Addition Of GSH Research Articles

Modification of myofibrillar protein gelation under oxidative stress using combined inulin and glutathione.

The effects of inulin (1.5%), glutathione (GSH, 0.05%), and their combination (1.5% inulin+0.05% GSH) on the conformational structure and gel performance of pork myofibrillar protein (MP) under oxidation condition were examined. The addition of GSH significantly prevented oxidation-induced carbonylation, reduction of α-helix content, and protein aggregation. As a result, treatment with GSH significantly reduced the particle size of oxidized MP by 35%, increased the solubility by 17.3%, and improved the gelling properties. The presence of inulin also obviously enhanced the gelling behavior of MP under oxidation condition, although it could hardly inhibit the modification of MP structure caused by oxidation. Treatment with inulin+GSH exhibited the highest cooking yield (84.2%) and the best textural characteristics, with a denser and more uniform network structure comprising evenly distributed small pores. The findings of this study provide a useful method for processing meat protein gel products with better oxidative stability and textural properties.

A copper(II) displacement approach for fluorescent turn-on sensing of glutathione using salicylaldehyde modified polydopamine nanoparticles

The salicylaldehyde modified green-fluorescent polydopamine nanoparticles (PDASA NPs) was synthesized, characterized and applied for the sensing of glutathione (GSH). The oxidative polymerization of dopamine in the presence of salicylaldehyde at pH = 8.5 (10 mM PBS solution) formed the spherical-shaped PDASA NPs with an average diameter of ∼ 150 nm. The addition of Cu(II) to the solution of PDASA NPs in HEPES buffer (10 mM, pH = 7.4) quenched the fluorescence at 490 nm (λex = 390 nm). Experimental evidence supported the fluorescence quenching was static in nature with the estimated Stern-Volmer constant (KSV) of 4.00 × 103 M−1. The fluorescence was restored upon addition of GSH to the solution containing PDASA NPs and Cu(II), among the other examined amino acids (alanine, aspartic acid, glutamic acid, arginine, glycine, cysteine, histidine, serine, leucine, proline, threonine, tryptophan, lysine and methionine). The nanoprobe Cu(II)-PDASA NPs showed a good linearity between 2.20 × 10−5 M and 2.49 × 10−6 M for GSH with an estimated limit of detection of 2.84 × 10−7 M. The Cu(II)-PDASA NPs was applied for the quantification of GSH in urine and saliva samples.

Ce doped polyaniline nanoparticles for absorption and photoacoustic imaging response to GSH in vitro and in vivo.

Glutathione (GSH) is an important biological thiol in cells, which is involved in many physiological processes in the organism and regulates pathological processes of cells. Rapid and accurate monitoring of GSH in vitro and in vivo is quite needed in investigating important biochemical events. In this contribution, innovative cerium (Ce) doped polyaniline (Ce–Fe@PANI NPs) were prepared via Fe(III) induced oxidization polymerization method. Upon addition of GSH, the absorption of Ce–Fe@PANI NPs red shifted from the visible to the NIR region, confirming the excellent absorption response to GSH. Moreover, Ce–Fe@PANI NPs exhibited excellent photoacoustic (PA) imaging enhancement in tube and shifted the PA intensity peak from 680 nm to 820 nm upon addition of GSH. In vitro and in vivo experiment verified that Ce–Fe@PANI NPs can monitor GSH in deep tissues via PA imaging technology. Collectively, this research provides Ce–Fe@PANI NPs would serve as a powerful nanoplatform to realize PA imaging detection of GSH in vitro and in vivo.

Stimuli-Responsive Drug Delivery of Doxorubicin Using Magnetic Nanoparticle Conjugated Poly(ethylene glycol)-g-Chitosan Copolymer.

