Journal List > Korean J Obstet Gynecol > v.53(11) > 1006497

Hwang, Na, Lee, Lee, Lee, Kim, Choi, and Hwang: Generation accumulation of murine ovarian genes in offspring exposed to microwave in uterus

Abstract

Objective

The aim of this study was to evaluate generational accumulation of murine fetal ovarian genes following prenatal exposure to 1.765-GHz microwave radiation.

Methods

A 1.765-GHz microwave generator was used. Twenty pregnant ICR mice were divided into two groups: the microwave-exposed experimental (irradiated) group, and the sham-exposed (sham) group. On the fifth day post-mating, dam mice were exposed to microwave irradiation in the insulated cage for 8 hours each day. The remaining mice were treated in the same way. Second generation mice were raised for 8 weeks then classified into four groups for examination. We removed the neonatal ovaries on the seventh day after the third delivery. We investigated the expression of six genes in the ovaries: Tnfaip 8, TNFsf 12, Cfd, CCL 11, Zfp 74, and Brd 3. Real time reverse transcription-polymerase chain reaction was performed using total RNA extracted from the removed ovaries.

Results

In the third-generation offspring, we detected some differences in ovarian gene expression between the first group and the fourth. Expression of CCL 11, and TNFsf 12 was decreased in the first group compared to the fourth group. Expression of Tnfaip 8, brd 3, Cfd, and Zfp 74 was higher in the first group than in the fourth group. We found differing results when we compared ovarian gene expression in mice of the second generation with those of the third.

Conclusion

The results suggest that there is no generational accumulation of murine ovarian genes in offspring exposed to 1.765-GHz microwaves in the uterus.

Figures and Tables

Figure 1
The comparison of birth weight in pregnant mice of the second generation. The birth weight of the first group is not different from that in the fourth group. However, that of the second group is decreased compared with other groups. aP<0.05 between 4 group and other groups, bP<0.05 between 1 group and other groups, cP<0.05 between 2 group and other groups.
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Figure 2
The comparison of number of offspring per pregnant mice of the second generation. The number of offspring in the first group is not different from that in the fourth group. However, the number of offspring in the second group is significantly increased compared with that in other groups. aP<0.05 between 4 group and other groups, bP<0.05 between 1 group and other groups, cP<0.05 between 2 group and other groups.
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Figure 3
The results of TNFaip 8 and CCL gene expression by real time reverse transcription-polymerase chain reaction. Expression of CCL 11, and TNFsf 12 was decreased in the first group compared to the fourth group. aP<0.05 between 4 group and other groups, bP<0.05 between 1 group and other groups, cP<0.05 between 2 group and other groups.
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Figure 4
The results of Tnfsf 12, Zfp 74, Cfd, and Brd 3 gene expression by real time reverse transcription-polymerase chain reaction. Expression of Tnfaip 8, brd 3, Cfd, and Zfp 74 was higher in the first group than in the fourth group. aP<0.05 between 4 group and other groups, bP<0.05 between 1 group and other groups, cP<0.05 between 2 group and other groups.
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Table 1
Primers used for reverse transcription-polymerase chain reaction
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Brd 3: bromodomain containing 3, CCL: chemokine (C-C motif) ligands, Cfd: complement factor D, TNFaip 8: tumor necrosis factor alpha induced protein 8, TNFsf 12: tumor necrosis factor superfamily 12, Zfp 74: zinc finger protein 74.

Table 2
The comparison of the body temperature between both groups
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Mann-Whitney U test.

Values are presented as mean±standard deviation.

Table 3
The comparison of the pregnancy period, the body weight at birth, the number of offspring each pregnant mouse between both groups on the 2nd generation
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*Student t-test, Mann-Whitney U test.

Values are presented as mean±standard deviation.

