Selective induction of manganous superoxide dismutase in human monocytes

1985 ◽  
Vol 249 (5) ◽  
pp. C393-C397 ◽  
Author(s):  
K. Asayama ◽  
R. L. Janco ◽  
I. M. Burr

Radioimmunoassays for both human copper-zinc and manganous superoxide dismutases (Cu-Zn SOD and Mn SOD, respectively) have been developed, validated, and utilized to measure the concentrations of these enzymes in cultured monocytes. Monocyte Mn SOD increased 4.7-fold over basal during 3 days of culture, an increase that was markedly enhanced by stimulation with bacterial lipopolysaccharide (LPS). Cu-Zn SOD showed a transient decrease over the culture period but was unaffected by LPS. Stimulation with muramyl dipeptide had minimal effect on Mn SOD and no effect on Cu-Zn SOD during culture, even at a concentration capable of activating the monocytes, as defined by zymosan-induced superoxide production.

1986 ◽  
Vol 234 (1) ◽  
pp. 225-228 ◽  
Author(s):  
J M C Gutteridge ◽  
J V Bannister

When OH. radicals are formed in a superoxide-driven Fenton reaction, in which O2.- is generated enzymically, deoxyribose degradation is effectively inhibited by CuZn- and Mn-superoxide dismutases. The products of this reaction are H2O2 and a Fe3+-EDTA chelate. The mixing of H2O2 and a Fe3+-EDTA chelate also generates OH. radicals able to degrade deoxyribose with the release of thiobarbituric acid-reactive material. This reaction too is inhibited by CuZn- and Mn-superoxide dismutases, suggesting that most of the OH. is formed by a non-enzymic O2.- -dependent reduction of the Fe3+-EDTA chelate. Since the reaction between the Fe3+-EDTA chelate and H2O2 leads to a superoxide dismutase-inhibitable formation of OH. radicals, it could suggest a much wider protective role for the superoxide dismutase enzymes in biological systems. Urate produced during the reaction of xanthine oxidase and hypoxanthine limits deoxyribose degradation as well as the effectiveness of the superoxide dismutase enzymes to inhibit damage to deoxyribose by H2O2 and the Fe3+-EDTA chelate. Some of this damage may result from an O2.--independent pathway to OH. formation in which urate reduces the ferric complex.


Hypertension ◽  
1995 ◽  
Vol 26 (6) ◽  
pp. 863-868 ◽  
Author(s):  
Carlos E. García ◽  
Crescence M. Kilcoyne ◽  
Carmine Cardillo ◽  
Richard O. Cannon ◽  
Arshed A. Quyyumi ◽  
...  

1989 ◽  
Vol 105 (1-2) ◽  
pp. 41-46 ◽  
Author(s):  
Irène Ceballos ◽  
France Javoy-Agid ◽  
Etienne C. Hirsch ◽  
Sylvie Dumas ◽  
Pierre P. Kamoun ◽  
...  

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