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   Table of Contents      
ORIGINAL ARTICLE
Year : 2014  |  Volume : 62  |  Issue : 1  |  Page : 12-15

Effects of melatonin on Wi-Fi-induced oxidative stress in lens of rats


1 Department of Ophthalmology, Medical Faculty, Süleyman Demirel University, Isparta, Turkey
2 Department of Biophysics, Medical Faculty, Süleyman Demirel University, Isparta, Turkey
3 Department of Biophysics, Medical Faculty, Izmir Katip Celebi University, Izmir, Turkey

Date of Submission14-Jul-2013
Date of Acceptance14-Dec-2013
Date of Web Publication31-Jan-2014

Correspondence Address:
Mustafa Nazıroğlu
Director of Neuroscience Research Center, Suleyman Demirel University, TR-32260 Isparta
Turkey
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0301-4738.126166

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  Abstract 

Introduction: Melatonin has been considered a potent antioxidant that detoxifies a variety of reactive oxygen species in many pathophysiological states of eye. The present study was designed to determine the effects of Wi-Fi exposure on the lens oxidant, antioxidant redox systems, as well as the possible protective effects of melatonin on the lens injury induced by electromagnetic radiation (EMR). Materials and Methods: Thirty-two rats were used in the current study and they were randomly divided into four equal groups as follows: First and second groups were cage-control and sham-control rats. Rats in third group were exposed to Wi-Fi (2.45 GHz) for duration of 60 min/day for 30 days. As in the third group, the fourth group was treated with melatonin. The one-hour exposure to irradiation in second, third and fourth took place at noon each day. Results: Lipid peroxidation levels in the lens were slightly higher in third (Wi-Fi) group than in cage and sham control groups although their concentrations were significantly (P < 0.05) decreased by melatonin supplementation. Glutathione peroxidase (GSH-Px) activity was significantly (P < 0.05) lower in Wi-Fi group than in cage and sham control groups although GSH-Px (P < 0.01) and reduced glutathione (P < 0.05) values were significantly higher in Wi-Fi + melatonin group than in Wi-Fi group. Conclusions: There are poor oxidative toxic effects of one hour of Wi-Fi exposure on the lens in the animals. However, melatonin supplementation in the lens seems to have protective effects on the oxidant system by modulation of GSH-Px activity.

Keywords: Antioxidants, electromagnetic ration, glutathione, lens, oxidative stress


How to cite this article:
Tök L, Nazıroğlu M, Doğan S, Kahya MC, Tök Ö. Effects of melatonin on Wi-Fi-induced oxidative stress in lens of rats. Indian J Ophthalmol 2014;62:12-5

How to cite this URL:
Tök L, Nazıroğlu M, Doğan S, Kahya MC, Tök Ö. Effects of melatonin on Wi-Fi-induced oxidative stress in lens of rats. Indian J Ophthalmol [serial online] 2014 [cited 2019 May 26];62:12-5. Available from: http://www.ijo.in/text.asp?2014/62/1/12/126166

People are intensely exposed to electromagnetic radiation particularly for the last two decades. Electromagnetic radiation (EMR) signals consist of extremely low frequency fields (between 1Hz up to 100 kHz) and high frequency fields, in the band of the radio frequency fields (RF, 100 kHz-3GHz) and of the microwaves (MW, above 3 GHz). Besides their use for technological applications (e.g, power lines, mobile phones), the EMFs are today widely used in medicine for diagnostic and therapeutic purposes. [1],[2] The World Health Organization Report (2007) and WHO Environmental Health Criteria Report (2007) issued precautions against EMR, considering the increased social and public interest in this subject, based on the epidemiological data, which associates the extra risk of amyotrophic lateral sclerosis, childhood leukemia, adult brain cancer, and miscarriage with EMR exposure of the power line radiation. [3]

