Oxidative Stress: from Life Sustainability to Life Unsustainability, from Blood Regulation in Brain to Alzheimer Disease
Christian
Amatore1;
1CNRS & PSL, FRENCH ACADEMY OF SCIENCES, Paris, France;
Type of Paper: General Plenary
Id Paper: 300
Topic: 46Abstract:
Oxidative stress is well known by medical doctors and biologists for its negative health issues. Unfortunately, this knowledge is mostly based on long-time hard consequences on patients’ well-being and observation of specific protein markers or metabolites. Conversely, though less publicized than its negative aspects, oxidative stress is also necessary for sustaining aerobic life through a series of critical processes undergoing at the single cell or tissue levels. This explains why, starting with cyanobacteria, the evolution of aerobic cells and organisms has retained oxidative stress mechanisms while enforcing various mechanisms (enzymes, anti-oxidants, etc.) to maintain a delicate balance (homeostasis) between its positive and negative consequences.
One good example of such delicate balance between life sustainability and life unsustainability is brought by the subtle mechanism of hyperemia that regulates blood distribution in the brain. Neurons cannot store the oxygen and nutrients amounts that are required to fulfil their high energy-demanding functions for more than 3-5 minutes (note that our brain consumes ca. 20 to 25% of our energy intake). Hence, when entering into a highly active status, neurons must send information to local blood capillaries to receive more energy than when less active. Besides its physiological function, the overall macroscopic outcome of this process allows observing the brain working through PET scans and functional magnetic resonance imaging (f-IRM). However, its fine details have long remained at the conjectural level. Thanks to the use of ultramicroelectrodes we have been able to investigate and quantitatively characterize this process and its dynamics at the level of single neurons. This confirmed that active neurons emit intense bursts of nitrogen monoxide (NO also known, though improperly, as ‘nitric oxide’) to entice local blood capillaries to deliver oxygen (O2) and nutrients. Hence, active neurons are usually bathed by an extracellular fluid simultaneously enriched in NO and O2.
In the absence of copper-containing Amyloid-β (Cu-Aβ), this process is beneficial by allowing neurons to perform their functions. However, when free Cu-Aβ peptides accumulates locally, this is expected to lead to a fast-catalytic formation of peroxynitrite, a highly toxic species, near active neurons. When diffusing into neuron membranes, peroxynitrite initiates therein fast and intense free-radical propagating chains that eventually results in the apoptotic neuron death. Though overseen by the biological and medical communities, this mechanism may well be at the origin of Alzheimer’s disease. In this respect, rather than being a causative factor, the formation of amyloid plaques may represent the best way for the brain to protect its neurons, by decreasing the availability in highly deleterious free Cu-Aβ peptides.
Keywords:
Oxidation;
References:
[1] C Amatore, S. Arbault, M. Guille and F. Lemaitre: Electrochemical Monitoring of Single Cell Secretion: Vesicular Exocytosis and Oxidative Stress, Chemical Reviews, 10 (2008), 2585–2621.
[2] Y.T. Li, S.H. Zhang, X.Y. Wang, X.W. Zhang, A.I. Oleinick, I. Svir, C. Amatore and W.H. Huang: Real-time Monitoring of Discrete Synaptic Release Events and Excitatory Potentials within Self-reconstructed Neuro-muscular Junctions, Angewandte Chemistry, 54 (2015), 9313–9318
[3] L. Ren, L. Mellander, J. Keighron, A-S. Cans, M. Kurczy, I. Svir, A. Oleinick, C. Amatore and A.G. Ewing: The Evidence for Open and Closed Exocytosis as the Primary Release Mechanism, Quarterly Reviews of Biophysics, 49 (2016), 1-27.
[4] Y. Wang, J.-M. Noël, J. Velmurugan, W. Nogala, M. V. Mirkin, C. Lu, M. Guille Collignon, F. Lemaitre and C. Amatore: Nanoelectrodes for Determination of Reactive Oxygen and Nitrogen Species inside Biological Cells, Proceedings of the National Academy of Sciences of the United States, 109 (2012), 11534-11539.
[5] C. Amatore, S. Arbault, D. Bruce, P. de Oliveira, M. Erard and M. Vuillaume: Characterization of the Electrochemical Oxidation of Peroxynitrite in Relevance with Oxidative Stress Bursts Measured at the Single Cell Level, Chemistry - A European Journal, 7 (2001), 4171-4179.
[6] C. Amatore, S. Arbault, C. Bouton, K. Coffi, J.-C. Drapier, H. Ghandour and Y. Tong: Monitoring the Release of Reactive Oxygen and Nitrogen Species by a Single Macrophage in Real-Time with a Microelectrode, ChemBioChem, 7 (2006), 653-661.
