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PubMed2004

UV light from 290 to 325 nm, but not broad-band UVA or visible light, augments the formation of melanocytic nevi in a guinea-pig model for human nevi.

We have previously described a guinea-pig model where pigmented nevi similar to human nevi can be produced by application of low-dose topical 7,12-dimethylbenzanthracene (DMBA) followed by solar-simulated light. Five groups of guinea-pigs were used to test the effect of various spectral bands of solar-simulated light on low-dose DMBA-induced melanocytic nevi. Animals were irradiated with either UVB to near UVA2 (290-325 nm), UVA, visible light, full solar spectrum or no irradiation three times per wk for 12 mo to determine the broad-band effect of nevi-inducing irradiation. There was a significant increase in nevi/animal in the UVB-treated group (mean 1.53) compared with all groups (versus UVA 0.3, p<0.001; versus visible light 0.24, p<0.001; versus full spectrum (UVB+UVA+visible) 0.68, p=0.02; versus control (nil irradiation) 0.37, p=0.01). No differences in skin thickness were found between any group (p=0.11). In conclusion, we present a report of the active waveband of melanocytic nevi induction; where UVB to near UVA2 is the likely responsible waveband. Furthermore, because there was a significant decrease in nevi/animal receiving the full solar spectrum compared with the UVB group, it is possible that broad-band UVA and or visible light may be inhibitory wavebands for nevi induction.

9,10-Dimethyl-1,2-benzanthracene↗
PubMed1996

Degradation of the light-stress protein is mediated by an ATP-independent, serine-type protease under low-light conditions.

Green plants respond to light stress by induction of the light-stress proteins (ELIPs). These proteins are stable as long as the light stress persists but are very rapidly degraded during subsequent low light conditions. Here we report that the degradation of ELIPs is mediated by an extrinsic, thylakoid-associated protease which is already present in the membranes during light stress conditions. Partial purification of the protease by perfusion chromatography indicates that this proteolytic activity may be represented by a protein with an apparent molecular mass of 65 kDa. The ELIP-directed protease is localized in the stroma lamellae of the thylakoid membranes and does not require ATP or additional stromal factors for proteolysis. The protease has an optimum activity at pH 7.5-9.5 and requires Mg2+ for its activity. The ELIP-degrading protease show an unusual temperature sensitivity and becomes reversibly inactivated at temperatures below 20 degree C and above 30 degree C. Studies with protease inhibitors indicate that this enzyme belongs to the serine class of proteases. The enhanced degradation of ELIP in isolated thylakoid membranes after addition of the ionophore nigericin suggests that a trans-thylakoid delta pH or changes in ionic strength may be involved in the mechanism of protease activation.

Adenosine Triphosphate↗
PubMed2004

Evening melatonin and bright light administration induce additive phase shifts in dim light melatonin onset.

In healthy young men, administration of a single light pulse (5000 lux for 3 hr) or a single melatonin pill (5 mg) at 20:40 hr under controlled constant routine conditions of <10 lux, yielded a phase delay and a phase advance, respectively, in the circadian marker of dim light melatonin onset 24 hr later. Phase shifts after combining the two interventions were additive. Melatonin suppression is not necessary for a phase shift by light, and melatonin is not a 'weak' Zeitgeber relative to bright light when ambient lighting is strictly controlled.

Adult↗
PubMed1995

Reversion profiles of coolwhite fluorescent light compared with far ultraviolet light: homologies and differences.

General Electric and Sylvania 15 W coolwhite fluorescent lamps emit roughly 6% of their total irradiance as light in the UV spectrum. Illumination of sensitive Salmonella tester strains results in both lethal and mutagenic activities. In contrast, comparable Philips lamps emit lower levels of UV light, especially UVB, and exhibit no detectable lethal or mutagenic effects. The spectra of mutations induced by General Electric coolwhite lamps in histidine-requiring base substitution mutants hisG46 and hisG428 ("reversion profiles") resemble mutagenesis by far UV light (UVC) and differ quite markedly from the spectra of mutations that occur spontaneously. Coolwhite and UVC reversion profiles are not identical, however. The percentage of C to A transversion mutations induced in hisG46 are elevated over those found after UVC treatment, and a strong bias for one particular class of tandem base substitutions (TAA-->TGT) prevails after treatment of hisG428 with coolwhite light, a bias not observed with UVC. Increased attention needs to be given to minimization of exposure to UV light from fluorescent lamps commonly used in homes and workplaces.