The interaction of the biological system and EMR in the molecular level can result in change in cell cycle, induction of cell death, modification of protein expression and mainly oxidative stress. [4],[5],[6],[7] EMR exposure of eye results in overproduction of reactive oxygen species (ROS), which can damage cellular components such as lipids, nucleic acids and proteins. [8] Lipid peroxidation in eye occurs because of elevated levels of ROS with the liberation of reactive aldehydes, such as malondialdehyde (MDA) and 4-hydroxy-2-nonenal. [9] ROS in eye can cause cellular damage by depleting enzymatic and/or non-enzymatic antioxidants triggering progressive dysfunction and eventually genotoxic events. [10],[11] ROS are also increasingly generated in the tissues in many vision impairing and blinding diseases including cataracts, glaucoma and retinopathies. Oxidative stress induced by ROS is a major risk factor for senile cataract, particularly nuclear cataract. [9] The level of ROS in eye is usually regulated by intracellular antioxidant defense system. The antioxidant defense system is composed of antioxidant molecules such as reduced glutathione (GSH) and of a variety of antioxidant enzymes such as superoxide dismutase and glutathione peroxidase (GSH-Px). [12] The eye lens has also evolved a wide range of protective and repair systems to protect its components from oxidative stress, including high levels of reduced GSH and abundant antioxidant enzymes such as superoxide dismutase and catalase. [13]

Melatonin (N-acetyl-5-methoxytryptamine), also an indoleamine, is a neurohormone secreted primarily by the pineal gland and has an effect on most biological and physiological processes. The biosynthesis of melatonin from serotonin proceeds via two key enzymes, arylalkylamine N-acetyltransferase and hydroxyindole-O-methyltransferase (5-hydroxytrypamine). [14] Melatonin in the eye is synthesized in the crystalline lens cortical fiber cells, retinal photoreceptor cells and ciliary body. Additionally, specific melatonin receptors are found in the retina, coroid, ciliary body, lens, sclera, which are targets for melatonin. [15]

We have recently observed modulator role of melatonin on Wi-Fi-induced oxidative stress in brain and dorsal root ganglion of rats. [16] To our knowledge, there is no report whether Wi-Fi induce oxidative stress in lens of experimental animals and humans. The aim of the present study was to determine the effects of Wi-Fi frequency (2.45 GHz) exposure on the lens oxidant, antioxidant redox systems, as well as the possible protective effects of melatonin on the lens injury induced by the EMR.


  Materials and Methods Top


Animals

In this study, 16 weeks old, 32 male albino rats of Wistar strain, weighing 220 ± 20 g were used. The study was approved by Ethical Committee of Suleyman Demirel University. Laboratory animals prepared by Ethical Committee of (Protocol Number; 2011-01). The rats were quarantined before irradiation, housed in individual stainless-steel cages in a pathogen-free environment in a windowless laboratory room with automatic temperature (22 ± 3°C) and lighting controls (12-h light/12-h dark) and fed standard laboratory chow and water ad libitum. Average light intensity was determined to be 4000 lux and humidity was 40 ± 10% in the laboratory. The authors confirm adherence to the Association for Research in Vision and Ophthalmology (ARVO) statement for the Use of Animals in Ophthalmic and Vision Research.

Experimental groups

After one week adaptation process, the animals were randomized into four groups of eight rats each. The rats in Group A1 (cage control) were not exposed to electromagnetic radiation (EMR) or did not receive melatonin. The rats in Group A2 (sham control) received an intraperitoneal injection of isotonic saline solution in the same volume and by the same scheme as that used in the group receiving melatonin without EMR exposure. Group B rats (the EMR group) were exposed to 1 hour of EMR from 9 am to 10 am for 30 days. Group C rats (treatment groups) were exposed to EMR in the same manner as Group B and received melatonin treatment. Melatonin was initially dissolved in 0.1 ml of dimethyl sulfoxide (DMSO) and then diluted with physiological saline solution. Melatonin was administered intraperitoneally at a dose of 10 μg/kg and in a 0.1 ml volume of DMSO. The injection was administered 24 hours after EMR exposure and continued for 30 days.