References

1. Heynick LN, Johnston SA, Mason PA. Radio frequency electromagnetic fields: cancer, mutagenesis, and genotoxicity. Bioelectromagnetics. 2003. Suppl 6. 74–100.
crossref
2. Wertheimer N, Leeper E. Electrical wiring configurations and childhood cancer. Am J Epidemiol. 1979. 109:273–284.
crossref
3. Merritt CR, Kremkau FW, Hobbins JC. Diagnostic ultrasound: bioeffects and safety. Ultrasound Obstet Gynecol. 1992. 2:366–374.
crossref
4. Robert E. Intrauterine effects of electromagnetic fields (low frequency, mid-frequency RF, and microwave): review of epidemiologic studies. Teratology. 1999. 59:292–298.
5. Ahlbom A, Green A, Kheifets L, Savitz D, Swerdlow A. Epidemiology of health effects of radiofrequency exposure. Environ Health Perspect. 2004. 112:1741–1754.
6. Hwang JY, Na SH, Lee HA, Lee DH, Lee HJ, Kim SI, et al. Microarray analysis of gene expression in mice ovaries exposed to a 1.765 GHz microwave in utero. Korean J Obstet Gynecol. 2009. 52:602.
7. Ortner MJ, Galvin MJ, McRee DI. Studies on acute in vivo exposure of rats to 2450-MHz microwave radiation. Radiat Res. 1981. 86:580–588.
8. Bergonie J, Tribondeau L. Interpretation of some results from radiotherapy and an attempt to determine a rational treatment technique. 1906. Yale J Biol Med. 2003. 76:181–182.
9. Michaelson SM. Health implications of exposure to radiofrequency/microwave energies. Br J Ind Med. 1982. 39:105–119.
crossref
10. Ritenour ER. Health effects of low level radiation: carcinogenesis, teratogenesis, and mutagenesis. Semin Nucl Med. 1986. 16:106–117.
11. Wertheimer N, Savitz DA, Leeper E. Childhood cancer in relation to indicators of magnetic fields from ground current sources. Bioelectromagnetics. 1995. 16:86–96.
crossref
12. Sigler AT, Lilienfield AM, Cohen BH, Westake IE. Radiation exposure in parents of children with mongolism (Down's syndrome). Bull Johns Hopk Hosp. 1965. 117:374–399.
13. Cohen BH, Lilienfield AM, Kramer S, Hyman LC. Hook EB, Porter IH, editors. Parental factors in Down's syndrome: results of the second 'Baltimore case-control study.'. Population cytogenetics studies in humans. 1977. New York: Academic Press;301–352.
14. Larsen AI, Olsen J, Svane O. Gender-specific reproductive outcome and exposure to high-frequency electromagnetic radiation among physiotherapists. Scand J Work Environ Health. 1991. 17:324–329.
crossref
15. Guberan E, Campana A, Faval P, Guberan M, Sweetnam PM, Tuyn JW, et al. Gender ratio of offspring and exposure to shortwave radiation among female physiotherapists. Scand J Work Environ Health. 1994. 20:345–348.
crossref
16. Larsen AI. Congenital malformations and exposure to high-frequency electromagnetic radiation among Danish physiotherapists. Scand J Work Environ Health. 1991. 17:318–323.
crossref
17. Lindbohm ML, Hietanen M, Kyyronen P, Sallmen M, von Nandelstadh P, Taskinen H, et al. Magnetic fields of video display terminals and spontaneous abortion. Am J Epidemiol. 1992. 136:1041–1051.
crossref
18. Berman E, Carter HB. Decreased body weight in fetal rats after irradiation with 2450-MHz (CW) microwaves. Health Phys. 1984. 46:537–542.
crossref
19. Nawrot PS, McRee DI, Staples RE. Effects of 2.45 GHz CW microwave radiation on embryofetal development in mice. Teratology. 1981. 24:303–314.
crossref
20. Heynick LN, Merritt JH. Radiofrequency fields and teratogenesis. Bioelectromagnetics. 2003. Suppl 6. S174–S186.
crossref
21. Nakamura H, Matsuzaki I, Hatta K, Nobukuni Y, Kambayashi Y, Ogino K. Nonthermal effects of mobile-phone frequency microwaves on uteroplacental functions in pregnant rats. Reprod Toxicol. 2003. 17:321–326.
crossref
22. Ono T, Saito Y, Komura J, Ikehata H, Tarusawa Y, Nojima T, et al. Absence of mutagenic effects of 2.45 GHz radiofrequency exposure in spleen, liver, brain, and testis of lacZ-transgenic mouse exposed in utero. Tohoku J Exp Med. 2004. 202:93–103.
crossref
23. Diem E, Schwarz C, Adlkofer F, Jahn O, Rudiger H. Non-thermal DNA breakage by mobile-phone radiation (1800 MHz) in human fibroblasts and in transformed GFSH-R17 rat granulosa cells in vitro. Mutat Res. 2005. 583:178–183.
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