Effect of ultraviolet-B radiation on intact cells of the cyanobacterium Spirulina platensis: characterization of the alterations in the thylakoid membranes

Intact trichomes of Spirulina platensis are exposed to ultraviolet- B (UV-B) radiation (270-320 nm; 1.9 mW m(-2)) for 9 h. This UV-B exposure results in alterations in the pigment-protein complexes and in the fluorescence emission profile of the chlorophyll-protein complexes of the thylakoids as compared with thylakoids isolated from control dark-adapted Spirulina cells. The UV-B exposure causes a significant decrease in photosystem II activity, but no loss in photosystem I activity. Although there is no change in the photosystem I activity in thylakoids from UV-B-exposed cells, the chlorophyll a emission at room temperature and at 77 K indicates alterations associated with photosystem I. Additionally, the results clearly demonstrate that the photosystem II core antennae of chlorophyll proteins CP47 and CP43 are affected by UV-B exposure, as revealed by Western blot analysis. Furthermore, a prominent 94 kDa protein band appears in the sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE) profile of UV-B-exposed cell thylakoids, which is absent from the control thylakoids. This 94 kDa protein appears not to be newly induced by UV-B exposure, but could possibly have originated from the UV-B-induced cross-linking of the thylakoid proteins. The exposure of isolated Spirulina thylakoids to the same intensity of UV-B radiation for 1-3 h induces losses in the CP47 and CP43 levels, but does not induce the appearance of the 94 kDa protein band in SDS-PAGE. These results clearly demonstrate that prolonged exposure of Spirulina cells to moderate levels of UV-B affects the chlorophyll a-protein complexes and alters the fluorescence emission spectral profile of the pigment-protein complexes of the thylakoid membranes. Thus, it is clear that chlorophyll a antennae of Spirulina platensis are significantly altered by UV-B radiation.     

Estimation of the annual solar UVR exposure dose of infants and small children in tropical Queensland, Australia

The solar ultraviolet radiation (UVR) exposure of infants and small children was measured for 1 week using UVR-sensitive polysulfone film attached to the shoulder and chest of the subjects. For the infant study, shoulder and chest badges received similar exposures, while the 2 1/2-year-olds received higher exposures on the shoulder than on the chest. Also, the 2 1/2-year-olds generally received higher exposures than the infants. The median total daily exposures for both groups were 39 and 92 J/m2. The maximum total daily exposures measured were 640 J/m2 (chest) and 240 J/m2 (shoulder) for the infants and 2060 J/m2 (shoulder) and 840 J/m2 (chest) for the 2 1/2 year-olds. Using this exposure data, monthly and annual exposure doses were calculated for both groups and compared to similar data from the UK. The annual exposure dose for infants is 8.4 kJ/m2 or 84 standard erythemal dose (SED) for both shoulder and chest. The annual exposure dose for 2 1/2 year-old children is 39.4 kJ/m2 or 394 SED for the shoulder and 28.8 kJ/m2 or 288 SED for the chest. Apart from the generally higher annual exposure doses experienced by the infants and 2 1/2 year-old children in Townsville, the main difference to the UK is the almost nonexistent drop in monthly exposure doses between summer and winter in Townsville compared to the UK. In the UK, the winter-month exposure dose is only 0.5% of the summer-month dose. However, in Townsville it is around 40%.     

Theoretical study of the effect of radiation on thymine

The possible effects of radiation exposure to DNA are studied by investigations for the thymine residue. Detailed analysis of the various addition and other products is undertaken theoretically, using the semiempirical AM1 procedure. The results agree with the experimental finding that the loss of hydrogen on radiation exposure occurs from the C₅-methyl group and hydroxyl radical addition occurs at C₆, yielding the ‘5-yl’ radical. This radical is nonplanar, the axial conformer being slightly preferred over the equatorial one. In contrast, the other possible radical, the ‘6-yl’ radical, is almost planar. These results are important in understanding the conformational changes in DNA as a consequence of radiation exposure.     

