Food Deprivation Promotes Oxidative Imbalance in Rat Brain

ABSTRACT:  The present study was aimed to evaluate the effect of food deprivation in brain oxidative status of Wistar and Goto-Kakizaki (GK) rats. For this purpose, we evaluated several oxidative stress parameters: lipid peroxidation (thiobarbituric acid reactive substances [TBARS]) and protein oxidation markers, hydrogen peroxide (H₂O₂) levels, nonenzymatic (reduced [GSH] and oxidized glutathione [GSSG] and vitamin E) and enzymatic (glutathione peroxidase [GPx], glutathione reductase [GRed], and manganese superoxide dismutase [MnSOD]) antioxidant defenses. Four-mo-old Wistar and GK rats were divided into 2 groups. One group of each rat strain was maintained under normal diet and the other groups were maintained under 50% food deprivation during 2 mo. GK rats under normal diet presented lower levels of vitamin E and higher GRed activity and GSH/GSSG ratio when compared with Wistar control rats. In Wistar rats, food deprivation induced a significant decrease in vitamin E levels and a significant increase in GPx activity, H₂O₂ production, and TBARS formation in the presence of the prooxidant pair ADP/Fe²⁺. However, GK rats under food deprivation presented a significant decrease in vitamin E levels and GRed activity and a significant increase in H₂O₂ production when compared with GK under normal diet. In summary, our results indicate that food deprivation affects brain oxidative status, which could predispose brain cells to degeneration and death.     

Antimicrobial Activity of Lactoperoxidase System Incorporated into Cross-Linked Alginate Films

ABSTRACT:  In this study, the antimicrobial effect of lactoperoxidase (LPS) incorporated alginate films was investigated on Escherichia coli (NRRL B-3008), Listeria innocua (NRRL B-33314), and Pseudomonas fluorescens (NRRL B-253) in presence of different concentrations of H₂O₂ (0.2, 0.4, and 0.8 mM) and KSCN (1, 2, and 4 mM). The incorporation of 70 nmol ABTS/min/cm² LPS into alginate films gave 0.66 to 0.85 nmol ABTS/min/cm² enzyme activity at 0.2 to 0.8 mM H₂O₂ concentration range. The antimicrobial activity of LPS system on target bacteria changed according to the concentrations of KSCN and H₂O₂. The growth of all tested bacteria was prevented for a 6-h period by applying LPS system in presence of 0.4 or 0.8 mM H₂O₂ and 4 mM KSCN. At 0.8 mM H₂O₂ and 4 mM KSCN, the LPS system also inhibited growth of L. innocua and P. fluorescens for a 24-h incubation period, whereas E. coli growth could not be inhibited for 24 h under these conditions. At 0.2 mM H₂O₂ and 1 to 4 mM KSCN, a considerable inhibitory effect was obtained only on P. fluorescens . The decreasing order of the resistance of studied bacteria to LPS system is as follows: E. coli , L. innocua , and P. fluorescens . The developed antimicrobial system has a good potential for use in meat, poultry, and seafood since alginate coatings are already used in these products. Further studies are needed to test the LPS incorporated edible films in real food systems.     

Effect of hydrogen peroxide on quality of fresh-cut tomato

ABSTRACT:  The effect of hydrogen peroxide (H₂O₂; 0, 0.1, 0.2, and 0.4 M) on selected nutritional quality of fresh-cut tomato was investigated. Microbial population of tomato slices stored at 10 °C and treated with H₂O₂ was lower than the control by 1-(0.2 and 0.4 M) and 5-log (0.4 M), 3 and 7 d after processing, respectively. Dipping fresh-cut tomato into H₂O₂ resulted in reduced phenolic and antioxidant levels after 7 d in storage by at least 5% and 20%, respectively, and produced an initial decline in vitamin C and lycopene. Change in color values in the H₂O₂ treatments were associated with reduced carotenoid content. Our results confirmed antimicrobial benefits of H₂O₂ but revealed a compromise in antioxidant and carotenoid contents of fresh-cut tomatoes.     

