Release Date: 2024-06-12

Brain and Oxidative Stress

Release Date: 2024-06-12

Brain tissue is more sensitive to oxidative damage due to many different properties than other tissues. So, the need for protection of brain tissue, which is more prone to oxidative damage than other tissues and organs, is greater than other tissues. Oxidative stress is brought on by a disturbance in the balance between antioxidants and [...]

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    Work TypeBook Chapter
    Published inBrain Biochemistry and Its Disease
    First Page149
    Last Page165
    DOIhttps://doi.org/10.69860/nobel.9786053359371.9
    Page Count17
    Copyright HolderNobel Tıp Kitabevleri
    Licensehttps://nobelpub.com/publish-with-us/copyright-and-licensing
    Brain tissue is more sensitive to oxidative damage due to many different properties than other tissues. So, the need for protection of brain tissue, which is more prone to oxidative damage than other tissues and organs, is greater than other tissues. Oxidative stress is brought on by a disturbance in the balance between antioxidants and free radicals, which have a scavenging effect on them in biological systems. Increased ROS causes cell damage by causing damage to cell membranes, deterioration in the structure and functions of intracellular proteins, and structural damage to DNA. Oxidative stress is responsible for the pathogenesis of many diseases, especially cancer, diabetes, neurological and cardiovascular diseases, atherosclerosis and inflammatory disorders. Brain tissue is prone to free radical damage because it produces more toxic radicals than other organs. Because the brain has a poorer antioxidant defense system and a higher oxidative metabolism than other organs, it is more vulnerable to ROS-induced damage that can lead to neuronal death. Regional differences in antioxidant system activities and variable metabolic rates in brain tissue may also cause regional accumulation of oxidative damage. In the light of this information, it is aimed to evaluate oxidative stress, the mechanism of oxidative stress formation and the mechanisms of action of oxidative stress on the brain, its effects on intracellular structures and the destruction products formed in oxidative stress with the results of biochemical studies.

    Songul Cetik Yildiz (Author)
    Assistant Professor, Mardin Artuklu University
    https://orcid.org/0000-0002-7855-5343
    3I graduated from Eskişehir Osmangazi University, Department of Biology (2005-2009). I also completed my master’s degree (2009-2011) and doctorate (2011-2014) education at Eskişehir Osmangazi University, Department of Biology. I have been working as an academician at Mardin Artuklu University since 2012. Throughout my academic life, I have carried out multidisciplinary projects with experimental studies. We aimed to benefit from the antitumor antioxidant and probiotic properties of alternative agents against multi-organ toxicity, mostly caused by cancer drugs. We evaluated possible oxidative stress parameters and apoptotic markers by measuring all parameters, especially biochemical and genetic. I am currently working as an assistant professor at the same university.

    • Sen CK. Antioxidant and redox regulation of cellular signaling: Introduction. Med Sci Sports Exerc. 2001;33:368.70.

    • Blakely WF. Hydrogen peroxide induced base damage in DNA. Radiat Res. 1990; 121:338- 43

    • Halliwel B, Gutterıdge JMC. Free Radicals in Biology and Medicine. New York. Oxford Science Publications. 1999

    • Yan LJ. Positive oxidative stress in aging and aging-re­lated disease tolerance. Redox Biol 2014:9;165-169

    • Cárdenas-Rodríguez N, Coballase-Urrutia E, Rivera-Espinosa L et al. Modulation of antioxidant enzymatic activities by certain antiepileptic drugs (valproic acid, oxcarbazepine, and topiramate): Evidence in humans and experimental models. Oxid Med Cell Longev. 2013; 598-493

    • Manwaring JD, Csallany AS. Malondialdehyde-containing proteins and their relationship to vitamin E. Lipids. 1988;23(7):651-655

    • Gutteridge JM. Lipid peroxidation and antioxi­dants as biomarkers of tissue damage. Clin Chem. 1995;41:1819-1828

    • Tamer L, Polat G, Eskandari G. Serbest radikaller. Mersin Ünv.Tıp Fakültesi Dergisi. 2000, 1: 52-58

    • Gupta RK, Patel AK, Shah N, et al. Oxidative stress and antioxidants in disease and cancer: a review. Asian Pac J Cancer Prev. 2014;15:4405-4409

    • Girotti AW. Lipid hydroperoxide generation, turnover, and effector action in biological systems, J Lipid Res. 1998;39:1529-1542

