The protective effects of melatonin against electromagnetic waves of cell phones in animal models: A systematic review

Mohammad Amiri , Habibolah Khazaie , Masoud Mohammadi

Animal Models and Experimental Medicine ›› 2025, Vol. 8 ›› Issue (4) : 629 -637.

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Animal Models and Experimental Medicine ›› 2025, Vol. 8 ›› Issue (4) : 629 -637. DOI: 10.1002/ame2.12552
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The protective effects of melatonin against electromagnetic waves of cell phones in animal models: A systematic review

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Abstract

Background: Due to the widespread use of cell phone devices today, numerous research studies have focused on the adverse effects of electromagnetic radiation on human neuropsychological and reproductive systems. In most studies, oxidative stress has been identified as the primary pathophysiological mechanism underlying the harmful effects of electromagnetic waves. This paper aims to provide a holistic review of the protective effects of melatonin against cell phone-induced electromagnetic waves on various organs.

Methods: This study is a systematic review of articles chosen by searching Google Scholar, PubMed, Embase, Scopus, Web of Science, and Science Direct using the keywords ‘melatonin’, ‘cell phone radiation’, and ‘animal model’. The search focused on articles written in English, which were reviewed and evaluated. The PRISMA process was used to review the articles chosen for the study, and the JBI checklist was used to check the quality of the reviewed articles.

Results: In the final review of 11 valid quality-checked articles, the effects of melatonin in the intervention group, the effects of electromagnetic waves in the case group, and the amount of melatonin in the chosen organ, i.e. brain, skin, eyes, testis and the kidney were thoroughly examined. The review showed that electromagnetic waves increase cellular anti-oxidative activity in different tissues such as the brain, the skin, the eyes, the testis, and the kidneys. Melatonin can considerably augment the anti-oxidative system of cells and protect tissues; these measurements were significantly increased in control groups. Electromagnetic waves can induce tissue atrophy and cell death in various organs including the brain and the skin and this effect was highly decreased by melatonin.

Conclusion: Our review confirms that melatonin effectively protects the organs of animal models against electromagnetic waves. In light of this conclusion and the current world-wide use of melatonin, future studies should advance to the stages of human clinical trials. We also recommend that more research in the field of melatonin physiology is conducted in order to protect exposed cells from dying and that melatonin should be considered as a pharmaceutical option for treating the complications resulting from electromagnetic waves in humans.

Keywords

animal model / cell phone radiation / melatonin

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Mohammad Amiri, Habibolah Khazaie, Masoud Mohammadi. The protective effects of melatonin against electromagnetic waves of cell phones in animal models: A systematic review. Animal Models and Experimental Medicine, 2025, 8(4): 629-637 DOI:10.1002/ame2.12552

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References

[1]

Belpomme D, Irigaray P. Electrohypersensitivity as a newly identified and characterized neurologic pathological disorder: how to diagnose, treat, and prevent it. Int J Mol Sci. 2020; 21(6): 1915.

[2]

Heuser G, Heuser SA. Functional brain MRI in patients complaining of electrohypersensitivity after long term exposure to electromagnetic fields. Rev Environ Health. 2017; 32(3): 291-299.

[3]

Havas M, Marrongelle J, Pollner B, et al. Provocation study using heart rate variability shows microwave radiation from 2.4 GHz cordless phone affects autonomic nervous system. Eur J Oncol. 2010; 5: 273-300.

[4]

Stein Y, Udasin IG. Electromagnetic hypersensitivity (EHS, microwave syndrome)—review of mechanisms. Environ Res. 2020; 186: 109445.

[5]

Genuis SJ, Lipp CT. Electromagnetic hypersensitivity: fact or fiction? Sci Total Environ. 2012; 414: 103-112.

[6]

Chavdoula ED, Panagopoulos DJ, Margaritis LH. Comparison of biological effects between continuous and intermittent exposure to GSM-900-MHz mobile phone radiation: detection of apoptotic cell-death features. Mutat Res. 2010; 700(1-2): 51-61.

[7]

Karinen A, Heinävaara S, Nylund R, Leszczynski D. Mobile phone radiation might alter protein expression in human skin. BMC Genomics. 2008; 9: 1-5.

[8]

Repar J, Supek F, Klanjscek T, Warnecke T, Zahradka K, Zahradka D. Elevated rate of genome rearrangements in radiation-resistant bacteria. Genetics. 2017; 205(4): 1677-1689.

[9]

Aly AA, Deris SB, Zaki N. The effects on cells mobility due to exposure to EMF radiation. Adv Comput. 2011; 2(4): 1-7.

[10]

Giraldo Acosta M, Cano A, Hernández-Ruiz J, Arnao MB. Melatonin as a possible natural safener in crops. Plants (Basel). 2022; 11(7): 890.

[11]

Skinner DC, Malpaux B. High melatonin concentrations in third ventricular cerebrospinal fluid are not due to Galen vein blood recirculating through the choroid plexus. Endocrinology. 1999; 140(10): 4399-4405.

