Literature DB >> 11976206

Nitrones as neuroprotectants and antiaging drugs.

Robert A Floyd1, Kenneth Hensley, Michael J Forster, Judith A Kelleher-Anderson, Paul L Wood.   

Abstract

Specific nitrones have been used for more than 30 years in analytical chemistry and biochemistry to trap and stabilize free radicals for the purpose of their identification and characterization. PBN (alpha-phenyl-tert-butyl nitrone), one of the more widely used nitrones for this purpose, has been shown to have potent pharmacologic activities in models of a number of aging-related diseases, most notably the neurodegenerative diseases of stroke and Alzheimer's disease. Studies in cell and animal models strongly suggest that PBN has potent antiaging activity. A novel nitrone, CPI-1429, has been shown to extend the life span of mice when administration was started in older animals. It has also shown efficacy in the prevention of memory dysfunction associated with normal aging in a mouse model. Mechanistic studies have shown that the neuroprotective activity of nitrones is not due to mass-action free radical-trapping activity, but due to cessation of enhanced signal transduction processes associated with neuroinflammatory processes known to be enhanced in several neurodegenerative conditions. Enhanced neuroinflammatory processes produce higher levels of neurotoxins, which cause death or dysfunction of neurons. Therefore, quelling of these processes is considered to have a beneficial effect allowing proper neuronal functioning. The possible antiaging activity of nitrones may reside in their ability to quell enhanced production of reactive oxygen species associated with age-related conditions. On the basis of novel ideas about the action of secretory products formed by senescent cells on bystander cells, it is postulated that nitrones will mitigate these processes and that this may be the mechanism of their antiaging activity.

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Year:  2002        PMID: 11976206     DOI: 10.1111/j.1749-6632.2002.tb02103.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  19 in total

1.  Interleukin-1beta-induced brain injury and neurobehavioral dysfunctions in juvenile rats can be attenuated by alpha-phenyl-n-tert-butyl-nitrone.

Authors:  L W Fan; L T Tien; B Zheng; Y Pang; P G Rhodes; Z Cai
Journal:  Neuroscience       Date:  2010-03-24       Impact factor: 3.590

Review 2.  Nitrones as therapeutics.

Authors:  Robert A Floyd; Richard D Kopke; Chul-Hee Choi; Steven B Foster; Sabrina Doblas; Rheal A Towner
Journal:  Free Radic Biol Med       Date:  2008-08-29       Impact factor: 7.376

3.  The nitrone spin trap 5,5-dimethyl-1-pyrroline N-oxide affects stress response and fate of lipopolysaccharide-primed RAW 264.7 macrophage cells.

Authors:  Zili Zhai; Sandra E Gomez-Mejiba; Dario C Ramirez
Journal:  Inflammation       Date:  2013-04       Impact factor: 4.092

4.  Accelerated decline in cognition in a mouse model of increased oxidative stress.

Authors:  Sreemathi Logan; Gordon H Royce; Daniel Owen; Julie Farley; Michelle Ranjo-Bishop; William E Sonntag; Sathyaseelan S Deepa
Journal:  Geroscience       Date:  2019-10-22       Impact factor: 7.713

5.  Phenyl-alpha-tert-butyl nitrone reverses mitochondrial decay in acute Chagas' disease.

Authors:  Jian-Jun Wen; Vandanajay Bhatia; Vsevolod L Popov; Nisha Jain Garg
Journal:  Am J Pathol       Date:  2006-12       Impact factor: 4.307

6.  Proteome expression and carbonylation changes during Trypanosoma cruzi infection and Chagas disease in rats.

Authors:  Jian-Jun Wen; Nisha Jain Garg
Journal:  Mol Cell Proteomics       Date:  2011-12-22       Impact factor: 5.911

7.  Mitochondrial complex III defects contribute to inefficient respiration and ATP synthesis in the myocardium of Trypanosoma cruzi-infected mice.

Authors:  Jian-Jun Wen; Nisha Jain Garg
Journal:  Antioxid Redox Signal       Date:  2010-01       Impact factor: 8.401

8.  Matrix metalloproteinase inhibition reduces oxidative stress associated with cerebral amyloid angiopathy in vivo in transgenic mice.

Authors:  Monica Garcia-Alloza; Claudia Prada; Carli Lattarulo; Sara Fine; Laura A Borrelli; Rebecca Betensky; Steven M Greenberg; Matthew P Frosch; Brian J Bacskai
Journal:  J Neurochem       Date:  2009-04-08       Impact factor: 5.372

9.  alpha-Phenyl-n-tert-butyl-nitrone attenuates lipopolysaccharide-induced brain injury and improves neurological reflexes and early sensorimotor behavioral performance in juvenile rats.

Authors:  Lir-Wan Fan; Ruei-Feng Chen; Helen J Mitchell; Rick C S Lin; Kimberly L Simpson; Philip G Rhodes; Zhengwei Cai
Journal:  J Neurosci Res       Date:  2008-12       Impact factor: 4.164

10.  [Not Available].

Authors:  Shivali Gupta; Jian-Jun Wen; Nisha Jain Garg
Journal:  Interdiscip Perspect Infect Dis       Date:  2009-06-14
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