Oxidative Stress in Iron-toxicity of Liver

Book chapter


Mehta, K (2018). Oxidative Stress in Iron-toxicity of Liver. in: Patel, V (ed.) The Liver: Oxidative stress and dietary antioxidants Elsevier. pp. 43-54
AuthorsMehta, K
EditorsPatel, V
Abstract

This chapter focuses on the pathophysiology of iron-induced oxidative stress in liver. • Iron plays a pivotal role in erythropoiesis, cell growth, and differentiation. • However, it is a redox active metal that can generate ROS via the Fenton chemistry and exert oxidative stress. Therefore, iron overload is toxic. • Excess-iron induced oxidative stress is the primary driving force for liver deterioration in the iron overload disease hereditary hemochromatosis. • In addition, elevated iron levels accelerate the pathological progression of other conditions, such as ALD, NAFLD, and NASH. • Regardless of the underlying etiology, excess iron crseates an inflammatory environment in the liver and activates the HSCs to cause increased deposition of ECM components, distortion of liver architecture, and paves the pathway for fibrosis and cirrhosis in untreated patients. •The future awaits more effective drugs with dual action; iron-chelating as well as antioxidant properties to decelerate iron-induced hepatic injury

Page range43-54
Year2018
Book titleThe Liver: Oxidative stress and dietary antioxidants
PublisherElsevier
Edition1
ISBN978-0128039519
Publication dates
Print04 Jan 2018
Publication process dates
Deposited12 Nov 2018
Accepted01 Jun 2017
Digital Object Identifier (DOI)https://doi.org/https://doi.org/10.1016/C2015-0-00760-2
Publisher's version
License
Permalink -

https://openresearch.lsbu.ac.uk/item/86w41

Restricted files

Publisher's version

  • 142
    total views
  • 0
    total downloads
  • 1
    views this month
  • 0
    downloads this month