羟自由基和高铁肌红蛋白氧化体系对牦牛肉肌原纤维蛋白氨基酸含量变化的影响

本研究比较分析了牦牛肉成熟过程中及羟自由基氧化体系(iron-catalyzed oxidizing system,IOS)和高铁肌红蛋白氧化体系(metmyoglobin oxidizing system,MOS)在特定氧化强度下牦牛肉肌原纤维蛋白氨基酸含量的变化.结果表明,在牦牛肉成熟过程中,苏氨酸、半胱氨酸、甘氨...     

Chemiluminescent determination of hydrogen peroxide in water

A method for determining low concentrations of hydrogen peroxide (H₂O₂) in water, based on the chemiluminescent oxidation of 3-aminophthalhydrazide (luminol) by H₂O₂ in the presence of a copper ion catalyst, is described. Levels of H₂O₂ down to 3 × 10^-8 mol/1 (1 ppb) can be determined. The method may be used to monitor the amount of residual H₂O₂ in aseptically filled packages sterilized with H₂O₂ before filling.     

Desulfiting Dried Apricots by Hydrogen Peroxide

ABSTRACT: Removal of sulfites from excessively sulfited dried apricots using hydrogen peroxide (H₂O₂) was studied. Dried apricots were dipped into 0.5, 1.0, and 1.5% H₂O₂ solutions at 20 °C and 40 °C for various times. At 60 °C, apricots were also treated with 1% H₂O₂ solution. Removal of sulfites by H₂O₂ followed a 1st-order kinetic model. At 20 °C to 60 °C and 1% H₂O₂ concentration, the E_a value was 22.46 kJ mol⁻¹. H₂O₂ treatment caused lighter, more yellow, and less red dried apricots. Critical factors for H₂O₂ application are choosing the appropriate H₂O₂ concentration, temperature, and exposure time and without bleaching the natural color of dried apricots.     

Production of Hydrogen Peroxide by Lactobacillus delbrueckii subsp. lactis as Influenced by Media Used for Propagation of Cells

ABSTRACT: Cells of Lactobacillus delbrueckii subsp. lactis I were grown in several media to determine the most suitable medium for production of H₂O₂ during refrigerated storage. H₂O₂ was detected from cells that were resuspended in phosphate buffer containing variable amounts of glucose. Cells grown in MRS broth produced more H₂O₂ during refrigerated storage than those grown in LBS pr PTM. Cells grown in LBS produced more H₂O₂ then those grown in PTM. For both MRS and LBS, cells inoculated in phosphate buffer containing 0% glucose produced significantly more H₂O₂ than those containing 1% or 10% glucose. MRS medium appears to be the best medium for growing cells for the production of H₂O₂.     

Use of microemulsions as vehicles for nucleophilic reagents in cosmetic formulations

The modifications of chemical reactivity induced in the human hair during its treatment with oxidative (H₂O₂) or reductive (HSO₃Na) agents via a micellar or a microemulsion system have been investigated. For this purpose, phase diagrams of micellar solutions and microcmulsions with H₂O₂ or NaSO₃H have been made in order to find out the corresponding areas of solubility. The properties of conductivity, surface tension and light scattering of various monophasic compositions as a function of their water content, have been studied.
As a result of the chemical reactivity data of human hair obtained through the reaction of H₂O₂ or HSO₃Na via a micellar or a microemulsion system, it appears reasonable to predict a more effective reaction of such agents with cystine residues existing in keratinic substrates, particularly when they are applied via a microemulsion. The decrease of the water content of the compositions considered, increases chemical reactivity of the keratinic proteins favouring the formation of cysteine and of cysteic acid in the reductive or oxidative treatments respectively.     

Reaction characteristics of a tooth-bleaching agent containing H2O2 and NaF: in vitro study of crystal structure change in treated hydroxyapatite and chemical states of incorporated fluorine

This in vitro study was performed to elucidate the reaction mechanism of sodium fluoride (NaF), which is added to tooth-bleaching agents to lessen the adverse effect of hydrogen peroxide (H₂O₂) on teeth. Both hydroxyapatite (HAP) and dihydrated dicalcium phosphate (DCPD), model substances for dental hard tissues, dissolved easily in a simple H₂O₂ solution. In the H₂O₂/NaF solutions, however, fluorine compounds that could not be identified by X-ray diffraction (XRD) due to the smallness of the products were formed on the surface of the HAP. X-ray photoelectron spectroscopy (XPS) studies demonstrated that fluoridated hydroxyapatite (FHAP) was formed on HAP, and that calcium fluoride (CaF₂) formation was accelerated by increasing the concentrations of fluorine and H₂O₂ along with the partial dissolution of HAP. In H₂O₂/NaF solution, DCPD also transformed easily to FHAP and CaF₂, which are favorable to the remineralization process on the tooth surface. Thus, the mechanism of NaF was elucidated, and its use together with H₂O₂ for tooth bleaching was proved to be effective. Methodologically, the XPS two-dimensional plot made it possible for the first time to directly estimate the ratio of FHAP and CaF₂ in the reaction products, in contrast to the conventional wet-analytical method, which is simply based on the difference in solubility of the two components.     