Improvement of the wetting and absorption properties of lignocellulosic fibers by means of gas phase ozonation

Gas phase ozonation was done on sheets made from chemical thermomechanical pulp in order to improve the wetting properties of the lignocellulosic fibers. The degree of modification was varied by letting the reaction continue for different lengths of time, ranging from 1 to 60 min. Changes in the chemistry of the fibers after ozone exposure were investigated using Fourier transform infrared (FT-IR) spectroscopy and electron spectroscopy for chemical analysis (ESCA). The evolution of a carbonyl signal and the decrease of aromatic absorption over time was observed with FT-IR spectroscopy. The carbonyl peak grew in intensity as the reaction continued throughout the whole range of treatment times. The ESCA showed that carbonyl and carboxyl functionalities were introduced after 10 min of ozone exposure and that the intensity of the peak from the aliphatic and aromatic carbons decreased. However, an ozone treatment longer than 15 min did not affect the chemical surface composition, as analyzed by ESCA. The single-fiber contact angle with water, measured using a Cahn balance, decreased with extended ozonation. Measuring the time required for the sheet to absorb a water droplet with a high speed camera showed that even a very short ozone exposure (1 min) dramatically affected the absorption behavior. The rate of absorption dramatically increased after as little as 1 min of ozone exposure. This improvement in absorption rate was most likely due to the formation of low molecular weight degradation products, acting as wetting agents, created during the ozonation.     

Determination of cyanide exposure by gas chromatography-mass spectrometry analysis of cyanide-exposed plasma proteins

Exposure to cyanide can occur in a variety of ways, including exposure to smoke from cigarettes or fires, accidental exposure during industrial processes, and exposure from the use of cyanide as a poison or chemical warfare agent. Confirmation of cyanide exposure is difficult because, in vivo, cyanide quickly breaks down by a number of pathways, including the formation of both free and protein-bound thiocyanate. A simple method was developed to confirm cyanide exposure by extraction of protein-bound thiocyanate moieties from cyanide-exposed plasma proteins. Thiocyanate was successfully extracted and subsequently derivatized with pentafluorobenzyl bromide for GC-MS analysis. Thiocyanate levels as low as 2.5 ng mL⁻¹ and cyanide exposure levels as low as 175 μg kg⁻¹ were detected. Samples analyzed from smokers and non-smokers using this method showed significantly different levels of protein-bound thiocyanate (p < 0.01). These results demonstrate the potential of this method to positively confirm chronic cyanide exposure through the analysis of protein-bound cyanide in human plasma.     

Kinetic study of the cationic photopolymerization of epoxy monomers

The photoinitiated cationic polymerization of di-epoxy monomers has been studied using real-time infrared (RTIR) spectroscopy. The polymerization rate and the amount of unreacted monomer were determined directly from the conversion vs. time curves recorded. The cure speed was greatly increased by using a Kr⁺ laser (337.4 nm) as radiation source. A 0.25 s exposure proved sufficient to make react more than 60% of the epoxy groups. The overall polymerization quantum yield was evaluated to be 200 mol photon^-1. Dark polymerization was shown to develop extensively after the UV exposure for about 30 min and may represent up to 80% of the total process. The hardening of the UV-cured tack-free coating was found to occur mainly in the dark, leading after 1 h to a very hard and glassy material. A bimolecular chain termination process is postulated to account for the decay profile of the reactive species observed after UV exposure.     

Sensitivity of the retina to radiation damage as a function of wavelength.

Abstract—Exposure of the retina of the rhesus monkey to visible and infrared radiation from CW optical sources like the Sun, xenon lamps, etc. produces small lesions or scotomata which may be classified as thermal or photochemical, depending on the wavelength and duration of exposure. The action spectrum for the production of retinal lesions has been determined for eight monochromatic laser wavelengths extending from 1064 to 441 nm. The corneal power required to produce a lesion decreases by three orders of magnitude in going from 1064 to 441 nm. Exposure to 1064 nm radiation for 1000 s produces a typical thermal lesion at elevated retinal temperatures. whereas a 1000 s exposure to 441 nm light produces a photochemical lesion at power levels too low to raise the retinal temperature by an appreciable amount (<0.1°). The two types of lesion have entirely different characteristics as will be discussed in some detail. The photopathology of thc photochemical lesion has been studied at postexposure times ranging from 1 h to 90 days and will be demonstrated in a number of histological slides. Moreover, this photopathology correlates well with monocular visual acuity tests in the rhesus monkey as defined by the Landolt ring technique. To further elucidate the differential effects on the retina of short vs long wavelength CW radiation, we have divided a simulated solar spectrum at sea level into two spectral bands. 400–800 nm and 700–1400 nm, and determined the radiant exposures required to produce very mild lcsions on the rhesus retina for exposure times of 1, 10, 100 and 1000 s. To correlate our data with solar retinitis and eclipse blindness the image diameter or spot size on the retina was 159 μm, corresponding to the image size of the Sun on the human retina. Exposure to the 400–800 nm spectrum for durations of 10 s or greater required approximately 400 J/cm² to produce a mild photochemical lesion. Reciprocity is maintained over the exposure range 10–1000 s. Radiant exposure to the 700–1400 nm spectrum, on the other hand, required roughly 69,100 J/cm² for a 1000 s exposure. This was a mild thermal lesion. We were unable to produce a lesion for exposure times less than 1000 s. We interpret these data to mean that solar retinitis and eclipse blindness are primarily photochemical events produced by the short wavelength component of the solar spectrum, and that the infrared component of the solar spectrum plays only a minor role in these retinal pathologies.     

