ultra-weak photon emission
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Ultra-weak photon emission originates from the relaxation of electronically excited species formed in the biological systems such as microorganisms, plants and animals including humans. Electronically excited species are formed during the oxidative metabolic processes and the oxidative stress reactions that are associated with the production of reactive oxygen species (ROS). The review attempts to overview experimental evidence on the involvement of superoxide anion radical, hydrogen peroxide, hydroxyl radical and singlet oxygen in both the spontaneous and the stress-induced ultra-weak photon emission. The oxidation of biomolecules comprising either the hydrogen abstraction by superoxide anion and hydroxyl radicals or the cycloaddition of singlet oxygen initiate a cascade of oxidative reactions that lead to the formation of electronically excited species such as triplet excited carbonyl, excited pigments and singlet oxygen. The photon emission of these electronically excited species is in the following regions of the spectrum (1) triplet excited carbonyl in the near UVA and blue-green areas (350-550nm), (2) singlet and triplet excited pigments in the green-red (550-750nm) and red-near IR (750-1000nm) areas, respectively and (3) singlet oxygen in the red (634 and 703nm) and near IR (1270nm) areas. The understanding of the role of ROS in photon emission allows us to use the spontaneous and stress-induced ultra-weak photon emission as a non-invasive tool for monitoring of the oxidative metabolic processes and the oxidative stress reactions in biological systems in vivo, respectively.
- MeSH
- elektrony MeSH
- fotobiologie metody MeSH
- fotony * MeSH
- lidé MeSH
- oxidace-redukce MeSH
- reaktivní formy kyslíku metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
Evolution has permitted a wide range of medium for communication between two living organism varying from information transfer via chemical, direct contact or through specialized receptors. Past decades have evidenced the existence of cell-to-cell communication in living system. Several studies have demonstrated the existence of one cell system influencing the other cells by means of electromagnetic radiations investigated by the stimulation of cell division, neutrophils activation, respiratory burst induction and alteration in the developmental stages, etc. The responses were evaluated by methods such as chemiluminescence, ultra-weak photon emission, generation of free oxygen radicals, and level of thiobarbituric acid-reactive substances (TBARS). The cellular communication is hypothesized to occur via several physical phenomenon's, however the current review attempts to provide thorough information and a detailed overview of experimental results on the cell-to-cell communication observed in different living system via ultra-weak photon emission to bring a better understanding and new perspective to the phenomenon.
Ultra-weak photon emission (UPE) is an endogenous bioluminescence phenomenon present in all biological samples with an active oxidative metabolism, even without an external pre-illumination. To verify the potential of UPE for non-invasive monitoring of metabolism and growth in germinating plants, the aim of this study was to investigate the UPE from a model system - germinating mung bean seedlings (Vigna radiata) - and analyze the statistical properties of UPE during the growth in two different conditions of imbibition (pure water and 1% sucrose). We found that in all days and in both conditions, photocount distributions of UPE time series follow the negative binomial distribution whose parameters changed during the growth due to the increasing ratio of signal-to-detector dark count. Correspondingly for both groups, the mean values of UPE increased during the seedlings growth, while the values of Fano factor show a decreasing trend towards 1 during the 6day period. While our results do not show any significant difference in hypocotyl length and weight gain between the two groups of mung seedlings, there is an indication of a tiny suppressing effect of sucrose on UPE intensity. We believe that UPE can be exploited for a sensitive non-invasive analysis of oxidative metabolism during the plant development and growth with potential applications in agricultural research.
- MeSH
- fotony * MeSH
- klíčení * MeSH
- vigna chemie růst a vývoj MeSH
- Publikační typ
- časopisecké články MeSH
Ultra-weak photon emission (UPE) is light emitted spontaneously by biological systems without the use of specific luminescent complexes. UPE is emitted in the near-UV/UV-Vis/near-IR spectra during oxidative metabolic reactions; however, the specific pathways involved in UPE remain poorly understood. Here, we used HL-60 cells, a human promyelocytic cell line that is often used to study respiratory burst, as a model system to measure UPE kinetics together with metabolic changes. HL-60 cells were differentiated into neutrophil-like cells by culturing in all-trans-retinoic acid for 7days. We then used a targeted metabolomics approach with capillary electrophoresis-mass spectrometry to profile intracellular metabolites in HL-60 cells and to investigate the biochemical changes based on the measured UPE profile. Our analysis revealed that the levels of specific metabolites, including putrescine, creatine, β-alanine, methionine, hydroxyproline, serine, and S-adenosylmethionine, were significantly altered in HL-60 cells after inducing respiratory burst. A comparison with recorded UPE data revealed that the changes in putrescine, glutathione, sarcosine, creatine, β-alanine, methionine, and hydroxyproline levels were inversely correlated with the change in UPE intensity. These results suggest that these metabolic pathways, particular the methionine pathway, may play a role in the observed changes in UPE in HL-60 cells and therefore demonstrate the potential for using UPE to monitor metabolic changes.