Hydroxyl Radical and Ferryl-Generating Systems Promote Gel Network Formation of Myofibrillar Protein

ABSTRACT: The objective of the study was to examine how oxidatively induced protein cross-linking would influence the gelation properties of myofibrillar protein (MP) under meat processing conditions. MP suspensions in 0.6 M NaCl at pH 6 were treated with an iron-catalyzed oxidizing system (IOS: 10 μM FeCl₃, 0.1 mM ascorbic acid, 0.05 to 5 mM H₂O₂) or a H₂O₂-activated metmyoglobin oxidizing system (MOS: 0.01 to 0.1 mM metmyoglobin/H₂O₂) that produced hydroxyl radical and ferryl species, respectively. Both oxidizing systems promoted MP thermal gelation, which was evidenced by rapid protein–protein interaction and the enhancement in storage modulus (elasticity) of the gel network as revealed by dynamic rheological testing in the 20 to 74 °C temperature range. This gelation-enhancing effect was attributed to the shift of myosin aggregation in the early stage of heating from predominantly head–head association (nonoxidized control samples) to prevalently tail–tail cross-linking through disulfide bonds. However, both hardness and water-holding capacity of chilled gels tended to decline when MP was exposed to ≥1 mM H₂O₂ in IOS and to all concentrations of metmyoglobin in MOS. Microscopic examination confirmed a more porous structure in oxidized gels when compared with nonoxidized protein gels. The results demonstrated that mild oxidation altered the mode of myosin aggregation in favor of an elastic gel network formation, but it did not improve or had a negative effect on water-binding properties of MP gels. Practical Application: Mild oxidation promotes protein network formation and enhances gelation of myofibrillar protein under normal salt and pH conditions used in meat processing. This oxidative effect, which involves disulfide linkages, is somewhat similar to that in bakery product processing where oxidants are used to improve dough performance through gluten protein interaction.     

Reaction characteristics of a tooth-bleaching agent containing H2O2 and NaF: in vitro study of crystal structure change in treated hydroxyapatite and chemical states of incorporated fluorine

This in vitro study was performed to elucidate the reaction mechanism of sodium fluoride (NaF), which is added to tooth-bleaching agents to lessen the adverse effect of hydrogen peroxide (H₂O₂) on teeth. Both hydroxyapatite (HAP) and dihydrated dicalcium phosphate (DCPD), model substances for dental hard tissues, dissolved easily in a simple H₂O₂ solution. In the H₂O₂/NaF solutions, however, fluorine compounds that could not be identified by X-ray diffraction (XRD) due to the smallness of the products were formed on the surface of the HAP. X-ray photoelectron spectroscopy (XPS) studies demonstrated that fluoridated hydroxyapatite (FHAP) was formed on HAP, and that calcium fluoride (CaF₂) formation was accelerated by increasing the concentrations of fluorine and H₂O₂ along with the partial dissolution of HAP. In H₂O₂/NaF solution, DCPD also transformed easily to FHAP and CaF₂, which are favorable to the remineralization process on the tooth surface. Thus, the mechanism of NaF was elucidated, and its use together with H₂O₂ for tooth bleaching was proved to be effective. Methodologically, the XPS two-dimensional plot made it possible for the first time to directly estimate the ratio of FHAP and CaF₂ in the reaction products, in contrast to the conventional wet-analytical method, which is simply based on the difference in solubility of the two components.     