[12]

Nakamura Y, Tamura H, Takayama H, Kato H. Increased endogenous level of melatonin in preovulatory human follicles does not directly influence progesterone production. Fertil Steril. 2003; 80(4): 1012-1016.

[13]

Reiter RJ. Melatonin: the chemical expression of darkness. Mol Cell Endocrinol. 1991; 79(1-3): C153-C158.

[14]

Reiter RJ, Paredes SD, Manchester LC, Tan DX. Reducing oxidative/nitrosative stress: a newly-discovered genre for melatonin. Crit Rev Biochem Mol Biol. 2009; 44(4): 175-200.

[15]

Jung KH, Hong SW, Zheng HM, et al. Melatonin ameliorates cerulein-induced pancreatitis by the modulation of nuclear erythroid 2-related factor 2 and nuclear factor-kappaB in rats. J Pineal Res. 2010; 48(3): 239-250.

[16]

Chahbouni M, Escames G, Venegas C, et al. Melatonin treatment normalizes plasma pro-inflammatory cytokines and nitrosative/oxidative stress in patients suffering from Duchenne muscular dystrophy. J Pineal Res. 2010; 48(3): 282-289.

[17]

Carrillo-Vico A, Guerrero JM, Lardone PJ, Reiter RJ. A review of the multiple actions of melatonin on the immune system. Endocrine. 2005; 27(2): 189-200.

[18]

Jung-Hynes B, Reiter RJ, Ahmad N. Sirtuins, melatonin and circadian rhythms: building a bridge between aging and cancer. J Pineal Res. 2010; 48(1): 9-19.

[19]

Jung-Hynes B, Huang W, Reiter RJ, Ahmad N. Melatonin resynchronizes dysregulated circadian rhythm circuitry in human prostate cancer cells. J Pineal Res. 2010; 49(1): 60-68.

[20]

Tan D-X, Chen LD, Poeggeler B, Manchester LC, Reiter R. Melatonin: a potent endogenous hydroxyl radical scavenger. Endocr J. 1993; 1: 57-60.

[21]

Scopus Citation Index hwsc. Elsevier.

[22]

Butterfield DA, Hensley K, Harris M, Mattson M, Carney J. Beta-amyloid peptide free radical fragments initiate synaptosomal lipoperoxidation in a sequence-specific fashion: implications to Alzheimer's disease. Biochem Biophys Res Commun. 1994; 200(2): 710-715.

[23]

Hensley K, Carney JM, Mattson MP, et al. A model for beta-amyloid aggregation and neurotoxicity based on free radical generation by the peptide: relevance to Alzheimer disease. Proc Natl Acad Sci USA. 1994; 91(8): 3270-3274.

[24]

Valko M, Izakovic M, Mazur M, Rhodes CJ, Telser J. Role of oxygen radicals in DNA damage and cancer incidence. Mol Cell Biochem. 2004; 266(1-2): 37-56.

[25]

Janero DR. Therapeutic potential of vitamin E in the pathogenesis of spontaneous atherosclerosis. Free Radic Biol Med. 1991; 11(1): 129-144.

[26]

Dröge W. Free radicals in the physiological control of cell function. Physiol Rev. 2002; 82(1): 47-95.

[27]

Galle J. Oxidative stress in chronic renal failure. Nephrol Dial Transplant. 2001; 16(11): 2135-2137.

[28]

Hoshino Y, Mishima M. Redox-based therapeutics for lung diseases. Antioxid Redox Signal. 2008; 10(4): 701-704.

[29]

Pruchniak MP, Aražna M, Demkow U. Biochemistry of oxidative stress. Adv Exp Med Biol. 2016; 878: 9-19.

[30]

Sies H. Oxidative stress: a concept in redox biology and medicine. Redox Biol. 2015; 4: 180-183.

[31]

Scaiano JC. Exploratory laser flash photolysis study of free radical reactions and magnetic field effects in melatonin chemistry. J Pineal Res. 1995; 19(4): 189-195.

[32]

Roberts JE, Hu DN, Wishart JF. Pulse radiolysis studies of melatonin and chloromelatonin. J Photochem Photobiol B. 1998; 42(2): 125-132.

[33]

Karbownik M, Reiter RJ. Antioxidative effects of melatonin in protection against cellular damage caused by ionizing radiation. Proc Soc Exp Biol Med. 2000; 225(1): 9-22.

[34]

Melchiorri D, Reiter RJ, Attia AM, Hara M, Burgos A, Nistico G. Potent protective effect of melatonin on in vivo paraquat-induced oxidative damage in rats. Life Sci. 1995; 56(2): 83-89.

[35]

Dubbels R, Reiter RJ, Klenke E, et al. Melatonin in edible plants identified by radioimmunoassay and by high performance liquid chromatography-mass spectrometry. J Pineal Res. 1995; 18(1): 28-31.

