Generic placeholder image

Pharmaceutical Nanotechnology

Editor-in-Chief

ISSN (Print): 2211-7385
ISSN (Online): 2211-7393

Research Article

Multi-organ Toxicity Attenuation by Cerium Oxide and Yttrium Oxide Nanoparticles: Comparing the Beneficial Effects on Tissues Oxidative Damage Induced by Sub-acute Exposure to Diazinon

Author(s): Mona Navaei-Nigjeh, Marzieh Daniali, Mahban Rahimifard and Mohammad R. Khaksar*

Volume 8, Issue 3, 2020

Page: [225 - 238] Pages: 14

DOI: 10.2174/2211738508666200808135226

Price: $65

Abstract

Background: Excessive use of diazinon, as an organophosphate pesticide (OP), contributes to cytotoxic and pathologic cellular damage and, in particular, oxidative stress. However, metal-oxide nanoparticles (NPs), such as cerium oxide (CeO2) and yttrium oxide (Y2O3), with the property of free radical scavenging demonstrated beneficial effects in the alleviation of oxidative stress biomarkers.

Objective: The aims of this study include evaluating beneficial effects of CeO2 NPs, Y2O3 NPs, and their combination against diazinon-induced oxidative stress in different tissues of brain, heart, lung, kidney, liver, and spleen.

Methods: Eight randomized groups of 6 adult male Wistar rats were formed. Each group of rats administered a different combination of diazinon, CeO2 and Y2O3 NPs daily and levels of oxidative stress markers, such as reactive oxygen species (ROS), lipid peroxidation (LPO), total thiol molecules (TTM) and total anti-oxidant power (TAP) and catalase enzyme, were measured after 2 weeks of the treatment.

Results: Measurements of the mentioned markers in the brain, heart, lung, kidney, liver, and spleen showed that the administration of NPs could significantly alleviate the oxidative stress induced by diazinon. However, the findings of this study illustrated that the combination of both CeO2 and Y2O3 NPs led to a better reduction in oxidative stress markers.

Conclusion: Sub-acute exposure of diazinon in rats led to increased levels of oxidative stress markers in pivotal tissues such as the brain, heart, lung, kidney, liver, and spleen. CeO2 and Y2O3 NPs neutralize the oxidative stress to compensate diazinon-induced tissue damages.

Lay Summary: Organophosphate pesticides (OPs), which are mainly used for pest control, are responsible for the entry of pesticides into the human food cycle. Organophosphate such as diazinon increases the molecular biomarkers of oxidative stress inside the cells of vital tissues such as the heart, liver, lungs, etc. Metal oxide nanoparticles (NPs) such as cerium oxide (CeO2) and yitrium oxide (Y2O3) can have free radical scavenging potential under oxidative stress and through various mechanisms. Although these nanoparticles reduce oxidative stress, it should be borne in the design of the study that additional doses of these substances reverse the beneficial effects.

Keywords: Cerium Oxide Nanoparticle, Diazinon, Lipid Peroxidation (LPO), Oxidative Stress, Reactive Oxygen Species (ROS), Total Antioxidant Power (TAP), Total Thiol Molecules (TTM), Yttrium Oxide Nanoparticles.