    • Esterbauer H, Cheeseman KH. Determination of alde­hydic lipid peroxidation products: malonaldehyde and 4-hydroxynonenal. Methods Enzymol. 1990;186:407-421

    • Dean RT, Fu S, Stocker R. Biochemistry and pathology of radical mediated protein oxidation. Biochemistry Journal. 1997;324:1-18

    • Rao RS, Moller IM. Pattern of occurrence and occu­pancy of carbonylation sites in proteins. Proteomics. 2011;11:4166-4173

    • Dalle-Donne I, Rossi R, Giustarini D, et al. Protein carbonyl groups as biomarkers of oxidative stress. Clin Chim Acta. 2003;329:23-38

    • Ozcan O, Erdal H, Cakırca G, Yonden Z. Oxidative stress and its impacts on intracellular lipids, proteins and DNA. J Clin Exp Invest. 2015;6(3):331-336

    • Kodydkova J, Vavrova L, Zeman M , Jirak R, Macasek J, Stankova B, et al. Antioxidative enzymes and increased oxidative stress in depressive women. Clin Biochem. 2009;42:1368-74

    • Galecki P, Szemraj J, Bieńkiewicz M, Florkowski A, Gałecka E. Lipid peroxidation and antioxidant protection in patients during acute depressive episodes and in remission after fluoxetine treatment. Pharmacol Rep. 2009;61(3):436-47

    • Haripriya D, Sangeetha P, Kanchana A, Balu M, Panneerselvam C. Modulation of age-associated oxidative DNA damage in rat brain cerebral cortex, striatum and hippocampus by L-karnitine. Exp Gerontol. 2005;40:129-135

    • Stamatovic SM, Shakui P, Keep RF, Moore BB, Kunkel SL, Van Rooijen N, et al. Monocyte chemoattractant protein-1 regulation of blood brain barrier permeability. JCBFM. 2005;25(5):593-606

    • Leutner S, Eckert A, Muller WE. ROS generation, lipid peroxidation and antioxidant enzyme activities in the aging brain. J Neural Transmis. 2001;108:955-967

    • Reiter RJ. Functional aspects of the pineal hormone melatonin in combating cell and tissue damage induced by free radicals. Eur J Endocrinol. 1996;134:412-420

    • Eren I, Nazıroglu M, Demirdas A, Celik O, Uğuz AC, Altunbasak A, et al. Venlafaxine modulates depression-induced oxidative stress in brain and medulla of rat. Neurochem Res. 2007;32:497-505

    • Longo N, Amat di San Filippo C, Pasquali M. Disorders of carnitine transport and the carnitine cycle. Am J Med Genet. 2006;142C(2):77-85

    • Meral I, Mert H, Mert N, Deger Y, Yoruk I, Yetkin A, Keskin S. Effects of 900-MHz electromagnetic field emitted from cellular phone on brain oxidative stress and some vitamin levels of guinea pigs. Brain Res. 2007;1169:120-124

    • Kuzay D, Sirav B, Ozer C. Effects of RF and ELF Radiation on Oxidative Stress of Brain Tissue and Plasma of Diabetic Rats. Kocaeli Üniv Sağlık Bil Derg. 2023;9(1):1-7

    • Ilhan A, Gurel A, Armutcu F, Kamilsi S, Iraz M, Akyol O, Ozen S. Ginkgo biloba prevents mobile phone-induced oxidative stress in rat brain. Clinica Chimica Acta. 2004;340:153-162

    • Gonthier B, Signorini Allibe N, et al. Ethanol can modify the effects of certain free radical generating systems on astrocytes. Alcohol Clin Exp Res. 2004;28:526-534

    • Kim GH, Kim JE, Rhie SJ, Yoon S. The role of oxidative stress in neurodegenerative diseases. Exp Neurobiol. 2015;24:325-340

    • Haorah J, Ramirez SH, Floreani N, Gorantla S, Morsey B, Persidsky Y. Mechanism of alcohol-induced oxidative stress and neuronal injury. Free Radic Biol Med .2008;45:1542-1550

    • Bilgin OA, Mammadov R, Suleyman B. Effect of taxifolin on ethanol-induced oxidative brain damage in rats. Sakarya Med J. 2018;8(3):638-643

