Short-wavelength Visible Light Research Articles

Trans–cis isomerization of an azoxybenzene liquid crystal

Trans–cis isomerization was investigated in a room temperature liquid crystal mixture of two azoxybenzene compounds. Experiments were performed on isolated molecules in dilute solutions and on the liquid crystal phase composed of the pure compounds. The absorption spectra of the trans and cis isomers were found to be similar to those of azobenzene compounds, as were the birefringence and order parameter of the nematic liquid crystal phase. The photo‐optic properties were also similar in that irradiation by ultraviolet light caused the conversion from trans to cis isomers, while short wavelength visible light incident on these compounds resulted in the conversion from cis to trans isomers. The activation energy for thermal relaxation from the cis to trans isomer in the liquid crystal phase was determined to be (66±7) kJ/mole, which is less than for azobenzene in solution. While a photostationary state in a dilute solution with approximately equal numbers of trans and cis isomers was achieved, the nematic–isotropic transition of the mixture of the pure compounds decreased from 70°C to room temperature with a cis concentration of only about 12%. One unusual finding was that the photostationary concentration of trans and cis isomers due to irradiation with light of a specific visible wavelength depended on the starting concentrations of the two isomers, indicating that there may be a molecular conformation that is not photo‐responsive and relaxes only thermally.

Ultraviolet and Short Wavelength Visible Light Exposure: Why Ultraviolet Protection Alone Is Not Adequate

The danger of exposure to ultraviolet (UV) radiation in both the natural environment and artificial occupational settings has long been recognized by national and international standards committees and worker safety agencies. There is an increasing body of literature that suggests that protection from UV exposure is not enough. Unprotected exposure to the short wavelengths of the visible spectrum, termed the "blue light hazard", is gaining acceptance as a true risk to long-term visual health. Global standards and experts in the field are now warning that those individuals who spend considerable time outdoors should seek sun filter eyewear with high impact resistant lenses that provide 100% UV filtration, high levels of blue light filtration, and full visual field lens/frame coverage as provided by high wrap eyewear. The Skin Cancer Foundation has endorsed certain sunglasses as "product[s]...effective [as] UV filter[s] for the eyes and surrounding skin". However, such endorsement does not necessarily mean that the eyewear meets all the protective needs for outdoor use. There are several brands that offer products with such protective characteristics. Performance sun eyewear by Nike Vision, available in both corrective and plano (nonprescription) forms, is one such brand incorporating these protective features.

Comparison of violet versus red laser exposures on visual search performance in humans

Previous research suggests that the visual impairment of a violet laser is not highly localized on the retina, because the lens absorbs most short-wavelength visible light and partly retransmits it as a diffuse fluorescence at approximately 500 nm. The present study investigated whether a 405 nm violet diode laser more greatly impairs visual search performance in humans than does a 670 nm red diode laser, depending on target eccentricity. Participants had to locate a square among 15 diamonds spread throughout a visual search display while being exposed to a violet or red laser beam that was either continuous or flickering and presented either on-axis or 33 degrees off-axis. Whereas the continuous on-axis violet and red lasers had comparable effects on search performance when the target was located near the center of the beam, the violet laser disrupted processing of eccentric targets more than did the red laser. The search decrements were reduced for both lasers when the beams were flickered or presented off-axis. Both the bluish appearance and greater spatial spread of effect of the violet laser suggest that the unique impairment caused by a violet laser beam derives from its induced lens fluorescence.

Measurement of carotenoids in the living primate eye using resonance Raman spectroscopy.

The xanthophyll carotenoids lutein and zeaxanthin (see Note 1) are specifically concentrated in the macula of the primate eye, the region of the retina responsible for high-resolution visual acuity necessary for reading, driving, and recognizing faces. They are thought to protect the macula from light-induced oxidative damage by acting as light-screening filters for short wavelength visible light and by acting as in situ antioxidants to prevent oxidative damage to polyunsaturated membrane lipids (,). Since high dietary intakes and blood levels of lutein and zeaxanthin have been epidemiologically associated with a lower risk of visual loss from age-related macular degeneration (AMD) (,), there has been considerable interest in measuring carotenoid macular pigment levels in living human eyes as a possible early test to detect individuals at high risk for visual loss from AMD. The current most commonly used method, psychophysical heterochromatic flicker photometry, has significant drawbacks since it is a subjective test that requires an attentive observer with good visual acuity, and it has a high intrasubject variability that may exceed ± 50% (,), which tends to limit its utility as a screening or diagnostic test. We have developed an alternative objective measurement method based on the principles of resonance Raman spectroscopy. This method is rapid, specific, sensitive, and highly reproducible, characteristics conducive to its use as a screening and diagnostic test on large populations with a wide range of visual acuities.