Base Sequence↗
PubMed1979

Interpretation of light diffraction by cross-striated muscle as Bragg reflexion of light by the lattice of contractile proteins.

1. The diffraction spectrum obtained by illuminating a cross-striated muscle fibre with a narrow beam of monochromatic light generally shows asymmetry of light intensity between left and right spectral lines. 2. The asymmetry of light intensity in left and right spectral lines is reversed when the fibre is rotated by 180 degrees. This indicates that intensities of the spectral lines are determined more by Bragg reflexion than by simple diffraction as in a plane grating. Populations of myofibrils with differing tilt of lattice planes must exist in each illuminated fibre segment to account for simultaneous Bragg reflexion to the left- and right-hand sides. 3. The light intensity of spectral lines shows a complicated dependence on the angle at which the incident beam is directed against the fibre. This 'intensity distribution' seems to reflect the specific myofibrillar arrangement at the site of illumination. 4. The intensity distributions of the left and right first order lines show close correlation if the deflexion of the incident beam differs by twice the Bragg angle. 5. The deflexion angle of the incident beam at which maximum intensity in spectral lines is obtained depends on sarcomere length as predicted by Bragg's formula. 6. Intensities of the first and second order lines are little correlated when recorded at the same beam deflexion, but are well correlated when recorded at beam deflexions calculated from Bragg's formula. 7. When a diffraction line is scanned perpendicularly to the meridional plane, the light intensity shows fluctuations resembling those obtained by beam deflexion within the meridional plane.

Animals↗
PubMed2005

Light responses and light adaptation in rat retinal rods at different temperatures.

Rod responses to brief pulses of light were recorded as electroretinogram (ERG) mass potentials across isolated, aspartate-superfused rat retinas at different temperatures and intensities of steady background light. The objective was to clarify to what extent differences in sensitivity, response kinetics and light adaptation between mammalian and amphibian rods can be explained by temperature and outer-segment size without assuming functional differences in the phototransduction molecules. Corresponding information for amphibian rods from the literature was supplemented by new recordings from toad retina. All light intensities were expressed as photoisomerizations per rod (Rh*). In the rat retina, an estimated 34% of incident photons at the wavelength of peak sensitivity caused isomerizations in rods, as the (hexagonally packed) outer segments measured 1.7 microm x 22 microm and had specific absorbance of 0.016 microm(-1) on average. Fractional sensitivity (S) in darkness increased with cooling in a similar manner in rat and toad rods, but the rat function as a whole was displaced to a ca 0.7 log unit higher sensitivity level. This difference can be fully explained by the smaller dimensions of rat rod outer segments, since the same rate of phosphodiesterase (PDE) activation by activated rhodopsin will produce a faster drop in cGMP concentration, hence a larger response in rat than in toad. In the range 15-25 degrees C, the waveform and absolute time scale of dark-adapted dim-flash photoresponses at any given temperature were similar in rat and toad, although the overall temperature dependence of the time to peak (t(p)) was somewhat steeper in rat (Q(10) approximately 4 versus 2-3). Light adaptation was similar in rat and amphibian rods when measured at the same temperature. The mean background intensity that depressed S by 1 log unit at 12 degrees C was in the range 20-50 Rh* s(-1) in both, compared with ca 4500 Rh* s(-1) in rat rods at 36 degrees C. We conclude that it is not necessary to assume major differences in the functional properties of the phototransduction molecules to account for the differences in response properties of mammalian and amphibian rods.

Adaptation, Ocular↗
PubMed1994

Reciprocal light-dark transcriptional control of nif and rbc expression and light-dependent posttranslational control of nitrogenase activity in Synechococcus sp. strain RF-1.

