Table 3.
Reference, year | Species (subject/tissue/cells/animals) | Light sources of irradiation, exposure times | Effect of blue light irradiation |
---|---|---|---|
Arnault et al., 2013 [16] |
Porcine eye RPE cells |
LED and filter, 10 nm illumination bands centered from 380 to 520 nm in 10 nm increments; The intensity of each band was calculated according to the solar intensity received by the retina after filtering by the optics of the eye; Exposure times: 18 h |
Loss of cell viability (maximal for wavelengths from 415 to 455 nm) |
Noell et al., 1966 [60] |
Rat |
Fluorescent lamps Monochromatic light of various wavelengths: 1200 to 2500 lx or green filter; Variation of the temperature; Exposures times: 1–2 days |
Continuous exposure to visible light to moderate levels of damaged photoreceptor cells Light damage classified into two types: class I (damage induced by low-intensity light exposure for long durations) and class II (damage induced by relatively high-intensity light exposure for short periods) |
Van Norren et al., 1990 [65] |
Rat |
Xenon light, white, irradiant dose from 4 J/cm2 at 379 nm to 2000 J/cm2 at 559 nm; Narrow band spectral light; Exposure times: 10 s to 1 h |
Susceptibility for damage sharply increased towards the ultraviolet Susceptibility to photic injury in rat is comparable to that in primates |
Marie et al., 2020 [66] |
Porcine retina cone receptors |
LED, 10 nm wavelength bands between 390 and 510 nm, plus the 630 nm band; Exposure times: 15 h |
The near UV visible range (415 and 455 nm) is the most toxic wavelengths; Toxicity occurred in the blue–violet light (425–445 nm) for exposures at intensities of sunlight received by the retina; Macular degeneration; Retinitis pigmentosa; The toxicity originates from a porphyrin |
Krigel et al., 2016 [67] |
Retina of albinos and pigmented rats |
LEDs (cold white, blue, and green), fluorocompact bulbs, fluorescent; Exposure times: 24 h; Exposure at high luminance was compared with a cyclic (dark/light) exposure at domestic levels for 1 week and 1 month |
Phototoxicity; Blue light component emitted by white LEDs at usual domestic luminance induced more retinal degeneration and the development of necrosis than other light sources |
Chamorro et al., 2013 [68] |
Human retinal pigment epithelial cells |
LED: 468 nm (blue), 525 nm (green), 616 nm (red), and white light; Exposure times: three cycles of light–darkness (12 h/12 h) |
LED radiations: Decrease in cellular viability; Increase in cellular apoptosis; Increase in ROS production; Increase in DNA damage; Apoptosis more important in cells exposed to white and blue Three light–darkness (12 h/12 h) cycles of exposure to LED lighting affect in vitro human retinal pigment epithelial cells |
Kuse et al., 2014 [69] |
Murine photoreceptor-derived cells (661 W) |
LEDs: 464 nm (blue), 456–553 nm (white), 522 nm (green); Exposure times: 24 h |
Blue LED light Increase of ROS production; Alteration of the protein expression level; Blue and white LED Aggregation of short-wavelength opsins (S-opsin), leading to severe cell damage; Damage of retinal cone photoreceptor cells; N-Acetylcysteine (antioxidant) protected against the cellular damage induced by blue LED light |
Abdhou et al., 2022 [70] |
Human RPE cells |
Solar simulator and blue light filtering IOL Cells were exposed or not to BL, with the absence or presence of either a CIOL < 400 nm, or a YIOL Exposure time: 30 minn |
Blue light is deleterious to RPE cells due to increased oxidative stress and cell death Blue light increased cellular and mitochondrial total ROS levels These effects were attenuated by filtering this radiation. YIOL decreased cellular and mitochondrial ROS levels The increase in ROS production was coupled with an increase in cell death, which decreased when cells were protected with YIOL Pretreatment of cells with N-acetylcysteine abolished the increase in cell death |
Wu et al., 1999 [71] |
Rat retina |
Fluorescent lamp, Blue light 400–480 nm of 0.64 W/m3; Exposure times: 3–6 h |
Photoreceptor cell apoptosis |
Shang et al., 2017 [93] |
Sprague–Dawley rat |
LEDs: 460 nm (blue), 530 nm (green), 620 nm (red); Exposure times: from 3–9 to 28 days under a 12 h dark/12 h light cycle |
Blue LED group induced more: functional damage photochemical injury (apoptosis and necrosis of photoreceptors and RPE) oxidative stress than that of green or red LED groups |
Jaardane et al., 2015 [94] |
Wistar Rats |
LEDs (blue region), and 449 nm, 467 nm, 473 nm, 507 nm; Exposure times: 6, 12, 18, 24, 48, and 72 h |
Oxidative damage and retinal injury; Retinal degeneration; Loss of photoreceptors: Activation of caspase-independent apoptosis, necrosis, necroptosis; Wavelength dependence of the effects |
AMD age-related macular degeneration, CCTs correlated color temperatures, CIOL clear UV-filtering IOL, DNA deoxyribonucleic acid, IOL intraocular filtering, K kelvin, LED light emitting diodes, nm nanometer, RCT randomized clinical trial, RPE retinal pigment epithelium, ROS reactive oxygen species, UV ultraviolet, VEGF vascular endothelial growth factor, YIOL yellow UV- and BL-filtering IOL