Effects of Microwave 10 GHz Radiation Exposure in the Skin of Rats: An Insight on Molecular Responses
← Research streamRats exposed to 10 GHz at 10 mW/cm2 (3 h/day for 30 days) showed increased skin surface temperature (~1.8°C) and significant changes in oxidative stress, inflammatory, metabolic, and stress-response signaling markers versus sham. Caspase-3 levels were unchang…
Study snapshot
Abstract
Effects of Microwave 10 GHz Radiation Exposure in the Skin of Rats: An Insight on Molecular Responses Saurabh Verma, Gaurav K Keshri, Santanu Karmakar, Kumar Vyonkesh Mani, Satish Chauhan, Anju Yadav, Manish Sharma, Asheesh Gupta. Effects of Microwave 10 GHz Radiation Exposure in the Skin of Rats: An Insight on Molecular Responses. Radiat Res. 2021 Aug 18. doi: 10.1667/RADE-20-00155.1. Abstract Microwave (MW) radiation poses the risk of potential hazards on human health. The present study investigated the effects of MW 10 GHz exposure for 3 h/day for 30 days at power densities of 5.23 ± 0.25 and 10.01 ± 0.15 mW/cm2 in the skin of rats. The animals exposed to 10 mW/cm2 (corresponded to twice the ICNIRP-2020 occupational reference level of MW exposure for humans) exhibited significant biophysical, biochemical, molecular and histological alterations compared to sham-irradiated animals. Infrared thermography revealed an increase in average skin surface temperature by 1.8°C and standard deviation of 0.3°C after 30 days of 10 mW/cm2 MW exposure compared to the sham-irradiated animals. MW exposure also led to oxidative stress (ROS, 4-HNE, LPO, AOPP), inflammatory responses (NFkB, iNOS/NOS2, COX-2) and metabolic alterations [hexokinase (HK), lactate dehydrogenase (LDH), citrate synthase (CS) and glucose-6-phospahte dehydrogenase (G6PD)] in 10 mW/cm2 irradiated rat skin. A significant alteration in expression of markers associated with cell survival (Akt/PKB) and HSP27/p38MAPK-related stress-response signaling cascade was observed in 10 mW/cm2 irradiated rat skin compared to sham-irradiated rat skin. However, MW-irradiated groups did not show apoptosis, evident by unchanged caspase-3 levels. Histopathological analysis revealed a mild cytoarchitectural alteration in epidermal layer and slight aggregation of leukocytes in 10 mW/cm2 irradiated rat skin. Altogether, the present findings demonstrated that 10 GHz exposure in continuous-wave mode at 10 mW/cm2 (3 h/day, 30 days) led to significant alterations in molecular markers associated with adaptive stress-response in rat skin. Furthermore, systematic scientific studies on more prevalent pulsed-mode of MW-radiation exposure for prolonged duration are warranted. pubmed.ncbi.nlm.nih.gov
AI evidence extraction
Structured fields below were generated from the paper’s abstract and metadata to make the evidence easier to inspect. Automated extraction may be incomplete or incorrect; verify important details against the original paper.
Main findings
Rats exposed to 10 GHz at 10 mW/cm2 (3 h/day for 30 days) showed increased skin surface temperature (~1.8°C) and significant changes in oxidative stress, inflammatory, metabolic, and stress-response signaling markers versus sham. Caspase-3 levels were unchanged (no evidence of apoptosis), and histology showed mild epidermal cytoarchitectural alteration with slight leukocyte aggregation at 10 mW/cm2.
Outcomes measured
- Skin surface temperature (infrared thermography)
- Biophysical/biochemical/molecular alterations in skin
- Oxidative stress markers (ROS, 4-HNE, LPO, AOPP)
- Inflammatory markers (NFkB, iNOS/NOS2, COX-2)
- Metabolic enzymes/markers (HK, LDH, CS, G6PD)
- Cell survival/stress signaling markers (Akt/PKB, HSP27/p38MAPK)
- Apoptosis marker (caspase-3)
- Histopathology (epidermal cytoarchitecture, leukocyte aggregation)
Limitations
- Sample size not reported in abstract
- Only rat skin studied; generalizability to humans not addressed in abstract
- Exposure described as continuous-wave; authors note need for studies on pulsed-mode exposure
- Lower power density group (5.23 mW/cm2) results not detailed in abstract
View raw extracted JSON
{
"study_type": "animal",
"exposure": {
"band": "microwave",
"source": null,
"frequency_mhz": 10000,
"sar_wkg": null,
"duration": "3 h/day for 30 days; continuous-wave; power densities 5.23 ± 0.25 and 10.01 ± 0.15 mW/cm2"
},
"population": "Rats (skin)",
"sample_size": null,
"outcomes": [
"Skin surface temperature (infrared thermography)",
"Biophysical/biochemical/molecular alterations in skin",
"Oxidative stress markers (ROS, 4-HNE, LPO, AOPP)",
"Inflammatory markers (NFkB, iNOS/NOS2, COX-2)",
"Metabolic enzymes/markers (HK, LDH, CS, G6PD)",
"Cell survival/stress signaling markers (Akt/PKB, HSP27/p38MAPK)",
"Apoptosis marker (caspase-3)",
"Histopathology (epidermal cytoarchitecture, leukocyte aggregation)"
],
"main_findings": "Rats exposed to 10 GHz at 10 mW/cm2 (3 h/day for 30 days) showed increased skin surface temperature (~1.8°C) and significant changes in oxidative stress, inflammatory, metabolic, and stress-response signaling markers versus sham. Caspase-3 levels were unchanged (no evidence of apoptosis), and histology showed mild epidermal cytoarchitectural alteration with slight leukocyte aggregation at 10 mW/cm2.",
"effect_direction": "harm",
"limitations": [
"Sample size not reported in abstract",
"Only rat skin studied; generalizability to humans not addressed in abstract",
"Exposure described as continuous-wave; authors note need for studies on pulsed-mode exposure",
"Lower power density group (5.23 mW/cm2) results not detailed in abstract"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"10 GHz",
"microwave radiation",
"rat skin",
"power density",
"continuous-wave",
"ICNIRP-2020 occupational reference level",
"oxidative stress",
"inflammation",
"NFkB",
"iNOS",
"COX-2",
"HSP27",
"p38MAPK",
"Akt/PKB",
"infrared thermography",
"histopathology"
],
"suggested_hubs": [
{
"slug": "who-icnirp",
"weight": 0.6,
"reason": "Abstract explicitly references ICNIRP-2020 occupational reference level."
},
{
"slug": "occupational-exposure",
"weight": 0.45,
"reason": "Exposure level is compared to an occupational reference level."
}
]
}AI-extracted fields are generated from the abstract and metadata and may be incomplete or incorrect. This material is for informational purposes and is not medical advice.
Identifiers and source
DOI: 10.1667/rade-20-00155.1
PubMed: 34407201
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