INACTIVATION AND REGENERATION OF IMMOBILIZED CATALASE

Catalase was immobilized on collagen membrane. The inactivation of immobilized catalase by 0.01M and 0.1M H₂O₂ was reported. After the initial stage of inactivation, a stable catalatic activity as measured in a continuous flow of 0.01M H₂O₂ through a modular reactor was observed for longer than 20 days (2.6 min residence time). The regeneration of catalatic activity from the O.1M H₂O₂ inactivated catalase occurred after incubating the inactivated modular reactor with 0.01M phosphate buffer, pH 6.8. The amount of activity regenerated is directly proportional to the time of incubation.     

Factors Limiting the Efficacy of Hydrogen Peroxide Washes for Decontamination of Apples Containing Escherichia coli

Factors limiting efficacy of H₂O₂ washes and alternative decontamination strategies were investigated with Golden Delicious apples, inoculated with nonpathogenic Escherichia coli. Post-treatment rinsing decreased efficacy by eliminating residual H₂O₂. A 2-stage wash incorporating a rinse to remove surfactant residues prior to H₂O₂ application was developed. Rapid attachment of E. coli to apples prevented effective removal by washing with water. Surviving E. coli following a 5% H₂O₂ wash were concentrated in stem and calyx areas. Survival was independent of the time interval between inoculation and washing. E. coli inoculation of punctured apple surfaces resulted in growth at 20 °C and greater survival after washing with 5% H₂O₂. Improved decontamination methods are needed.     

Degradation Kinetics of Anthocyanins from Sour Cherry, Pomegranate, and Strawberry Juices by Hydrogen Peroxide

ABSTRACT: Degradations were studied at different hydrogen peroxide (H₂O₂) concentrations (9.31 to 27.92 mmol. L¹) over a range of 10° to 30 °C. Degradation of anthocyanins by H₂O₂ was described by first-order function. Comparison of t_1/2 values revealed that sour cherry anthocyanins were the most resistant to H₂O₂, followed by pomegranate and strawberry anthocyanins. Thus, the removal of residual H₂O₂ from the juice contact surfaces of aseptically packaged strawberry juices should be controlled more carefully to prevent anthocyanin degradation. Respective E_a values were between 9.4 to 11.1, 9.5 to 11.4, and 11.4 to 12.2 kcal.mol¹; and Q₁₀ values between 1.59 to 2.22, 1.62 to 2.05, and 1.76 to 2.36 for strawberry, sour cherry, and pomegranate anthocyanins.     

Efficacy of Sulfuric Acid Scarification and Disinfectant Treatments in Eliminating Escherichia coli O157: H7 from Alfalfa Seeds Prior to Sprouting

ABSTRACT: E. coli O157:H7 reduction on inoculated alfalfa seeds was investigated using acid scarification treatments with or without subsequent application of sanitizers. Scarification with 0.1 to 2N H₂SO₄ for 2.5 to 45 min did not affect (p ≤ 0.05) seed viability. E. coli O157:H7 was reduced by 2.1 to 5.0 logs after treating with 0.1 to 2N H₂SO₄ for 5 to 20 min. Combined scarification (0.5N H₂SO₄) and H₂O₂ or CH₃COOH treatments enhanced microbial destruction by less than 1 log compared to sanitizer alone. Chlorine, Na₂CO₃, or Na₃PO₄ treatments preceded by scarification did not significantly increase microbial destruction compared to sanitizer alone. Appreciable reductions in seed germination were only observed with chlorine treatments.     

Comparative Flavonoids Contents of Selected Herbs and Associations of Their Radical Scavenging Activity with Antiproliferative Actions in V79-4 Cells

ABSTRACT:  To elucidate the health benefit of herbal teas on the cytotoxicity induced by H₂O₂ in V79-4 cells, herbal extracts and its flavonoids were tested using lactate dehydrogenase release and determining intracellular reactive oxygen species generation and antioxidant activity with superoxide radical scavenging assay. Significant decrease in cell viability was observed on V79-4 cells treated with H₂O₂ (1 mM), while herbal extracts and its flavonoids including catechin and epigallocatechin gallate prevented the LDH release from H₂O₂ cytotoxicity. Total catechin contents of green tea (65.6 mg/g of dry matter) were significantly higher than other herbal teas (35.8 to 1.2 mg/g of DM). The relative concentration of the 4 major tea catechins ranked EGCG > EGC > EC > C. Green tea exhibited the lowest IC₅₀ values (2 g fresh herb/100 mL) of superoxide radical scavenging activity among the tested herbal tea, which indicates powerful antioxidant activity in O₂^·− radicals scavenging, followed by black tea, dandelion, hawthorn, rose hip, chamomile.     