Methods for the isolation and detection of etheno adducts in nucleotide pools in vivo following exposure to ethyl carbamate

Cellular extraction and high-performance liquid chromatographic methods were developed for the isolation of etheno adducts from nucleotide pools formed in vivo following exposure to the chemical carcinogen ethyl carbamate. These techniques were employed to detect etheno adduct formation using BDF1 mice and rainbow trout (Salmo gairdneri) as test species following inter-peritoneal injection of the chemical. Ethenoadenine was detected in splenocyte nucleotide pools of mice after acute (24 h) exposure and chronic (two weeks) exposure. Several etheno adducts (i.e. ethenoadenine, etheno-AMP, etheno-ADP and etheno-ATP) were also detected in total spleen cell nucleotide pools of trout following acute ethyl carbamate exposure.     

Patterns in the received facial UV exposure of school children measured at a subtropical latitude

Polysulfone (PS) dosimeters have been employed to measure the erythemally effective UV exposure to the vertex, nose, cheek, chin and side facial sites of 45 volunteer high school students from Hervey Bay, Australia (25.3 degrees S 152.9 degrees E). The results of a series of 1 h outdoor sport trials (basketball and soccer) found the mean student facial exposure, determined as the arithmetic average of facial site exposures of unprotected students (no hat) to protected students (hat), varied from 140 +/- 82 J m(-2) (1sigma) to 99 +/- 33 J m(-2) (1sigma), respectively. All hourly student facial exposures recorded over the study period were found to exceed the National Health and Medical Research Council's adopted safe daily limit of 30 J m(-2). Facial exposure relative to the received ambient UV increased to the nose at higher (winter) solar zenith angles (SZAs) compared with lower (summer) SZA ranges for both protected and unprotected students. The protection offered by the broad-brimmed hats was reduced significantly to the lower chin facial site at the higher SZA range, indicating that the style of hat used offers best protection in summer to the upper facial regions at most risk of receiving a high exposure when no hat protection is used. Variations to specific student facial exposure sites were measured between both basketball and soccer players. Variation in student facial exposure was further examined with respect to cloud cover and comparisons to manikin headform measurements were also made. The study results indicate that hats alone are not adequate forms of sun protection in a school environment. Schools aiming to achieve acceptable safe limits of facial exposure may need to further consider the effectiveness of hat protection with increasing SZA, cloud cover and head position relative to the sun that is specific to the scheduled outdoor activity.     

Absorption kinetics of uranium tri-n-butyl phosphate in the rat: Implications for occupational exposure

The absorption kinetics for uranium into blood after deposition as tri-n-butylphosphate (UTBP) in the rat lung were combined with human data on particle deposition and clearance from the ICRP Publication 66 respiratory tract model and information from the most recent ICRP biokinetic model for uranium to predict the consequences for exposure of workers. These predictions suggest that, (1) the biokinetics of UTBP are similar to those for a Type F compound as defined by ICRP, (2) the dose coefficient is essentially independent of the aerosol size and isotopic composition, (3) the mass of uranium equivalent to the ALI can vary by 13 fold depending upon the isotopic composition, (4) intakes of uranium as UTBP other than chronic intakes as highly enriched forms should be restricted on the basis of the chemical toxicity of uranium, (5) the assessment of intake by urine bioassay measurements should be interpreted with caution unless the exposure conditions are well defined and (6) severe kidney damage is unlikely at intakes corresponding to the ALI or daily limit.     