Exposure system and design

We used six rats in the exposure system in the same time [Figure 1]. Details of exposure system have been described in detail elsewhere. [16],[17] We used power values as 1 mW/m 2 in the experiments as described below. A "SET ELECO" generator from Set Electronic Co, Istanbul (Turkey), provided with a half-wave dipole antenna system was used to irradiate the cells with a 2.45 GHz radio frequency with 217 Hz pulses. The electric field density was set at 11 V/m in order to get a 0.1 W/kg whole-body average specific absorption rate (SAR) and electromagnetic radiation values estimated for 2.45 GHz set up.
Figure 1: The experimental setup for irradiation of rats[5,6]

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The EMR dose was calculated from the measured electric field density (V/m). SAR values were calculated by using electric properties of tissue sample and measured electric field intensities for every distance in certain frequency. These values were shown in [Table 1].
Table 1

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The rats of Group A2 were placed in the cylindrical restrainer with the radio frequency source switched off during times similar to those used for irradiation. The A1 control animals were kept in their cage without any treatment or restraint of any kind.

Preparation of lens samples

Head of all animals were cut and the lens samples were dissected as described in own previous study. [18] The lens tissues were placed into glass bottles, labeled and stored in a deep freeze (−33°C) until processing (maximum 15 days). After weighing, The lens samples were placed on ice, and homogenized (2 minutes at 5000 rpm) in a five volumes (1:5, w/v) of ice-cold Tris-HCl buffer (50 mM, pH 7.4), by using a glass ultrasonic homogenizer (HD 2070, Bandelin Ultrasonic homogenizer, Bandelin Electronics GmbH and Co. KG, Berlin, Germany). All preparation procedures were performed on ice. The lens homogenate samples were used for immediate lipid peroxidation, GSH levels and enzyme activities.

Lipid peroxidation determinations

Lipid peroxidation levels in the lens homogenate were spectrophotometrically (at 532 nm) measured with the thiobarbituric-acid reaction by the method of Placer et al. [19]

Reduced glutathione (GSH), glutathione peroxidase (GSH-Px) and protein assays

The GSH content in the lens samples was spectrophotometrically measured at 412 nm using the method of Sedlak and Lindsay. [20] Standard curve of the GSH were prepared with different concentrations of GSH. GSH-Px activities of the lens homogenate were measured spectrophotometrically at 37 °C and 412 nm according to the Lawrence and Burk. [21] The protein content in the lens homogenate was measured by method of Lowry et al.,[22] with bovine serum albumin as the standard.

Statistical analyses

All results are expressed as means ± standard deviation (SD). To determine the effect of treatment, data were analyzed using analysis of Mann-Whitney U test. P values of less than 0.05 were regarded as significant. Data was analyzed using the Statistical Package for the Social Sciences software (SPSS) statistical program (version 17.0 software, SPSS Inc. Chicago, IL, USA).


  Results and Discussion Top


In this study, we found firstly in the literature that 2.45 GHz EMR, to which people are intensely Wi-Fi exposed in daily life, increased malondialdehyde (MDA), the indicator of lipid peroxidation and oxidative stress on the lens, and decreased antioxidants including GSH level and GSH-Px activity. Oxidative stress and thus, ROS, are believed to be a principal cause of noncongenital cataract. ROS have been implicated in the development of lens opacification, which has been demonstrated in both experimental animal models [18],[23] and in cultured lens systems. [24],[25] Cataract patients also exhibited elevated levels of oxidative stress. [18] ROS including superoxide and singlet oxygen can also be generated in the lens and aqueous humor, which explains why areas of the world with higher intensity of EMR irradiation have higher incidence of cataracts. [26]

Levels of lipid peroxidation are shown in [Figure 2]. Mean values of cage control, sham control, Wi-Fi and Wi-Fi + melatonin groups as μM/g protein were 10.8, 10.7, 11.4 and 9.8, respectively. The lipid peroxidation levels were insignificantly higher in Wi-Fi group than in cage and sham control groups. However, lipid peroxidation levels were significantly (P < 0.05) lower in Wi-Fi + melatonin group than in Wi-Fi and control groups.
Figure 2: The effects of melatonin on lipid peroxidation levels on lens of Wi-Fi-induced EMR. (Mean ± SD). (mean ± SD). aP < 0.05 versus Wi-Fi and control groups