Two-dimensional imaging of spontaneous ultra-weak photon emission was measured in the yeast cells, Arabidopsis plant and the human hand using highly sensitive charge coupled device (CCD) camera. For the first time, the detail analysis of measuring parameters such as accumulation time and binning is provided with the aim to achieve two-dimensional images of spontaneous ultra-weak photon emission of good quality. We present data showing that using a hardware binning with binning factor 4 × 4, the accumulation time decreases in the following order: yeast cells (30 min) > the human hand (20 min) > Arabidopsis plant (10 min). Analysis of measuring parameters provides a detailed description of standard condition to be used for two-dimensional spontaneous ultra-weak photon imaging in microbes, plants and animals. Thus, CCD imaging can be employed as a unique tool to examine the oxidative state of the living organism with the application in microbiological, plant and medical research.
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- Arabidopsis fyziologie MeSH
- časové faktory MeSH
- fotony * MeSH
- lidé MeSH
- oxidace-redukce MeSH
- ruka fyziologie MeSH
- Saccharomyces cerevisiae fyziologie MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
In the human skin, reactive oxygen species (ROS) produced continuously during oxidative metabolic processes (cellular respiration, oxidative burst) are essential for various cellular processes such as defense against infection, cellular signaling and apoptosis. On the other hand, when the formation of ROS exceeds a capacity of the non-enzymatic and the enzymatic antioxidant defense system, ROS cause the damage to the human skin known to initiate premature skin aging and skin cancer. In this study, two-dimensional spontaneous ultra-weak photon emission from the human skin has been measured using a highly sensitive charged coupled device (CCD) camera. It is demonstrated here that two-dimensional ultra-weak photon emission from the human skin increases with the topical application of exogenous ROS in the following order: hydrogen peroxide (H₂O₂) < superoxide anion radical (O₂•⁻) < hydroxyl radical (HO•). We propose here that the two-dimensional ultra-weak photon emission can be used as a non-invasive tool for the spatial and temporal monitoring of oxidative stress in the human skin.
- MeSH
- diagnostické zobrazování metody MeSH
- dospělí MeSH
- elektronová paramagnetická rezonance MeSH
- fotometrie přístrojové vybavení metody MeSH
- fotony MeSH
- fyziologie kůže účinky léků MeSH
- hlava fyziologie MeSH
- hydroxylový radikál metabolismus MeSH
- kůže účinky léků metabolismus MeSH
- lidé MeSH
- oxidační stres účinky léků MeSH
- peroxid vodíku aplikace a dávkování farmakokinetika farmakologie MeSH
- reaktivní formy kyslíku aplikace a dávkování metabolismus farmakologie MeSH
- ruka fyziologie MeSH
- superoxidy metabolismus MeSH
- trup fyziologie MeSH
- xanthin aplikace a dávkování farmakologie MeSH
- xanthinoxidasa aplikace a dávkování farmakologie MeSH
- železo aplikace a dávkování farmakologie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Reactive oxygen species formed as a response to various abiotic and biotic stresses cause an oxidative damage of cellular component such are lipids, proteins and nucleic acids. Lipid peroxidation is considered as one of the major processes responsible for the oxidative damage of the polyunsaturated fatty acid in the cell membranes. Various methods such as a loss of polyunsaturated fatty acids, amount of the primary and the secondary products are used to monitor the level of lipid peroxidation. To investigate the use of ultra-weak photon emission as a non-invasive tool for monitoring of lipid peroxidation, the involvement of lipid peroxidation in ultra-weak photon emission was studied in the unicellular green alga Chlamydomonas reinhardtii. Lipid peroxidation initiated by addition of exogenous linoleic acid to the cells was monitored by ultra-weak photon emission measured with the employment of highly sensitive charged couple device camera and photomultiplier tube. It was found that the addition of linoleic acid to the cells significantly increased the ultra-weak photon emission that correlates with the accumulation of lipid peroxidation product as measured using thiobarbituric acid assay. Scavenging of hydroxyl radical by mannitol, inhibition of intrinsic lipoxygenase by catechol and removal of molecular oxygen considerably suppressed ultra-weak photon emission measured after the addition of linoleic acid. The photon emission dominated at the red region of the spectrum with emission maximum at 680 nm. These observations reveal that the oxidation of linoleic acid by hydroxyl radical and intrinsic lipoxygenase results in the ultra-weak photon emission. Electronically excited species such as excited triplet carbonyls are the likely candidates for the primary excited species formed during the lipid peroxidation, whereas chlorophylls are the final emitters of photons. We propose here that the ultra-weak photon emission can be used as a non-invasive tool for the detection of lipid peroxidation in the cell membranes.