[7] Y. Li, C. Sella, F. Lemaitre, M. Guille Collignon, L.Thouin and C. Amatore: Highly Sensitive Pt-black Electrodes for Detection in Microchannel. Application to the Electrochemical Detection of Hydrogen Peroxyde and Nitrites, Electroanalysis, 25 (2013), 895–902.
[8] J.S. Beckman and W.H. Koppenol: Nitric Oxide, Superoxide, and Peroxynitrite: the Good, the Bad, and Ugly, American Journal of Physiology – Cell Physiology, 271 (1996), C1424–C1437.
[9] R. Giacovazzi, I. Ciofini, L. Rao, C. Adamo and C. Amatore: Copper-Amyloid-β Complex May Catalyze Peroxynitrite Production in Brain: Evidence from Molecular Modeling, Physical Chemistry Chemical Physics (PCCP), 16 (2014), 10169-10174.
[10] W.H. Koppenol: The Centenial of the Fenton Reaction, Free Radical Biology & Medicine, 15 (1993), 645-651
[11] J.F. Torres-Roca, H. Lecoeur, C. Amatore and M.L. Gougeon: The Early Intracellular Production of a Reactive Oxygen Intermediate Mediates Apoptosis in Dexamethasone Treated Thymocytes. Cell Death and Differentiation, 2 (1995), 309-319.
[12] M.F. Beal: Mitochondria take center stage in aging and neurodegeneration, Annals of Neurology, 58 (2005) 495-505.
[13] T. Finkel and N.J. Holbrook: Oxidants, oxidative stress and the biology of ageing, Nature, 408 (2000), 239-247.
[14] B. Lassegue and K.K. Griendling: NADPH Oxidases: Functions and Pathologies in the Vasculature, Arteriosclerosis, Thrombosis, and Vascular Biology, 30 (2010), 653–661.
[15] U. Forstermann and W.C. Sessa: Nitric oxide synthases: regulation and function, European Heart Journal, 33 (2012), 829–837.
[16] C. Amatore, S. Arbault, D. Bruce, P. de Oliveira, M. Erard and M. Vuillaume: Analysis of Individual Biochemical Events Based on Artificial Synapses using Ultramicroelectrodes: Cellular Oxidative Burst, Faraday Discussions, 116 (2000), 319-303.
[17] Real Time Monitoring of Peroxynitrite by Stimulation of Macrophages with Ultramicroelectrodes. C. Amatore, M. Guille-Collignon and F. Lemaître, Peroxynitrite Detection in Biological Media (S. Peteu, S. Szunerits and M. Bayachou, Eds.), 2015, RSC Books, London, chapter 6.
[18] C.S. Roy and C.S. Sherrington: On the Regulation of the Blood-supply of the Brain, The Journal of Physiology, 11 (1890) 85-108, 158-7-158-17.
[19] D.E. Koshland Jr.: The molecule of the year, Science, 258 (1992), 1861 & front cover of issue 5090.
[20] Nobelprize.org, Nobel Media AB 2014: The Nobel Prize in Physiology or Medicine 1998, http://www.nobelprize.org/nobel_prizes/medicine/laureates/1998/
[21] W.H. Koppenol, J.J. Moreno, W.A. Pryor, H. Ischiropoulos and J.S. Beckman: Peroxynitrite, a Cloaked Oxidant Formed by Nitric Oxide and Superoxide, Chemical Research in Toxicology, 5 (1992), 834-842.
[22] R.E. Huie, and S. Padmaja: Free Radical Research Communications. 18 (1993), 195-199.
[23] C. Amatore, S. Arbault, C. Bouton, J.-C. Drapier, H. Ghandour and A. C. W. Koh: Real-time Amperometric Analysis of Reactive Oxygen and Nitrogen Species Released by Single Immunostimulated Macrophages, ChemBioChem, 9 (2008), 1472-1480.
[24] C. Amatore, S. Arbault, Y. Bouret, B. Cauli, M. Guille, A. Rancillac and J. Rossier: Detection of Nitric Oxide Release During Neuronal Activity with Platinized Carbon Fiber Microelectrodes, ChemPhysChem, 7 (2006), 181-187.
[25] A. Rancillac, M. Guille, X.-K. Tong, H. Geoffroy, E. Hamel, C. Amatore, S. Arbault, J. Rossier and B. Cauli: Glutamatergic Control of Microvascular Tone by Distinct GABA Neurons in the Cerebellum, Journal of Neuroscience, 26 (2006), 6997-7006.
[26] C. Amatore, R.S. Kelly, E.W. Kristensen, W.G. Kuhr and R.M. Wightman: Effect of Restricted Diffusion at Ultramicroelectrodes in Brain Tissue. The Pool Model: Theory and Experiment for Chronoamperometry, Journal of Electroanalytical Chemistry, 213 (1986), 31-42.