Photocytotoxicity of lipofuscin in human retinal pigment epithelial cells

Lipofuscin accumulates with age in a variety of highly metabolically active cells, including the retinal pigment epithelium (RPE) of the eye, where its photoreactivity has the potential for cellular damage. The aim of this study was to assess the phototoxic potential of lipofuscin in the retina. RPE cell cultures were fed isolated lipofuscin granules and maintained in basal medium for 7 d. Control cells lacking granules were cultured in an identical manner. Cultures were either maintained in the dark or exposed to visible light (2.8 mWcm 2) at 37°C for up to 48 h. Cells were subsequently assessed for alterations in cell morphology, cell viability, lysosomal stability, lipid peroxidation, and protein oxidation. Exposure of lipofuscin-fed cells to short wavelength visible light (390–550 nm) caused lipid peroxidation (increased levels of malondialdehyde and 4-hydroxy-nonenal), protein oxidation (protein carbonyl formation), loss of lysosomal integrity, cytoplasmic vacuolation, and membrane blebbing culminating in cell death. This effect was wavelength-dependent because light exposure at 550 to 800 nm had no adverse effect on lipofuscin-loaded cells. These results confirm the photoxicity of lipofuscin in a cellular system and implicate it in cell dysfunction such as occurs in ageing and retinal diseases.

Identification and Quantitation of Carotenoids and their Metabolites in the Tissues of the Human Eye

There is increasing evidence that the macular pigment carotenoids, lutein and zeaxanthin, may play an important role in the prevention of age-related macular degeneration, cataract, and other blinding disorders. Although it is well known that the retina and lens are enriched in these carotenoids, relatively little is known about carotenoid levels in the uveal tract and in other ocular tissues. Also, the oxidative metabolism and physiological functions of the ocular carotenoids are not fully understood. Thus, we have set out to identify and quantify the complete spectrum of dietary carotenoids and their oxidative metabolites in a systematic manner in all tissues of the human eye in order to gain better insight into their ocular physiology.Human donor eyes were dissected, and carotenoid extracts from ocular tissues [retinal pigment epithelium/choroid (RPE/choroid), macula, peripheral retina, ciliary body, iris, lens, vitreous, cornea, and sclera] were analysed by high-performance liquid chromatography (HPLC). Carotenoids were identified and quantified by comparing their chromatographic and spectral profiles with those of authentic standards.Nearly all ocular structures examined with the exception of vitreous, cornea, and sclera had quantifiable levels of dietary (3R,3′R,6′R)-lutein, zeaxanthin, their geometrical (E / Z) isomers, as well as their metabolites, (3R,3′S,6′R)-lutein (3′-epilutein) and 3-hydroxy-β,ϵ-caroten-3′-one. In addition, human ciliary body revealed the presence of monohydroxycarotenoids and hydrocarbon carotenoids, while only the latter group was detected in human RPE/choroid. Uveal structures (iris, ciliary body, and RPE/choroid) account for ∼50% of the eye’s total carotenoids and ∼30% of the lutein and zeaxanthin. In the iris, these pigments are likely to play a role in filtering out phototoxic short-wavelength visible light, while they are more likely to act as antioxidants in the ciliary body. Both mechanisms, light screening and antioxidant, may be operative in the RPE/choroid in addition to a possible function of this tissue in the transport of dihydroxycarotenoids from the circulating blood to the retina. This report lends further support for the critical role of lutein, zeaxanthin, and other ocular carotenoids in protecting the eye from light-induced oxidative damage and aging.

Ein Retinoidbestandteil von Lipofuszin, A2-E, ist ein Photosensitizer in humanen RPE-Zellen

A fluorescent compound of lipofuscin, A2-E, has been shown to impair lysosomal function and to increase the intralysosomal pH of human retinal pigment epithelial (RPE) cells. This study addressed the phototoxic potential of A2-E on RPE cells. A2-E accumulation was confirmed by fluorescence microscopy and fluorescence-activated cell sorter analysis. Acridine orange staining allowed assessment of lysosomal integrity and intralysosomal pH. Phototoxic properties of A2-E were determined by exposing A2-E-free and A2-E-fed RPE cell cultures to short-wavelength visible light and assessing cell viability and lysosomal integrity. Intralysosomal accumulation of A2-E was confirmed. Acridine orange staining showed that the A2-E was located in the lysosomal compartment and induced an elevation of intralysosomal pH. Exposure of A2-E fed cells to light resulted in a significant loss of cell viability by 72 h which was not observed in either RPE cells maintained in the dark or A2-E-free cultures exposed to light. Toxicity was associated with a loss of lysosomal integrity. A2-E is detrimental to RPE cell function by a variety of mechanisms including inhibition of lysosomal degrading capacity, loss of membrane integrity, and phototoxicity. Such mechanisms could contribute to retinal aging and to retinal diseases associated with excessive lipofuscin accumulation.