Export as

Related outputs

Iron and liver fibrosis: mechanistic and clinical aspects
Mehta, K, Farnaud, S and Sharp, P A (2019). Iron and liver fibrosis: mechanistic and clinical aspects. World Journal of Gastroenterology. 25 (5), pp. 521-538. https://doi.org/10.3748/wjg.v25.i5.521
A Novel Human Neuronal Cell Model to Study Iron Accumulation in Parkinson’s Disease
Mehta, K, Ahmed, B and Farnaud, S (2019). A Novel Human Neuronal Cell Model to Study Iron Accumulation in Parkinson’s Disease. Journal of Alzheimers Disease & Parkinsonism. 9 (1), p. 461. https://doi.org/10.4172/2161-0460.1000461
Measurement of 4-hydroxynonenal (4-HNE) protein adducts by ELISA
Mehta, K and Patel, V (2019). Measurement of 4-hydroxynonenal (4-HNE) protein adducts by ELISA. in: Hancock, John and Conway, Myra (ed.) Redox-Mediated Signal Transduction: Methods and Protocols, Methods in Molecular Biology, vol. 1990 Springer.
Betaine, in context.
Mehta, K and Patel, V (2015). Betaine, in context. in: Preedy, V (ed.) Betaine: Chemistry, Analysis, Function and Effects The Royal Society of Chemistry.
Molecular and cellular insights into iron regulation
Mehta, K (2012). Molecular and cellular insights into iron regulation. PhD Thesis University of Westminster School of Life Sciences
Molecular Effects of Alcohol on Iron Metabolism
Mehta, K, Farnaud, S and Patel, VB (2016). Molecular Effects of Alcohol on Iron Metabolism. in: Molecular Aspects of Alcohol and Nutrition: A Volume in the Molecular Nutrition Series Academic Press. pp. 355-368
Characterisation of hepcidin response to holotransferrin treatment in CHO TRVb-1 cells
Mehta, K, Greenwell, P, Renshaw, D, Busbridge, M, Garcia, M, Farnaud, S and Patel, VB (2015). Characterisation of hepcidin response to holotransferrin treatment in CHO TRVb-1 cells. Blood Cells, Molecules, and Diseases. 55 (2), pp. 110-118. https://doi.org/10.1016/j.bcmd.2015.05.002
Iron Enhances Hepatic Fibrogenesis and Activates Transforming Growth Factor-β Signaling in Murine Hepatic Stellate Cells.
Mehta, K, Coombes, JD, Briones-Orta, M, Manka, PP, Williams, R., Patel, VB and Syn, W-K (2018). Iron Enhances Hepatic Fibrogenesis and Activates Transforming Growth Factor-β Signaling in Murine Hepatic Stellate Cells. American Journal of the Medical Sciences. 355 (2), pp. 183-190. https://doi.org/10.1016/j.amjms.2017.08.012
Case Studies: Effects of Beef, Whey and Carbohydrate Supplementation in Female Master Triathletes
Mehta, K, Seijo, M, Larumbe-Zabala, E, Ashrafi, N, Christides, T, Karsten, B, Nielsen, BV and Naclerio, F (2018). Case Studies: Effects of Beef, Whey and Carbohydrate Supplementation in Female Master Triathletes. Journal of Human Sport and Exercise. 14 (1), pp. 170-184. https://doi.org/10.14198/jhse.2019.141.14
HFE mRNA expression is responsive to intracellular and extracellular iron loading: short communication
Mehta, K, Farnaud, S and Patel, VB (2017). HFE mRNA expression is responsive to intracellular and extracellular iron loading: short communication. Molecular Biology Reports. 44 (5), pp. 399-403. https://doi.org/10.1007/s11033-017-4123-2
Erratum to: HFE mRNA expression is responsive to intracellular and extracellular iron loading: short communication
Mehta, K, Farnaud, S and Patel, VB (2017). Erratum to: HFE mRNA expression is responsive to intracellular and extracellular iron loading: short communication. Molecular Biology Reports. 44 (5), pp. 405-405. https://doi.org/10.1007/s11033-017-4127-y
Mucosa-associated invariant T cells link intestinal immunity with antibacterial immune defects in alcoholic liver disease
Riva, A, Patel, V, Kurioka, A, Jeffery, HC, Wright, G, Tarff, S, Shawcross, D, Ryan, JM, Evans, A, Azarian, S, Bajaj, JS, Fagan, A, Patel, V, Mehta, K, Lopez, C, Simonova, M, Katzarov, K, Hadzhiolova, T, Pavlova, S, Wendon, JA, Oo, YH, Klenerman, P, Williams, R. and Chokshi, S (2017). Mucosa-associated invariant T cells link intestinal immunity with antibacterial immune defects in alcoholic liver disease. Gut. Williams, R. (5), pp. 918-930. https://doi.org/10.1136/gutjnl-2017-314458
Characterization of hepcidin response to holotransferrin in novel recombinant TfR1 HepG2 cells
Mehta, K, Busbridge, M, Renshaw, D, Evans, RW, Farnaud, S and Patel, VB (2016). Characterization of hepcidin response to holotransferrin in novel recombinant TfR1 HepG2 cells. Blood Cells, Molecules, and Diseases. 61, pp. 37-45. https://doi.org/10.1016/j.bcmd.2016.06.008
Thyroid Hormone Receptor (TR): a regulator in Liver Fibrogenesis
Manka, P, Coombes, JD, Bechmann, L, Swiderska-Syn, M, Reid, D, Claridge, LC, Younis, R, Mehta, K, Briones, MA, Kitamura, N, Mi, Z, Kuo, PC, Williams, R., Eksteen, B, Diehl, AM, Gerken, G, Canbay, A, Flamant, F, Gauthier, K and Syn, WK (2016). Thyroid Hormone Receptor (TR): a regulator in Liver Fibrogenesis. Fibrogenesis. New York 01 - 02 Jan 2016 https://doi.org/10.1055/s-0036-1597375