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Levels of GSH are shown in [Figure 3]. Mean values of cage control, sham control, Wi-Fi and Wi-Fi + melatonin groups as μM/g protein were 3.08, 3.12, 2.95 and 3.41, respectively. The GSH levels were insignificantly decreased in Wi-Fi group. However, GSH levels were significantly (P < 0.05) higher in Wi-Fi + melatonin group than in Wi-Fi group.
Figure 3: The effects of melatonin on reduced glutathione (GSH) levels on lens of Wi-Fi-induced EMR. (Mean ± SD). (mean ± SD). aP < 0.05 versus Wi-Fi group

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Activities of GSH-Px are shown in [Figure 4]. Mean values of cage control, sham control, Wi-Fi and Wi-Fi + melatonin groups as IU/g protein were 9.8, 10.4, 8.8 and 11.4, respectively. The GSH-Px activities were significantly (P < 0.05) lower in Wi-Fi group than in cage and sham control groups. The antioxidant enzyme activities were modulated by melatonin administration and their activities were significantly higher in Wi-Fi + melatonin group than in Wi-Fi (P < 0.01) and control groups (P < 0.05).
Figure 4: The effects of melatonin on reduced glutathione peroxidase (GSH-Px) activities on lens of 2.45 GHz induced EMR. (Mean ± SD). (mean ± SD). aP < 0.05 versus controls. bP < 0.01 versus Wi-Fi group

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GSH is the most prevalent low molecular weight thiol containing antioxidant within mammalian cells. The GSH acts to protect cellular constituents from oxidative damage by directly reacting with oxidants or as the substrate for GSH-Px to scavenge peroxides. [27] It is believed that the high content of GSH in the lens protects thiols in structural proteins and enzymes for proper biological functions. The endogenous high level of GSH plays a crucial role as the first line of defense against exogenous and endogenous ROS and enables lens proteins to remain in a reduced state. [27] The ROS are continuously formed and are detoxified by superoxide dismutase, GSH-Px and catalase. Excessive production of free-radicals and the consumption of antioxidants lead to insufficient endogenous defense mechanisms. Lipid peroxidation values as MDA were increased in the lens samples by the Wi-Fi frequency exposure although GSH-Px activity was decreased by the exposure. The GSH-Px activity decreased in the lens samples because it may relate to the used antioxidants due to decrease ROS production and the compensatory in the antioxidant redox system.

Melatonin, as well as its metabolites, act directly to detoxify ROS such as hydroxyl radicals, peroxynitrite anion, singlet oxygen and reactive nitrogen species such as nitric oxide. [2],[28] Melatonin possesses an electron-rich aromatic indole ring and acts as an electron-donor, thus having the ability to reduce and repair electrophilic radicals. [28] In addition, melatonin stimulates antioxidant enzymes such as superoxide dismutase and GSH-Px and they exert an antioxidative effect, indirectly. [27] Melatonin, as well as its metabolites, terminates the initiation and propagation of lipid peroxidation. [2] Melatonin is a stabilizer of cell membranes against oxidative stress. [28] In the current study we observed GSH and GSH-Px values were increased by melatonin administration although lipid peroxidation levels decreased due to its antioxidant protector effects and free radical scavenger effects. Consistent with results of the current study, studies using ultraviolet radiation [29] and ionize radiation [30] as the oxidant agent, in which antioxidant efficacy of melatonin on the lens was demonstrated, reported that oxidant-antioxidant indicators were similarly affected.

In conclusion, the results presented for Wi-Fi on lens are not consistent with a generalized antioxidant abnormality although melatonin induced modulator role on the over production of ROS. The beneficial effects of melatonin on antioxidant systems included regulation of the lipid peroxidation, GSH-Px and GSH values in the lens.


