Ultra-weak Photon Emission Measurement Research Articles

Skin lightness affects ultraviolet A-induced oxidative stress: Evaluation using ultraweak photon emission measurement.

The human skin is usually exposed to ultraviolet A (UVA) in the sunlight and experiences oxidative stress associated with skin disorders and aging. Although oxidative stress caused by UVA exposure is assumed to be dependent on skin colour, few studies have demonstrated this dependency. We investigated the effects of skin colour on UVA-induced oxidative stress using ultraweak photon emission (UPE) generated from the skin during oxidation processes. The UPE intensities of skin samples were detected using a photomultiplier tube every second without any labelling. We irradiated skin tissue of different colours with UVA and measured UPE over time. UVA-induced UPE could be detected from immediately after irradiation to 2h after irradiation, indicating persistent oxidative stress. Skin lightness (L*) positively correlates with UPE intensity. Lighter-coloured skin exhibited more UVA-induced UPE, indicating higher oxidative stress. Additionally, oxidative stress persisted significantly more in lighter skin compared with darker skin. Skin tissues exhibited pigment darkening after UVA irradiation. Our results suggest that skin lightness affects oxidative stress induced by UV irradiation. Our study demonstrated the relationship between skin lightness and UVA-induced oxidative stress for the first time and offers new photodermatological insights into the human skin.

Effects of silver nanoparticles on wheat seedlings growth evaluated using ultra-weak photon emissions measurements / Efeitos das nanopartículas de prata no crescimento das plântulas de trigo avaliadas através de medições de emissões de fótons ultra fracos

Ultra-weak photon emission (UWPE) is used to evaluate the effects of silver nanoparticles (AgNP) on wheat seeds germination. Three test series, using wheat seed samples in triplicate, irrigated by three different solutions: AgNP colloid, deionized water and sodium citrate dihydrate solution, had their UWPE data acquired for 24 hours at the fifth day of germination, inside an especially designed dark chamber. The photon-counts summation of each test was calculated, and correlated to its respective germination parameters – total biomass gain and total elongation of seedling aerial part. AgNP tests presented inferior total photon-counts summation and germination parameters levels, as compared to the tests using the other two solutions. Besides, the UWPE temporal profiles decreased over time for the AgNP tests, while for the other two test solutions the emission increased over time. Those results points changes in physiologic functions as deleterious effects of the AgNP contaminant. Principal Component Analysis (PCA) was applied, and the AgNP tests could be separated of the other tests due to germination parameters and UWPE data. The proposed method using UWPE measurements seems to be feasible to evaluate germination parameters of wheat seed in the presence of AgNP, and potentially in the presence of other contaminants.

Non-invasive evaluation of skin oxidative stress using ultra-weak photon emission measurement

Non-invasive evaluation of skin oxidative stress using ultra-weak photon emission measurement

Non-invasive evaluation of skin oxidative stress using ultra-weak photon emission measurement

Non-invasive evaluation of skin oxidative stress using ultra-weak photon emission measurement

An Experimental Investigation of Ultraweak Photon Emission from Adult Murine Neural Stem Cells