Stimuli-responsive nanoparticles are regarded as an ideal candidate for anticancer drug targeting. We synthesized glutathione (GSH) and magnetic-sensitive nanocomposites for a dual-targeting strategy. To achieve this goal, methoxy poly (ethylene glycol) (MePEG) was grafted to water-soluble chitosan (abbreviated as ChitoPEG). Then doxorubicin (DOX) was conjugated to the backbone of chitosan via disulfide linkage. Iron oxide (IO) magnetic nanoparticles were also conjugated to the backbone of chitosan to provide magnetic sensitivity. In morphological observation, images from a transmission electron microscope (TEM) showed that IO nanoparticles were embedded in the ChitoPEG/DOX/IO nanocomposites. In a drug release study, GSH addition accelerated DOX release rate from nanocomposites, indicating that nanocomposites have redox-responsiveness. Furthermore, external magnetic stimulus concentrated nanocomposites in the magnetic field and then provided efficient internalization of nanocomposites into cancer cells in cell culture experiments. In an animal study with CT26 cell-bearing mice, nanocomposites showed superior magnetic sensitivity and then preferentially targeted tumor tissues in the field of external magnetic stimulus. Nanocomposites composed of ChitoPEG/DOX/IO nanoparticle conjugates have excellent anticancer drug targeting properties.

GSH Levels Serve As a Biological Redox Switch Regulating Sulforaphane-Induced Cell Fate in Human Lens Cells.

PurposeSulforaphane (SFN) is a therapeutic phytochemical agent for many health conditions. SFN-induced cytotoxicity is shown to have promise in preventing posterior capsule opacification (PCO). In the current study, we aimed to elucidate key processes and mechanisms linking SFN treatment to lens cell death.MethodsThe human lens epithelial cell line FHL124 and central anterior epithelium were used as experimental models. Cell death was assessed by microscopic observation and cell damage/viability assays. Gene or protein levels were assessed by TaqMan RT-PCR or immunoblotting. Mitochondrial networks and DNA damage were assessed by immunofluorescence. Mitochondrial membrane potential, activating transcription factor 6 (ATF6) activity, ratio of reduced glutathione (GSH) to oxidized glutathione (GSSG), and glutathione reductase (GR) activity were measured using different light reporter assays. SFN metabolites were analyzed by LC-MS/MS.ResultsTreatment with N-acetylcysteine (NAC), a reactive oxygen species scavenger, prevented SFN-induced cell death in both models. NAC also significantly protected FHL124 cells from SFN-induced mitochondrial dysfunctions, endoplasmic reticulum stress (ERS), DNA damage and autophagy. SFN significantly depleted GSH, the major antioxidant in the eye, and reduced GR activity, despite doubling its protein levels. The most abundant SFN conjugate detected in lens cells following SFN application was SFN–GSH. The addition of GSH protected lens cells from all SFN-induced cellular events.ConclusionsSFN depletes GSH levels in lens cells through conjugation and inhibition of GR activity. This leads to increased reactive oxygen species and oxidative stress that trigger mitochondrial dysfunction, ERS, autophagy, and DNA damage, leading to cell death. In summary, the work presented provides a mechanistic understanding to support the therapeutic application of SFN for PCO and other disorders.

Study on the Photochemical Reaction Process of 4-methyl-7-Hydroxycoumarin and Its Mechanism by Multi-Spectroscopic Technologies

The photochemical reaction process of 4-methyl-7-hydroxycoumarin (7H4MC) was studied by UV-Vis spectrometer and fluorescence spectroscopy. The results have shown that the characteristic peak of the UV-Vis spectra at 323 nm of 7H4MC undergoes a significant decrease in absorbance and a slight blue shift when was illuminated; the absorbance of the absorption peak at 279 nm rises, and there is a tendency for new peaks to appear. May be, there are structural changes or new materials generation. The addition of imidazole, VC, 3-indole methanol, GSH and other substances also have different effects on the photochemical reaction of 7H4MC. Among them, only imidazole has a certain inhibitory effect on the process of its photochemical reaction.

