Chunhai CHEN, Qinlong MA, Jiawen TAO, et al. Effects of terahertz exposure on skin injury in mouse model[J]. Journal of Third Military Medical University, 2020, 43(23): 2282-2289.
DOI:
Chunhai CHEN, Qinlong MA, Jiawen TAO, et al. Effects of terahertz exposure on skin injury in mouse model[J]. Journal of Third Military Medical University, 2020, 43(23): 2282-2289. DOI: 10.16016/j.1000-5404.202008138.
Effects of terahertz exposure on skin injury in mouse model
To explore the characteristics of biological effects of terahertz (THz) exposure on the skin injury
and investigate the underlying mechanisms.
Methods
2
The hair-removed skin of C57BL/6J mice were exposed to 0.22 THz irradiation
at an average power density of 0
25 and 50 mW/cm
2
respectively
for 5 min. The temperature curve and pathological changes in the exposed area were observed and analyzed. The gene expression in the skin area was detected using RNA-seq analysis and bioinformatics analysis for global changes of the impairment and underlying molecular mechanisms. Finally
ELISA was used to verify inflammatory responses in the skin revealed by RNA-seq.
Results
2
Though 25 mW/cm
2
THz irradiation did not induce obvious temperature change
50 mW/cm
2
THz irradiation exposure significantly raised the temperature higher than 2 ℃
and caused epithelial detachment and bleeding in the exposed area. RNA-seq analysis found 49 genes up-regulated and 27 genes down-regulated in the injured skin area. The following Gene Ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis revealed that these genes were majorly involved in immune responses and inflammatory responses. The results of ELISA indicated that the expression levels of IL-1β
IL-6
and TNF-α were increased remarkably after exposure.
Conclusion
2
THz irradiation exposure causes significant thermal effects and other injuries
including inflammatory responses
and induces abnormal expression of a series of genes in the exposed skin area.
关键词
Keywords
references
CROWE T W, GLOBUS T, WOOLARD D L, et al . Terahertz sources and detectors and their application to biological sensing[J ] . Philos Trans A Math Phys Eng Sci, 2004, 362(1815): 365-377. DOI:10.1098/rsta. 2003.1327.
ZHAO G Z, SHEN Y C, LIU Y. Application of terahertz technology in military and security field[J]. J Electron Meas Instrum, 2015, 29(8): 1097-1101. DOI:10.13382/j.jemi.2015. 08.001.
PLUSQUELLIC D F, SIEGRIST K, HEILWEIL E J, et al . Applications of terahertz spectroscopy in biosystems[J ] . ChemPhysChem, 2007, 8(17): 2412-2431. DOI:10.1002/cphc. 200700332.
SUN J H. Applications and developments of terahertzelectromagnetic wave in biological and medical fields[J]. J Cap Norm Univ Nat Sci Ed, 2004, 25(4): 17-22. DOI:10.3969/j.issn.1004-9398.2004.04.006.
SUN Q, HE Y, LIU K, et al . Recent advances in terahertz technology for biomedical applications[J ] . Quant Imaging Med Surg, 2017, 7(3): 345-355. DOI:10.21037/qims. 2017.06.02.
ROMANENKO S, BEGLEY R, HARVEY A R, et al . The interaction between electromagnetic fields at megahertz, gigahertz and terahertz frequencies with cells, tissues and organisms: risks and potential[J ] . J Royal Soc Interface, 2017, 14(137): 20170585. DOI:10.1098/rsif.2017.0585.
PARKER J E, BEASON C W, STURGEON S P, et al . Revisiting 35 and 94 GHz millimeter wave exposure to the non-human primate eye[J ] . Heal Phys, 2020, 119(2): 206 -215. DOI:10.1097/hp.0000000000001216.
TITOVA L V, AYESHESHIM A K, GOLUBOV A, et al . Intense THz pulses cause H2AX phosphorylation and activate DNA damage response in human skin tissue[J ] . Biomed Opt Express, 2013, 4(4): 559-568. DOI:10.1364/boe.4.000559.