Neurons like other living cells may have ultraweak photon emission (UPE) during neuronal activity. This study is aimed to evaluate UPE from neural stem cells (NSC) during their serial passaging and differentiation. We also investigate whether the addition of silver nanoparticles (AgNPs) or enhancement of UPE (by AgNPs or mirror) affect the differentiation of NSC. In our method, neural stem and progenitor cells of subventricular zone (SVZ) are isolated and expanded using the neurosphere assay. The obtained dissociated cells allocated and cultivated into three groups: groups: I: cell (control), II: cell + mirror, and III: cell + AgNPs. After seven days, the primary neurospheres were counted and their mean number was obtained. Serial passages continuous up to sixth passages in the control group. Differentiation capacity of the resulting neurospheres were evaluated in vitro by immunocytochemistry techniques. Measurement of UPE was carried out by photomultiplier tube (PMT) in the following steps: at the end of primary culture, six serial cell passages of the control group, before and after of the differentiation for 5 minutes. The results show that neither mirror nor AgNPs affect on the neurosphere number. The UPE of the NSC in the sixth subculturing passage was significantly higher than in the primary passage (P < 0.05). AgNPs significantly increased the UPE of the NSC compared to the control group before and after the differentiation (P < 0.05). Also, the treatment with AgNPs increased 44% neuronal differentiation of the harvested NSCs. UPE of NSC after the differentiation was significantly lower than that before the differentiation in each groups, which is in appropriate to the cell numbers (P < 0.0001). The mirror did not significantly increase UPE, neither before nor after the differentiation of NSC. As a conclusion, NSC have UPE-properties and the intensity is increased by serial passaging that are significant in the sixth passage. The AgNPs increases the UPE intensity of NSC that pushes more differentiation of NSC to the neurons. The mirror was not effective in enhancement of UPE. As a result, UPE measurement may be suitable for assessing and studying the effects of nanoparticles in living cells and neurons.

Imaging of ultraweak photon emission for evaluating the oxidative stress of human skin

Ultraweak photon emission (UPE) is generally observed in living organisms and often designated as biophoton emission. UPE is detectable from human skin, and its intensity increases by external stress such as ultraviolet (UV) irradiation. Presently, UPE measurement is used to evaluate oxidation status. The fact that the electronically excited species responsible for UPE are formed by reactive oxygen species (ROS)-induced lipid peroxidation and protein and nucleic acid oxidation is well known. The human skin undergoes oxidative stress by UV irradiation, resulting in various skin complications; therefore, it is essential to know the oxidation status of the skin. In this study, we assessed the characteristics of UV-induced UPE in the skin by the imaging and spectroscopy systems. Two-dimensional images obtained by a highly sensitive imaging system using a cooled charge-coupled device (CCD) camera revealed that UPE intensity increases with the amount of UV and is suppressed by antioxidants. Additionally, it is indicated that UPE is generated not only from the epidermis but also from the dermis. The spectra of UPE induced by UVA or UVB showed similar peaks in the visible light region. Furthermore, we confirmed the efficiency of sunscreen by the imaging technique. UPE measurement is a useful method to evaluate UV-induced oxidation in the human skin, and UPE imaging is an effective method to visually evaluate oxidative stress in the human skin.

Traditional Chinese Medicine-Based Subtyping of Early-Stage Type 2 Diabetes Using Plasma Metabolomics Combined with Ultra-Weak Photon Emission

The prevalence of type 2 diabetes mellitus (T2DM) is increasing rapidly worldwide. Because of the limited success of generic interventions, the focus of the disease study has shifted toward personalized strategies, particularly in the early stages of the disease. Traditional Chinese medicine (TCM) is based on a systems view combined with personalized strategies and has improved our knowledge of personalized diagnostics. From a systems biology perspective, the understanding of personalized diagnostics can be improved to yield a biochemical basis for such strategies; for example, metabolomics can be used in combination with other system-based diagnostic methods such as ultra-weak photon emission (UPE). In this study, we investigated the feasibility of using plasma metabolomics obtained from 44 pre-T2DM subjects to stratify the following TCM-based subtypes: Qi-Yin deficiency, Qi-Yin deficiency with dampness, and Qi-Yin deficiency with stagnation. We studied the relationship between plasma metabolomics and UPE with respect to TCM-based subtyping in order to obtain biochemical information for further interpreting disease subtypes. Principal component analysis of plasma metabolites revealed differences among the TCM-based pre-T2DM subtypes. Relatively high levels of lipids (e.g., cholesterol esters and triglycerides) were important discriminators of two of the three subtypes and may be associated with a higher risk of cardiovascular disease. Plasma metabolomics data indicate that the lipid profile is an essential component captured by UPE with respect to stratifying subtypes of T2DM. The results suggest that metabolic differences exist among different TCM-based subtypes of pre-T2DM, and profiling plasma metabolites can be used to discriminate among these subtypes. Plasma metabolomics thus provides biochemical insights into system-based UPE measurements. (C) 2019 THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company.

