Moderate radioprotective role of zeolite in rats

  • Miloš Pavlović University of Belgrade, Faculty of Veterinary Medicine, Department of Reproduction, Fertility and Artificial Insemination, Belgrade, Serbia
  • Mirjana Djukic University of Belgrade, Faculty of Pharmacy, Department of Toxicology, Belgrade, Serbia
  • Danilo Vojvodić University of Defense, Faculty of Medicine of the Military Medical Academy, Belgrade, Serbia
  • Milica Ninković University of Defense, Faculty of Medicine of the Military Medical Academy, Belgrade, Serbia
  • Ivana Stevanović University of Defense, Faculty of Medicine of the Military Medical Academy, Belgrade, Serbia
  • Ana Djurić University of Belgrade, Faculty of Pharmacy, Department of Toxicology, Belgrade, Serbia
  • Boban Stanojević University of Belgrade, Institute of Nuclear Sciences “Vinča”, Department for Radiobiology and Molecular Genetics (080), Belgrade, Serbia
Keywords: brain, oxidative stress, plasma, radiation, ionizing, rats, zeolites

Abstract


Background/Aim. Exposure of living organisms to γ-radiation results in the overproduction of free radicals. The aim of the study was to test if the subacute administration of micronized zeolite (MZC) accomplishes radioprotective role based on the evaluation of the status of oxidative stress (OS) in the brain and 8-hydroxyguanosine (8-OH-dG) in the plasma of the rats exposed to the single γ-ray irradiation of 2 and/or 10 Gray (Gy). Methods. Wistar rats were on a four-week normal or 5% MZC supplemented diet and afterward exposed to the single γ-ray irradiation of 2 and 10 Gy. Groups of rats were: a) on a normal diet (the control group, and 2Gy and 10Gy groups); b) on 5% MZC supplemented diet (the control group – MZC, MZC + 2Gy, and MZC + 10Gy groups). We measured malondialdehyde (MDA), glutathione (GSH) total, and activity of total superoxide dismutase (tSOD) and manganese superoxide dismutase (MnSOD) in vulnerable brain regions (cerebellum, hippocampus, and cerebral cortex) and 8-OH-dG in plasma. Results. Lower MDA was found in the MZC+2Gy and MZC+10Gy groups compared to the 2Gy and 10Gy groups. Activity od total SOD was higher in the MZC+10Gy group than in the 10Gy one. GSH was the highest in the 10Gy group. Compared to the control group, 8-OH-dG was extremely higher in groups radiated with 10 Gy regardless of a diet, but slightly lower in the MZC+2Gy and 2Gy groups. Conclusion. Subacute MZC pretreatment accomplished partial radioprotective effect in irradiated rats compared to non-irradiated rats, based on suppressed SOD activity at 2 Gy, and reduced brain MDA when exposed to 2 Gy and 10 Gy.

 

References

Kim JH, Jenrow KA, Brown SL. Mechanisms of radiation-induced normal tissue toxicity and implications for future clinical trials. Radiat Oncol J 2014; 32(3): 103‒15.

Han J, Won EJ, Lee BY, Hwang UK, Kim IC, Yim JH, et al. Gamma rays induce DNA damage and oxidative stress associ-ated with impaired growth and reproduction in the copepod Tigriopus japonicus. Aquat Toxicol 2014; 152: 264‒72.

Azzam EI, Jay-Gerin JP, Pain D. Ionizing radiation-induced metabolic oxidative stress and prolonged cell injury. Cancer Lett 2012; 327(1‒2): 48‒60.

Đukić M, Ninković M, Jovanović M. Oxidative stress - clinical di-agnostic significance. J Med Biochem 2008; 27(4): 409‒25.

Lamprecht M, Bogner S, Steinbauer K, Schuetz B, Greilberger JF, Leber B, et al. Effects of zeolite supplementation on parame-ters of intestinal barrier integrity, inflammation, redoxbiology and performance in aerobically trained subjects. J Int Soc Sports Nutr 2015; 12(1): 40.

Kraljević Pavelić S, Simović Medica J, Gumbarević D, Filošević A, Przulj N, Pavelić K. Critical Review on Zeolite Clinoptilolite Safety and Medical Applications in vivo. Front Pharmacol 2018; 9: 1350.

Mastinu A, Kumar A, Maccarinelli G, Bonini SA, Premoli M, Aria F, et al. Zeolite Clinoptilolite: Therapeutic Virtues of an An-cient Mineral. Molecules 2019; 24(8): E1517.

Garbarino VR, Orr ME, Rodriguez KA, Buffenstein R. Mecha-nisms of oxidative stress resistance in the brain: lessons learned from hypoxia tolerant extremophilic vertebrates. Arch Biochem Biophys 2015; 576: 8‒16.