UV Radiation and Mouse Models of Herpes Simplex Virus Infection

Orolabial human infections with herpes simplex virus type 1 (HSV-1) are very common; following the primary epidermal infection, the virus is retained in a latent form in the trigeminal ganglia from where it can reactivate and cause a recrudescent lesion. Recrudescences are triggered by various stimuli including exposure to sunlight. In this review three categories of mouse models are used to examine the effects of UV irradiation on HSV infections: these are UV exposure prior to primary infection, UV exposure as a triggering event for recrudescence and UV exposure prior to challenge with virus in mice already immunized to HSV. In each of these models immunosuppression occurs, which is manifest, in some instances, in increased morbidity or an increased rate of recrudescence. Where known, the immunological mechanisms involved in the models are summarized and their relevance to human infections considered.     

Determination of the herbicide diclofop in human urine

A simple and sensitive method for the gas chromatographic determination of diclofop residues in human urine is described. Recoveries of diclofop, as its methyl ester, from fortified urine were greater than 85% at 100, 50, 10 and 1 μg kg⁻¹, and were similar with and without the inclusion of a hydrolytic step in the analytical method. However, a hydrolytic step was necessary for analysis of 24-h urine samples collected from a male applicator following a single exposure to diclofop-methyl during application to wheat using a tractor-pulled sprayer. Diclofop residues determined with hydrolysis were approximately double those without hydrolysis, suggesting that a significant portion of diclofop was excreted in the conjugated form.     

A study on the dispersion, preparation, characterization and photo-degradation of polypropylene traced with rare earth oxides

This research work deals with the effect of rare earth oxides on the PP matrix with respect to the thermal and mechanical properties and to the photo-degradation under UV irradiation exposure. The rare earth oxides are used as tracers for the identification of polymer materials, in order to have an economically efficient recycling and high speed automatic sorting of plastic wastes. The addition of 0.1 wt% of such particles of a micrometric size has a minor effect on the mechanical and thermal properties of the traced materials, as well as on the photo-degradation of the polymer after UV irradiation exposure. For 1 wt% tracer content, before UV irradiation treatment, the melting and crystallization temperatures as well as the thermal stability of the PP matrix are slightly increased, whereas the elongation at break decreases from 10 to 50% for a cross-head speed of 250 mm/min. However, the addition of 1 wt% of CeO₂ improves the photo-degradation resistance of the PP matrix to UV exposure due to the UV light screening effects offered by these particles. The SEM images together with the results obtained from image processing show a homogenous dispersion of tracers in the PP matrix.     

Surfactant removal and silica condensation during the photochemical calcination of thin film silica mesophases

The evolution of photochemical surfactant removal and silica condensation from organically templated thin film silica nanocomposites with mesoscopic ordering has been probed using a combined application of Fourier transform infrared (FT-IR) spectroscopy and single wavelength ellipsometry. Thin films of silica nanocomposites were prepared by a previously reported evaporation-induced self-assembly process. Specifically, oxidized silicon and gold substrates were withdrawn at 25 mm/min from a subcritical micelle concentration solution containing an ethylene oxide surfactant as a structure-directing agent and tetraethyl orthosilicate as a silica precursor. Real-time grazing incidence difference FT-IR spectra of the nanocomposite films on gold taken during exposure to short-wavelength ultraviolet light (184-257 nm) show that surfactant removal and silica condensation occur gradually and concomitantly. Surfactant removal and silica reconstructions were found to be nearly complete after 90 min of exposure. Further, a transient feature was observed in the FT-IR spectra around 1713 cm(-1) during the UV exposure process and was assigned to a carbonyl (C=O) stretching mode absorption, reflecting the transient formation of a partially oxidized surfactant intermediate. From these data we propose a stepwise model for surfactant removal from the nanocomposite films. Ellipsometrically determined index of refraction values collected as a function of UV exposure are also shown to support such a stepwise mechanism of surfactant removal from the ordered nanocomposite silica thin film mesophases studied here.     