Application of ultra-weak photon emission measurements in agriculture

Here we report our two applications of ultra-weak photon emission (UPE) measurements in agriculture. One is to find new types of agrochemicals that potentiate plants’ defense, so-called “plant activator”. We first analyzed the relation between plant defense and Elicitor-Responsive Photon Emission (ERPE) using a combination of rice cells and a chitin elicitor. Pharmacological analyses clarified that ERPE was generated as a part of the chitin elicitor-responsive defense in close relation with the generation of reactive oxygen species (ROS). Then we successfully detected the activity of plant activators as the potentiation of ERPE, and developed a new screening system for plant activators based on this principle. Another UPE application is to distinguish herbicide-resistant weeds from susceptible ones by measuring UPE in weeds. In our study, it was revealed that the weed biotypes resistant to sulfonylurea (SU) herbicides, one of the major herbicide groups, showed stronger UPE than susceptible ones after an SU herbicide treatment. By further analysis with a pharmacological and RNAi study, we found that the detoxifying enzyme P450s contributed to the UPE increase in SU herbicide resistant weeds. It is considered that weeds resistant to herbicides other than SU might also be able to be distinguished from susceptible ones by UPE measurement, as long as the herbicides are subject to detoxification by P450s.

Using multifractal analysis of ultra-weak photon emission from germinating wheat seedlings to differentiate between two grades of intoxication with potassium dichromate

The aim of the present study was to test whether the multifractal properties of ultra-weak photon emission (UPE) from germinating wheat seedlings (Triticum aestivum) change when the seedlings are treated with different concentrations of the toxin potassium dichromate (PD). To this end, UPE was measured (50 seedlings in one Petri dish, duration: approx. 16.6- 28 h) from samples of three groups: (i) control (group C, N = 9), (ii) treated with 25 ppm of PD (group G25, N = 32), and (iii) treated with 150 ppm of PD (group G150, N = 23). For the multifractal analysis, the following steps where performed: (i) each UPE time series was trimmed to a final length of 1000 min; (ii) each UPE time series was filtered, linear detrended and normalized; (iii) the multifractal spectrum (f(α)) was calculated for every UPE time series using the backward multifractal detrended moving average (MFDMA) method; (iv) each multifractal spectrum was characterized by calculating the mode (αmode) of the spectrum and the degree of multifractality (Δα); (v) for every UPE time series its mean, skewness and kurtosis were also calculated; finally (vi) all obtained parameters where analyzed to determine their ability to differentiate between the three groups. This was based on Fisher's discriminant ratio (FDR), which was calculated for each parameter combination. Additionally, a non-parametric test was used to test whether the parameter values are significantly different or not. The analysis showed that when comparing all the three groups, FDR had the highest values for the multifractal parameters (αmode, Δα). Furthermore, the differences in these parameters between the groups were statistically significant (p < 0.05). The classical parameters (mean, skewness and kurtosis) had lower FDR values than the multifractal parameters in all cases and showed no significant difference between the groups (except for the skewness between group C and G150). In conclusion, multifractal analysis enables changes in UPE time series to be detected even when they are hidden for normal linear signal analysis methods. The analysis of changes in the multifractal properties might be a basis to design a classification system enabling the intoxication of cell cultures to be quantified based on UPE measurements.