Hulbert A, Pamplona R, Buffenstein R, Buttemer W. Life and death: metabolic rate, membrane composition, and life span of animals. Physiol Rev 2007; 87(4): 1175‒213.

Das TK, Wati MR, Fatima-Shad K. Oxidative stress gated by Fenton and Haber Weiss reactions and its association with Alzheimer’s disease. Arch Neurosci 2015; 2(2): e60038.

Jovanović M, Malicević Z, Jovicić A, Dukić M, Ninković M, Jelenković A, et al. Selective sensitivity of the striatum to oxidative stress. Vojnosanit Pregl 1997; 54(6 Suppl): 33‒43. (Serbian)

National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory Animals. Guide for the Care and Use of Laboratory Animals. 8th ed. Washington (DC): National Academies Press (US); 2011.

Pavelic K, Katic M, Sverko V, Marotti T, Bosnjak B, Balog T, et al. Immunostimulatory effect of natural clinoptilolite as a possi-ble mechanism of its antimetastatic ability. J Cancer Res Clin Oncol 2002; 128(1): 37‒44.

Kassayová M, Ahlersová E, Ahlers I. Two-phase response of rat pineal melatonin to lethal whole-body irradiation with gamma rays. Physiol Res 1999; 48(3): 227‒30.

Alya G, Azroony R, Kasies F. Role of dose-rate on survival of lethally gamma irradiated (Male and Female) rats. Damascus: Atomic Energy Commission; 2003. (Arabic)

Mason KA, Withers HR, McBride WH, Davis CA, Smathers JB. Comparison of the gastrointestinal syndrome after total-body or total-abdominal irradiation. Radiat Res 1989; 117(3): 480‒8.

McBride WH, Chiang CS, Olson JL, Wang CC, Hong JH, Pajonk F, et al. A sense of danger from radiation. Radiat Res 2004; 162(1): 1‒19.

Gurd JW, Jones LR, Mahler HR, Moore WJ. Isolation and par-tial characterization of rat brain synaptic plasma membranes. J Neurochem 1974; 22(2): 281‒90.

Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein meas-urement with the Folin phenol reagent. J Biol Chem 1951; 193(1): 265‒75.

Sun M, Zigman S. An improved spectrophotometric assay for superoxide dismutase based on epinephrine autoxidation. Anal Biochem 1978; 90(1): 81‒9.

Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in ani-mal tissues by thiobarbituric acid reaction. Anal Biochem 1979; 95(2): 351‒8.

Anderson M. The DTNB-GSSG reductase recycling assay for total glutathione (GSH+ 1/2 GSSG). In: Greenwald RA, edi-tor. CRC Handbook of Methods for Oxygen Radical Re-search. 1st ed. Boca Raton, FL: CRC Press; 1986. p. 319‒23.

"Radiation Sickness". National Organization for Rare Disor-ders. Retrieved 6 June 2019. [citated 2019 Nov 14]. Available from: https://rarediseases.org/rare-diseases/radiation-sickness/.

Coleman CN, Blakely WF, Fike JR, MacVittie TJ, Metting NF, Mitchell JB, et al. Molecular and cellular biology of moderate-dose (1–10 Gy) radiation and potential mechanisms of radia-tion protection: report of a workshop at Bethesda, Maryland, December 17–18, 2001. Radiat Res 2003; 159(6): 812‒34.

Stanojević B, Đukić M, Stevanović I, Ninković M, Đurić A, Gobeljić B, et al. Zeolite pretreatment accomplishes partial brain radi-oprotective role by reducing iron and oxidative/nitrosative stress in rats. Hrana i ishrana 2018; 59(1): 26‒32.

Hill JM, Switzer RC 3rd. The regional distribution and cellular localization of iron in the rat brain. Neuroscience 1984; 11(3): 595‒603.

Djukic MM, Jovanovic MD, Ninkovic M, Stevanovic I, Ilic K, Curcic M, et al. Protective role of glutathione reductase in paraquat induced neurotoxicity. Chem Biol Interact 2012; 199(2): 74‒86.

Djuric A, Begic A, Gobeljic B, Stanojevic I, Ninkovic M, Vojvodic D, et al. Oxidative stress, bioelements and androgen status in testes of rats subacutely exposed to cadmium. Food Chem Toxicol 2015; 86: 25‒33.

Michalska–Mosiej M, Socha K, Soroczyńska J, Karpińska E, Łazarczyk B, Borawska MH. Selenium, Zinc, Copper, and total antioxidant status in the serum of patients with chronic tonsil-litis. Biol Trace Elem Res 2016; 173(1): 30‒4.