Synechococcus sp. strain RF-1 exhibits a circadian rhythm of N2 fixation when cells are grown under a light-dark cycle, with nitrogenase activity observed only during the dark period. This dark-dependent activity correlated with nif gene transcription in strain RF-1. By using antibodies against dinitrogenase reductase (the Fe protein of the nitrogenase complex), it was found that there was a distinct shift in the mobility of this protein on sodium dodecyl sulfate gels during the light-dark cycle. The Fe protein was present only when cells were incubated in the dark. Upon illumination, there was a conversion of all Fe protein to a modified form, after which it rapidly disappeared from extracts. These studies indicated that all nitrogenase activity present during the dark cycle resulted from de novo synthesis of nitrogenase. Upon entering the light phase, cells appeared to quickly degrade the modified form of Fe protein, perhaps as a result of activating or inducing a protease. By contrast, transcription of the rbcL gene, which encodes the catalytic subunit of the key enzyme of CO2 fixation (a light-dependent process), was enhanced in the light.

Bacterial Proteins↗
PubMed1983

Light adaptation in cells of macaque lateral geniculate nucleus and its relation to human light adaptation.

Responses of macaque lateral geniculate nucleus (LGN) cells to stimuli of different incremental intensities and wavelength compositions were studied at different levels of light adaptation from scotopic to low photopic levels. Stimuli were large in comparison with receptive-field size. Human increment thresholds were measured for comparison. The strength of responses grew in many cells from threshold up to a saturation level as a logarithmic function of incremental intensity. More complex intensity-response functions were also obtained, particularly from parvocellular layer (PCL) cells, but the shape and slope of the intensity-response function changed as a function of adaptation level only with chromatic backgrounds. As a function of adaptation level, the intensity-response functions shifted along the logarithmic abscissa but not sufficiently for a complete contrast constancy. Thus responses to any constant contrast became smaller when adaptation level decreased. The change from cone to rod responses, when possible, took place without noticeable change in shape of intensity-response functions, and much of the adaptive shift of the functions could be attributed to the change-over between rods and cones. Differences between different cells in light adaptation and dark-adapted sensitivity were large, mostly because of variation in the strength of rod input. The strongest excitatory rod inputs were found in PCL cells activated by short-wavelength light, so that the highest sensitivity at low levels of illumination occurred in blue- and blue-green-sensitive cells. The lowest increment thresholds based on cones matched the thresholds of macaque cone late receptor potentials recorded by Boynton and Whitten (3). They were also similar to human cone thresholds measured psychophysically but only for small stimulus sizes that may approximate the size of the receptive-field centers. Human sensitivity was much higher when measured with large stimulus sizes, indicating integration at post-geniculate neural levels. Light adaptation, as evaluated with respect to contrast constancy and Weber law behavior, was similarly incomplete in monkey single cells and human perception. A few cat LGN cells were studied in a control experiment; results agreed with previous findings. The light adaptation of cat cels was more complete and sensitivity higher than those observed under comparable conditions in macaque single cells and human. The maintained activity level of cells was little affected by the intensity of steady backgrounds. Thus, the steady-state hyper-polarisation of receptors was not transmitted to LGN cells.

Adaptation, Ocular↗
PubMed1982

Bence Jones proteins and light chains of immunoglobulins. Preferential association of the V lambda VI subgroup of human light chains with amyloidosis AL (lambda).