WILMINK G J, RIVEST B D, ROTH C C, et al . In vitro investigation of the biological effects associated with human dermal fibroblasts exposed to 2.52 THz radiation[J ] . Lasers Surg Med, 2011, 43(2): 152-163. DOI:10.1002/lsm.20960..
BONDAR N P, KOVALENKO I L, AVGUSTINOVICH D F, et al . Behavioral effect of terahertz waves in male mice[J ] . Bull Exp Biol Med, 2008, 145(4): 401-405. DOI:10.1007/s10517-008-0102-x.
KIRICHUK V F, ANTIPOVA O N, KRYLOVA Y A. Effect of continuous irradiation with terahertz electromagnetic waves of the NO frequency range on behavioral reactions of male albino rats under stress conditions[J]. Bull Exp Biol Med, 2014, 157(2): 184-189. DOI:10.1007/s10517-014- 2521-1.
ALEXANDROV B S, PHIPPS M L, ALEXANDROV L B, et al . Specificity and heterogeneity of terahertz radiation e ffect on gene expression in mouse mesenchymal stem cells[J ] . Sci Rep, 2013, 3: 1184. DOI:10.1038/srep01184.
FRANCHINI V, DE SANCTIS S, MARINACCIO J, et al . Study of the effects of 0.15 terahertz radiation on genome integrity of adult fibroblasts[J ] . Environ Mol Mutagen, 2018, 59(6): 476-487. DOI:10.1002/em.22192.
KOYAMA S, NARITA E, SHIMIZU Y, et al . Twenty four-hour exposure to a 0.12 THz electromagnetic field does not affect the genotoxicity, morphological changes, or expression of heat shock protein in HCE-T cells[J ] . Int J Environ Res Public Heal, 2016, 13(8): 793. DOI:10.3390/ijerph13080793.
BOGOMAZOVA A N, VASSINA E M, GORYACHKOV-SKAYA T N, et al . No DNA damage response and negligible genome-wide transcriptional changes in human embryonic stem cells exposed to terahertz radiation[J ] . Sci Rep, 2015, 5: 7749. DOI:10.1038/srep07749.
TITOVA L V, AYESHESHIM A K, GOLUBOV A, et al . Intense THz pulses down-regulate genes associated with skin cancer and psoriasis: a new therapeutic avenue?[J ] . Sci Rep, 2013, 3: 2363. DOI:10.1038/srep02363.
TSOY A, SAL IEV T, ABZHANOVA E, et al . The effects of mobile phone radiofrequency electromagnetic fields on β-amyloid-induced oxidative stress in human and rat primary astrocytes[J ] . Neuroscience, 2019, 408: 46-57. DOI:10.1016/j.neuroscience.2019.03.058.
JEONG Y, SON Y, HAN N K, et al . Impact of long-term RF-EMF on oxidative stress and neuroinflammation in aging brains of C57BL/6 mice[J ] . Int J Mol Sci, 2018, 19(7): 2103. DOI:10.3390/ijms19072103.
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Related Author
Peng GAO
Yonghui LU
Qinlong MA
Min LI
Chunhai CHEN
Mindi HE
Zhengping YU
张彦文
Related Institution
Graduate Institute, Chinese PLA Medical School
Department of Laboratory Medicine, First Medical Center, Chinese PLA General Hospital
Department of Nutrition, Nutrition and Food Safety Research Center, Chongqing Medical Nutrition Research Center, Chongqing Key Laboratory of Nutrition and Health, Faculty of Military Preventive Medicine, Army Medical University (Third Military Medical University)
Department of Cardiovascular Surgery, Second Affiliated Hospital, Army Medical University (Third Military Medical University), Chongqing, Nutrition and Food Safety Research Center, Chongqing Medical Nutrition Research Center, Chongqing Key Laboratory of Nutrition and Health, Faculty of Military Preventive Medicine, Army Medical University (Third Military Medical University)
Department of Military Nutrition and Food Hygiene, Nutrition and Food Safety Research Center, Chongqing Medical Nutrition Research Center, Chongqing Key Laboratory of Nutrition and Health, Faculty of Military Preventive Medicine, Army Medical University (Third Military Medical University)