Method of modulating radical formation by mutant cuznsod enzymes

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

514184, 514499, A01N 4304

Patent

active

058344578

ABSTRACT:
Familial amyotrophic lateral sclerosis (FALS)-associated mutant CuZnSODs, A4V and G93A, have been discovered to catalyze the generation of hydroxyl radical from hydrogen peroxide at higher rates than that of wild type CuZnSOD. The copper chelator diethyldithiocarbamate (DDC) has been found to inhibit both radical generation and SOD activity of mutant CuZnSODs A4V and G93A at DDC concentrations significantly lower than those required to inhibit wild type CuZnSOD enzyme. In a neural cell culture model of FALS, DDC reverses the effect of four FALS-associated mutants, but does not alter the survival of cells expressing only wild type CuZnSOD. Thus, radical formation may be modulated and ALS treated in subjects with a mutant CuZnSOD enzyme by the administration of copper chelating agents. Treatment can also be affected by the administration of radical scavenging agents, or the administration of expression inhibitors specific for the mutant genes.

REFERENCES:
Zhong et al., "bcl-2 inhibits death of central neural cells induced by multiple agents," Proc. Natl. Acad. Sci. USA, vol. 90, pp. 4533-4537, May 1993.
Gurney et al., "Motor Neuron Degeneration in Mice That Express a Human Cu,Zn Superoxide Dismutase Mutation," Science, vol. 264, pp. 1772-1775, 17 Jun. 1994.
Borchelt et al., "Superoxide dismutase 1 with mutations linked to familial amyotrohic lateral sclerosis possesses significant activity," Proc. Natl. Acad. Sci. USA, vol. 91, pp. 8292-8296, Aug. 1994.
Rabizadeh, S., "Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptoitic gene: Studies in yeast and neural cells," Proc. Natl. Acad. Sci. USA, vol. 92, pp. 3024-3028, Mar. 1995.
Nishida et al. "Characterization of three yeast copper-zinc superoxide dismutase mutatns analogous to those coded for in familial amyotrophic lateral sclerosis" Pro. Natl. Acad. Sci. USA. 91:9906-9910 (1994).
Pardo et al. "Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons" Proc. Natl. Acad. Sci. USA 92: 954-958 (1995).
Misra. "Reaction of Copper-Zinc Superoxide Dismutase with Diethyldithiocarbamate" The Journal of Biological Chemistry 254 No. 22:11623-11628 (1979).
Collard et al. "Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis" Nature 375:61-64 (1995).
Yim et al. "Enzyme Function of Copper, Zinc Superoxide Dismutase as a Free Radical Generator" The Journal of Biological Chemistry 268 No. 6:4099-4105 (1993).
Conradi, et al., "Long-tme penicallamine-treatment in amyotrophic lateral sclerosis with parallel determination of lead in blood, plasma and urine", Acta Neurol. Scandinav., vol. 65, pp. 203-211, 1983.
Deng et al., "Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis", Human Molecular Genetics, vol. 4, No. 6, pp. 1113-1116, 1995.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Method of modulating radical formation by mutant cuznsod enzymes does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Method of modulating radical formation by mutant cuznsod enzymes, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Method of modulating radical formation by mutant cuznsod enzymes will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-1516893

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.