Using ultra-weak photon emission to determine the effect of oligomeric proanthocyanidins on oxidative stress of human skin

Exposure of skin to ultraviolet (UV) radiation triggers oxidative stress in skin tissue that can lead to erythema, early skin aging or even cancer. It is suggested that oligomeric proanthocyanidins (OPCs), phytonutrients that belong to the polyphenol family have an anti-oxidant/anti-inflammatory activity on the skin. Measuring ultra-weak photon emission (UPE) is a non-invasive, fairly-sensitive and convenient technique for continuously monitoring oxidative stress. The present study was undertaken to confirm anti-oxidant activity of the specific OPCs cream formulation in human skin by measuring UPE of skin. In the present study 25 healthy female subjects participated. As a baseline measurement of skin, UPE was recorded from the dorsal surface of the subjects’ hands before (spontaneous UPE) and after exposure to UV (UV-induced UPE). The effects of the OPCs cream on spontaneous and UV-induced UPE were measured using a fractionated UV exposure protocol. UV exposure resulted in an increase in UPE from both hands. Repeat UV exposure also resulted in a long-term increase of spontaneous UPE. This is likely due to depletion of anti-oxidant capacity of skin resulting in sensitization of skin to UV. It was assessed by measuring spontaneous UPE at 80 min after each UV exposure. Application of the OPCs cream immediately after UV exposure resulted in a significant (approx. 30%) decrease in UV-induced UPE. Topical OPCs cream application also reduced sensitization of skin to UV following repeated UV exposure (i.e., reduced long-term increase in spontaneous UPE). This study indicates that the specific OPCs cream formulation significantly decreases UV-induced oxidative stress in human skin based on UPE measurement. It therefore suggests that regular use of this OPCs cream might protect skin from harmful effects of UV.

Topical formulation containing natural oligomeric proanthocyanidins (OPCS) reduces UV-induced oxidative stress in skin as assessed by ultra-weak photon emission (UPE)

Background OPCs are natural phytonutrients of the flavanol family. The dietary supplement ingredient MASQUELIER's ® OPCs has been demonstrated to exhibit antioxidant, anti-inflammatory and vasculo-protective properties in humans, which suggested potential benefits as a topical formulation for skin health. Exposure of skin to UV triggers oxidative stress in skin tissue that can lead to erythema, skin aging or even cancer. Our previous studies have shown that a specific topical formulation (cream containing MASQUELIER's ® OPCs) can significantly reduce UV-induced erythema in skin of human subjects and in animals, indicating it has antioxidant activity in skin. Objective This study was undertaken to further establish antioxidant activity of the specific OPCs cream formulation in human skin by measuring ultra-weak photon emission (UPE) of skin. UPE measurement in skin is a non-invasive, fairly-sensitive and convenient technique for continuously monitoring oxidative stress (Sauermann, 1999). Methods The study was an open-label study in 25 healthy volunteers. Measurement of skin UPE was performed on the dorsal surface of the subjects’ hands before (spontaneous UPE) and after exposure to UV (UV-induced UPE). The effects of the OPCs cream on spontaneous and UV-induced UPE were measured using a fractionated UV exposure protocol. Results Within each subject, spontaneous UPE of the right and left hand were found to be significantly correlated ( r =0.9; p =0.000). UV-induced UPE of the right and left hand were also significantly correlated ( r =0.87; p =0.000). UV exposure resulted in a long-term (>80 min) increase of spontaneous UPE. This is likely due to depletion of antioxidant capacity of skin, which is quantifiable by the fractionated UV-exposure protocol. Application of the OPCs cream immediately after UV exposure resulted in a significant (approx. 30%) decrease in UV-induced UPE. Topical OPCs application also reduced UV-induced long-term increase in spontaneous UPE, indicating prevention depletion of antioxidant capacity of skin by UV. Conclusions This study indicates that the specific OPCs cream formulation significantly decreases UV-induced oxidative stress in human skin based on UPE measurement, thereby suggesting that regular use of this OPCs cream might protect skin from harmful effects of UV.

