AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
PDF (2 MB)
Collect
Submit Manuscript AI Chat Paper
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Review Article | Open Access

The inorganic chemicals that surround us: role of tellurium, selenium and zinc on behavioural functions in mammals

Edgardo O. Alvarez1( )Osvaldo J. Sacchi1,2Silvia G. Ratti1,3
Laboratorio de Epigénesis y Neuropsicofarmacología Experimental, Facultad de Ciencias Médicas, Universidad Católica de Cuyo, sede San Luis, Argentina
IMBECU, CONICET, Mendoza, Argentina
Área de Farmacología, Facultad de Ciencias Médicas, Universidad Nacional de Cuyo, Mendoza, Argentina
Show Author Information

Abstract

Living organisms live in continuous interaction with its environment. During this process changes in one can induce adaptive responses on the other. Many factors in the environment have been studied with the notorious distinction of been rare or to be of high intensity strength in its interaction with living organisms. However, little attention has been put on some factors that have constant interaction with organisms but usually have low intensity strength, such as the case of the inorganic chemical environment that surrounds us. In this review, the interaction between the chemical element and living organisms is discussed under a theoretical model of interaction between compartments, giving attention to tellurium (Te), zinc (Zn) and selenium (Se) on some cognitive functions in human and animals. After studies in our laboratory of the phenotypic expression of the HSR (Hand Skill Relative) gene in school children community living in geographic zone rich in minerals and mines of La Rioja province, Argentine, where Te was found to be in higher non-toxic concentrations, a translational experimental model to maturing rats exposed to this trace element was made. Te was found to increase some parameters related to locomotion in an open field induced by novelty and exploratory motivation. At the same time, inhibition of lateralized responses, survival responses and social activity was also observed. Some of these changes, particularly those related to lateralization had similarity with that found previously in children of La Rioja province. Discussion of similarities and discrepancies of biologic effects between animals and humans, about the possible meaning of Te and its interaction with Zn and Se with relevance to humans was analyzed.