    • Srinivasan M, Rukkumani A, Sudheer R, Menon VP. Ferulic acid, a natural protector against carbon tetrachloride induced toxicity. Fundament Clin Pharmacol. 2005;19:491-496

    • Karadeniz A, Yıldırım A, Karakoc A, et al. Protective effect of Panax ginseng on carbon tetrachloride induced liver, heart and kidney injury in rats. Revue Med Vet. 2009;160:237-243

    • Cetin E, Cetin N. Protective effect of ghrelin against the oxidative brain and kidney injuries induced by carbon tetrachloride in rats. Atatürk Unv Vet Bil Derg. 2011;6(3):195-200

    • Ozdek E, IHan S. Molecular mechanisms in brain aging. J Fac Pharm. 2023;47(1):284-294

    • Liguori I, Russo G, Curcio F, Bulli G, Aran L, Della-Morte D, et al. Oxidative stress, aging, and diseases. Clin Interv Aging, 2018;13:757-772

    • onescu-Tucker A, Cotman CW. Emerging roles of oxidative stress in brain aging and alzheimer’s disease. Neurobiol Aging. 2021;107:86-95

    • Moreira PI. Alzheimer’s disease and diabetes: an integrative view of the role of mitochondria, oxidative stress, and insulin. J Alzheimers Dis. 2012;30(2):199-215

    • Wallace DC. A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine. Annu Rev Genet. 2005;39:359-407

    • Zhao B, Pan BS, Shen SW, Sun X, Hou ZZ, Yan R, et al. Diabetes induced central neuritic dystrophy and cognitive deficits are associated with the formation of oligomeric reticulon-3 via oxidative stress. J Biol Chem. 2013;288:15590-15599

    • Braughler JM, Hall ED. Central nervous systems trauma and stroke: I. Biochemical considerations for oxygen radical formation and lipid peroxidation. Free Radical Biol Med. 1989;6(3):289-301

    • Liang HY, Chen ZJ, Xiao H, et al. nNOS-expressing neurons in the vmPFC transform pPVT derived chronic pain signals into anxiety behaviors. Nat Commun. 2020;11(1):2501

    • Qu W, Liu NK, Wu X, et al. Disrupting nNOS–PSD95 interaction improves neurological and cognitive recoveries after traumatic brain injury. Cereb Cortex. 2020;30(7):3859-3871

    • Khanzode SD, Dakhale GN, Khanzode SS, Saoji A, Palasodkar R. Oxidative damage and major depression: the potential antioxidant action of selective serotonin reuptake inhibitors. Redox Rep. 2003;8(6):365-370

    • Uzumluoglu CM. Şizofreni etyopatogenezinde oksidatif stresin rolü. Sağlık Bak. Bakırköy Prof. Dr. Mazhar Osman Ruh Sağlığı ve Sinir Hast. Eğit. Araş. Hastanesi 12. Psikiyatri Birimi, Uzmanlık Tezi. 2008.

    • Alnahdi HS, Sharaf IA. Possible prophylactic effect of omega-3 fatty acids on cadmium-induced neurotoxicity in rats’ brains. Environ Sci Pollut Res Int. 2019;26(30):31254-31262.

    • Al Olayan EM, Aloufi AS, AlAmri OD, El-Habit OH, Abdel Moneim AE. Protocatechuic acid mitigates cadmium-induced neurotoxicity in rats: role of oxidative stress, inflammation and apoptosis. Sci Total Environ. 2020;723:137969

    • Bolat I, Yıldırım S. Investigation of neurotoxicity oxidative stress and oxidative dna damage in cadmium-induced brain injury in rats. Vet Sci Pract. 2023;18(1):19-24

    • Karoui-Kharrat D, Kaddour H, Hamdi Y, Mokni M, Amri M, Mezghani S. Response of antioxidant enzymes to cadmium-induced cytotoxicity in rat cerebellar granule neurons. Open Life Sci. 2017;12:113-119

    • Shagirtha K, Bashir N, Milton Prabu S. Neuroprotective efficacy of hesperetin against cadmium induced oxidative stress in the brain of rats. Toxicol Industr Health. 2017;33(5):454-468

    • Beyatli A, Gulec Peker EG, Gül N, Cevher SC. Morin (2′,3,4′,5,7-Pentahydroxyflavon) antioxidant effect in streptozotocin-ınduced diabetic rat brain and heart tissues. J Anatol Envir Animal Sci. 2022;7(3):257-262

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