Histopathological study of the effects of administering heme iron and ferrous sulfate with vitamin C in rat liver and brain
DOI:
https://doi.org/10.24265/horizmed.2019.v19n2.03Keywords:
Iron, Heme, Ascorbic acid, ToxicityAbstract
Objective: To determine the effect exerted by the administration of heme iron and ferrous sulfate with vitamin C in rat liver and brain. Materials and methods: The study used Holtzman albino rats housed in a bioterium with a temperature of 22 ± 2 °C, humidity between 50 and 70 %, and 12 hours of light and 12 hours of darkness. They received elemental iron 4.0 mg/kg b.w. as heme iron or ferrous sulfate + vitamin C 10 mg for seven days, at which time they were sacrificed, and blood, liver and brain were extracted. Histological sections were made and treated with hematoxylin-eosin for microscopic observation, and serum antioxidant capacity was measured. Results: The brains of the rats treated with heme iron and ferrous sulfate + vitamin C did not undergo significant changes, while the histological sections of the livers of the rats treated with heme iron showed a parenchyma without polar distribution, some nuclei lacking cytoplasm and numerous Küpffer cells at the sinusoidal level. In contrast, the rats treated with ferrous sulfate + vitamin C had a significantly deteriorated hepatic parenchyma, some areas with loose nuclei without cytoplasm and others with disappeared cytoplasmic membranes. In addition, in some areas, the liver parenchyma was homogenized. Conclusions: The brains of the rats treated with heme iron and those with ferrous sulfate + vitamin C did not practically undergo any change. In contrast, the liver of the rats treated with ferrous sulfate + vitamin C had greater liver damage than those treated with heme iron.
Downloads
References
Instituto Nacional de Estadística e Informática. Encuesta Demográfica y de Salud Familiar. ENDES-2016. Perú: Lima; 2017.
Lane DJR, Richardson DR. The active role of vitamin C in mammalian iron metabolism: much more than just enhanced iron absorption! Free Radic Biol Med. 2014 Oct;75:69-83.
Lane DJR, Robinson SR, Czerwinska H, Bishop GM, Lawen A. Two routes of iron accumulation in astrocytes: Ascorbate- dependent ferrous iron uptake via the divalent metal transporter (DMT1) plus an independent route for ferric iron. Biochem J. 2010 Nov;432(1):123–32.
Hallberg L, Brune M, Rossander L. The role of vitamin C in iron absorption. Int J Vitam Nutr Res Suppl. 1989 Feb;30:103-8.
Troesch B, Egli I, Zeder C, Hurrell RF, Zimmermann MB. Fortification iron as ferrous sulfate plus ascorbic acid is more rapidly absorbed than as sodium iron EDTA but neither increases serum nontransferrin-bound iron in women. J Nutr. 2011 May;141(5):822-7.
Wolff NA, Garrick MD, Zhao L, Garrick LM, Ghio AJ, Thévenod F. A role for divalent metal transporter (DMT1) in mitochondrial uptake of iron and manganese. Sci Rep. 2018 Jan 9;8:211.
Nam TS, Shim JY, Kim BJ, Rah Y, Hyun PK, Kim SY, et al. Clinical Study on the iron absorption from heme-iron polypeptide and nonheme-iron. Nut Sci. 2006 Nov;9(4):295-300.
Seligman PA, Moore GM, Schleicher RB. Clinical studies of HIP: An oral-iron product. Nut Res. 2000;20(9)-86.
West AR, Oates PS. Mechanisms heme iron absorption: current questions and controversies. World J Gastroenterol. 2008 Jul 14;14(26):4101-10.
Carr A, Frei B. Does vitamin C act as a pro-oxidant under physiological conditions?. FASEB J. 1999 Jun;13(9):1007-24.
Nimse SB, Pal D. Free radicals, natural antioxidants, and their reaction mechanisms. RSC Adv. 2015 Jan5(35)27986–28006.
Hernández-García D, Wood CD, Castro-Obregón S, Covarrubias L. Reactive oxygen species: A radical role in development?. Free Radic Biol Med. 2010 Jul 15;49(2):130-43.
Kalyanaraman B. Teaching the basics of redox biology to medical and graduate students: Oxidants, antioxidants and diseases mechanisms. Redox Biology. 2013 Feb;1(1):244-57.
Fehér J, Csomós G, Vereckei A. Free Radicals Reactions in Medicine. 1987. Germany: Springer-Verlag Berlin. pp 199.
Halliwell B, Gutteridge JMC. Free Radical in Biology and Medicine. 2007. 4th ed. Oxford: Oxford University Press.
Benzie IF, Strain JJ. The ferric reducing ability of plasma (FRAP) as a measure of "antioxidant power": The FRAP assay. Anal Biochem. 1996 Jul 15;239(1):70-6.
Galaris D, Evangelou A. The role of oxidative stress in mechanisms of metal-induced carcinogenesis. Crit Rev Oncol Hematol. 2002 Apr;42(1):93-103.
Gholampour F, Keikha S. Berberine protects the liver and kidney against functional disorders and histological damages induced by ferrous sulfate. Iran J Basic Med Sci. 2018 May;21(5):476-82.
Abdel-Reheim MA, Shehata Messiha BA, Abo-Saif AA. Hepatoprotective effect of Diosmin on iron-induced liver damage. Int J Pharm. 2017 Jul;13(6):529-40.
He H, Qiao Y, Zhang Z, Wu Z, Liu D, Liao Z, et al. Dual action of vitamin C in iron supplement therapeutics for iron deficiency anemia: prevention of liver damage induced by iron overload. Food Funct. 2018 Oct 17; 9(10): 5390-5401.
Whittaker P, Hines FA, Robl MG, Dunkel VG. Histopathological evaluation of liver, pancreas, spleen, and heart from iron- overloaded Sprague-Dawley rats. Toxicol Pathol. 1996 Sep- Oct;24(5):558-63.
Khoshfetrat MR, Mortazavi S, Neyestani T, Mahmoodi MR, Zerafati-Shoae N, Mohammadi-Nasrabadi F. Iron and vitamin C Co-Supplementation increased serum vitamin C without adverse effect on zinc level in iron deficient female youth. Int J Prev Med. 2014 Aug;5(8):1037-44.
Yatmark P, Morales NP, Chaisri U, Wichaiyo S, Hemstapat W, Srichairatanakool S, et al. Iron distribution and histopathological characterization of the liver and heart of β-thalassemic mice with parenteral iron overload: Effects of deferoxamine and deferiprone. Exp Toxicol Pathol. 2014 Sep;66(7):333-43.
Srigiridhar K, Nair KM. Supplementation with alpha- tocopherol or a combination of alpha-tocopherol and ascorbic acid protects the gastrointestinal tract of iron-deficient rats against iron-induced oxidative damage during iron repletion. Br J Nutr. 2000 Aug;84(2):165-73.
Courtois F, Delvin E, Ledoux M, Seidman E, Lavoie JC, Levy E. The antioxidant BHT normalizes some oxidative effects of iron + ascorbate on lipid metabolism in Caco-2 cells. J Nutr. 2002 Jun;132(6):1289-92.
Cardoso SM, Pereira C, Oliveira R. Mitochondrial function is differentially affected upon oxidative stress. Free Radic Biol Med.1999 Jan;26(1-2):3-13.
Published
How to Cite
Issue
Section
License
Copyright (c) 2019 Horizonte Médico (Lima)

This work is licensed under a Creative Commons Attribution 4.0 International License.
Horizonte Médico (Lima) (Horiz. Med.) journal’s research outputs are published free of charge and are freely available to download under the open access model, aimed at disseminating works and experiences developed in biomedical and public health areas, both nationally and internationally, and promoting research in the different fields of human medicine. All manuscripts accepted and published in the journal are distributed free of charge under the terms of a Creative Commons license – Attribution 4.0 International (CC BY 4.0).