  Acknowledgment Top


Authorship: MN formulated the present hypothesis. MN and LT were responsible for writing the report. SD was responsible for analysis of the data. ΦT and MCK made critical revision for the manuscript.

 
  References Top

1.
Consales C, Merla C, Marino C, Benassi B. Electromagnetic fields, oxidative stress, and neurodegeneration. Int J Cell Biol 2012;2012:683897.  Back to cited text no. 1
[PUBMED]    
2.
Espino J, Pariente JA, Rodríguez AB. Oxidative stress and immunosenescence: Therapeutic effects of melatonin. Oxid Med Cell Longev 2012.  Back to cited text no. 2
    
3.
The World Health Organization Report. Extremely low frequency fields. Environmental health criteria; 238, 2007. Available from: http://www.who.int/peh-emf/publications/Complet_DEC_2007.pdf  Back to cited text no. 3
    
4.
Li HW, Yao K, Jin HY, Sun LX, Lu DQ, Yu YB. Proteomic analysis of human lens epithelial cells exposed to microwaves. Jpn J Ophthalmol 2007;51:412-6.  Back to cited text no. 4
[PUBMED]    
5.
Nazýroðlu M, Gümral N. Modulator effects of L-carnitine and selenium on wireless devices (2.45 GHz)-induced oxidative stress and electroencephalography records in brain of rat. Int J Radiat Biol 2009;85:680-9.  Back to cited text no. 5
    
6.
Türker Y, Nazýroðlu M, Gümral N, Celik O, Saygýn M, Cömlekçi S, et al. Selenium and L-carnitine reduce oxidative stress in the heart of rat induced by 2.45-GHz radiation from wireless devices. Biol Trace Elem Res 2011;143:1640-50.  Back to cited text no. 6
    
7.
Nazýroðlu M, Yüksel M, Köse SA, Özkaya MO. Recent reports of Wi-Fi and mobile phone-induced radiation on oxidative stress and reproductive signaling pathways in females and males. J Membr Biol. 2013;246:869-75.  Back to cited text no. 7
    
8.
Kocer I, Taysi S, Ertekin MV, Karslioglu I, Gepdiremen A, Sezen O, et al. The effect of L-carnitine in the prevention of ionizing radiation-induced cataracts: A rat model. Graefes Arch Clin Exp Ophthalmol 2007;245:588-94.  Back to cited text no. 8
[PUBMED]    
9.
Kovacic P, Somanathan R. Unifying mechanism for eye toxicity: Electron transfer, reactive oxygen species, antioxidant benefits, cell signaling and cell membranes. Cell Membr Free Radic Res 2008;2:56-69.  Back to cited text no. 9
    
10.
Özkaya D, Nazýroðlu M, Armaðan A, Demirel A, Köroglu BK, Çolakoðlu N, et al. Dietary vitamin C and E modulates oxidative stress induced-kidney and lens injury in diabetic aged male rats through modulating glucose homeostasis and antioxidant systems. Cell Biochem Funct 2011;29:287-93.  Back to cited text no. 10
    
11.
Nazýroðlu M, Dilsiz N, Cay M. Protective role of intraperitoneally administered vitamins C and E and selenium on the levels of lipid peroxidation in the lens of rats made diabetic with streptozotocin. Biol Trace Elem Res 1999;70:223-32.  Back to cited text no. 11
    
12.
Nordberg J, Arner ES. Reactive oxygen species, antioxidants, and the mammalian thioredoxin system. Free Radic Biol Med 2001;31:1287-12.  Back to cited text no. 12
    