- MeSH
- buněčná membrána účinky léků metabolismus MeSH
- Chlamydomonas reinhardtii cytologie účinky léků metabolismus MeSH
- fotony MeSH
- histidin farmakologie MeSH
- hydroxylový radikál metabolismus MeSH
- inhibitory lipoxygenas farmakologie MeSH
- kyselina linolová farmakologie MeSH
- kyslík metabolismus MeSH
- lipoxygenasa metabolismus MeSH
- malondialdehyd metabolismus MeSH
- mannitol farmakologie MeSH
- peroxidace lipidů účinky léků MeSH
- thiobarbituráty metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
This review attempts to summarize molecular mechanisms, spectral and intensity properties, detection techniques and applications of ultra-weak photon emission. Ultra-weak photon emission is the chemiluminescence from biological systems where electronically excited species are formed during oxidative metabolic or oxidative stress processes. It is generally accepted that photons are emitted (1) at near UVA, visible, and near IR spectral ranges from 350 to 1300nm and (2) at the intensity of photon emission in the range of several units to several hundreds (oxidative metabolic process) and several hundreds to several thousands (oxidative stress process) photons s(-1)cm(-2). Current development in detection using low-noise photomultiplier tubes and imaging using highly sensitive charge coupled device cameras allows temporal and spatial visualization of oxidative metabolic or oxidative stress processes, respectively. As the phenomenon of ultra-weak photon emission reflects oxidative metabolic or oxidative stress processes, it can be widely used as a non-invasive tool for monitoring of the physiological state of biological systems.
- MeSH
- fotobiologie metody MeSH
- fotony * MeSH
- lidé MeSH
- spektrální analýza MeSH
- terminologie jako téma * MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
In recent years, excessive oxidative metabolism has been reported as a critical determinant of pathogenicity in many diseases. The advent of a simple tool that can provide a physiological readout of oxidative stress would be a major step towards monitoring this dynamic process in biological systems, while also improving our understanding of this process. Ultra-weak photon emission (UPE) has been proposed as a potential tool for measuring oxidative processes due to the association between UPE and reactive oxygen species. Here, we used HL-60 cells as an in vitro model to test the potential of using UPE as readout for dynamically monitoring oxidative stress after inducing respiratory burst. In addition, to probe for possible changes in oxidative metabolism, we performed targeted metabolomics on cell extracts and culture medium. Lastly, we tested the effects of treating cells with the NADPH oxidase inhibitor diphenyleneiodonium chloride (DPI). Our results show that UPE can be used as readout for measuring oxidative stress metabolism and related processes.
All living organisms emit ultra-weak photon emission as a result of oxidative processes caused by the physical or chemical stress factors. In the present study, the effect of oxidative stress induced by the exposure of the plant model Arabidopsis thaliana to ultraviolet A (UVA) radiation was studied using ultra-weak photon emission. When Arabidopsis plants and leaves were exposed to UVA radiation, two kinetically distinguished phases in the ultra-weak photon emission decay were observed: the fast decay phase (τ1=0.805±0.024 min) and slow decay phase (τ2=4.321±0.166 min). The spectral analysis of the UVA radiation-induced ultra-weak photon emission showed that the photon emission during the fast decay phase is from both blue-green and red regions of the spectrum, whereas the photon emission during the slow decay phase is solely from the blue-green region of the spectrum. These observations reveal that triplet excited carbonyls contribute to ultra-weak photon emission during both fast and slow decay phases, whereas chlorophylls participate in the ultra-weak photon emission solely during the fast decay phase. It is illustrated here that the ultra-weak photon emission serves as a non-invasive method for the monitoring of oxidative stress in plants caused by UVA radiation.