Smartphone-assisted ratiometric fluorescence sensing platform and logical device based on polydopamine nanoparticles and carbonized polymer dots for visual and point-of-care testing of glutathione

As a crucial biothiol, glutathione (GSH) plays a key role in the organisms. Monitoring GSH level is of great significance for disease diagnosis and biomedical research. In this work, polydopamine (PDA) nanoparticles-red fluorescent carbonized polymer dots (r-CPDs) based ratiometric fluorescence sensing platform was constructed and employed for GSH assay. Dopamine (DA) could be oxidized by cobalt oxyhydroxide (CoOOH) nanosheets and further polymerized into PDA nanoparticles with green fluorescence. However, in the presence of GSH, CoOOH nanosheets were reduced and decomposed, which prevented the production of PDA nanoparticles. In the sensing system, green-emitting PDA nanoparticles were employed as a response unit and r-CPDs were used as an internal reference unit. With the addition of GSH, the green fluorescence of PDA nanoparticles decreased as well as the red fluorescence of system remained relatively stable. Importantly, a distinct fluorescence color evolution from green to red was presented with a serious of GSH concentrations. Based on this, a portable smartphone-assisted ratiometric chromaticity analytical method was developed to achieve the on-site visual detection of GSH. Both the established ratiometric fluorescence and ratiometric chromaticity sensing methods for GSH assay have the merits of wide linear range, high sensitivity and excellent accuracy, which are suitable for the determination of GSH in human serum and exhibit great application potential in rapid and accurate monitoring of the GSH levels in clinical. Moreover, an ingenious logical device reflecting GSH levels was designed based on the two different fluorescence signals, which provided a new strategy for the intelligent online detection of GSH in complex biological matrices.

BSA-stabilized manganese phosphate nanoflower with enhanced nanozyme activity for highly sensitive and rapid detection of glutathione

The development of an efficient protein-inorganic nanohybrid with superior nanozyme activity for highly sensitive detection of glutathione (GSH) is essential for early diagnosis of human diseases. Herein, a rapid and highly sensitive colorimetric assay using self-assembled bovine serum albumin-hydrated manganese phosphate nanoflowers (MnPNF) as a biomimic oxidase is developed for GSH detection in human serum. The BSA can complex with Mn2+ to serve the nucleation center to produce MnPNF in the presence of phosphate-buffered saline (PBS). The morphology and surface characterization results show that the MnPNF is assembled with hierarchical nanoplates to form 500 nm nanoflowers. The oxidase-like activity of MnPNF is based on the redox reaction with 3,3′,5,5′-tetramethylbenzidine. However, the addition of GSH can reduce MnPNF to Mn2+, and subsequently supresses the oxidase-like activity and a yellow color at 450 nm is observed in the presence of H2SO4. The MnPNF-based nanozyme exhibits excellent sensing ability toward GSH detection, and a good linear relationship between the change in absorbance at 450 nm and the added amounts of GSH at 50 nM–10 μM with low limits of detection of 20 and 26.6 nM in the PBS and diluted human serum, respectively, is observed. Moreover, the sensing probe shows a superior selectivity over the other 16 interferences, which drive the determination of GSH feasible in real human serum. Since the MnPNF can be simply prepared at room temperature and no functionalization is required, this assay can be used to design the highly efficient biomimic oxidase for effective sensing of GSH and other disease-related biomolecules in biological fluid samples.

Effectiveness of cauda epididymal plasma-2 and lecithin based diluents to minimize abnormality of sexing albumin spermatozoa during cold storage