An antiserum prepared against a lambda-Bence Jones protein from a patient (SUT) who had multiple myeloma and amyloidosis had specificity for lambda-light chains of the chemically defined variable (V) region lambda-chain subgroup lambda VI. Sequence analyses of protein SUT and of five other lambda-light chains recognized immunologically as of the V lambda VI subgroup revealed that all six proteins had the N-terminal sequence characteristic for prototype lambda VI proteins. The isotypic nature of the V lambda VI subgroup was demonstrated immunochemically: lambda VI molecules were detected among light chains isolated from the IgG proteins of each of 12 normal individuals and lambda VI antigenic determinants were also detectable on the intact IgG proteins. The frequency of lambda VI molecules among lambda-type light chains is estimated to be approximately 5% based on the finding that 5 of 91 lambda Bence Jones proteins were of the V lambda VI subgroup. Proteins of the V lambda VI subgroup, in contrast to those of the other five chemically-classified lambda chain subgroup, appear to be preferentially associated with the amyloid process as evidenced by the fact that all six lambda VI proteins were obtained from patients with amyloidosis AL and, in addition, 5 of 42 lambda-type monoclonal immunoglobulins from patients with primary or myeloma-associated amyloidosis were classified by immunodiffusion analyses as having lambda VI-type light chains.

Amino Acid Sequence↗
PubMed1976

Hepatic hydroxylation of 3beta-hydroxy-5-androsten-17-one in orchiectomized or adrenalectomized rats exposed to a reversed light cycle, constant light, or constant darkness.

The oxidative metabolism of 3beta-hydroxy-5-androsten-17-one (DHA)2 by liver microsomes in vitro was studied in sham-operated, castrated, or adrenalectomized rats maintained for 21 days in a normal light cycle, a reverse light cycle, constant light, or constant darkness and killed either at 0600 or 1800 h. Statistical analysis of the data (3-way analysis of variance) indicated the following significant effects: 1) exposure to a reverse light cycle resulted in lower body weights and increased rates of formaation of 7alpha-OH-DHA and 7-oxo-DHA; 2) despite an increase in microsomal protein content, livers from rats in constant light had the lowest rates of formation of all DHA products; 3) rats kept in constant darkness exhibited the highest rates of DHA metabolism; 4) castration decreased the microsomal protein content and the rates of formation of 16alpha-OH-DHA, 7alpha-OH-DHA, and 7-oxo-DHA; 5) adrenalectomized rats exhibited high rates of 7alpha-OH-DHA formation although microsomal protein and liver and body weights decreased; and 6) the formation of 7-oxygenated products of DHA was greater in the rats killed at 1800 than at 0600 h. We conclude that the type of illumination is quantitatively more important in determining the magnitude of DHA metabolism by the adult male rat liver than either the adrenals or the testes.

Adrenalectomy↗
PubMed1983

Influence of intraocular scattered light on lightness-scaling experiments.

Following Munsell's bisection procedure [J. Opt. Soc. Am. 23, 394 (1933)], we established a nine-step gray scale in which each step is an equal increment in lightness. We calculated retinal illuminances after intraocular scatter by using the point-spread function of Vos et al. [Vision Res. 16, 215-219 (1976)]. After this correction for intraocular scatter, we find a logarithmic relationship between retinal illuminance and achromatic lightness scales that are determined by the bisection method. Additional bisection experiments with a series of different backgrounds corroborate this result. We find that lightness depends linearly on the logarithm of scatter-corrected retinal illuminance, with different slopes for backgrounds of different lightness. This study also highlights the importance of using scatter-corrected illuminance in any quantitative model of lightness.

Adult↗
PubMed1984

The light-harvesting polypeptides of Rhodospirillum rubrum. I. The amino-acid sequence of the second light-harvestng polypeptide B 880-beta (B 870-beta) of Rhodospirillum rubrum S 1 and the carotenoidless mutant G-9+. carotenoidless mutant G-9+.

