Literature DB >> 11028919

Signaling by reactive oxygen species in the nervous system.

P Maher1, D Schubert.   

Abstract

Free radicals and reactive oxygen species (ROS) are involved in a variety of different cellular processes ranging from apoptosis and necrosis to cell proliferation and carcinogenesis. Cells contain multiple sites for ROS production and a few mechanisms for their degradation. Which of these sites is activated by a given stimulus may play a role in dictating the subsequent downstream effects of the ROS generated on cellular function. Even when the ultimate outcome is similar, such as when ROS production leads to cell death, the specific cellular changes can be quite different depending on the initial stimulus and the type of cell involved. These data, along with the evidence that ROS can modify a number of intracellular signaling pathways including protein phosphatases, protein kinases and transcription factors, suggest that the majority of the effects of ROS on cells are through their actions on signaling pathways rather than via nonspecific damage of intracellular macromolecules.

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Year:  2000        PMID: 11028919     DOI: 10.1007/pl00000766

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  46 in total

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Journal:  Antioxid Redox Signal       Date:  2012-08-03       Impact factor: 8.401

2.  Defects in mitochondrial axonal transport and membrane potential without increased reactive oxygen species production in a Drosophila model of Friedreich ataxia.

Authors:  Yujiro Shidara; Peter J Hollenbeck
Journal:  J Neurosci       Date:  2010-08-25       Impact factor: 6.167

3.  Downregulation in components of the mitochondrial electron transport chain in the postmortem frontal cortex of subjects with bipolar disorder.

Authors:  Xiujun Sun; Jun-Feng Wang; Michael Tseng; L Trevor Young
Journal:  J Psychiatry Neurosci       Date:  2006-05       Impact factor: 6.186

4.  Nitric oxide signaling participates in norepinephrine-induced activity of neuronal intracellular survival pathways.

Authors:  Michael J Chen; Amelia A Russo-Neustadt
Journal:  Life Sci       Date:  2007-09-15       Impact factor: 5.037

5.  Reactive oxygen species regulate F-actin dynamics in neuronal growth cones and neurite outgrowth.

Authors:  Vidhya Munnamalai; Daniel M Suter
Journal:  J Neurochem       Date:  2008-11-17       Impact factor: 5.372

6.  Functional CRH variation increases stress-induced alcohol consumption in primates.

Authors:  Christina S Barr; Rachel L Dvoskin; Manisha Gupte; Wolfgang Sommer; Hui Sun; Melanie L Schwandt; Stephen G Lindell; John W Kasckow; Stephen J Suomi; David Goldman; J Dee Higley; Markus Heilig
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-17       Impact factor: 11.205

7.  CRH haplotype as a factor influencing cerebrospinal fluid levels of corticotropin-releasing hormone, hypothalamic-pituitary-adrenal axis activity, temperament, and alcohol consumption in rhesus macaques.

Authors:  Christina S Barr; Rachel L Dvoskin; Qiaoping Yuan; Robert H Lipsky; Manisha Gupte; Xian Hu; Zhifeng Zhou; Melanie L Schwandt; Stephen G Lindell; Megan McKee; Michelle L Becker; Mitchel A Kling; Phillip W Gold; Dee Higley; Markus Heilig; Stephen J Suomi; David Goldman
Journal:  Arch Gen Psychiatry       Date:  2008-08

8.  Impact of central and peripheral TRPV1 and ROS levels on proinflammatory mediators and nociceptive behavior.

Authors:  Karin N Westlund; Mikhail Y Kochukov; Ying Lu; Terry A McNearney
Journal:  Mol Pain       Date:  2010-08-06       Impact factor: 3.395

9.  Distinct contributions of reactive oxygen species in amygdala to bee venom-induced spontaneous pain-related behaviors.

Authors:  Yun-Fei Lu; Volker Neugebauer; Jun Chen; Zhen Li
Journal:  Neurosci Lett       Date:  2016-03-10       Impact factor: 3.046

10.  Reactive oxygen species mediate TNFR1 increase after TRPV1 activation in mouse DRG neurons.

Authors:  Fei Ma; Liping Zhang; Karin N Westlund
Journal:  Mol Pain       Date:  2009-06-17       Impact factor: 3.395

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