Background and Aim:Lecithin based diluent such as AndroMed, is a semen diluent made without animal components to prevent the risk of disease transmission, while glutathione (GSH) is an intracellular non-enzymatic antioxidant that prevents cell damage due to reactive oxygen species. Meanwhile, the specific impact of AndroMed and GSH combinations on spermatozoa abnormalities has not been fully studied. Therefore, this study aims to determine the effect of using cauda epididymal plasma-2 (CEP-2) and AndroMed diluents with or without the addition of GSH on the abnormalities of sexing semen of Ongole crossbred bulls in cold storage.Materials and Methods:This study used a factorial completely randomized design 2×2, the first factor was types of diluent and the second was with or without the addition of GSH. Observation of spermatozoa abnormalities was carried out at a storage time of 0-5 days using 297 ejaculations of liquid semen, with 100 spermatozoa observed per smear of each ejaculate. Furthermore, the data were analyzed using a two-way analysis of variance and the significant threshold (p-value) for statistical analysis was set at <0.05.Results:The results showed that there was a significant difference (p<0.05) between AndroMed and CEP-2 in minimizing the abnormalities of upper layer spermatozoa (X), with parameters DH and AD on day 0, damage of spermatozoa (DMR) on days 1-5, and dag-like defect (DLD) on day 5. Furthermore, spermatozoa abnormalities in the lower layer (Y) showed a significant difference between diluents in the parameters of AD on day 1, DMR on days 0-5, and DLD on days 1-5. The significant difference between with or without the addition of GSH in the X sperm was observed in the DH parameters on day 0 and DMR on 5, while there was no significant difference in the Y sperm.Conclusion:Based on the results, AndroMed has the potential to minimize spermatozoa abnormalities compared to CEP-2 diluent in sexed liquid semen. Therefore, AndroMed diluents with or without the addition of 1 mM GSH have no significant effect on spermatozoa abnormalities.

Electrochemical biosensor based on singlet oxygen generated by molecular photosensitizers

Here a sensing strategy with the integration of photosensitizer and electrochemical analysis was present. The photosensitizer, Zinc(II) tetraphenylporphyrin (ZnTCPP), was functionalized graphene oxide (GO) to form complex (ZnTCPP/GO) as the electrode material and generated singlet-oxygen (1O2) in the presence of air under light illumination. Due to the special electronic structure of 1O2, hydroquinone (HQ) could react with 1O2 to produce electrochemically-detectable products, benzoquinone (BQ). Meanwhile, the formed BQ could be reduced on the electrode, completing the redox cycling. The ZnTCPP/GO modified ITO electrode produces a stable and enhanced photocurrent signal under 420 nm irradiation in air-saturated buffer, compared with in N2-saturated buffer. On the other hand, l-glutathione (GSH) as a signalling molecule plays important role in physiological process, which was employed as model to investigated the sensing performance. Coupling with HQ oxidized by 1O2, a GSH sensor was constructed on the basis the redox cycling of HQ. A sensitive reduction of photocurrent is observed with the addition of GSH, due to the GSH could be oxidized by the generated 1O2 to form GSSG. The biosensor displayed good performance in a broad concentration range of 0–150 μM, with a lower detection limit of 1.3 μM at an S/N ratio of 3, and could be used in practical application. This work affords a platform for constructing the biosensor with 1O2 instead of enzyme via on/off light switching.

Smartphone-Assisted Colorimetric Detection of Glutathione and Glutathione Reductase Activity in Human Serum and Mouse Liver Using Hemin/G-Quadruplex DNAzyme.

Abnormal levels of reduced glutathione (GSH) and glutathione reductase (GR) are usually related to a variety of diseases, so it is of great significance to determine the GSH concentration and GR activity. We herein develop a smartphone-assisted colorimetric biosensor for the detection of GSH and GR activity in human serum and mouse liver using hemin/G-quadruplex DNAzyme. Firstly, an obvious color change from colorless to green can be observed, owing to the high peroxidase-like activity of hemin/G-quadruplex DNAzyme toward 2,2′-azino-bis(3-ethylbenzothiozoline-6-sulfonic acid) (ABTS). With the addition of GSH or GR, the H2O2-mediated oxidation of ABTS catalyzed by hemin/G-quadruplex DNAzyme is significantly inhibited, resulting in remarkable color fading. Therefore, the detection of GSH and GR activity can be achieved by observing the color transition or measuring the absorbance at 420 nm. The detection limit was estimated to be as low as 0.1 μM and 10 μU/mL for GSH and GR, respectively. More interestingly, the RGB values of the sensing system can be identified by the smartphone application (APP, color collect), which makes it an ideal format for on-site determination and point-of-care testing (POCT). In addition, the proposed method shows excellent selectivity and acceptable applicability for the determination of GSH concentration and GR activity in human serum samples and mouse liver tissues, which might hold great application potential in clinical diagnosis and drug screening.