Vapor Treatment of Electrospray Droplets: Evidence for the Folding of Initially Denatured Proteins on the Sub-Millisecond Time-Scale

The exposure of electrospray droplets generated from either highly acidic or highly basic solutions to basic or acidic vapors, respectively, admitted into the counter-current drying gas, has been shown to lead to significant changes in the observed charge state distributions of proteins. In both cases, distributions of charge states changed from relatively high charge states, indicative of largely denatured proteins, to lower charge state distributions that are more consistent with native protein conformations. Ubiquitin, cytochrome c, myoglobin, and carbonic anhydrase were used as model systems. In some cases, bimodal distributions were observed that are not noted under any solution pH conditions. The extent to which changes in charge state distributions occur depends upon the initial solution pH and the pK_a or pK_b of the acidic or basic reagent, respectively. The evolution of charged droplets in the sampling region of the mass spectrometer inlet aperture, where the vapor exposure takes place, occurs within roughly 1 ms. The observed changes in the spectra, therefore, are a function of the magnitude of the pH change as well as the rates at which the proteins can respond to this change. The exposure of electrospray droplets in this fashion may provide means for accessing transient folding states for further characterization by mass spectrometry.     

A Case–Sibling Assessment of the Association Between Skin Pigmentation and Other Vitamin D-related Factors and Type 1 Diabetes Mellitus

Fair skin pigmentation has been associated with a higher risk of type 1 diabetes mellitus (T1DM). The aim is to compare children with T1DM directly to a sibling in relation to their skin pigmentation in sun-exposed and unexposed sites, past sun exposure and methylation of the VDR gene promoter. The sample consisted of children with T1DM attending a diabetes outpatient clinic and siblings (total n  = 42). Cutaneous melanin density was estimated using a spectrophotometer. Parental report on past sun exposure was obtained. DNA methylation analysis of the VDR gene promoter was conducted. Matched data analysis was performed comparing each case directly to their sibling. Cases were significantly more likely to have lighter skin pigmentation at the upper arm (AOR 0.69 [95% CI: 0.52, 0.90]; P  = 0.01). Low infant sun exposure was imprecisely associated with a two-fold increase in T1DM risk (AOR 2.43 [95% CI: 0.91, 6.51]; P  = 0.08 for under 1 h of winter sun exposure per leisure day). The VDR gene promoter was completely unmethylated in both cases and siblings. The previously demonstrated association between light skin pigmentation and T1DM risk was evident even in this comparison across sibling pairs. Further work on past UVR exposure and related factors such as skin pigmentation is required.     

Investigation of the stability of polyelectrolyte multilayer coatings in open-tubular capillary electrochromatography using laser scanning confocal microscopy

A simple polyelectrolyte multilayer (PEM) coating procedure was used for the development of stable modified capillaries. PEM coatings were constructed in fused-silica capillaries using alternating rinses of cationic and anionic polyelectrolytes. The multilayer coatings investigated in this study consisted of two and twenty layer pairs, or bilayers. A bilayer is one layer of a cationic polymer and one layer of an anionic polymer. Poly(diallyldimethylammonium chloride) was used as the cationic polymer, and the polymeric surfactant poly(sodium N-undecanoyl-L-leucylvalinate) was used as the anionic polymer. Previous studies for both chiral and achiral separations have shown that PEM-coated capillaries have excellent reproducibilities, remarkable endurance, and strong stabilities against extreme pH values when used in open-tubular capillary electrochromatography (OT-CEC). In this study, the stability of the coatings was further investigated after exposure to 0.1 M and 1.0 M NaOH. Structural changes of these coatings were monitored using laser scanning confocal microscopy (LSCM) after flushing the capillaries with NaOH. This technique allowed observation of the degradation of the coatings. Observations are discussed in terms of separations using OT-CEC. Electropherograms obtained from the chiral separation of 1,1'-binaphthyl-2,2'-dihydrogenphosphate in OT-CEC showed a decrease in selectivity and an increase in electroosmotic mobility after long exposure to NaOH. The ability to recover the capillaries by exposure to NaOH was also demonstrated. Measurements of electroosmotic mobility and selectivity showed that 2-bilayer and 20-bilayer PEM coatings could be completely removed from the capillary surface after approximately 3.5 and 9.5 h, respectively, of continuous exposure to 1 M NaOH.     

