material. This synthetic method produces 2-methyl-2-[15N]nitropropane which is useful for the synthesis of many other PBN-15N type spin traps for the purpose of increasing spin trapping sensitivity. EPR spin trapping with PBN-15N in benzene and in phosphate buffer has been investigated. The 15N hyperfine splitting constant (15N-hfsc) is larger than 14N-hfsc by 40%. The larger 15N-hfsc gives more opportunity to identify different radical addends within the same system.


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