Michael addition reaction of symmetrically halogenated bischalcones with reduced glutathione assessed by RP-HPLC and RP-HPLC-ESI-MS

Chalcones and derivatives are promising drugs, demonstrating, among others, antiviral, anticancer, anti-inflammatory, and antioxidant effects. The bioactivity of chalcones and derivatives are associated with their reactivity with cellular thiols, such as the reduced glutathione (GSH), the most important non-protein thiol compound present in mammals. Here, three symmetrically halogenated bischalcones (SHBCs) were synthesized, and their Michael addition reaction with GSH was studied to investigate if the cytotoxic effects of the compounds were correlated with their GSH-reactivity. Formation of two diastereomeric adducts (GS) was observed as a result of the addition of GSH to one of the unsaturated carbon–carbon bonds and other diastereomeric adducts (BS) were formed on addition of another GSH molecule to the second carbon–carbon double bond. However, reactivity of the compounds with GSH did not directly correlate with their in vitro cancer cell toxicity.

MnO2 Nanospheres Assisted by Cysteine Combined with MnO2 Nanosheets as a Fluorescence Resonance Energy Transfer System for "Switch-on" Detection of Glutathione.

Manganese dioxide nanosheets combined with cysteine-assisted emitting manganese dioxide nanospheres (Cys-MnO2 nanospheres) is fabricated for the first time as an "off-on" fluorescence detection platform for glutathione (GSH). In this sensing system, Cys-MnO2 nanospheres served as energy donors, while MnO2 nanosheets were used as both energy acceptors and recognition units. MnO2 nanosheets can effectively quench the fluorescence of Cys-MnO2 nanospheres through the fluorescence resonance energy transfer (FRET). The addition of GSH could reduce MnO2 nanosheets into Mn2+, disrupting the FRET process and restoring the fluorescence of Cys-MnO2 nanospheres. Under the optimum conditions, the "switch-on" platform we established has a wide response to GSH with a range of 5-50 μM and 150-800 μM, as well as a superior specificity. Importantly, all components of the sensor are nontoxic, biocompatible, easily prepared, and have a high utilization of raw materials. Moreover, the sensing system achieved satisfactory results in human serum, showing a tremendous potential in the field of biomedicine.

NCL-based mitochondrial-targeting fluorescent probe for the detection of Glutathione in living cells

Glutathione (GSH) plays a critical role in maintaining cellular redox homeostasis in biological system. Mitochondrion is a pivotal organelle for cellular aerobic respiration and its disorder is associated with impaired redox balance, leading to cell death. In this work, we designed and synthesized a non-invasive “off-on” mitochondrial-targeting fluorescent probe QZ for the detection of GSH in living cells. Based on the mechanism of native chemical ligation (NCL) and fluorescence resonance energy transfer (FRET), a rhodamine B derivative, QZ was prepared, by choosing aromatic thioester bond as the selective reaction site. QZ exhibited excellent detection capability for GSH over Cys and Hcy. Upon addition of GSH to QZ solution, a remarkably enhanced fluorescence was observed with a limit of detection of 2.98 µmol/L. Furthermore, QZ was found to possess the specific mitochondrial localization ability in cell imaging experiments. Moreover, with exogenous and endogenous stimulations, QZ could image GSH in living cells.

Glutathione-mediated formation of disulfide bonds modulates the properties of myofibrillar protein gels at different temperatures

The present study illustrated modulation of protein aggregation by affecting disulfide/sulfhydryl exchange reactions by adding different concentrations of free thiol represented by reduced-glutathione (GSH) for modulating myofibrillar protein (MP) gel properties at 75 °C or 95 °C. Gel strength and rheological results showed the effects of GSH were dependent on the concentrations (5, 10, 20, 40, and 80 g/kg) and heating temperatures. SEM results showed that the addition of GSH improved the gel microstructure at 95 °C. AFM and DLS results indicated that protein aggregation was also inhibited. At 75 °C, the addition of GSH influenced both MP aggregation and gel properties. Low concentrations (5, 10 g/kg) of GSH promoted aggregation, whereas high concentrations (20, 40, and 80 g/kg) of GSH inhibited this. By analyzing the protein structure and cross-linking pattern changes of MP and MP/GSH composites, a pathway involving GSH influencing MP gel properties was determined.

