Toxic effect of copper-zinc pyrite ore on erythropoiesis in chronic experiment
https://doi.org/10.15372/SSMJ20200607
Abstract
Natural ores contain a large number of harmful components for human health. Workers of mining and processing enterprises, who have long-term contact with these natural elements, are often diagnosed with anemia, that pathogenesis is not sufficiently studied. Aim of the study was to detail the mechanisms of rats’ erythron disorders in the long-termintoxication by natural complex of heavy metal compounds of copper-zinc pyrite ore.
Material and methods. The work was performed on 60 white non-linear male rats aged 3-4 months weighing 220,52 ± 15,51 g. The experimental group of animals (n = 40) were injected orally with water suspension of copper-zinc powder in a bread crumb an hour before standard feeding during 75-120 days. The blood and bone marrow of experimental groups of rats were carried out on the 75-th, 90-th, 105-th and 120-th days of the experiment. The blood and bone marrow of rats’ control groups were studied on the 75-th and 105-th day. The central part of erythron was assessed by the number and composition of the erythroblastic islets (EI) of bone marrow, the number of free macrophages, the coefficients of involvement of colonyforming units of red blood cells (CFU-E) and macrophages into erythropoiesis.
Results. In the peripheral blood of experimental rats the number of red blood cells and the content of hemoglobin were reliably less than the control values on the 90-th and 120-th day, the number of reticulocytes was exceeded the control group on the 75-th, 105-th and 120-th day. In the bone marrow of experimental rats there were only a single EI1 and EI2 classes of maturity. Throughout the experiment, the content of free macrophages and EI with reticulocytes «crown» in the bone marrow of rats was elevated, and the concentration of iron and erythropoietin in the blood, on the contrary, was reduced. The intensity of CFU-E involvement in the erythropoiesis was less than the control level by 2 times on 105th and 120th days of the experiment.
Conclusion. With long-term introduction of copper-zinc pyrite ore in the bone marrow of rats the process of formation of EI de novo is suppressed by destabilizing the contact of free bone macrophages with young red blood cells. There is reduces in the content of serum erythropoietin and bound iron, that combines with the change of erythropoiesis nature, leads to decreasing of the number of mature red blood cells and content of hemoglobin in the peripheral blood.
About the Authors
K. R. ZiyakaevaRussian Federation
Klara R. Ziyakaeva
450008, Ufa, Lenin str., 3
A. F. Kayumova
Russian Federation
Aliya F. Kayumova - doctor of medical sciences, professor.
450008, Ufa, Lenin str., 3
References
1. Ostrovskaya S.S., Shatornaya V.F., Belskaya Yu.A. Effects of heavy metals and radiation on rat’s hemotosis. Svit meditsini ta biologii = World of Medicine and Biology. 2014; 47 (4): 177-179. [In Russian].
2. Ryspekova N.N., Nurmukhambetov A.N., Askarova A.E., Akanov A.A. Role of heavy metals in anemia (Review). Vestnik Kazakhskogo Natsional’nogo meditsinskogo universiteta = Bulletin of the Kazakh National Medical University. 2013; 3 (2): 46-51. [In Russian].
3. Medina S., Xu H., Wang S.C., Lauer F.T., Liu K.J., Burchiel S.W. Low level arsenite exposures suppress the development of bone marrow erythroid progenitors and result in anemia in adult male mice. Toxicol. Lett. 2017; 273: 106-111. doi: 10.1016/j.toxlet.2017.03.021
4. Zhang Y., Wang S., Chen C., Wu X., Zhang Q., Jiang F. Arsenic primes human bone marrow CD34+ cells for erythroid differentiation. Bioinorg. Chem. Appl. 2015; 2015: 751013. doi: 10.1155/2015/751013
5. Bakirov A.B., Suleimanov R.A.,Valeyev T.K. Experience of assessing water-related health risks to the population of the surrounding areas of mining. Meditsina truda i ekologiya cheloveka = Occupational Medicine and Human Ecology. 2016; 2: 5-13. [In Russian].
6. Tishevskaya N.V., Shevyakov S.A., Zakharov Yu.M. The effect of erythropoietin and macrophage colony stimulating factor on the proliferative activity of erythroid cells in cultures of erythroblastic islets. Meditsins-kiy akademicheskiy zhurnal = Medical Academic Journal. 2003; 3 (3): 67-72. [In Russian].
7. Yeo J.H., Cosgriff M.P., Fraser S.T. Analyzing the formation, morphology, and integrity of erythroblastic islands. Methods Mol. Biol. 2018; 1698: 133152. doi: 10.1007/978-1-4939-7428-3_8
8. Hom J., Dulmovits B.M., Mohandas N., Blanc L. The erythroblastic island as an emerging paradigm in the anemia of inflammation. Immunol. Res. 2015; 63 (1-3): 75-89. doi: 10.1007/s12026-015-8697-2
9. Zakharov Yu.M., Tishevskaya N.V., Shevyakov S.A. The effect of humoral factors on phagocytic activity of central macrophages in the erythroblast islet culture. Rossiyskiy fiziologicheskiy zhurnal imeni Ivana Mikhaylovicha Sechenova = Russian Journal of Physiology. 2002; 88 (9): 1191-1198. [In Russian].
