scholarly journals Prokaryotic iron superoxide dismutase replaces cytosolic copper, zinc superoxide dismutase in protecting yeast cells against oxidative stress

IUBMB Life ◽  
1998 ◽  
Vol 44 (1) ◽  
pp. 41-49
Author(s):  
Dolores Agius ◽  
William Bannister ◽  
Rena Balzan
2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Fábio Cangeri Di Naso ◽  
Alexandre Simões Dias ◽  
Marilene Porawski ◽  
Norma Anair Possa Marroni

Aim. To investigate the effects of exogenous antioxidant copper zinc superoxide dismutase (Cu/Zn SOD) on oxidative stress in the experimental model of diabetes mellitus (DM).Methods. Twenty eight male Wistar rats divided in four groups were used: control (CO), controls treated with SOD (CO + SOD), diabetics (DM), and diabetics treated with SOD (DM + SOD). SOD (orgotein, 13 mg/Kg body weight was administered. DM was induced by a single streptozotocin injection (i.p., 70 mg/kg), and 60 days later, we evaluated liver oxidative stress.Results. Liver lipoperoxidation was increased in the DM group and significantly decreased in the DM + SOD group. Nitrite and nitrate measures were reduced in the DM and increased in the DM + SOD group, while iNOS expression in the DM group was 32% greater than in the CO and 53% greater in the DM + SOD group than in the DM group (P<.01). P65 expression was 37% higher in the DM (P<.05), and there was no significant difference between the DM and DM + SOD groups.Conclusion. SOD treatment reduced liver oxidative stress in diabetic animals, even though it did not change NFκB. SOD also increased NO, probably by the increased dismutation of the superoxide radical. The iNOS expression increase, which became even more evident after SOD administration.


Biochemistry ◽  
1991 ◽  
Vol 30 (38) ◽  
pp. 9305-9313 ◽  
Author(s):  
Paul Amstad ◽  
A. Peskin ◽  
Girish Shah ◽  
Marc Edouard Mirault ◽  
Remy Moret ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (94) ◽  
pp. 91141-91149 ◽  
Author(s):  
Xingren Pan ◽  
Pengfei Qin ◽  
Rutao Liu ◽  
Jianfeng Li ◽  
Fucui Zhang

The combination of molecular and cellular analysis suggested that the structural and functional alterations of Cu/Zn-SOD were closely associated with increased risk of oxidative stress initiated by both CPFX and ENFX.


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