Morphology-Dependent Performance of MnO2 Nanostructure-Carbon Dot-Based Biosensors for the Detection of Glutathione.

Herein, we develop a facile, sensitive, and selective fluorescent nanosensor for the detection of glutathione (GSH). In this protocol, carbon dots (Cdots) with a fairly high quantum yield were synthesized by a microwave-assisted pyrolysis technique. Moreover, different shapes of the MnO2 nanostructure were also prepared by the hydrothermal technique. A comparative photophysical study of different morphology-dependent Cdots@MnO2 nanostructure-based biosensors was explored, which showed different results for the quenching values of ("turn-off") fluorescence intensity, quantum yields, electron transfer rate, and average lifetime. The structure, property, and performance of nanomaterials are interdependent. Therefore, the different shapes of MnO2, that is, nanoflowers (NFs), nanorods (NRs), and a mixture of NFs/NRs was prepared by the hydrothermal method owing to different specific surface areas (23-69 m2 g-1) which put the impact on their sensing activity. It was observed that the variation in the different photophysical parameters of fluorescent Cdots such as quantum yield (Φ), average lifetime values [τav (ns)], radiative (kr) rate constant, nonradiative (knr) rate constant, rate of electron transfer (kET), the efficiency of electron transfer (ΦEET), FRET efficiency (E), and Förster distance (R0) were dependent on the different shapes of the MnO2 nanostructure. These results indicate that the transfer of energy occurs between the Cdots and different shapes of MnO2 nanostructures based on fluorescence resonance energy transfer at different charge-transfer rates. The recovery rate ("turn-on") of fluorescence of Cdots with the addition of GSH was obtained best for the NF structure by conversion of MnO2 to Mn2+, and the limit of detection was obtained as ∼19 μM for GSH. The developed sensing probes were rapid, easy, cheap, and eco-friendly for the determination of GSH.

Caloric restriction increases levels of taurine in the intestine and stimulates taurine uptake by conjugation to glutathione

Our previous study indicated increased levels of taurine-conjugated bile acids (BA) in the intestine content of mice submitted to caloric restriction (CR). In the current project, we found increased levels of free taurine and taurine conjugates, including glutathione (GSH)-taurine, in CR compared to ad libitum fed animals in the mucosa along the intestine but not in the liver. The levels of free GSH were decreased in the intestine of CR compared to ad libitum fed mice. However, the levels of oxidized GSH were not affected and were complemented by the lack of changes in the antioxidative parameters. Glutathione-S transferases (GST) enzymatic activity was increased as was the expression of GST genes along the gastrointestinal tract of CR mice. In the CR intestine, addition of GSH to taurine solution enhanced taurine uptake. Accordingly, the expression of taurine transporter (TauT) was increased in the ileum of CR animals and the levels of free and BA-conjugated taurine were lower in the feces of CR compared to ad libitum fed mice. Fittingly, BA- and GSH-conjugated taurine levels were increased in the plasma of CR mice, however, free taurine remained unaffected. We conclude that CR-triggered production and release of taurine-conjugated BA in the intestine results in increased levels of free taurine what stimulates GST to conjugate and enhance uptake of taurine from the intestine.

Ascorbate and glutathione independently alleviate arsenate toxicity in brinjal but both require endogenous nitric oxide.

