Literature DB >> 15691590

An epigrammatic (abridged) recounting of the myriad tales of astonishing deeds and dire consequences pertaining to nitric oxide and reactive oxygen species in mitochondria with an ancillary missive concerning the origins of apoptosis.

Diane E Heck1, Valerian E Kagan, Anna A Shvedova, Jeffrey D Laskin.   

Abstract

Mitochondria play a central role in the life and death of cells. These organelles serve as the major energy-producing power-house, whereby the generation of ATP is associated with the utilization of molecular oxygen. A significant fraction (2-3%) of molecular oxygen consumed by mitochondria may be reduced in a one-electron fashion to yield a series of reactive oxygen species (ROS) such as superoxide anion radical, hydrogen peroxide, and hydroxyl radical. ROS are capable of damaging components of the electron transport apparatus and can, in turn, disrupt mitochondrial functioning, limiting cellular ATP levels and ultimately resulting in cell death. ROS-induced disruption of electron transport can perpetuate production of deleterious ROS and propagate mitochondrial damage. Consequently, mitochondria are highly enriched with water-soluble and lipid-soluble antioxidants (glutathione, ascorbate, Vitamin E, and coenzyme Q) and antioxidant enzymes, such as superoxide dismutase, glutathione peroxidase, catalase, thioredoxins, and peroxiredoxin. Another important antioxidant acting as a very effective scavenger of reactive lipid (peroxyl, alkoxyl) radicals is nitric oxide (NO) generated by mitochondrial nitric oxide synthase. However, NO can also be very disruptive to mitochondria function, a process facilitated by its high reactivity with superoxide. This interaction results in the formation of peroxynitrite, an oxidant capable of causing oxidative/nitrosative stress, further aggravating mitochondrial dysfunction, causing ATP depletion and damage to cells. Thus, in the most general sense, the effects of NO in mitochondria may be either protective or deleterious depending on specific conditions of local redox environment (redox potential, ratio of oxidized to reduced glutathione, transition metals, and the presence of other oxygen- and nitrogen-centered radicals).

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Year:  2005        PMID: 15691590     DOI: 10.1016/j.tox.2004.11.027

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  8 in total

1.  Cardiolipin switch in mitochondria: shutting off the reduction of cytochrome c and turning on the peroxidase activity.

Authors:  Liana V Basova; Igor V Kurnikov; Lei Wang; Vladimir B Ritov; Natalia A Belikova; Irina I Vlasova; Andy A Pacheco; Daniel E Winnica; Jim Peterson; Hülya Bayir; David H Waldeck; Valerian E Kagan
Journal:  Biochemistry       Date:  2007-02-24       Impact factor: 3.162

Review 2.  Nitric oxide and peroxynitrite in health and disease.

Authors:  Pál Pacher; Joseph S Beckman; Lucas Liaudet
Journal:  Physiol Rev       Date:  2007-01       Impact factor: 37.312

Review 3.  Mechanisms of oxidant generation by catalase.

Authors:  Diane E Heck; Michael Shakarjian; Hong Duck Kim; Jeffrey D Laskin; Anna M Vetrano
Journal:  Ann N Y Acad Sci       Date:  2010-08       Impact factor: 5.691

4.  miR-638 Inhibits immature Sertoli cell growth by indirectly inactivating PI3K/AKT pathway via SPAG1 gene.

Authors:  Pandi Hu; Kaifeng Guan; Yue Feng; Changping Ma; Huibin Song; Yang Li; Xuanyan Xia; Jialian Li; Fenge Li
Journal:  Cell Cycle       Date:  2017-11-09       Impact factor: 4.534

Review 5.  Modulation of cGMP in heart failure: a new therapeutic paradigm.

Authors:  Guido Boerrigter; Harald Lapp; John C Burnett
Journal:  Handb Exp Pharmacol       Date:  2009

6.  Antitumor effect of manumycin on colorectal cancer cells by increasing the reactive oxygen species production and blocking PI3K-AKT pathway.

Authors:  Jingyu Zhang; Hua Jiang; Li Xie; Jing Hu; Li Li; Mi Yang; Lei Cheng; Baorui Liu; Xiaoping Qian
Journal:  Onco Targets Ther       Date:  2016-05-24       Impact factor: 4.147

Review 7.  NADPH and Mitochondrial Quality Control as Targets for a Circadian-Based Fasting and Exercise Therapy for the Treatment of Parkinson's Disease.

Authors:  William M Curtis; William A Seeds; Mark P Mattson; Patrick C Bradshaw
Journal:  Cells       Date:  2022-08-04       Impact factor: 7.666

Review 8.  Induction of oxidative stress as a mechanism of action of chemopreventive agents against cancer.

Authors:  B Rigas; Y Sun
Journal:  Br J Cancer       Date:  2008-02-05       Impact factor: 7.640

  8 in total

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