Lee EK, Kim JA, Kim JS, Park SJ, Heo K, Yang KM, et al. Acti-vation of denovo GSH synthesis pathway in mouse spleen af-ter long term low-dose γ-ray irradiation. Free Radic Res 2013; 47(2): 89‒94.

Lindenau J, Noack H, Possel H, Asayama K, Wolf G. Cellular dis-tribution of superoxide dismutases in the rat CNS. Glia 2000; 29(1): 25‒34.

Melov S, Schneider JA, Day BJ, Hinerfeld D, Coskun P, Mirra SS, et al. A novel neurological phenotype in mice lacking mito-chondrial manganese superoxide dismutase. Nat Genet 1998; 18(2): 159.

Floyd RA, Carney JM. Age influence on oxidative events dur-ing brain ischemia/reperfusion. Arch Gerontol Geriatr 1991; 12(2‒3): 155‒77.

Wang X, Michaelis EK. Selective neuronal vulnerability to oxi-dative stress in the brain. Front Aging Neurosci 2010; 2: 12.

Wang X, Zaidi A, Pal R, Garrett AS, Braceras R, Chen XW, et al. Genomic and biochemical approaches in the discovery of mechanisms for selective neuronal vulnerability to oxidative stress. BMC Neurosci 2009; 10: 12.

Andersen BB, Gundersen HJ, Pakkenberg B. Aging of the human cerebellum: a stereological study. J Comp Neurol 2003; 466(3): 356‒65.

Weydert CJ, Waugh TA, Ritchie JM, Iyer KS, Smith JL, Li L, et al. Overexpression of manganese or copper–zinc superoxide dismutase inhibits breast cancer growth. Free Rad Biol Med 2006; 41(2): 226‒37.

Pathak CM, Avti PK, Kumar S, Khanduja KL, Sharma SC. Whole body exposure to low-dose gamma radiation promotes kidney antioxidant status in Balb/c mice. J Radiat Res 2007; 48(2): 113‒20.

Wu L, Navrotsky A. Synthesis and thermodynamic study of transition metal ion (Mn 2+, Co 2+, Cu 2+, and Zn 2+) ex-changed zeolites A and Y. Phys Chem Chem Phys 2016; 18(15): 10116‒22.

Jacobs PH, Waite TD. The role of aqueous iron (II) and manga-nese (II) in sub-aqueous active barrier systems containing nat-ural clinoptilolite. Chemosphere 2004; 54(3): 313‒24.

Ballatori N, Krance SM, Marchan R, Hammond CL. Plasma membrane glutathione transporters and their roles in cell phys-iology and pathophysiology. Mol Aspects Med 2009; 30(1‒2): 13‒28.

Kojima S, Matsuki O, Nomura T, Shimura N, Kubodera A, Yamaoka K, et al. Localization of glutathione and induction of glutathione synthesis-related proteins in mouse brain by low doses of gamma-rays. Brain Res 1998; 808(2): 262‒9.

Kawakita Y, Ikekita M, Kurozumi R, Kojima S. Increase of intra-cellular glutathione by low-dose γ-ray irradiation is mediated by transcription factor AP-1 in RAW 264.7 cells. Biol Pharm Bull 2003; 26(1): 19‒23.

Yamaoka K, Kojima S, Takahashi M, Nomura T, Iriyama K. Change of glutathione peroxidase synthesis along with that of superoxide dismutase synthesis in mice spleens after low-dose X-ray irradiation. Biochim Biophys Acta 1998; 1381(2): 265‒70.

Avti P, Pathak CM, Kumar S, Kaushik G, Kaushik T, Farooque A, et al. Low dose gamma-irradiation differentially modulates an-tioxidant defense in liver and lungs of Balb/c mice. Int J Ra-diat Biol 2005; 81(12): 901‒10.

Patt HM, Tyree EB, Straube RL, Smith DE. Cysteine Protection against X Irradiation. Science 1949; 110(2852): 213‒4.

Teshima K, Yamamoto A, Yamaoka K, Honda Y, Honda S, Sasaki T, et al. Involvement of calcium ion in elevation of mRNA for gamma-glutamylcysteine synthetase (gamma-GCS) induced by low-dose gamma-rays. Int J Radiat Biol 2000; 76(12): 1631‒9.

Floyd RA, Carney JM. Free radical damage to protein and DNA: mechanisms involved and relevant observations on brain undergoing oxidative stress. Ann Neurol 1992; 32 Suppl: S22‒7.

Cuttler JM, Pollycove M. Can cancer be treated with low doses of radiation J Am Phys Surg 2003; 8(4): 108‒11.

Published
2021/08/06
Section
Original Paper