The light-harvesting complex B 880 from Rhodospirillum rubrum S 1 (wild type) and B 870 from the carotenoidless mutant G-9+ was shown to consist mainly of an organic solvent-(chloroform/methanol-) soluble and an organic solvent-insoluble polypeptide. The isolation and separation of these two low-molecular-mass polypeptides (Mr 6101 and Mr 6079) were achieved by a two-step extraction procedure of chromatophores using in the first step chloroform/methanol containing 0.1M ammonium acetate. Following Sephadex LH-60 chromatography of this first extract a light-harvesting polypeptide (B 870-alpha) was isolated and its complete amino acid sequence was determined (R. Brunisholz et al. (1981) FEBS Lett. 129/1, 150-154, B 880-alpha: G. Gogel et al. (1983) Biochim. Biophys. Acta 746, 32-39). Upon reextraction of the chromatophore pellet with chloroform/methanol/ammonium acetate containing in addition acetic acid a second low-molecular-mass polypeptide (B 880-beta of B 870-beta) was generated. The complete amino acid sequences of the chloroform/methanol-insoluble light-harvesting polypeptide of Rs. rubrum S 1 (B 880-beta) and of Rs. rubrum G-9+ (B 870-beta) were determined. They are identical and consist of 54 amino acid residues. The conserved histidine residue within the hydrophobic stretch raises more evidence for ligand complexation of bacteriochlorophyll to this specific histidine residue which therefore possibly plays the key role in pigment-protein interactions. Both polypeptides (B 880-alpha and B 880-beta) are part of the light-harvesting complex B 880 in an apparent ratio of 1:1. Based on the primary structure data a possible arrangement of both light-harvesting polypeptides within the membrane will be discussed.

Amino Acid Sequence↗
PubMed1991

Significance of nonparametric light effects in entrainment of circadian rhythms in owl monkeys (Aotus lemurinus griseimembra) by light-dark cycles.

In a total of 12 adult Colombian owl monkeys, Aotus lemurinus griseimembra, the significance of nonparametric light effects for the entrainment of the circadian system by light-dark (LD) cycles was studied by carrying out (a) phase-response experiments testing the phase-shifting effect of 30-min light pulses (LPs) of 250 lx applied at various phases of the free-running circadian activity rhythm (LL 0.2 lx) and (b) synchronization experiments testing the entraining effect of 24-h single LP photoperiods consisting of 30-min L of 80 lx and 23.5-h D of 0.5 lx (sP 0.5) and skeleton photoperiods consisting of two 30-min LPs of 80 lx, given against a background illuminance of 0.5 lx either symmetrically at 12-h intervals (PP 12:12) or asymmetrically at 9- and 15-h intervals (PP 9:15). The phase-response characteristics in Aotus, as evidenced by the phase-response curve, generally correspond to those of nocturnal rodents, providing that this neotropical simian primate chronobiologically is a genuine nocturnal species. When free-running with a spontaneous period close to 24 h (24.3 +/- 0.1 h), the PP 12:12 produced entrainment in only two of five owl monkeys, whereas the sP 0.5 entrained four of them. The PP 9:15, however, brought about stable entrainment of the circadian rhythms of locomotor activity, feeding activity, and core temperature in all animals tested (n = 8). Changes in phase position of the activity time with the endogenous rhythm entrained by a PP 12:12, by an sP 0.5, or by a PP 9:15 give evidence that both LPs of a skeleton photoperiod contribute to the phase setting of the circadian system. When free-running with a considerably lengthened spontaneous period (tau greater than or equal to 25.5 h), even the sP 0.5 and the PP 9:15 failed to entrain the owl monkeys' circadian rhythms, whereas a 24-h photoperiod with a very long LP of 3 h caused entrainment. The results indicate that in Aotus lemurinus griseimembra, in addition to the nonparametric light effects, parametric light effects play a significant role in the entrainment of circadian rhythms by LD cycles.

Animals↗
PubMed1991

Research note: evaluation of humoral and delayed hypersensitivity responses in cockerels reared under constant light or a twelve hour light:twelve hour dark photoperiod.

Immature cockerels were reared under constant light [24 h light (L):0 h dark (D)] or a 12L:12D photoperiod in order to evaluate the effect of constant light on immunoresponsiveness. At 10 wk of age males were immunized with SRBC, with reimmunization occurring either 3 or 8 wk later. Animals reared under constant light had lower (P less than .05) anti-SRBC antibody titers than the 12L:12D males. Additionally, the pattern of the antibody response following secondary immunizations were different, with 24L:0D males exhibiting no increase in antibody titers between Days 3 and 9 postinjection. Delayed hypersensitivity responses of 24L:0D males were lower (P less than .05) than those of 12- or 16-wk-old 12L:12D males. Taken together, these results suggest that circadian light:dark cycles may play a role in modulating the immune system.