[36]

Hattori A, Migitaka H, Iigo M, et al. Identification of melatonin in plants and its effects on plasma melatonin levels and binding to melatonin receptors in vertebrates. Biochem Mol Biol Int. 1995; 35(3): 627-634.

[37]

statista.com.

[38]

Karaman MI, Gökçe AM, Koca O, et al. The effects of electromagnetic waves emitted by the cell phones on the testicular tissue. Arch Ital Urol Androl. 2014; 86(4): 274-277.

[39]

Maluin SM, Osman K, Jaffar FHF, Ibrahim SF. Effect of radiation emitted by wireless devices on male reproductive hormones: a systematic review. Front Physiol. 2021; 12: 732420.

[40]

Bahaodini A, Owjfard M, Tamadon A, Jafari SM. Low frequency electromagnetic fields long-term exposure effects on testicular histology, sperm quality and testosterone levels of male rats. Asian Pacific Journal of Reproduction. 2015; 4(3): 195-200.

[41]

Köylü H, Mollaoglu H, Ozguner F, Nazýroölu M, Delibap N. Melatonin modulates 900 Mhz microwave-induced lipid peroxidation changes in rat brain. Toxicol Ind Health. 2006; 22(5): 211-216.

[42]

Altun G, Kaplan S, Deniz OG, et al. Protective effects of melatonin and omega-3 on the hippocampus and the cerebellum of adult Wistar albino rats exposed to electromagnetic fields. J Microsc Ultrastruct. 2017; 5(4): 230-241.

[43]

Ayata A, Mollaoglu H, Yilmaz HR, Akturk O, Ozguner F, Altuntas I. Oxidative stress-mediated skin damage in an experimental mobile phone model can be prevented by melatonin. J Dermatol. 2004; 31(11): 878-883.

[44]

Kerman M, Senol N. Oxidative stress in hippocampus induced by 900 MHz electromagnetic field emitting mobile phone: protection by melatonin. Biomed Res. 2012; 23(1): 147-151.

[45]

Seymen CM, Ilgaz C, Erdogan D, et al. Melatonin modulates NMDA-receptor 2B/Calpain-1/Caspase-12 pathways in rat brain after long time exposure to GSM radiation. Turk Neurosurg. 2019; 29(6): 887-900.

[46]

Oktem F, Ozguner F, Mollaoglu H, Koyu A, Uz E. Oxidative damage in the kidney induced by 900-MHz-emitted mobile phone: protection by melatonin. Arch Med Res. 2005; 36(4): 350-355.

[47]

Ozguner F, Aydin G, Mollaoglu H, Gökalp O, Koyu A, Cesur G. Prevention of mobile phone induced skin tissue changes by melatonin in rat: an experimental study. Toxicol Ind Health. 2004; 20(6-10): 133-139.

[48]

Ozguner F, Bardak Y, Comlekci S. Protective effects of melatonin and caffeic acid phenethyl ester against retinal oxidative stress in long-term use of mobile phone: a comparative study. Mol Cell Biochem. 2006; 282: 83-88.

[49]

Pandey N, Giri S. Melatonin attenuates radiofrequency radiation (900 MHz)-induced oxidative stress, DNA damage and cell cycle arrest in germ cells of male Swiss albino mice. Toxicol Ind Health. 2018; 34(5): 315-327.

[50]

Shokri M, Shamsaei ME, Malekshah AK, Amiri FT. The protective effect of melatonin on radiofrequency electromagnetic fields of mobile phone-induced testicular damage in an experimental mouse model. Andrologia. 2020; 52(11): e13834.

[51]

Sokolovic D, Djindjic B, Nikolic J, et al. Melatonin reduces oxidative stress induced by chronic exposure of microwave radiation from mobile phones in rat brain. J Radiat Res. 2008; 49(6): 579-586.

[52]

Gundersen HJ, Jensen EB. The efficiency of systematic sampling in stereology and its prediction. J Microsc. 1987; 147(Pt 3): 229-263.

[53]

Levine RL, Williams JA, Stadtman ER, Shacter E. Carbonyl assays for determination of oxidatively modified proteins. Methods Enzymol. 1994; 233: 346-357.

[54]

Góth L. A simple method for determination of serum catalase activity and revision of reference range. Clin Chim Acta. 1991; 196(2-3): 143-151.

[55]

Draper HH, Hadley M. Malondialdehyde determination as index of lipid peroxidation. Methods Enzymol. 1990; 186: 421-431.

[56]

Sun Y, Oberley LW, Li Y. A simple method for clinical assay of superoxide dismutase. Clin Chem. 1988; 34(3): 497-500.

[57]

Aebi H. Catalase in vitro. Methods Enzymol. 1984; 105: 121-126.

[58]

Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967; 70(1): 158-169.

[59]

Woessner JF. The determination of hydroxyproline in tissue and protein samples containing small proportions of this imino acid. Arch Biochem Biophys. 1961; 93: 440-447.

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2025 The Author(s). Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences.

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