Volume 18, Issue 2 (Mar-Apr 2024)                   mljgoums 2024, 18(2): 32-35 | Back to browse issues page


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Hematyar Tabatabaie F, Moshtaghie A A, Rastegari A A, Nayeri H. Cerium interfering effect on iron intestinal absorption in rats using the Everted Gut Sac (EGS) method. mljgoums 2024; 18 (2) :32-35
URL: http://mlj.goums.ac.ir/article-1-1403-en.html
1- Department of Biochemistry, Falavarjan Branch.Islamic Azad University, Isfahan, Iran
2- Department of Biochemistry, Falavarjan Branch.Islamic Azad University, Isfahan, Iran , moshtaghie@Pharm.mui.ac.ir
Abstract:   (301 Views)
Background: Certain trace elements, like cerium, have the potential to disrupt iron metabolism. This study explored the impact of cerium on intestinal iron absorption, focusing on the initial stage of iron metabolism. We employed the rat everted gut sac (EGS) segments to assess the interference caused by cerium. The primary objectives of this study were to examine the absorption of cerium in the intestines and to compare iron absorption in the presence and absence of cerium.
Methods: For the EGS experiment, segments of the rat's duodenum, ileum, or jejunum were promptly excised, cut into 5-6 cm segments, and rinsed with a physiological solution. These freshly prepared rat EGS segments were then incubated in Earle's medium containing iron (III) and/or cerium (III). We examined the impact of ascorbic acid, glucose, and different time intervals on the intestinal absorption of cerium and iron. Specifically, we investigated how glucose (5 mM) and ascorbic acid (2.8 mM) affected the absorption of cerium and iron at various concentrations (ranging from 0 to 200 mg/L). Additionally, we assessed the interfering effect of cerium on iron absorption.
Results: The results indicated that the maximum intestinal absorption of Fe (III) and Ce (III) occurred at a concentration of 200 mg/L. Furthermore, it was observed that their uptake increased following the reduction by ascorbic acid. The absorption of these elements also rose in the presence of glucose, suggesting energy-dependent transport. Additionally, a consistent cerium concentration was found to decrease iron absorption by 24.3% (P ≤ 0.05).
Conclusion: Based on the results, cerium likely reduces iron uptake by competing with iron. Cerium can also disrupt iron metabolism and lead to iron-related metabolic disorders. However, further studies at the molecular and intracellular levels are needed to gain a better understanding of this mechanism.

 
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Research Article: Research Article | Subject: Biochemistry
Received: 2021/07/5 | Accepted: 2024/01/7 | Published: 2024/04/28 | ePublished: 2024/04/28

References
1. Brown CJ, Chenery SR, Smith B, Mason C, Tomkins A, Roberts GJ, et al. Environmental influences on the trace element content of teeth-implications for disease and nutritional status. Arch Oral Biol. 2004;49(9):705-17. [View at Publisher] [DOI] [PMID] [Google Scholar]
2. Beaser SB, Segel A, Vandam L. The anticoagulant effects in rabbits and man of the intravenous injection of salts of the rare earths. J Clin Invest. 1942;21(4):447-54. [View at Publisher] [DOI] [PMID] [Google Scholar]
3. Blinova I, Muna M, Heinlaan M, Lukjanova A, Kahru A. Potential Hazard of Lanthanides and Lanthanide-Based Nanoparticles to Aquatic Ecosystems: Data Gaps, Challenges and Future Research Needs Derived from Bibliometric Analysis. Nanomaterials (Basel). 2020;10(2):328. [View at Publisher] [DOI] [PMID] [Google Scholar]
4. Doguer C, Ha J-H, Collins JF. Intersection of Iron and Copper Metabolism in the Mammalian Intestine and Liver. Compr Physiol. 2018;8(4):1433-61. [View at Publisher] [DOI] [PMID] [Google Scholar]
5. Aslam MF, Frazer DM, Faria N, Bruggraber SFA, Wilkins SJ, Mirciov C, et al. Ferroportin mediates the intestinal absorption of iron from a nanoparticulate ferritin core mimetic in mice. FASEB J. 2014;28(8):3671-8. [View at Publisher] [DOI] [PMID] [Google Scholar]
6. Moshtaghie AA, Taher M. Aluminium Interference with Iron Absorption by Everted Gut Sac. Med J Islamic World Acad Sci. 1993; 6(4): 277-281. Med J Islamic World Acad Sci. 1993;6(4):277-81. [View at Publisher] [Google Scholar]
7. Moshtaghie AA, Badii AA, Hassanzadeh T. Investigation of Manganese and Iron Absorption by Rat Everted Gut Sac. Pakistan J Biol Sci. 2006;9(7):1346-9. [View at Publisher] [DOI] [Google Scholar]
8. Ahmadvand H, Ani M, Moshtaghie S. The Efffect of Titanium on Stearic Acid Transport in Rat Everted Gut Sac. J Adv Med Biomed Res. 2010;18(72):34-41. [View at Publisher] [Google Scholar]
9. Piskin E, Cianciosi D, Gulec S, Tomas M, Capanoglu E. Iron absorption: factors, limitations, and improvement methods. ACS Omega. 2022;7(24):20441-56. [View at Publisher] [DOI] [PMID] [Google Scholar]
10. Cook JD, Reddy MB. Effect of ascorbic acid intake on nonheme-iron absorption from a complete diet. Am J Clin Nutr. 2001;73(1):93-8. [View at Publisher] [DOI] [PMID] [Google Scholar]
11. Trischitta F, Denaro MG, Faggio C. Ion transport in the intestine of Gobius niger in both isotonic and hypotonic conditions. J Exp Zool A Comp Exp Biol. 2004;301(1):49-62. [View at Publisher] [DOI] [PMID] [Google Scholar]
12. Arnich N, Cunat L, Lanhers M-C, Burnel D. Comparative in situ study of the intestinal absorption of aluminum, manganese, nickel, and lead in rats. Biol Trace Elem Res. 2004;99(1-3):157-71. [View at Publisher] [DOI] [PMID] [Google Scholar]
13. Vafaei-Pour Z, Shokrzadeh M, Jahani M, Shaki F. Embryo-protective effects of cerium oxide nanoparticles against gestational diabetes in mice. Iran J Pharm Res. 2018;17(3):964-75. [View at Publisher] [PMID] [Google Scholar]
14. Najafi R, Hosseini A, Ghaznavi H, Mehrzadi S, Sharifi AM. Neuroprotective effect of cerium oxide nanoparticles in a rat model of experimental diabetic neuropathy. Brain Res Bull. 2017;131:117-22. [View at Publisher] [DOI] [PMID] [Google Scholar]
15. Salvetti A, Gambino G, Rossi L, De Pasquale D, Pucci C, Linsalata S, et al. Stem cell and tissue regeneration analysis in low-dose irradiated planarians treated with cerium oxide nanoparticles. Mater Sci Eng C Mater Biol Appl. 2020;115:111113. [View at Publisher] [DOI] [PMID] [Google Scholar]
16. Zhao H, Cheng Z, Cheng J, Hu R, Che Y, Cui Y, et al. The toxicological effects in brain of mice following exposure to cerium chloride. Biol Trace Elem Res. 2011;144(1-3):872-84. [View at Publisher] [DOI] [PMID] [Google Scholar]
17. Alam MA, Al‐Jenoobi FI, Al‐mohizea AM. Everted gut sac model as a tool in pharmaceutical research: limitations and applications. J Pharm Pharmacol. 2012;64(3):326-36. [View at Publisher] [DOI] [PMID] [Google Scholar]
18. Singh VK, Rai PK. Kidney stone analysis techniques and the role of major and trace elements on their pathogenesis: a review. Biophys Rev. 2014;6(3-4):291-310. [View at Publisher] [DOI] [PMID] [Google Scholar]
19. Moshtaghie A, Taghikhani M, Sandughchin M. Cadmium interaction with iron metabolism, in vitro and in vivo studies. Journal of Islamic Academy of Sciences. 1994;7(3):145-50. [View at Publisher] [Google Scholar]