Use of hydrogen peroxide detection strips to determine the extent of pasteurization in whole milk

Commercially available hydrogen peroxide (H₂O₂) detection strips were shown to be effective in determining known levels of H₂O₂ in milks where the lactoperoxidase system (LPS) had been inactivated. In addition, the strips were evaluated for determination of residual H₂O₂ in LPS-activated milks, following a range of heat treatments. The detection of residual H₂O₂ corresponded with results of zero lactoperoxidase activity. Hence, the detection strips offer a simple and accurate method for detecting the absence of lactoperoxidase, and therefore can be used to determine whether the milk has been subjected to overpasteurization. The technique provides a more convenient method than the standard procedure based on oxidation of 1,4-phenylenediamine.     

Shelf-Life Extension of Fresh Mushrooms (Agaricus bisporus) By Application of Hydrogen Peroxide and Browning Inhibitors

ABSTRACT: An experimental washing process for fresh mushrooms entailing immersion in 5% H₂O₂, followed by application of a sodium erythorbate-based browning inhibitor, was optimized, scaled up, and made continuous. The laboratory process described previously was modified by adding a pre-wash step using 0.5% to 1% H₂O₂, increasing the wash solution H₂O₂ concentration from 3% to 5%, and substituting 4% sodium erythorbate + 0.1% NaCl for the more complex browning inhibitor formulation used previously. A continuous, commercial-scale washing facility was built to test the new process. Mushrooms washed by this process were free of adhering soil, less subject to brown blotch than conventionally washed mushrooms, and at least as resistant to enzymatic browning as unwashed mushrooms during storage at 4 °C. Storage at 10 °C accelerated development of brown blotch and browning.     

Improved Sanitizing Treatments for Fresh Tomatoes

ABSTRACT:  Fresh tomatoes repeatedly have been associated with major outbreaks of salmonellosis; however, efforts to disinfect them with chlorine or other sanitizing agents have had only mixed success. Our objective was to determine whether hydrogen peroxide (H₂O₂) treatments would be more efficacious than conventional methods in disinfecting tomatoes containing human pathogens and, at the same time, be noninjurious to quality. Tomatoes were dip inoculated with Escherichia coli NRRL B-766 or a Salmonella cocktail and then held for 0, 24, or 48 h at 4 or 24 °C prior to treatment. Treatments included 200 ppm chlorine (Cl₂) at 20 °C for 3 min, water at 20 °C for 3 min or at 60 °C for 2 min, 1% H₂O₂ at 20 °C for 15 min or at 60 °C for 2 min, and 5% H₂O₂ at 60 °C for 2, 3, or 5 min. In tomatoes held 48 h postinoculation, the chlorine treatment was only marginally more effective than an equivalent water rinse in reducing the target bacterial population, while the hot water and 1% H₂O₂ treatments achieved reductions no greater than 1.3 logs. However, application of 5% H₂O₂ at 60 °C resulted in larger reductions. Efficacy of all treatments decreased as the time interval between inoculation and treatment increased. Greater reductions could not be achieved with 5% H₂O₂ at 60 °C by increasing the contact time or addition of surfactants, and these treatments caused some quality loss.     

Antioxidant Activity of Soy Protein Hydrolysates in a Liposomal System

ABSTRACT: Native and heated soy protein isolate was hydrolyzed with 3 purified (pepsin, papain, and chymotrypsin) and 3 crude (Alcalase®, Protamex^TM, and Flavourzyme^TM) proteases. The hydrolysates were incubated (37 °C, 1 h) with a liposome-oxidizing system (50 μM FeCl₃/0.1 mM ascorbate, pH 7.0) to test antioxidant activities by determining the concentrations of TBARS. Degree of hydrolysis of SPI hydrolysates ranged from 1.7 to 20.6%. Both hydrolyzed and nonhydrolyzed SPI decreased TBARS (by 28 to 65%), except for papain-hydrolyzed samples. Samples of chymotrypsin- and Flavourzyme-hydrolyzed (0.5 h) preheated SPI had the greatest inhibitory effect on lipid oxidation.