Influence of Wavelength and Packaging Material on Lipid Oxidation and Colour Changes in Low-fat Mayonnaise

The influence of light of different wavelengths on lipid oxidation and colour changes in unpacked low-fat mayonnaise was studied using fluorescent light tubes emitting ultraviolet radiation and blue, yellow and red light. The protective effect of the polyester materials PET (polyethylene terephtalate), PEN (polyethylene naphtalate) and PET/PEN copolymer was evaluated by exposing mayonnaise packed in these materials to cool white fluorescent light. The change in colour of samples representing all storage conditions was almost entirely due to a decrease in yellowness, presumably as a result of photobleaching of β -carotene. The colour was affected by wavelengths shorter than 470 nm with the greatest effect produced by wavelengths in the 410–450 nm range. The concentration of hexanal in the headspace was used as an indicator of lipid oxidation. The effect on lipid oxidation was most pronounced with ultraviolet radiation, although short wavelength visible light also had a significant effect. The polyester materials offered some protection against lipid oxidation by filtering out the ultraviolet radiation to varying degrees. PEN and PET/PEN copolymer offered better protection than PET. None of the materials offered sufficient protection against colour changes.

Retinal pigment epithelium pigment granules stimulate the photo-oxidation of unsaturated fatty acids

The cellular pigments of the retinal pigment epithelium (RPE) have been shown to catalyze free radical activity, especially when illuminated with visible or ultraviolet light. This activity is sufficient to cause photooxidation of several major cellular components. The present investigation determined the relative ability of melanin, lipofuscin, and melanolipofuscin granules isolated from human and bovine eyes to oxidize polyunsaturated fatty acids, specifically linoleic and docosahexaenoic acids. The dark reactivity as well as the light-stimulated reactions were determined. The production of hydroperoxide derivatives of the linoleic and docosahexaenoic acids were determined by NADPH oxidation coupled to the activity of glutathione peroxidase, and also by production of thiobarbituric acid reactive substances. All RPE pigment granules stimulated fatty acid oxidation when irradiated with short wavelength (<550 nm) visible light, with the melanosomes exhibiting the greatest light-induced activity. Only lipofuscin granules, however, caused peroxidation of fatty acids in the dark. These findings provide additional support for the role of RPE pigments in “blue light toxicity” as well as indicating that accumulation of lipofuscin may contribute to increased photooxidation in the aging RPE.

Colour tuning in human visual cortex measured with functional magnetic resonance imaging.

The primate retina contains three classes of cones, the L, M and S cones, which respond preferentially to long-, middle- and short-wavelength visible light, respectively. Colour appearance results from neural processing of these cone signals within the retina and the brain. Perceptual experiments have identified three types of neural pathways that represent colour: a red-green pathway that signals differences between L- and M-cone responses; a blue-yellow pathway that signals differences between S-cone responses and a sum of L- and M-cone responses; and a luminance pathway that signals a sum of L- and M-cone responses. It might be expected that there are neurons in the primary visual cortex with response properties that resemble these three perceptual pathways, but attempts to find them have led to inconsistent results. We have therefore used functional magnetic resonance imaging (fMRI) to examine responses in the human brain to a large number of colours. In visual cortical areas V1 and V2, the strongest response is to red-green stimuli, and much of this activity is from neurons receiving opposing inputs from L and M cones. A strong response is also seen with blue-yellow stimuli, and this response declines rapidly as the temporal frequency of the stimulus is increased. These responses resemble psychophysical measurements, suggesting that colour signals relevant for perception are encoded in a large population of neurons in areas V1 and V2.