[27] K. Shibuki: An Electrochemical Probe for Detecting Nitric Oxide Release in Brain Tissue, Neuroscience Research, 9 (1990), 69-76.
[28] K. Shibuki and D. Okada: Endogenous Nitric Oxide Release Required for Long-Term Synaptic Depression in the Cerebellum, Nature, 349 (1991), 326-328.
[29] C. Amatore, S. Arbault and A. Koh: Simultaneous Detection and Quantification of Reactive Oxygen and Nitrogen Species Released by a Single Macrophage by Triple Potential-Step Amperometry, Analytical Chemistry, 82 (2010), 1411-1419.
[30] Long-Term Synaptic Plasticity in Cerebellar Stellate Cells. S.J. Liu, P. Lachamp, Y. Liu, I. Savtchouk and L. Sun, Cerebellum, 7 (2008), 559-62.
[31] A.I. Oleinick, C. Amatore, M. Guille, S. Arbault, O.V. Klymenko and I. Svir: Modelling Release of Nitric Oxide in a Slice of Rat’s Brain: Describing Stimulated Functional Hyperemia with Diffusion-Reaction Equations, Mathematical Medicine and Biology, 23 (2006), 27-44.
[32] R.F. Schmidt and G. Thews, Human Physiology, Second Edition, 1989, Springer-Verlag, New York.
[33] S. Caccia, I. Denisov and M. Perrella: The Kinetics of the Reaction between NO and O2 as Studied by a Novel Approach, Biophysical Chemistry, 76 (1999), 63-72.
[34] R. Vassar, B.D. Bennett, S. Babu-Khan, S. Kahn, E.A. Mendiaz, P. Denis, D.B. Teplow, S. Ross, P. Amarante, R. Loeloff, Y. Luo, S. Fisher, J. Fuller, S. Edenson, J. Lile, M.A. Jarosinski, A.L. Biere, E. Curran, T. Burgess, J.C. Louis, F. Collins, J. Treanor, G. Rogers and M. Citron: β-Secretase Cleavage of Alzheimer's Amyloid Precursor Protein by the Transmembrane Aspartic Protease BACE, Science, 286 (1999), 735-41.
[35] C.L. Masters, G. Multhaup, G. Simms, J. Pottgiesser, R.N. Martins and K. Beyreuther: Neuronal Origin of a Cerebral Amyloid: Neurofibrillary Tangles of Alzheimer’s Disease Contain the Same Protein as the Amyloid of Plaque Cores and Blood Vessels, The EMBO Journal, 4 (1985), 2757–2763.
[36] M.O. Murphy and H. LeVine, III: Alzheimer’s Disease and the β-Amyloid Peptide, Journal of Alzheimer's Disease, 19 (2010), 311-323.
[37] M.A. Lovell, J.D. Robertson, W J. Teesdale, J.L. Campbell and W.R. Markesbery: Copper, Iron and Zinc in Alzheimer's Disease Senile Plaques, Journal of the Neurological Sciences, 158 (1998), 47-52.
[38] M.E. Rice and I. Russo-Menna: Differential Compartmentalization of Brain Ascorbate and Glutathione between Neurons and Glia, Neuroscience, 82 (1998) 1213–1223.
[39] V. Balland, C. Hureau and J.M. Savéant: Electrochemical and Homogeneous Electron Transfers to the Alzheimer Amyloid-β Copper Complex Follow a Preorganization Mechanism, Proceedings of the National Academy of Sciences of the United States of America, 107 (2010), 17113–17118.
[40] J.H.M. Tsai, J.G. Harrison, J.C. Martin, T.P. Hamilton, M. van der Woerd, M.J. Jablonsky and J.S. Beckman: Role of Conformation of Peroxynitrite Anion (ONOO-) with its Stability and Toxicity, Journal of the American Chemical Society, 116 (1994), 4115-4116.
[41] H. Yin, L. Xu and N.A. Porter: Free Radical Lipid Peroxidation: Mechanisms and Analysis, Chemical Reviews, 111 (2011), 5944–5972.
[42] J.R. Rittenhouse, W. Lobunez, D. Swern and J.G. Miller: The Electric Moments of Organic Peroxides. II. Aliphatic Peracids, Journal of the American Chemical Society, 80 (1958), 4850–4852.Full Text:
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Amatore C. (2017).
Oxidative Stress: from Life Sustainability to Life Unsustainability, from Blood Regulation in Brain to Alzheimer Disease.
In Kongoli F, Marquis F, Chikhradze N
(Eds.), Sustainable Industrial Processing Summit
SIPS 2017 Volume 5. Marquis Intl. Symp. / New and Advanced Materials and Technologies
(pp. 26-41).
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