Graphical Abstract
[1]
Khaksar MR, Rahimifard M, Baeeri M, et al. Protective effects of cerium oxide and yttrium oxide nanoparticles on reduction of oxidative stress induced by sub-acute exposure to diazinon in the rat pancreas. J Trace Elem Med Biol 2017; 41: 79-90.
[http://dx.doi.org/10.1016/j.jtemb.2017.02.013] [PMID: 28347467]
[2]
Abdollahi M, Ranjbar A, Shadnia S, Nikfar S, Rezaie A. Pesticides and oxidative stress: a review. Med Sci Monit 2004; 10(6): RA141-7.
[PMID: 15173684]
[3]
Pakzad M, Fouladdel S, Nili-Ahmadabadi A, et al. Sublethal exposures of diazinon alters glucose homostasis in Wistar rats: biochemical and molecular evidences of oxidative stress in adipose tissues. Pestic Biochem Physiol 2013; 105(1): 57-61.
[http://dx.doi.org/10.1016/j.pestbp.2012.11.008] [PMID: 24238291]
[4]
Hung DZ, Yang HJ, Li YF, et al. The long-term effects of organophosphates poisoning as a risk factor of CVDs: a nationwide population-based cohort study. PLoS One 2015; 10(9): e0137632
[http://dx.doi.org/10.1371/journal.pone.0137632] [PMID: 26339906]
[5]
Shiri M, Navaei-Nigjeh M, Baeeri M, et al. Blockage of both the extrinsic and intrinsic pathways of diazinon-induced apoptosis in PaTu cells by magnesium oxide and selenium nanoparticles. Int J Nanomedicine 2016; 11: 6239-50.
[http://dx.doi.org/10.2147/IJN.S119680] [PMID: 27920530]
[6]
Judge SJ, Savy CY, Campbell M, et al. Mechanism for the acute effects of organophosphate pesticides on the adult 5-HT system. Chem Biol Interact 2016; 245: 82-9.
[http://dx.doi.org/10.1016/j.cbi.2015.12.014] [PMID: 26721196]
[7]
Slotkin TA, Skavicus S, Seidler FJ. Diazinon and parathion diverge in their effects on development of noradrenergic systems. Brain Res Bull 2017; 130: 268-73.
[http://dx.doi.org/10.1016/j.brainresbull.2017.02.004] [PMID: 28235599]
[8]
Guyton KZ, Loomis D, Grosse Y, et al. Carcinogenicity of tetrachlorvinphos, parathion, malathion, diazinon, and glyphosate. Lancet Oncol 2015; 16(5): 490-1.
[http://dx.doi.org/10.1016/S1470-2045(15)70134-8] [PMID: 25801782]
[9]
Vahidirad M, Arab-Nozari M, Mohammadi H, Zamani E, Shaki F. Protective effect of captopril against diazinon induced nephrotoxicity and neurotoxicity via inhibition of ROS-NO pathway. Drug Chem Toxicol 2018; 41(3): 287-93.
[http://dx.doi.org/10.1080/01480545.2017.1391830] [PMID: 29115169]
[10]
Velki M, Di Paolo C, Nelles J, Seiler TB, Hollert H. Diuron and diazinon alter the behavior of zebrafish embryos and larvae in the absence of acute toxicity. Chemosphere 2017; 180: 65-76.
[http://dx.doi.org/10.1016/j.chemosphere.2017.04.017] [PMID: 28391154]
[11]
Ahmadi-Naji R, Heidarian E, Ghatreh-Samani K. Evaluation of the effects of the hydroalcoholic extract of Terminalia chebula fruits on diazinon-induced liver toxicity and oxidative stress in rats. Avicenna J Phytomed (AJP) 2017; 7(5): 454-66.
[12]
Harchegani AB, Rahmani A, Tahmasbpour E, Kabootaraki HB, Rostami H, Shahriary A. Mechanisms of diazinon effects on impaired spermatogenesis and male infertility. Toxicol Ind Health 2018; 34(9): 653-64.
[http://dx.doi.org/10.1177/0748233718778665] [PMID: 29996728]
[13]
Estevez AY, Erlichman JS. The potential of cerium oxide nanoparticles (nanoceria) for neurodegenerative disease therapy. Nanomedicine (Lond) 2014; 9(10): 1437-40.
[http://dx.doi.org/10.2217/nnm.14.87] [PMID: 25253491]
[14]
Navaei-Nigjeh M, Gholami M, Fakhri-Bafghi MS, Baeeri M, Abdollahi M. Molecular and biochemical evidences for beneficial effects of zinc oxide nanoparticles in modulation of chlorpyrifos toxicity in human lymphocytes. Iran J Pharm Res 2018; 17(3): 927-39.
[PMID: 30127816]
[15]
Rzigalinski BA, Carfagna CS, Ehrich M. Cerium oxide nanoparticles in neuroprotection and considerations for efficacy and safety. Wiley Interdiscip Rev Nanomed Nanobiotechnol 2017; 9(4): 1444.
[http://dx.doi.org/10.1002/wnan.1444] [PMID: 27860449]
[16]
Köhrle J, Jakob F, Contempré B, Dumont JE. Selenium, the thyroid, and the endocrine system. Endocr Rev 2005; 26(7): 944-84.
[http://dx.doi.org/10.1210/er.2001-0034] [PMID: 16174820]
[17]