10. Tishevskaya N.V., Zakharov Yu.M., Golubotovskii E.V., Kolesnikov O.L., Trofimova N.V., Arkhipenko Yu.V., Sazontova T.G. Effects of fullerenol C60(OH)24 on erythropoiesis in vitro. Bull. Exp. Biol. Med. 2014; 157 (1): 49-51. doi: 10.1007/s10517-014-2489-x
11. Volchegorskii I.A., Tishevskaya N.V., Dement’eva E.V. Antianemic effect of reamberin in rats with acute alloxan-induced diabetes. Eksperimental’naya i klinicheskaya farmakologiya = Experimental and Clinical Pharmacology. 2008; 71 (6): 23-27. [In Russian]. doi: 10.30906/0869-2092-2008-71-6-23-27
12. Suldina T.I. The content of heavy metals in food and their effects on the body. Ratsional’noye pitaniye, pishchevyye dobavki i biostimulyatory = Rational Nutrition, Nutritional Supplements and Biostimulants. 2016; 1: 136-140. [In Russian].
13. Zakharov Yu.M., Rassokhin A.G. Erythroblastic Island. Moscow: Meditsina, 2002. 280 p. [In Russian].
14. Ziyakaeva K.R., Kayumova A.F. Copper-Zinc pyrite ore intoxication affects erythron of rats. Rossiyskiy fiziologicheskiy zhurnal imeni Ivana Mikhaylovicha Sechenova = Russian Journal of Physiology. 2019; 105 (6): 780-789. [In Russian]. doi: 10.1134/S0869813919 0 60128
15. Ziyakaeva K.R., Kayumova A.F. Changes in erythron of experimental rats under influence of pyrite ore. «Agritech-II-2019: Agribusiness, environmental engineering and biotechnologies»: coll. thes. rep. 2nd international scientific conf., Krasnoyarsk, Nowember 13-14, 2019. Krasnoyarsk; 2020. 052026. doi:10.1088/1755-1315/421/5/052026
16. Xu J., Yang J., Nyga A., Ehteramyan M., Moraga A., Wu Y., Zeng L., Knight M.M., Shelton J.C. Cobalt (II) ions and nanoparticles induce macrophage retention by ROS-mediated down-regulation of RhoA expression. Acta Biomater. 2018; 72: 434-446. doi: 10.1016/j.actbio.2018.03.054
17. Bourdonnay E., Morzadec C., Sparfel L., Galibert M.D., Jouneau S., Martin-Chouly C., Fardel O., Vernhet L. Global effects of inorganic arsenic on gene expression profile in human macrophages. Mol. Immunol. 2009; 46 (4): 649-656. doi: 10.1016/j.molimm.2008.08.268
18. Gardner R.M., Nyland J.F., Evans S.L., Wang S.B., Doyle K.M., Crainiceanu C.M., Silbergeld E.K. Mercury induces an unopposed inflammatory response in human peripheral blood mononuclear cells in vitro. Environmental Health Perspectives. 2009; 117 (12): 1932-1938. doi: 10.1289/ehp.0900855
19. Xu H., Wang X., Wang W. Functional suppression of macrophages derived from THP-1 cells by envi-ronmentally-relevant concentrations of arsenite. Comp. Biochem. Physiol. C. Toxicol. Pharmacol. 2018; 214: 36-42. doi: 10.1016/j.cbpc.2018.08.010
20. Tishevskaya N.V., Gevorkyan N.M., Kozlova N.I. A modern view of the role of T-lymphocytes in regulation of erythropoiesis. Uspekhi sovremennoy biologii = Biology Bulletin Reviews. 2016; 136 (1): 83-96. [In Russian].
21. Tishevskaya N.V., Gevorkyan N.M., Kozlova N.I. The role of T-lymphocytes in hormonal regulation of morphogenetic processes. Uspekhi sovremennoy biologii = Biology Bulletin Reviews. 2015; 135 (2): 189202. [In Russian].
22. Kim S.H., Sharma R.P. Cytotoxicity of inorganic mercury in murine T and B lymphoma cell lines: involvement of reactive oxygen species, Ca(2+) homeostasis, and cytokine gene expression. Toxicol. In Vitro. 2003; 17 (4): 385-395. doi: 10.1016/S0887-2333(03)00040-7
23. Baskey S.J., Lehoux E.A., Catelas I. Effects of cobalt and chromium ions on lymphocyte migration. J. Orthop. Res. 2017; 35 (4): 916-924. doi: 10.1002/jor.23336
24. Horiguchi H., Kayama F., Oguma E., Willmore W.G., Hradecky P., Bunn H.F. Cadmium and platinum suppression of erythropoietin production in cell culture: clinical implications. Blood. 2000; 96 (12): 3743-3747.
25. Ziyakaeva K.R., Gabdulkhakova I.R., Zainetdi-nova A.T., Mullayanova A.N., Shamratova V.G., Kayumova A. F. The influence of copperzink pyrite ore on some haemotological indices and acid resistance of erythrocytes in experiment. Sovremennye problemy nauki i obrazovaniya = Modern Problems of Science and Education. 2018; 3: 28. [In Russian].
26. Chumakova S.P., Urazova O.I., Zima A.P., Novitskiy V.V. Features of the physiology of erythrocytes. Hemolysis and eryptosis. Gematologiya i transfuziologiya = Hematology and Transfusiology. 20182018; 63 (4): 343-351. [In Russian]. doi: 10.25837/HAT.2019.51.80.003