Light Induces Peroxidation in Retina by Activating Prostaglandin G/H Synthase

Prostaglandin G/H synthase (PGHS) has been shown to generate peroxides to a significant extent in the retina and absorbs light at the lower end of the visible spectrum. We postulated that PGHS could be an important initial source of peroxidation in the retina exposed to light, which would in turn alter retinal function. Exposure of pig eyes (in vivo) to light (350 fc/3770 lx) caused after 3 h a 50% increase and by 5 h a 30% decrease in a- and b-wave amplitudes of the electroretinogram (ERG) which were comparable at 380–650 nm and 380–440 nm but were not observed at wavelengths > 450 nm. These effects of light were prevented by free radical scavengers (dimethylthiourea and high-dose allopurinol) and PGHS inhibitors (naproxen and diclofenac), but stable analogs of prostaglandins did not affect the ERG. Both increases and subsequent decreases in ERG wave amplitudes following light exposure in vivo were associated with increases in retinal prostaglandin and malondialdehyde (peroxidation product) levels, which were inhibited by the nonselective PGHS blockers, naproxen and diclofenac. Similar observations were made in vitro on isolated porcine eyecups as well as on retinal membranes exposed to light (250 fc/2700 lx) 380–650 nm and 380–440 nm but not at >500 nm. Both PGHS-1 and PGHS-2 contributed equivalently to light-induced prostaglandin synthesis, as shown after selective PGHS-2 blockers, but mRNA expression of PGHS-1 and 2 was not affected by light. Finally, light stimulated activities of pure PGHS-1 and PGHS-2 isozymes, and these were also shown to produce superoxide radical (detected with fluorogenic spin trap, proxyl fluorescamine). Taken together, data suggest that PGHS-(1 and 2) is activated by short wavelength visible light, and in the retina is an important source of reactive oxygen species which in turn alter retinal electrophysiological function. PGHS thus seems a likely chromophore in setting forth photic-induced retinal injury. Findings provide an explanation for increased sensitivity of the retina to visible light predominantly at the far blue range of its spectrum.

Light damage revisited: converging evidence, diverging views?

Are observations on ultraviolet (UV)- and visible light-induced ocular changes in animals relevant for human pathology? Different conclusions are drawn by different groups, depending on their perspective: while in the epidemiologist's view the evidence for those lesions is mostly limited or insufficient, laboratory scientists continually extend observations on radiation damage in animals. Consequently, there are diverging views on the necessity and specifications for eye protection. In this review, problems of epidemiological surveys and observations in humans and animal studies are discussed, and natural and artificial protection of the eye is outlined. The human and animal eye has an inherent potential for photochemical lesions due to chromophores including the visual pigments that are present at birth. Lifelong light exposure gives rise to additional absorbing molecules. With decreasing wavelengths of the electromagnetic spectrum the number of absorbing molecules rises; therefore, the likelihood of a photochemical reaction grows. As the spectral energy is augmented, more damage will occur. In our view, the knowledge gained from laboratory studies is a significant component of the total evidence from different fields-epidemiology, clinical observations, model studies and theoretical calculations-that UV radiation and short-wavelength visible light can cause acute and chronic changes in ocular structures. Such changes may comprise irreversible damage. Following recently issued recommendations of the major visual health organizations in the United States, protection against UV and blue light should be incorporated into the spectrum of safety considerations for sunglasses.

Rat lens glycolysis after in vivo exposure to narrow band UV or blue light radiation

UV radiation and short wavelength visible light are known to damage various tissues in the eye. This paper investigates the effect on rat lens glycolysis after in vivo exposure with 90 kJ m −2 narrow band UV radiation (UVB, 300 nm) and 90 kJ m −2 blue light (435 nm) radiation. After exposure, all lenses were incubated in Medium 199. Samples of culture medium were withdrawn after 2, 4, 6 h and 5, 10, 20 h in two UVB studies and after 5, 10 and 20 h in a blue light study. Lactate is the major end product of lens glycolysis. Lactate was determined with a modified enzymatic-photometric method. Intralenticular lactate was determined in one UVB experiment. In the UVB experiments we found a lower lactate production in the exposed lenses 2–6 h after exposure. There was an accumulation of lactate inside UVB-exposed lenses after 6 h incubation compared with their contralateral lenses. No significant effect on lactate production was observed in the blue light experiment. Conclusions. UVB induced a reversible inhibition of glycolysis. UVB also induced an accumulation of lactate inside the lens. Blue light tended to increase glycolysis.

Updating on intraoperative light-induced retinal injury.

We are presenting the state of knowledge concerning intraoperative light-induced retinal injury, considered to be a combination of photic retinopathy and retinal photocoagulation. It may arise from retinal light exposure to the operating microscope or to the fiberoptic endoilluminator. Ultraviolet and short-wavelength visible light are more dangerous than longer wavelength light. Many risk factors may facilitate the onset of this iatrogenic disease following surgery. Many aspects of the retinal damage are still poorly understood. Many mid light-induced retinal injuries probably remain undiagnosed in routine postoperative examination. Current appropriate light filters are not the definitive solution. Appropriate precautions should be taken during both anterior segment and vitreoretinal surgery.