13.
Zheng Y, Liu Y, Ge J, Wang X, Liu L, Bu Z, et al. Resveratrol protects human lens epithelial cells against H2O2-induced oxidative stress by increasing catalase, SOD-1, and HO-1 expression. Mol Vis 2010;16:1467-74.  Back to cited text no. 13
[PUBMED]    
14.
Itoh MT, Takahashi N, Abe M, Shimizu K. Expression and cellular localization of melatonin-synthesizing enzymes in the rat lens. J Pineal Res 2007;42:92-6.  Back to cited text no. 14
[PUBMED]    
15.
Alarma-Estrany P, Pintor J. Melatonin receptors in the eye: Location, second messengers and role in ocular physiology. Pharmacol Ther 2007;113:507-22.  Back to cited text no. 15
[PUBMED]    
16.
Nazýroðlu M, Çelik Ö, Özgül C, Çið B, Doðan S, Bal R, et al. Melatonin modulates wireless (2.45 GHz)-induced oxidative injury through TRPM2 and voltage gated Ca (2+) channels in brain and dorsal root ganglion in rat. Physiol Behav 2012;105:683-92.  Back to cited text no. 16
    
17.
Nazýroðlu M, Cið B, Doðan S, Uðuz AC, Dilek S, Faouzi D. 2.45-Gz wireless devices induce oxidative stress and proliferation through cytosolic Ca²⁺ influx in human leukemia cancer cells. Int J Radiat Biol 2012;88:449-56.  Back to cited text no. 17
    
18.
Simþek M, Naziroðlu M, Erdinç A. Moderate exercise with a dietary vitamin C and E combination protects against streptozotocin-induced oxidative damage to the kidney and lens in pregnant rats. Exp Clin Endocrinol Diabetes 2005;113:53-9.  Back to cited text no. 18
    
19.
Placer ZA, Cushman L, Johnson BC. Estimation of products of lipid peroxidation (malonyldialdehyde) in biological fluids. Anal Biochem 1966;16:359-64.  Back to cited text no. 19
    
20.
Sedlak J, Lindsay RH. Estimation of total, protein bound and non-protein sulfhydryl groups in tissue with Ellmann's reagent. Anal Biochem 1968;25:192-205.  Back to cited text no. 20
[PUBMED]    
21.
Lawrence RA, Burk RF. Glutathione peroxidase activity in selenium-deficient rat liver. Biochem Biophys Res Commun 1976;71:952-8.  Back to cited text no. 21
[PUBMED]    
22.
Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin- Phenol reagent. J Biol Chem 1951;193:265-75.  Back to cited text no. 22
[PUBMED]    
23.
Truscott RJ. Age-related nuclear cataract-oxidation is the key. Exp Eye Res 2005;80:709-25.  Back to cited text no. 23
[PUBMED]    
24.
Spector A, Wang GM, Wang RR, Li WC, Kuszak JR. A brief photochemically induced oxidative insult causes irreversible lens damage and cataract. I. Transparency and epithelial cell layer. Exp Eye Res 1995;60:471-81.  Back to cited text no. 24
    
25.
Gupta SK, Trivedi D, Srivastava S, Joshi S, Halder N, Verma SD. Lycopene attenuates oxidative stress induced experimental cataract development: An in vitro and in vivo study. Nutrition 2003;19:794-79.  Back to cited text no. 25
[PUBMED]    
26.
Taylor HR, West SK, Rosenthal FS, Muñoz B, Newland HS, Abbey H, et al. Effect of ultraviolet radiation on cataract formation. N Engl J Med 1999;319:1429-33.  Back to cited text no. 26
    
27.
Lou MF. Redox regulation in the lens. Prog Retin Eye Res 2003;657-82.  Back to cited text no. 27
    
28.
Ekmekcioglu C. Melatonin receptors in humans: Biological role and clinical relevance. Biomed Pharmacother 2006;60:97-108.  Back to cited text no. 28
[PUBMED]    
29.
Bardak Y, Ozertürk Y, Ozgüner F, Durmuº M, Delibaº N. Effect of melatonin against oxidative stress in ultraviolet-B exposed rat lens. Curr Eye Res 2000;20:225-30.  Back to cited text no. 29
    
30.
Karslioglu I, Ertekin MV, Taysi S, Koçer I, Sezen O, Gepdiremen A, et al. Radioprotective effects of melatonin on radiation-induced cataract. J Radiat Res 2005;46:277-82.  Back to cited text no. 30
    


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