20. Singh AK, Singh SK, Rai SB. Role of Li+ ion in the luminescence enhancement of lanthanide ions: favorable modifications in host matrices. RSC advances. 2014;4(51):27039-61. [View at Publisher] [DOI] [Google Scholar]
21. Schubert D, Dargusch R, Raitano J, Chan S-W. Cerium and yttrium oxide nanoparticles are neuroprotective. Biochem Biophysi Res Commun. 2006;342(1):86-91. [View at Publisher] [DOI] [PMID] [Google Scholar]
22. Maynar M, Bartolomé I, Alves J, Barrientos G, Grijota FJ, Robles MC, et al. Influence of a 6-month physical training program on serum and urinary concentrations of trace metals in middle distance elite runners. J Int Soc Sports Nutr. 2019;16(1):53. [View at Publisher] [DOI] [PMID] [Google Scholar]
23. Tsukamoto Y, Iwanami S, Marumo F. Disturbances of trace element concentrations in plasma of patients with chronic renal failure. Nephron. 1980;26(4):174-9. [View at Publisher] [DOI] [PMID] [Google Scholar]
24. Bjørklund G, Aaseth J, Skalny AV, Suliburska J, Skalnaya MG, Nikonorov AA, et al. Interactions of iron with manganese, zinc, chromium, and selenium as related to prophylaxis and treatment of iron deficiency. J Trace Elem Med Biol. 2017;41:41-53. [View at Publisher] [DOI] [PMID] [Google Scholar]
25. González-Domínguez Á, Visiedo-García FM, Domínguez-Riscart J, González-Domínguez R, Mateos RM, Lechuga-Sancho AM. Iron Metabolism in Obesity and Metabolic Syndrome. Int J Mol Sci. 2020;21(15):5529. [View at Publisher] [DOI] [PMID] [Google Scholar]
26. Park K, Park J, Lee H, Choi J, Yu WJ, Lee J. Toxicity and tissue distribution of cerium oxide nanoparticles in rats by two different routes: single intravenous injection and single oral administration. Arch Pharm Res. 2018;41(11):1108-16. [View at Publisher] [DOI] [PMID] [Google Scholar]
27. Elmagirbi A, Sulistyarti H, Atikah A. Study of Ascorbic Acid as Iron(III) Reducing Agent for Spectrophotometric Iron Speciation. J Pure Appl Chem Res. 2012;1(1):11-7. [View at Publisher] [DOI] [Google Scholar]
28. Ems T, St Lucia K, Huecker MR. Biochemistry, Iron Absorption. Treasure Island (FL): StatPearls; 2020. [View at Publisher] [PMID] [Google Scholar]
29. Lesjak M, Hoque R, Balesaria S, Skinner V, Debnam ES, Srai SKS, et al. Quercetin inhibits intestinal iron absorption and ferroportin transporter expression in vivo and in vitro. PLoS One. 2014;9(7):e102900. [View at Publisher] [DOI] [PMID] [Google Scholar]
30. Leung F, Hodsman A, Muirhead N, Henderson A. Ultrafiltration studies in vitro of serum aluminum in dialysis patients after deferoxamine chelation therapy. Clin Chem. 1985;31(1):20-3. [View at Publisher] [DOI] [PMID] [Google Scholar]
31. Dahle JT, Arai Y. Environmental geochemistry of cerium: applications and toxicology of cerium oxide nanoparticles. Int J Environ Res Public Health. 2015;12(2):1253-78. [View at Publisher] [DOI] [PMID] [Google Scholar]
32. Estevez AY, Pritchard S, Harper K, Aston JW, Lynch A, Lucky JJ, et al. Neuroprotective mechanisms of cerium oxide nanoparticles in a mouse hippocampal brain slice model of ischemia. Free Radic Biol Med. 2011;51(6):1155-63. [View at Publisher] [DOI] [PMID] [Google Scholar]
33. Lanone S, Rogerieux F, Geys J, Dupont A, Maillot-Marechal E, Boczkowski J, et al. Comparative toxicity of 24 manufactured nanoparticles in human alveolar epithelial and macrophage cell lines. Part Fibre Toxicol. 2009;6:14. [View at Publisher] [DOI] [PMID] [Google Scholar]

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