Nontargeted effects of ionizing radiation: implications for low-dose exposures

The traditional thinking has been that the biological effects of ionizing radiation occur in irradiated cells as a consequence of the DNA damage they incur. This implies that: 1) biological effects occur only in irratiated cells, 2) radiation traversal through the nucleus of the cell is a prerequisite to produce a biological response, and 3) DNA is the target molecule in the cell. Evidence has been emerging, however, for non-DNA targeted effects of radiation; that is, effects including mutations, chromosomal aberrations, and changes in gene expression which occur in cells that in themselves receive no radiation exposure. Two of these phenomena will be described in this paper. The first is radiation-induced genomic instability whereby biological effects, including elevated frequencies of mutations and chromosomal aberrations, arise in the distant descendants of irradiated cells. The second phenomenon has been termed the "bystander effect", whereby in a mixed population of irradiated and nonirradiated cells, biological effects arise in those cells that receive no radiation exposure. The damage signals are transmitted from cell to cell through gap junction channels, and the genetic effects observed in bystander cells appear to result from an upregulation of oxidative stress. The possible influence of these non-targeted effects of radiation of the respounse to low-dose exposures is discussed.     

The effects of short-term exposures to ultraviolet radiation in the Hawaiian Coral Montipora verrucosa

Exposure to ultraviolet radiation (UVR, 290–400 nm) is an important abiotic factor that tropical marine organisms have been exposed to over evolutionary time. Additionally, UVR is known to cause coral bleaching independently and is an important synergistic factor in bleaching caused by thermal stress. Corals can avoid some of the damage associated with exposure to UVR by producing UVR-absorbing compounds such as mycosporine-like amino acids (MAAs). To examine the role of MAAs in the UVR photobiology of corals we conducted experiments on the Hawaiian coral Montipora verrucosa. M. verrucosa colonies were collected from 1, 5 and 10 m and exposed to three different UVR treatments for 3 days under constant visible irradiances equivalent to a depth of 0.15 m depth in Kane'ohe Bay. In addition to quantifying the MAA concentration of these corals several types of UVR-induced damage were measured to assess whether MAAs were providing protection. Quantum yields of photosystem II (PSII) fluorescence and excitation pressure on PSII were measured for each coral, and the formation of direct UVR damage to DNA was measured as cyclobutane pyrimidine dimers (CPDs) and (6-4) pyrimidine–pyrimidone photoproducts for the holobiont. All corals exhibited midday depressions in quantum yields, developed DNA photoproducts, and increased their MAA concentrations significantly as a result of UVR exposures. CPD accumulation in M. verrucosa was highest in corals from 1 m, which had the lowest MAA concentrations at the end of the experiment. Corals originally from 10 m showed the highest MAA concentration and lowest DNA damage in response to exposure to UVR. While corals from all collection depths displayed some sensitivity to increased irradiances of UVR, their respective levels of tolerance were clearly dependant on their previous light history.     

Assessment of the immune responsiveness of mice irradiated with continuous wave or pulse-modulated 425-MHz radio frequency radiation

Groups of female BALB/C mice were irradiated with 425-MHz radio frequency (RF) radiation either continuous wave (CW) or pulse modulated (PM, 1-ms pulse width, 250 pulses/s). Mice were irradiated in a rectangular strip-transmission line at average forward powers of 78, 17.7, or 5 W for CW and 17.7, 5, or 1.25 W for PM. The mean specific absorption rate, as measured using twin-well calorimetry was 7.7 W/kg for a forward power of 70 W. No differences in the mitogen-stimulated response of lymphocytes or in the primary antibody response to sheep erythrocytes or polyvinylpyrrolidone were observed between irradiated and sham-irradiated mice, nor between mice exposed to either CW or PM 425-MHz RF radiation.     

Non-parametric estimation of thresholds for radiation effects in vertebrate species under chronic low-LET exposures

Databases on effects of chronic low-LET radiation exposure were analyzed by non-parametric statistical methods, to estimate the threshold dose rates above which radiation effects can be expected in vertebrate organisms. Data were grouped under three umbrella endpoints: effects on morbidity, reproduction, and life shortening. The data sets were compiled on a simple ‘yes’ or ‘no’ basis. Each data set included dose rates at which effects were reported without further details about the size or peculiarity of the effects. In total, the data sets include 84 values for endpoint “morbidity”, 77 values for reproduction, and 41 values for life shortening. The dose rates in each set were ranked from low to higher values. The threshold TDR5 for radiation effects of a given umbrella type was estimated as a dose rate below which only a small percentage (5%) of data reported statistically significant radiation effects. The statistical treatment of the data sets was performed using non-parametric order statistics, and the bootstrap method. The resulting thresholds estimated by the order statistics are for morbidity effects 8.1 × 10⁻⁴ Gy day⁻¹ (2.0 × 10⁻⁴–1.0 × 10⁻³), reproduction effects 6.0 × 10⁻⁴ Gy day⁻¹ (4.0 × 10⁻⁴–1.5 × 10⁻³), and life shortening 3.0 × 10⁻³ Gy day⁻¹ (1.0 × 10⁻³–6.0 × 10⁻³), respectively. The bootstrap method gave slightly lower values: 2.1 × 10⁻⁴ Gy day⁻¹ (1.4 × 10⁻⁴–3.2 × 10⁻⁴) (morbidity), 4.1 × 10⁻⁴ Gy day⁻¹ (3.0 × 10⁻⁴–5.7 × 10⁻⁴) (reproduction), and 1.1 × 10⁻³ Gy day⁻¹ (7.9 × 10⁻⁴–1.3 × 10⁻³) (life shortening), respectively. The generic threshold dose rate (based on all umbrella types of effects) was estimated at 1.0 × 10⁻³ Gy day⁻¹.     

Postirradiation change in the radiosensitivity of rats in relation to the preliminary radiation dose in the cutaneous form of radiation injury

The experimental animals were exposed two times to soft 17kV X-radiation. Post-irradiation changes in radiosensitivity were shown to depend upon dose of preliminary irradiation (10, 18 and 25 Gy). The state of radiosensitive tissues was studied and a comparison was made of a residual damage curve with a change in the proliferative activity of dividing tissue elements during 30 days after irradiation.