In this study, we have explored the possible role of ascorbic acid (ASC) and glutathione (GSH) in alleviating arsenate (AsV ) toxicity in brinjal roots. Moreover, we have also focused our attention on the possible involvement of endogenous nitric oxide (NO) in accomplishing this task. AsV treatment negatively impacts the length and fresh weight of roots and shoots as well as the dry weight and fitness of roots, and this was accompanied by greater As accumulation in roots and shoots of brinjal. AsV treatment also declined the endogenous NO level by inhibiting Nitric Oxide Synthase-like (NOS-like) activity. Furthermore, AsV stimulated oxidative stress markers, caused protein damage by their carbonylation due to downregulation in antioxidants [particularly ascorbate (AsA)-GSH cycle], leading to disturbed cellular redox status. This, collectively, led to root cell death in brinjal. However, the addition of either ASC or GSH rescued brinjal roots from the toxic effects of AsV in. Interestingly, lycorine (an inhibitor of ASC biosynthesis) further increased AsV toxicity, while ASC rescued its effects. Moreover, buthionine sulphoximine (BSO, an inhibitor of GSH biosynthesis) interestingly increased further AsV toxicity, while GSH rescued the plant from the As toxic effects. An interesting notion of this study was that GSH rescued the toxic effect of lycorine, while ASC rescued the toxic effect of BSO, though the AsV toxicity mediated by either ASC or GSH was always accompanied by high endogenous NO level and NOS-like activity. All together, these results suggest that ASC and GSH independently mitigate AsV toxicity in brinjal roots, but both might be dependent on endogenous NO for accomplishing the AsV toxicity alleviatory tasks.

Modulating skin colour: role of the thioredoxin and glutathione systems in regulating melanogenesis.

Different skin colour among individuals is determined by the varying amount and types of melanin pigment. Melanin is produced in melanocytes, a type of dendritic cell located in the basal layer of the epidermis, through the process of melanogenesis. Melanogenesis consists of a series of biochemical and enzymatic reactions catalysed by tyrosinase and other tyrosinase-related proteins, leading to the formation of two types of melanin, eumelanin and pheomelanin. Melanogenesis can be regulated intrinsically by several signalling pathways, including the cyclic adenosine monophosphate (cAMP)/protein kinase A (PKA), stem cell factor (SCF)/c-kit and wingless-related integration site (Wnt)/β-catenin signalling pathways. Ultraviolet radiation (UVR) is the major extrinsic factor in the regulation of melanogenesis, through the generation of reactive oxygen species (ROS). Antioxidants or antioxidant systems, with the ability to scavenge ROS, may decrease melanogenesis. This review focuses on the two main cellular antioxidant systems, the thioredoxin (Trx) and glutathione (GSH) systems, and discusses their roles in melanogenesis. In the Trx system, high levels/activities of thioredoxin reductase (TrxR) are correlated with melanin formation. The GSH system is linked with regulating pheomelanin formation. Exogenous addition of GSH has been shown to act as a depigmenting agent, suggesting that other antioxidants may also have the potential to act as depigmenting agents for the treatment of human hyperpigmentation disorders.

Dual-signaling amplification strategy for glutathione sensing by using single gold nanoelectrodes

A new nanosensor for glutathione (GSH) detection by use of single nanoelectrodes has been developed through a dual-signaling ratiometric amplification strategy. Ag nanoparticles (Ag NPs) metalized DNA1 was modified on an Au nanoelectrode surface. Due to the strong affinity between Ag NP and GSH, Ag NPs could be removed by the addition of GSH. The remaining metalized DNA1 could hardly form a double strand, while the de-metalized DNA1 could hybrid with DNA2 and DNA3 to form a complex structure to adsorb methylene blue (MB), and then the electrochemical signal of differential pulse voltammetry (DPV) from MB oxidation could be observed. With the addition of GSH, the peak current of MB oxidation at about −0.27 V (IMB) increases, while the signal of Ag oxidation at about 0.1 V (IAg) decreases. It was found that there had a linear relationship between the ratio of dual-signal (IMB/IAg) and the GSH concentrations, which could be used to detect GSH. The ratiometric nanosensor is label-free, easy to operate, and can eliminate inherent system errors. Considering the advantages of nanoelectrodes, such as low IR drop, fast response, and small overall dimension, this developed nanosensor can be used for GSH detection living systems (e.g., cell lysate).