Animals↗
PubMed1997

Lighting test partnership: Southern California/Kaiser Permanente lighting study.

Energy-reduction conservation efforts are in the interest of any well-run health care facility. Energy-efficient lighting and lighting systems can deliver significant energy savings while maintaining optimum lighting levels. This document is a result of a lighting study conducted by Southern California Edison's Customer Solution's Group and Kaiser Permanente to help resolve some issues relating to future lighting projects. In particular, specular reflectors as an issue was addressed.

California↗
PubMedDate not supplied

Effect of glutaraldehyde-based cold sterilization solutions on light transmission of single-use, plastic light-curing tips.

Previous research has demonstrated that autoclaving of conventional curing tips results in the build-up of an opaque scale on the curing tips ends, greatly reducing light intensity output. Cold sterilization of conventional light-curing tips in most glutaraldehyde-based solutions did not damage the tip or decrease light-transmission quality. However, the specific brand of cold sterilant was found to be of importance, as one specific product was shown to decrease light-tip intensity values irreversibly, even after subsequent tip polishing. A decrease in light intensity output from the curing source significantly affects polymer cure and the biological properties of the restorative material.

Analysis of Variance↗
PubMed1995

Balancing photosynthetic light-harvesting and light-utilization capacities in potato leaf tissue during acclimation to different growth temperatures.

We investigated the effect of temperature during growth and development on the relationship between light-harvesting capacity, indicated by chlorophyll concentration, and light-utilization potential, indicated by light- and bicarbonate-saturated photosynthetic oxygen evolution, in Solanum tuberosum L. cv. Norland. Clonal plantlets were transplanted and grown at 20 degrees C for 2 weeks before transfer to 12, 16, 20, 24 and 28 degrees C for 6 weeks. After 4 weeks of the temperature treatments, leaf tissue fresh weights per area were one-third higher in plants grown at 12 degrees C vs those grown at 28 degrees C. Conversely, chlorophyll content per area in tissue grown at 12 degrees C was less than one-half of that of tissue grown at 28 degrees C at 4 weeks. Photosynthetic capacity measured at a common temperature of 20 degrees C and expressed on a chlorophyll basis was inversely proportional to growth temperature. Leaf tissue from plants grown at 12 degrees C for 4 weeks had photosynthetic rates that were 3-fold higher on a chlorophyll basis than comparable tissue from plants grown at 28 degrees C. These results suggest that the relationship between light-harvesting capacity and light-utilization potential varies 3-fold in response to the growth temperatures examined. The role of this response in avoidance of photoinhibition is discussed.

Acclimatization↗
PubMedDate not supplied

Two-year color changes of light-cured composites: influence of different light-curing units.

This study determined color changes in a composite cured with various types of curing units after two years. A hybrid (Clearfil AP-X) composite was cured with a conventional halogen, a high intensity halogen, a plasma arc and a light emitting diode unit. The specimens were stored in light-proof boxes after the curing procedure to avoid further exposure to light and stored in 37 degrees C in 100% humidity. Colorimetric values of the specimens immediately after curing and after two years were measured using a colorimeter. The CIE 1976 L*a*b color system was used to determine color differences. Differences from baseline were calculated as deltaE*ab. Data were analyzed with two-way analysis of variance (p<0.05). The deltaE*ab values varied significantly, depending on the curing unit used. The specimens cured with a plasma arc curing unit induced significantly higher color changes than any other specimen and the color differences were also visually appreciable by the non-skilled operator (deltaE*ab >2.5). The specimens cured with a high intensity halogen curing unit produced the lowest color change; however, there were no statistically significant differences among the color changes of specimens cured with conventional halogen, high intensity halogen and the light emitting diode unit, and the color changes were not clinically relevant (deltaE*ab <2.5). The results of this study suggest that composite materials undergo measurable changes due to curing unit exposure. The specimens cured with a plasma arc light showed the highest color changes as compared to specimens cured with other curing units.

Analysis of Variance↗