References

[1]
Alvarez EO, Lario-Galvez RG, Ratti SG. The biological role of trace elements in epigenetic modulation of cognitive functions. Curr Trends Neurology 2018, 12: 81-91.
[2]
Zollo A, Furno FM, Grandola G, et al. Factores ambientales generadores de radicales libres y factores clínico-sanitarios y ocupacionales de riesgo de irradiaciones: prevención y protección (in Spanish). Hig Sanid Ambient 2004, 4: 65-71.
[3]
von Bertalanffy L. The theory of open systems in physics and biology. Science 1950, 111(2872): 23-29.
[4]
Beattie JA, Stockmayer WH. An account of the thermodynamic properties of gases, principally in terms of the Beattie-Bridgeman equation. A Treatise on Physical Chemistry. Taylor HS, Glasstone S, Eds. New York: Van Nostrand, 1951.
[5]
Steele EJ, Gorczynski RM, Lindley RA, et al. Lamarck and panspermia - on the efficient spread of living systems throughout the Cosmos. Prog Biophys Mol Biol 2019, 149: 10-32.
[6]
Masud N, Ellison A, Pope EC, et al. Cost of a deprived environment-increased intraspecific aggression and susceptibility to pathogen infections. J Exp Biol 2020, 223(Pt 20): jeb229450.
[7]
Beltrán I, Durand V, Loiseleur R, et al. Effect of early thermal environment on the morphology and performance of a lizard species with bimodal reproduction. J Comp Physiol B 2020, 190(6): 795-809.
[8]
Salliot C, Nguyen Y, Boutron-Ruault MC, et al. Environment and lifestyle: their influence on the risk of RA. J Clin Med 2020, 9(10): 3109.
[9]
Ferreira AS, Lima AP, Jehle R, et al. The influence of environmental variation on the genetic structure of a poison frog distributed across continuous Amazonian rainforest. J Hered 2020, 111(5): 457-470.
[10]
Wright RO, Baccarelli A. Metals and neurotoxicology. J Nutr 2007, 137(12): 2809-2813.
[11]
Chasteen TG, Fuentes DE, Tantaleán JC, et al. Tellurite: history, oxidative stress, and molecular mechanisms of resistance. FEMS Microbiol Rev 2009, 33(4): 820-832.
[12]
Selinus O, Alloway BJ, Centeno JA, et al. Essential of Medical Geology: Impact of the Natural Environment on Public Health. Amsterdam: Elsevier Academic Press, 2005.
[13]
Daniel N, Tandoh KK, Blestmond BA. Geochemistry of minor and trace elements in soils of Akuse area, southeastern Ghana. Geosciences 2019, 9(1): 8-17.
[14]
Reimann C, Siewers U, Skarphagen H, et al. Influence of filtration on concentrations of 62 elements analysed on crystalline bedrock groundwater samples by ICP-MS. Sci Total Environ 1999, 234(1-3): 155-173.
[15]
Anastassopoulou J. Metal-DNA interactions. J Mol Struct 2003, 651-653: 19-26.
[16]
Chen HB, Ke QD, Kluz T, et al. Nickel ions increase histone H3 lysine 9 dimethylation and induce transgene silencing. Mol Cell Biol 2006, 26(10): 3728-3737.
[17]
Bhai S, Ganguly B. Role of backbones on the interaction of metal ions with deoxyribonucleic acid and peptide nucleic acid: a DFT study. J Mol Graph Model 2019, 93: 107445.
[18]
Liu YF, Ran SY. Divalent metal ions and intermolecular interactions facilitate DNA network formation. Colloids Surf B Biointerfaces 2020, 194: 111117.
[19]
Rosenbach H, Borggräfe J, Victor J, et al. Influence of monovalent metal ions on metal binding and catalytic activity of the 10-23 DNAzyme. Biol Chem 2020, 402(1): 99-111.
[20]
Dittimer DC. Tellurium. Chem Eng News 2003, (accessed 27 March, 2021)
[21]
Munn LE, Hopkins BS. Studies on tellurium the value of some tellurium compounds as disinfectants. J Bacteriol 1925, 10(1): 79-86.
[22]
Frazer AD. Tellurium in the treatment of syphilis. Lancet 1930, 216(5577): 133-134.
[23]
Schroeder HA, Buckman J, Balassa JJ. Abnormal trace elements in man: tellurium. J Chronic Dis 1967, 20(3): 147-161.
[24]
Newman RA, Osborn S, Siddik ZH. Determination of tellurium in biological fluids by means of electrothermal vaporization-inductively coupled plasma-mass spectrometry (ETV-ICP-MS). Clin Chim Acta 1989, 179(2): 191-196.
[25]
Siddik ZH, Newman RA. Use of platinum as a modifier in the sensitive detection of tellurium in biological samples. Anal Biochem 1988, 172(1): 190-196.
[26]
Boles JO, Lebioda L, Dunlap RB, et al. Telluromethionine in structural biochemistry. SAAS Bull Biochem Biotechnol 1995, 8: 29-34.
[27]
Budisa N, Steipe B, Demange P, et al. High-level biosynthetic substitution of methionine in proteins by its analogs 2-aminohexanoic acid, selenomethionine, telluromethionine and ethionine in Escherichia coli. Eur J Biochem 1995, 230(2): 788-796.
[28]
Sredni B, Gal R, Cohen IJ, et al. Hair growth induction by the tellurium immunomodulator AS101: association with delayed terminal differentiation of follicular keratinocytes and ras-dependent up-regulation of KGF expression. FASEB J 2004, 18(2): 400-402.
[29]
Xie L, Chen J, McMickle A, et al. The immunomodulator AS101 suppresses production of inflammatory cytokines and ameliorates the pathogenesis of experimental autoimmune encephalomyelitis. J Neuroimmunol 2014, 273(1/2): 31-41.
[30]
Sredni B, Geffen-Aricha R, Duan WZ, et al. Multifunctional tellurium molecule protects and restores dopaminergic neurons in Parkinson's disease models. FASEB J 2007, 21(8): 1870-1883.
[31]
Yossipof TE, Bazak ZR, Kenigsbuch-Sredni D, et al. Tellurium compounds prevent and reverse type-1 diabetes in NOD mice by modulating α4β7 integrin activity, IL-1β, and T regulatory cells. Front Immunol 2019, 10: 979.
[32]
Fernández-Turiel JL, López-Soler A, Llorens JF, et al. Environmental monitoring using surface water, river sediments, and vegetation: a case study in the Famatina Range, La Rioja, NW Argentina. Environ Int 1995, 21(6): 807-820.
[33]
Laden BP, Porter TD. Inhibition of human squalene monooxygenase by tellurium compounds: evidence of interaction with vicinal sulfhydryls. J Lipid Res 2001, 42(2): 235-240.
[34]
Perez-D'Gregorio RE, Miller RK. Teratogenicity of tellurium dioxide: prenatal assessment. Teratology 1988, 37(4): 307-316.
[35]
Ratti SG, Cordoba P, Rearte S, et al. Differential expression of handedness, scalp hair-whorl direction, and cognitive abilities in primary school children. Int J Neuroprotection Neuroregeneration 2007, 4(1): 52-60.
[36]
Ratti SG, Vizioli NM, Álvarez EO. Epigenetic modulation expressed as methylation changes in DNA from primary school children of two different geographical environments II. Am J Neuroprotect Neuroregen 2010, 2(1): 65-70.
[37]
Ratti SG, Vizioli NM, Gaglio E, et al. Biological effects of trace elements on lateralized exploratory activity, defensive behaviour, and epigenetic DNA molecular changes in maturing rats. Am J Neuroprotect Neuroregen 2012, 4(2): 167-175.
[38]
Ratti SG, Alvarez EO. The behavioural responses displayed by litter rats after chronic administration of non-toxic concentrations of ZnTe to parent rats are mediated primarily by Te. Am J Neuroprotect Neuroregen 2014, 6(1): 33-42.
[39]
Ratti SG, Alvarez EO. Short administration of ZnTe to male and female rats previous to mating and fertilization affects behavioural responses of litters during the prepuberal period. Am J Neuroprotect Neuroregen 2014, 6(1): 54-61.
[40]
Ratti SG, Alvarez EO. Differential effects of zinc and tellurium on epigenetic changes of coping behaviour in maturing rats. J Neurorestoratol 2019, 7(1): 37-46.
[41]
Cravo M, Fidalgo P, Pereira AD, et al. DNA methylation as an intermediate biomarker in colorectal cancer: modulation by folic acid supplementation. Eur J Cancer Prev 1994, 3(6): 473-479.
[42]
Crider KS, Yang TP, Berry RJ, et al. Folate and DNA methylation: a review of molecular mechanisms and the evidence for folate's role. Adv Nutr 2012, 3(1): 21-38.
[43]
Iskandar BJ, Rizk E, Meier B, et al. Folate regulation of axonal regeneration in the rodent central nervous system through DNA methylation. J Clin Investig 2010, 120(5): 1603-1616.
[44]
Kim KC, Friso S, Choi SW. DNA methylation, an epigenetic mechanism connecting folate to healthy embryonic development and aging. J Nutr Biochem 2009, 20(12): 917-926.
[45]
Lubecka-Pietruszewska K, Kaufman-Szymczyk A, Stefanska B, et al. Folic acid enforces DNA methylation-mediated transcriptional silencing of PTEN, APC and RARbeta2 tumour suppressor genes in breast cancer. Biochem Biophys Res Commun 2013, 430(2): 623-628.
[46]
Ratti SG, Alvarez EO. The altered behavioural responses displayed by litter rats after chronic administration of non-toxic concentrations of ZnTe to parent rats are reversed by simultaneous folic acid treatment. Am J Neuroprotect Neuroregen 2015, 7(1): 56-64.
[47]
Ratti SG, Alvarez EO. Tellurium epigenetic transgenerational effects on behavioral expression of coping behavior in rats. Prog Brain Res 2019, 245: 247-261.
[48]
Ratti SG, Sacchi OJ, Alvarez EO. Behavioural multigenerational effects induced by the administration of very low doses of zinc during pregnancy, lactation, and prepuberal period in the rat. J Neurorestoratol 2021, 9(1): 72-80.
[49]
Tyszka-Czochara M, Grzywacz A, Gdula-Argasińska J, et al. The role of zinc in the pathogenesis and treatment of central nervous system (CNS) diseases. Implications of zinc homeostasis for proper CNS function. Acta Pol Pharm 2014, 71(3): 369-377.
[50]
Rubio C, Weller DG, Martín-Izquierdo RE, et al. El zinc: oligoelemento esencial (in Spanish). Nutr Hosp 2007, 22: 101-107.
[51]
Gower-Winter SD, Levenson CW. Zinc in the central nervous system: From molecules to behavior. Biofactors 2012, 38(3): 186-193.
[52]
McCall KA, Huang C, Fierke CA. Function and mechanism of zinc metalloenzymes. J Nutr 2000, 130(5S Suppl): 1437S-1446S.
[53]
Brayer KJ, Segal DJ. Keep your fingers off my DNA: protein-protein interactions mediated by C2H2 zinc finger domains. Cell Biochem Biophys 2008, 50(3): 111-131.
[54]
Cherasse Y, Urade Y. Dietary zinc Acts as a sleep modulator. Int J Mol Sci 2017, 18(11): 2334.
[55]
Nakamura M, Miura A, Nagahata T, et al. Low zinc, copper, and manganese intake is associated with depression and anxiety symptoms in the Japanese working population: findings from the eating habit and well-being study. Nutrients 2019, 11(4): E847.
[56]
Hassan A, Sada KK, Ketheeswaran S, et al. Role of zinc in mucosal health and disease: a review of physiological, biochemical, and molecular processes. Cureus 2020, 12(5): e8197.
[57]
Kurokawa S, Berry MJ. Selenium. Role of the essential metalloid in health. Met Ions Life Sci 2013, 13: 499-534.
[58]
van Rij AM, Thomson CD, McKenzie JM, et al. Selenium deficiency in total parenteral nutrition. Am J Clin Nutr 1979, 32(10): 2076-2085.
[59]
Schwarz K, Foltz CM. Selenium as an integral part of factor 3 against dietary necrotic liver degeneration. 1951. Nutrition 1999, 15(3): 255.
[60]
Chen J, Berry MJ. Selenium and selenoproteins in the brain and brain diseases. J Neurochem 2003, 86(1): 1-12.
[61]
Köhrle J, Gärtner R. Selenium and thyroid. Best Pract Res Clin Endocrinol Metab 2009, 23(6): 815-827.
[62]
Papp LV, Lu J, Holmgren A, et al. From selenium to selenoproteins: synthesis, identity, and their role in human health. Antioxid Redox Signal 2007, 9(7): 775-806.
[63]
Howell GO, Hill CH. Biological interaction of selenium with other trace elements in chicks. Environ Health Perspect 1978, 25: 147-150.
[64]
Hille R. Molybdenum and tungsten in biology. Trends Biochem Sci 2002, 27(7): 360-367.
[65]
Lane TW, Morel FM. A biological function for cadmium in marine diatoms. PNAS 2000, 97(9): 4627-4631.
[66]
Price NM, Morel FMM. Cadmium and cobalt substitution for zinc in a marine diatom. Nature 1990, 344(6267): 658-660.
[67]
Wolfe-Simon F, Switzer Blum J, Kulp TR, et al. A bacterium that can grow by using arsenic instead of phosphorus. Science 2011, 332(6034): 1163-1166.
[67]
Ratti SG, Alvarez EO. Selenium treatment modifies the epigenetic behavioural changes induced by chronic non-toxic administration of ZnTe to prepuberal rats. Am J Neuroprot Neuroregen 2016, 8(1): 66-74.
Journal of Neurorestoratology
Pages 151-163
Cite this article:
Alvarez EO, Sacchi OJ, Ratti SG. The inorganic chemicals that surround us: role of tellurium, selenium and zinc on behavioural functions in mammals. Journal of Neurorestoratology, 2021, 9(2): 151-163. https://doi.org/10.26599/JNR.2021.9040015

738

Views

21

Downloads

6

Crossref

5

Web of Science

0

Scopus

Altmetrics

Received: 27 March 2021
Revised: 21 June 2021
Accepted: 05 July 2021
Published: 05 June 2021
© The authors 2021

This article is published with open access at http://jnr.tsinghuajournals.com

Return