Doping of Wide-Gap II-VI Compounds for Short-Wavelength Visible Light Emitting Devices

Doping of Wide-Gap II-VI Compounds for Short-Wavelength Visible Light Emitting Devices

Large photoinduced birefringence in an optically nonlinear polyester polymer

A nonlinear optical polyester with disperse red side groups exhibited a stable photoinduced birefringence, from 0.14 at 850 nm to 0.21 at 633 nm, after exposure to linearly polarized short-wavelength visible or ultraviolet light. Thin-film wave plates, birefringent diffraction gratings and waveguides were written in this polymer using photoexposure. Thin- film wave plates of &amp;lt;1 μm thickness showed ≳π/4 phase delay and good temporal stability. A 9:1 diffraction efficiency ratio of the two polarization eigenmodes was measured from thin birefringent gratings. This ratio is in good agreement with the theoretical prediction obtained using a simple three-level model.

Characterization of cisplatin degradation as affected by pH and light

The stability of cisplatin in 0.9% sodium chloride solution was studied. Cisplatin was reconstituted with sterile water for injection to achieve a concentration of approximately 1 mg/mL in 0.9% sodium chloride solution. The solutions were placed in flexible polyvinyl chloride containers, clear and amber glass flasks, and plastic syringes and stored at 22-25 degrees C in the dark or exposed to measured amounts of light and assayed periodically for up to 96 days. The initial pH of some of the solutions was adjusted. The stability of cisplatin in the solutions was determined by measuring the concentrations of cisplatin, trichloroammineplatinate(II) (TCAP), and trans-dichlorodiammineplatinum(II) (transplatin) with high-performance liquid chromatography and by measuring solution pH. The effect of adding ethylene oxide and other materials was also determined. TCAP was identified as the predominant degradation product of cisplatin in all the solutions. The rate of degradation was dependent on pH: In the dark, about 0.04% and 0.21% of the cisplatin degraded to TCAP per week at pH 4.3 and 6.3, respectively. The presence of ethylene oxide accelerated cisplatin degradation. Degradation also occurred during exposure to short-wavelength (350-490-nm) visible light. Storage in amber glass flasks offered more protection than storage in clear flasks. Isomerization of cisplatin to transplatin was not observed. The major degradation product of cisplatin was trichloroammineplatinate(II). Solution pH was the predominant factor affecting cisplatin stability.

Photodegradation of poly( o-(trimethylsilyl)phenylacetylene) in solutions

Poly( o-(trimethylsilyl)phenylacetylene), poly(TMSPA) has been found to be highly stable in organic solvents in the absence of light and also in film form under ultra-violet/visible light irradiation. However, when poly(TMSPA) in chlorinated solvents is irradiated with ultra-violet and short-wavelength visible light, the polymer degrades and the rate of degradation is highest in the more highly chlorinated solvents such as CHCl 3 and CCl 4. After 2 h irradiation of a 2 × 10 −3 M CCl 4 solution the molecular weight of poly(TMSPA) may decrease by almost two orders of magnitude. Ultra-violet/visible absorption spectroscopy suggests the presence of charge-transfer interaction between CHCl 3 and CH 2Cl 2 with the poly(TMSPA) after irradiation. X-ray photoelectron spectroscopy results indicate that chlorine is incorporated into the polymer during the degradation process.

Influences of artificial lighting on the seaward orientation of hatchling loggerhead turtles Caretta caretta

The seaward orientation behavior of hatchling loggerhead turtles Caretta caretta when exposed to five different artificial light sources (high-pressure) and low-pressure sodium vapor, and yellow, red, and white incandescent lamps) was examined. Each light source affected hatchling sea-finding performance either in direction of orientation or width of dispersion. Hatchlings were attracted to light sources emitting short-wavelength visible light and long-wavelength sources that excluded intermediate wavelengths. A negative response was observed toward sources emitting predominately yellow light. For this reason, low-pressure sodium vapor (LPS) luminaires, which emit only yellow light, are expected to affect loggerhead hatchling sea-finding minimally, if positioned behind the primary dune. LPS luminaires positioned between emerging hatchlings and the ocean, however, will disrupt hatchling orientation.

Stability and degradation of trans-polyphenylacetylene in organic solvents and under light illumination

The stability of a semiconducting photoconductor, trans-polyphenylacetylene (PPA), in organic solvents and under light illumination has been studied. When chloroform is used as solvent, loss of effective conjugation and decrease in molecular weight are detectable after less than an hour. The degradation is slowed down considerably at — 20°C with only minimal changes detected after 48h. On the other hand, the presence of near-UV and short wavelength visible light strongly accelerates the degradation of PPA samples in solution and of solution-cast PPA films. The photoconductivity of solution-cast PPA films decreases rapidly on illumination with near-UV and short wavelength visible light but not with red light.