Investigation of the hydrothermal stability of cross-linked liquid silicone rubber (LSR)

We investigate the hydrothermal stability of cross-linked liquid silicone rubber (LSR) in water at 100 °C up to period of two years. Optical microscopy of cross-sections of the exposed samples reveal that only the outer 100 μm of the surface layer is affected after two years. However, the surface chemistry of the material after prolonged exposure becomes significantly modified, as monitored by X-ray photoelectron spectroscopy (XPS) and attenuated total reflectance Fourier transform infrared (ATR-FTIR), which probes depths of 10 nm and 1 μm, respectively. In addition, changes to the bulk physical properties of the rubber samples, prior to and after the exposure, were investigated by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). Micro-hardness analysis showed that surface roughness of the two year exposed sample increased from 60 (IRHD) to 75 (IRHD). Furthermore, the volume change (%) measurement showed a significant decrease in the course of exposure at prolonged time. The results provide the experimental basis for development of LSR materials suitable for numerous technical applications.     

Performance evaluation of the GastroPlusTM software tool for prediction of the toxicokinetic parameters of chemicals

ABSTRACT

The accurate prediction of toxicokinetic parameters arising from oral, dermal and inhalation routes of chemical exposure is a key element in chemical safety assessments. In this research, the physiologically based pharmacokinetic (PBPK) GastroPlus^TM software was evaluated against a series of chemicals for the prediction of toxicokinetic parameters. Overall, 67% of predicted intrinsic clearance (Clint) values were within 1- to 10-fold of empirical data for 463 compounds, and 87% of the predicted fraction unbounded in plasma (Fup) values were 1- to 3-fold of empirical data for 441 compounds. The r² (coefficient of determination) of predicted C_max (maximum plasma concentration) and AUC (Area Under Curve) values versus the corresponding empirical values from oral, inhalation and dermal exposures ranged from 0.04 to 0.92. Among the three exposures, the highest r² values, ranging from 0.80 to 0.92, were observed for oral exposure predictions, where 88% of the compounds had 1- to 10-fold differences between predicted and empirical values for C_max and AUC. The predicted plasma C_ss (steady-state plasma concentration) values were consistent with those C_ss values calculated by in vitro-to-in vivo extrapolation (IVIVE) approaches using experimental parameters. Based on the evaluation results, GastroPlus? can be used as a QSAR/PBPK tool for toxicokinetic parameter predictions.     

Effects of isothermal 2.45 GHz microwave radiation on the mammalian cell cycle: comparison with effects of isothermal 27 MHz radiofrequency radiation exposure

Synchronized Chinese hamster ovary (CHO) cells were exposed to continuous wave (CH) 2.45 GHz microwave radiation (MWR) or CW 27 MHz radiofrequency radiation (RFR) under isothermal conditions (37±0.2°) to test the following hypotheses: (1) high frequency electromagnetic radiation exposure directly affects the mammalian cell cycle in the absence of radiation-induced heating; and (2) the magnitude of the cell cycle alteration is frequency dependent. CHO cells in either G₀/G₁-, S−, or G₂/M-phase of the cell cycle were simultaneously exposed to CW 27 MHz RFR or CW 2.45 GHz MWR at specific absorption rates (SARs) of 5 or 25 W kg⁻¹, or sham exposed, at 37±0.2°C. Cell cycle alterations were determined by flow cytofluorometry over a 4 d period after exposure. The DNA distributions of RFR, MWR, and sham exposed cells were compared to detect qualitative effects on the cell cycle. Quantitative measures of the effects of isothermal radiation exposure were determined from differences in the number of exposed and sham exposed cells in various cell cycle phases as well as comparison of the mean DNA content of exposed and sham exposed cell samples. Flow cytofluorometric assay precision and accuracy were determined by comparison of DNA distributions of replicate CHO control cell samples and by the use of internal DNA standards.Exposure to 27 MHz RFR or 2.45 GHz MWR altered the CHO cell cycle for periods of up to 4 d following exposure at SARs of 5 or 25 W kg⁻¹. There were significant differences in temporal responses, cell cycle phase sensitivity, and overall degree of cell cycle alteration for 27 MHz compared with 2.45 GHz radiation exposure. In contrast to the effect of 27 MHz RFR, which did not affect G₂/M-phase CHO cells, 2.45 GHz MWR altered all cell cycle phases to varying degrees. Exposure to 2.45 GHz MWR at 5 or 25 W kg⁻¹ was twice as effective as 27 MHz RFR in inducing cell cycle alterations as determined by differences in the number of exposed versus sham-exposed cells in various cell cycle phases.