Venkatachalam P, Jayaraj M, Manikandan R, et al. Zinc oxide nanoparticles (ZnONPs) alleviate heavy metal-induced toxicity in Leucaena leucocephala seedlings: a physiochemical analysis. Plant Physiol Biochem 2017; 110: 59-69.
[http://dx.doi.org/10.1016/j.plaphy.2016.08.022] [PMID: 27622846]
[18]
Tunçsoy M, Duran S, Ay Ö, Cicik B, Erdem C. Effects of copper oxide nanoparticles on antioxidant enzyme activities and on tissue accumulation of Oreochromis niloticus. Bull Environ Contam Toxicol 2017; 99(3): 360-4.
[http://dx.doi.org/10.1007/s00128-017-2129-z] [PMID: 28685220]
[19]
Rubio L, Marcos R, Hernández A. Nanoceria acts as antioxidant in tumoral and transformed cells. Chem Biol Interact 2018; 291: 7-15.
[http://dx.doi.org/10.1016/j.cbi.2018.06.002] [PMID: 29879412]
[20]
Ghaznavi H, Najafi R, Mehrzadi S. Neuro-protective effects of cerium and yttrium oxide nanoparticles on high glucose-induced oxidative stress and apoptosis in undifferentiated PC12 cells. Neurol Res 2015; 37(7): 624-32.
[21]
Tavoosi S, Baghsheikhi AH, Shetab-Boushehri SV, et al. Cerium and yttrium oxide nanoparticles and nano-selenium produce protective effects against h2o2-induced oxidative stress in pancreatic beta cells by modulating mitochondrial dysfunction. Pharm Nanotechnol 2020; 8(1): 63-75.
[http://dx.doi.org/10.2174/2211738507666191002154659] [PMID: 31577213]
[22]
Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976; 72: 248-54.
[http://dx.doi.org/10.1016/0003-2697(76)90527-3] [PMID: 942051]
[23]
Rashedinia M, Hosseinzadeh H, Imenshahidi M, Lari P, Razavi BM, Abnous K. Effect of exposure to diazinon on adult rat’s brain. Toxicol Ind Health 2016; 32(4): 714-20.
[http://dx.doi.org/10.1177/0748233713504806] [PMID: 24217015]
[24]
Jafari M, Salehi M, Ahmadi S, Asgari A, Abasnezhad M, Hajigholamali M. The role of oxidative stress in diazinon-induced tissues toxicity in Wistar and Norway rats. Toxicol Mech Methods 2012; 22(8): 638-47.
[http://dx.doi.org/10.3109/15376516.2012.716090] [PMID: 22871176]
[25]
Dam K, Seidler FJ, Slotkin TA. Developmental neurotoxicity of chlorpyrifos: delayed targeting of DNA synthesis after repeated administration. Brain Res Dev Brain Res 1998; 108(1-2): 39-45.
[http://dx.doi.org/10.1016/S0165-3806(98)00028-5] [PMID: 9693782]
[26]
Slotkin TA, Seidler FJ. Oxidative and excitatory mechanisms of developmental neurotoxicity: transcriptional profiles for chlorpyrifos, diazinon, dieldrin, and divalent nickel in PC12 cells. Environ Health Perspect 2009; 117(4): 587-96.
[http://dx.doi.org/10.1289/ehp.0800251] [PMID: 19440498]
[27]
Dowding JM, Song W, Bossy K, et al. Cerium oxide nanoparticles protect against Aβ-induced mitochondrial fragmentation and neuronal cell death. Cell Death Differ 2014; 21(10): 1622-32.
[http://dx.doi.org/10.1038/cdd.2014.72] [PMID: 24902900]
[28]
Grulke E, Reed K, Beck M, Huang X, Cormack A, Seal S. Nanoceria: factors affecting its pro-and anti-oxidant properties. Environ Sci Nano 2014; 1(5): 429-44.
[http://dx.doi.org/10.1039/C4EN00105B]
[29]
Hashem RM, Rashd LA, Hashem KS, Soliman HM. Cerium oxide nanoparticles alleviate oxidative stress and decreases Nrf-2/HO-1 in D-GALN/LPS induced hepatotoxicity. Biomed Pharmacother 2015; 73: 80-6.
[http://dx.doi.org/10.1016/j.biopha.2015.05.006] [PMID: 26211586]
[30]
Hosseini A, Sharifi AM, Abdollahi M, et al. Cerium and yttrium oxide nanoparticles against lead-induced oxidative stress and apoptosis in rat hippocampus. Biol Trace Elem Res 2015; 164(1): 80-9.
[http://dx.doi.org/10.1007/s12011-014-0197-z] [PMID: 25516117]
[31]
Schubert D, Dargusch R, Raitano J, Chan S-W. Cerium and yttrium oxide nanoparticles are neuroprotective. Biochem Biophys Res Commun 2006; 342(1): 86-91.
[http://dx.doi.org/10.1016/j.bbrc.2006.01.129] [PMID: 16480682]
[32]
Xie Y, Wang B, Li F, et al. Molecular mechanisms of reduced nerve toxicity by titanium dioxide nanoparticles in the phoxim-exposed brain of Bombyx mori. PLoS One 2014; 9(6): e101062
[http://dx.doi.org/10.1371/journal.pone.0101062] [PMID: 24971466]
[33]