Non‐invasive monitoring of oxidative skin stress by ultraweak photon emission measurement. II: biological validation on ultraviolet A‐stressed skin

Several physical or chemical environmental stressors generate reactive oxygen species, which trigger oxidation reactions of cells or tissues and thereby induce a correlated ultraweak photon emission (UPE) signal. The present study was designed to qualify and validate UPE measurement following ultraviolet (UV) excitation of porcine and human skin as an analytical method to assess the potency of topical antioxidants in vivo. UPE of porcine skin in vitro and human skin in vivo following excitation with UVA was recorded using sensitive photomultiplier systems. For validation purposes, the effects of variation of extrinsic and intrinsic parameters encompassing skin thickness, humidity, temperature, pH, and composition of the surrounding atmosphere were assessed. Signals were analyzed with regard to overall signal intensity and spectral distribution. In two clinical trials enrolling 20 volunteers each, the effects of topical antioxidant treatment on UVA-induced UPE were validated. Different stressors encompassing exposition to ozone, UVA irradiation, or even cigarette smoke induced UPE of skin. Critical parameters affecting the quality and quantity of the UPE signal were the spectral composition of the exciting UV light, skin temperature, skin humidity, and the O(2) concentration of the surrounding atmosphere. Generally, UVA-induced UPE decreased with increasing temperature, humidity, and O(2) concentration. Skin pH had no significant effect on UPE with regard to signal quality and quantity over a pH range of 2.8-8.2. In a clinical study UPE measurement following UVA excitation could precisely reflect a dose-dependent antioxidant effect of topically applied vitamin C and alpha-glucosylrutin. Our data indicate that UVA irradiation induces UPE especially in deeper (living) skin layers, where antioxidants must be active in order to interfere with accelerated skin ageing. Based on the clinical data, and with knowledge of modulating external variables, UPE measurement following UV excitation can be qualified as a reliable and valid method for the non-invasive measurement of antioxidant efficacy on the skin.

Effect of long-term storage on induced photon emission of boar spermatozoa

Ultraweak photon emission measurements were found to be a useful tool for investigating the influence of stress factors on cells. In the present study, induced photon emission of boar spermatozoa was investigated using a luminometer during a 12-day storage at 15&amp;deg;C in Biosolwens extender. It was shown that the day of storage had a significant effect on some photon emission parameters. During storage, a significant increase in the Integral, Peak max. and Slope max. parameters and a decline in the T.-half (fall) parameter were observed. A significant correlation was observed between photon emission parameters and sperm motility. In conclusion, the results of the present study indicate that the measurement of induced photon emission can be an alternative, sensitive and relatively simple method for assessing the effect of preservation on oxidative damage to boar spermatozoa. &amp;nbsp;

Changes in ATP level and iron-induced ultra-weak photon emission in bull spermatozoa, caused by membrane peroxidation during thermal stress.

ATP level, cell motility and viability, oxygen uptake, pyruvate kinase activity, and ultra-weak photon emission (UPE) induced by red-ox Fe(2+)-ascorbate cycling system were studied in fresh, in previously equilibrated in a glycerol diluent, and in cryopreserved bull spermatozoa, exposed to thermal stress by incubation of the cells at 44 degrees C. A sharp drop in motility and viability of fresh spermatozoa and even more so, of equilibrated and cryopreserved cells was accompanied by accumulation of ATP. When cell movement was totally inhibited, ATP utilization was decreased, while chemical energy continued to be produced by cell pyruvate kinase, one of the key glycolytic enzymes, which in spermatozoa is very active (6500 IU/g protein) and insensitive to feed-back inhibition by excess of ATP and L-cysteine. Accumulation of ATP during incubation at 44 degrees C in 0.9% NaCl was accompanied by rapid decrease in oxygen consumption by fresh spermatozoa and an increase in Fe(2+)-ascorbate induced UPE, followed by a sharp decrease in ATP level observed at the end of induced UPE measurement. The increase in photon emission due to lipid peroxidation was highly correlated with the increase in cell ATP level caused by thermal stress.