Abdel-Diam MM, Samak DH, El-Sayed YS, Aleya L, Alarifi S, Alkahtani S. Curcumin and quercetin synergistically attenuate subacute diazinon-induced inflammation and oxidative neurohepatic damage, and acetylcholinesterase inhibition in albino rats. Environ Sci Pollut Res Int 2019; 26(4): 3659-65.
[http://dx.doi.org/10.1007/s11356-018-3907-9] [PMID: 30535736]
[34]
Zafiropoulos A, Tsarouhas K, Tsitsimpikou C, et al. Cardiotoxicity in rabbits after a low-level exposure to diazinon, propoxur, and chlorpyrifos. Hum Exp Toxicol 2014; 33(12): 1241-52.
[http://dx.doi.org/10.1177/0960327114532384] [PMID: 24818614]
[35]
Abdel-Daim MM, Taha R, Ghazy EW, El-Sayed YS. Synergistic ameliorative effects of sesame oil and alpha-lipoic acid against subacute diazinon toxicity in rats: hematological, biochemical, and antioxidant studies. Can J Physiol Pharmacol 2016; 94(1): 81-8.
[http://dx.doi.org/10.1139/cjpp-2015-0131] [PMID: 26550680]
[36]
Nemmar A, Yuvaraju P, Beegam S, Fahim MA, Ali BH. Cerium oxide nanoparticles in lung acutely induce oxidative stress, inflammation, and DNA damage in various organs of mice. Oxid Med Cell Longev 2017.: 20179639035
[http://dx.doi.org/10.1155/2017/9639035] [PMID: 28392888]
[37]
Hernández-Moreno D, Míguez MP, Soler F, Pérez-López M. Influence of sex on biomarkers of oxidative stress in the kidney, lungs, and liver of rabbits after exposure to diazinon. Environ Sci Pollut Res Int 2018; 25(32): 32458-65.
[http://dx.doi.org/10.1007/s11356-018-3258-6] [PMID: 30232776]
[38]
El Shaer SS, Salaheldin TA, Saied NM, Abdelazim SM. In vivo ameliorative effect of cerium oxide nanoparticles in isoproterenol-induced cardiac toxicity. Exp Toxicol Pathol 2017; 69(7): 435-41.
[http://dx.doi.org/10.1016/j.etp.2017.03.001] [PMID: 28431810]
[39]
Al-Otaibi AM, Al-Balawi HFA, Ahmad Z, Suliman EM. Toxicity bioassay and sub-lethal effects of diazinon on blood profile and histology of liver, gills and kidney of catfish, Clarias gariepinus. Braz J Biol 2019; 79(2): 326-36.
[http://dx.doi.org/10.1590/1519-6984.185408] [PMID: 30427380]
[40]
Karimani A, Heidarpour M, Moghaddam Jafari A. Protective effects of glycyrrhizin on sub-chronic diazinon-induced biochemical, hematological alterations and oxidative stress indices in male Wistar rats. Drug Chem Toxicol 2019; 42(3): 300-8.
[http://dx.doi.org/10.1080/01480545.2018.1497053] [PMID: 30203683]
[41]
Contreras-Zentella ML, Hernández-Muñoz R. Is liver enzyme release really associated with cell necrosis induced by oxidant stress? Oxid Med Cell Longev 2016; 2016: 3529149
[http://dx.doi.org/10.1155/2016/3529149] [PMID: 26798419]
[42]
Abdel-Daim MM, Abushouk AI, Alkhalf MI, et al. Antagonistic effects of Spirulina platensis on diazinon-induced hemato-biochemical alterations and oxidative stress in rats. Environ Sci Pollut Res Int 2018; 25(27): 27463-70.
[http://dx.doi.org/10.1007/s11356-018-2761-0] [PMID: 30043347]
[43]
Banaee M, Sureda A, Mirvagefei AR. Ahmadi, Histopathological Alterations Induced by Diazinon in Rainbow trout (Oncorhynchus mykiss). Int J Environ Res 2013; 7(3): 735-44.
[44]
Girón-Pérez MI, Zaitseva G, Casas-Solis J, Santerre A. Effects of diazinon and diazoxon on the lymphoproliferation rate of splenocytes from Nile tilapia (Oreochromis niloticus): the immunosuppresive effect could involve an increase in acetylcholine levels. Fish Shellfish Immunol 2008; 25(5): 517-21.
[http://dx.doi.org/10.1016/j.fsi.2008.07.002] [PMID: 18674623]
[45]
Díaz-Resendiz KJG, Ortiz-Lazareno PC, Covantes-Rosales CE, et al. Effect of diazinon, an organophosphate pesticide, on signal transduction and death induction in mononuclear cells of Nile tilapia fish (Oreochromis niloticus). Fish Shellfish Immunol 2019; 89: 12-7.
[http://dx.doi.org/10.1016/j.fsi.2019.03.036] [PMID: 30890431]
[46]
Khazaie S, Jafari M, Heydari J, et al. Modulatory effects of vitamin C on biochemical and oxidative changes induced by acute exposure to diazinon in rat various tissues: prophylactic and therapeutic roles. J Anim Physiol Anim Nutr (Berl) 2019; 103(5): 1619-28.
[http://dx.doi.org/10.1111/jpn.13144] [PMID: 31218763]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy