Intracellular ROS scavenging and antioxidant enzyme regulating capacities of corn gluten meal-derived antioxidant peptides in HepG2 cells

The objective of this study was to investigate the intracellular reactive oxygen species (ROS) scavenging activities and antioxidant enzyme regulating capacities of corn gluten peptide fractions (CPFs) in HepG2 cells. A cellular antioxidant activity (CAA) assay was used to assess their antioxidant activities and revealed that both CPF1 (molecular weight < 1 kDa) and CPF2 (molecular weight between 1 and 3 kDa) exhibited high cellular antioxidant activities with EC₅₀ values of 2.85 ± 0.19 mg/mL and 5.05 ± 0.32 mg/mL, respectively. Both CPFs also exhibited cytoprotective effects and intracellular ROS scavenging activities in HepG2 cells subjected to oxidative stress by oxidation with H₂O₂. In addition, at concentrations of 2.50 mg/mL, the CPFs increased the activity levels of superoxide dismutase (SOD), catalase (CAT), and glutathione reductase (GR), as well as the total glutathione (GSH) levels in oxidized HepG2 cells (from 86.54% to 114.14% (CPF1) or 109.72% (CPF2) for SOD activity; from 71.91% to 107.64% (CPF1) or 106.50% (CPF2) for CAT activity; from 70.52% to 103.01% (CPF1) or 104.10% (CPF2) for GR activity; and from 81.39% to 114.00% (CPF1) or 108.82% (CPF2) for total GSH levels). These results suggested that both CPF1 and CPF2 exhibited positive effects on the activities of the intracellular antioxidant enzymes SOD, CAT and GR, as well as on the total GSH levels in HepG2 cells under conditions of oxidative stress. Furthermore, size exclusion gel chromatography and MALDI-TOF/TOF mass spectrometry revealed that the molecular weights of the antioxidant peptides in CPF1 were between 500 Da to 900 Da, and a novel antioxidant peptide consisting of GLLLPH (Gly-Leu-Leu-Leu-Pro-His) was identified in CPF1.     

Peptides derived from high oleic acid soybean meals inhibit colon,liver and lung cancer cell growth

Soybean meal, a co-product after oil extraction from seeds, is rich in protein. Our objective was to utilize this co-product, obtain gastrointestinal (GI) resistant peptides from the isolated protein, and test for bioactivity against colon, liver and lung cancer cell lines. N98-4445A, S03-543CR high oleic acid soybean lines, and R95-1705 high protein soybean line were used for this study. Protein isolates were prepared at alkaline pH and hydrolyzed using alcalase enzyme to generate peptide hydrolysates. After determining gastrointestinal resistance of the peptide hydrolysates they were fractionated into definite molecular sizes of < 5 kDa, 5–10 kDa, and 10–50 kDa and tested against human colon (HCT-116, Caco-2), liver (HepG-2) and lung (NCL-H1299) cancer cell lines. MTS, 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2 H-tetrazolium, cytotoxicity assay was performed to test in vitro cancer cell viability upon treatment with peptide fractions. The peptide fractions from N98-4445A and S03-543CR lines showed cell growth inhibition of 73% of colon cancer (HCT-116), 70% of liver cancer cells and 68% of lung cancer cells. Dose response showed that the peptides had significant inhibitory effect at higher concentrations (1000 μg/mL to 600 μg/mL) and gradually decreased with decreased dosage (500 μg/mL to 100 μg/mL). Reverse phase HPLC identified three single peptides from the 10–50 kDa fractions of N98-4445A soy line that have potential for enhanced activity. Soybean peptide fractions can thus be a source of bioactivity against colon, liver and lung cancer cell proliferation.     

Cocoa brew inhibits in vitro α-glucosidase activity: The role of polyphenols and high molecular weight compounds

Cocoa brew showed a dose-dependent inhibitory activity against α-glucosidase (IC₅₀ 7.87 mg/mL). The cocoa brew was fractionated by ultrafiltration in a low molecular weight fraction (LMW < 10 kDa) and two melanoidin-rich fractions called high molecular weight (HMW > 30 kDa) and intermediate molecular weight (IMW 10–30 kDa) fractions. All fractions tested caused some inhibition with IMW that was the most active (IC₅₀ 2.37 mg/mL). LMW fraction was separated with Sephadex LH-20 in an unbound (containing monomeric and dimeric catechins) and a bound fraction. All the inhibitory activity was recovered in the unbound fraction. All the phenolic compounds identified with HPLC showed α-glucosidase inhibitory activity. IMW and HMW fractions were fractionated by ethanol precipitation. The fractions from IMW precipitated with 75 and 25% ethanol were found to contain power inhibitors of α-glucosidase activity (IC₅₀ 0.87 and 1.01 mg/mL, respectively). In the HMW sample, the fractions precipitated with 50 and 75% ethanol were found to be active against α-glucosidase activity. Most of the inhibitory activity against α-glucosidase of cocoa brew was due to the LMW fraction (56%) whereas IMW and HMW contributed for about 47% of the inhibitory activity. This study suggests that different components of cocoa may influence α-glucosidase activity.     

Antioxidant activities of enzymatic rapeseed protein hydrolysates and the membrane ultrafiltration fractions

In this study, rapeseed protein isolate was hydrolyzed with various proteases to obtain hydrolysates that were separated by membrane ultrafiltration into four molecular size fractions (<1, 1–3, 3–5, and 5–10 kDa). Alcalase hydrolysis significantly (p < 0.05) produced the highest yield of protein hydrolysate while Flavourzyme produced the least. The <1 kDa fraction was the most abundant after the membrane ultrafiltration of the protein hydrolysates, which indicates that the proteases were efficient at reducing the native rapeseed proteins into low molecular weight peptides. Antioxidant properties of the resulting hydrolysates and membrane fractions were characterized and results showed the Pepsin + Pancreatin (P + P) protein hydrolysate had significantly highest (p < 0.05) scavenging activity against DPPH radical among the unfractionated enzymatic hydrolysates. But the P + P hydrolysate was not as effective as other hydrolysates during long-term inhibition of linoleic acid oxidation. For most of the samples, fractionation into the <1 kDa peptides significantly (p < 0.05) improved DPPH and superoxide scavenging properties when compared to the unfractionated protein hydrolysates. Only the <1 kDa fraction showed ferric reducing antioxidant power and the effect was dose-dependent. Overall, Alcalase and Proteinase K seem to be more efficient proteases to release antioxidant peptides from rapeseed proteins when compared to P + P, Flavourzyme and Thermolysin.     

Chemical characterization and chemo-protective activity of cranberry phenolic powders in a model cell culture. Response of the antioxidant defenses and regulation of signaling pathways

Oxidative stress and reactive oxygen species (ROS)-mediated cell damage are implicated in various chronic pathologies. Emerging studies show that polyphenols may act by increasing endogenous antioxidant defense potential. Cranberry has one of the highest polyphenol content among commonly consumed fruits. In this study, the hepato-protective activity of a cranberry juice (CJ) and cranberry extract (CE) powders against oxidative stress was screened using HepG2 cells, looking at ROS production, intracellular non-enzymatic and enzymatic antioxidant defenses by reduced glutathione concentration (GSH), glutathione peroxidase (GPx) and glutathione reductase (GR) activity and lipid peroxidation biomarker malondialdehyde (MDA). Involvement of major protein kinase signaling pathways was also evaluated. Both powders in basal conditions did not affect cell viability but decreased ROS production and increased GPx activity, conditions that may place the cells in favorable conditions against oxidative stress. Powder pre-treatment of HepG2 cells for 20 h significantly reduced cell damage induced by 400 μM tert-butylhydroperoxide (t-BOOH) for 2 h. Both powders (5–50 μg/ml) reduced t-BOOH-induced increase of MDA by 20% (CJ) and 25% (CE), and significantly reduced over-activated GPx and GR. CE, with a significantly higher amount of polyphenols than CJ, prevented a reduction in GSH and significantly reduced ROS production. CJ reversed the t-BOOH-induced increase in phospho-c-Jun N-terminal kinase. This study demonstrates that cranberry polyphenols may help protect liver cells against oxidative insult by modulating GSH concentration, ROS and MDA generation, antioxidant enzyme activity and cell signaling pathways.     

Production and fractionation of tuna by-product protein hydrolysate by ultrafiltration and nanofiltration: Impact on interesting peptides fractions and nutritional properties

The production of fish protein hydrolysates (FPH) is a promising route to add value to fish by-products due to their potential application as a source of interest peptide fractions. Using Alcalase for hydrolysis of tuna dark muscle by-product, the influence of enzyme/substrate ratio and hydrolysis time on the rate of interest peptide fractions (1–4 kDa) was studied. The rate of this fraction obtained under optimized conditions (temperature 55 °C, pH 8.5, enzyme/substrate ratio of 1% and 60 min of hydrolysis reaction) was 26%. The performance of the combined process associating ultrafiltration and nanofiltration membranes was evaluated for fractionation of produced hydrolysate in order to isolate fractions enriched in peptides of specific molecular weight (MW). The interest peptide fraction (1–4 kDa) was isolated and the positive effect of diafiltration on peptide purification process was underlined. The peptide fractions produced have a high nutritional quality which can be used in human nutrition and they have a potential for applications in aquaculture diets.     

Prenylation preserves antioxidant properties and effect on cell viability of the natural dietary phenol curcumin

Curcumin (CRM) is a naturally occurring phenolic compound with a variety of biological and pharmacological activities. We have investigated the effect of aromatic C-prenylation on the antioxidant activity of this natural compound. The protective effect of CRM and its diprenyl derivative (PCRM) was investigated against neat cholesterol degradation (at 140 °C) and Cu^2 +-induced oxidation (at 37 °C) of liposomes and human low density lipoproteins. The activity of two simplified vanilloid analogs (vanillin and vanillyl alcohol) was also compared in the same systems. Cytotoxicity and cell permeation of both curcuminoids were also assessed using differentiated Caco-2 cell monolayers. PCRM, like CRM, significantly inhibited the oxidative degradation of polyunsaturated fatty acids and cholesterol, and the formation of their oxidation products in the oxidative stress systems, acting as scavenger of peroxyl radicals, without toxic effect (in the range 10–100 μM) on differentiated Caco-2 cell viability. Nevertheless, the structural modification of the lead compound severely affected membrane permeation through the Caco-2 monolayers, with apparent permeability coefficient (P_app) values in the apical-to-basolateral direction (2-h incubation) of 2.93 ± 0.94 × 10^− 6 cm/s and < 10^− 7 cm/s for CRM and PCRM, respectively. Taken together, our observations reveal a surprising bioactivity of PCRM, and qualify this compound as an interesting probe to explore the antioxidant pharmacophore of curcuminoids.     

Hepatoprotection using sweet orange peel and its bioactive compound,hesperidin, for CCl4-induced liver injury in vivo

The hepatoprotective effect of water extracts of sweet orange (Citrus sinensis) peel (WESP) and its biological compound, hesperidin (HD), on oxidative stress in vivo, were investigated. HD was the major compounds among the ten compounds identified using HPLC-DAD and HPLC-MS/MS analysis. Oral administration of WESP to rats at 10 and 100 mg/kg bw for 28 consecutive days before a single dose of CCl₄ (2 ml/kg bw) demonstrates a significant protective effect by lowering the levels of aspartate aminotransferase (AST) and alanine aminotransferase (ALT), and by improving the histological architecture of the rat liver. WESP attenuated oxidative stress by increasing the content of hepatic glutathione (GSH), and by a dramatic increase in the activities of superoxide dismutase (SOD) and glutathione peroxidase (GPx). WESP induced a significant CYP2E1 activity, which suggests that WESP may be a substrate of CYP2E1. WESP at a dose of 1.0 mg/kg bw and HD at 0.1 mg/kg bw did not sustain the protective effect against oxidative stress, in vivo. This study demonstrated that citrus peel protects rat liver from CCl₄-induced injury by attenuating hepatic oxidative stress, which suggests that WESP can be used as a therapeutic antihepatotoxic agent for the treatment of hepatic injury.     

Effects of controlled pepsin hydrolysis on antioxidant potential and fractional changes of chickpea proteins

This study investigated the effects of controlled pepsin hydrolysis on antioxidant potential and fractional changes of chickpea protein extracts (CPE). The enzyme hydrolysis increased soluble protein content (1.2 to 2-fold) and free radical scavenging activity (1.9 to 3-fold) of hydrolyzed chickpea protein extract (HCPE), but almost unaffected its antioxidant potential in oil-in-water emulsion system and reduced its iron chelating capacity (1.3-fold) and functional properties. The chromatographic fractions of CPE are mainly acidic, while those of HCPE are mainly basic and neutral. The majority of chickpea proteins had pI between 4.5 and 5.5, and molecular weight (MW) between 15 and 40 kDa, while MW of their pepsin hydrolysis products ranged between 6.5 and 14.2 kDa. The main antioxidant proteins in CPE and HCPE fractionated by ultrafiltration had MW greater than 30 kDa and between 2 and 10 kDa, respectively. The chickpea proteins and hydrolysates showed different potentials as functional food ingredients.     

Dihydrocaffeic acid,a major microbial metabolite of chlorogenic acids,shows similar protective effect than a yerba mate phenolic extract against oxidative stress in HepG2 cells

The hepatoprotective effect of a yerba mate phenolic extract (YMPE), rich in chlorogenic acids, and its main circulating metabolites dihydrocaffeic (DHCA) and dihydroferulic (DHFA) acids were assessed in human hepatoma HepG2 cells subjected to oxidative damage induced by tert-butylhydroperoxide (t-BOOH). Direct treatment of HepG2 cells with realistic concentrations of YMPE (1, 10 and 50 μg/mL), DHCA or DHFA (0.2, 1, 10 μM) for 20 h was not cytotoxic and significantly decreased ROS generation. Pre-treatment with YMPE and DHCA prevented the cytotoxicity and macromolecular damage induced by t-BOOH. Moreover, decreased levels of reduced glutathione (GSH), and increased ROS levels and antioxidant enzyme activity induced by t-BOOH were dose-dependently recovered. DHFA only showed a slight protection against cell cytotoxicity, lipid oxidation and GSH depletion. In conclusion, YMPE and one of its major microbial metabolites, DHCA, confer significant protection against oxidative damage, adding evidences to the beneficial health effects associated with mate intake.     

Production,analysis and in vivo evaluation of novel angiotensin-I-converting enzyme inhibitory peptides from bovine casein

Novel angiotensin-I-converting enzyme inhibitory peptides were isolated from bovine casein hydrolysate prepared by AS1.398 neutral protease. The active hydrolysate obtained at 12 h hydrolysis showed the highest ACE-inhibitory activity and was further consecutively separated by ultrafiltration, and the 3 kDa permeate showed the highest ACE-inhibiting activity. This active fraction was further purified to yield two novel ACE-inhibiting peptides, whose amino acid sequences were Arg-Tyr-Pro-Ser-Tyr-Gly (κ-casein; f25–30) and Asp-Glu-Arg-Phe (κ-casein; f15–18), respectively. The IC₅₀ value of the peptides were 54 ± 1.2 μg/mL and 21 ± 0.8 μg/mL, respectively. The Lineweaver–Burk plots revealed that the peptides acts as a non-competitive inhibitor. Antihypertensive effect in spontaneously hypertensive rats also revealed that single and repeated oral administrations of hydrolysates of bovine casein decreased systolic blood pressure significantly in spontaneously hypertensive rats (P < 0.01, P < 0.05). These results suggested that the peptide derived from peptides from bovine casein would be a beneficial ingredient for functional food or pharmaceuticals against hypertension.     

Oxidative stability of virgin olive oil enriched with carnosic acid

The aim of this study was to evaluate the effect of the addition of carnosic acid on the oxidative stability of virgin olive oil. Two different amounts of carnosic acid (0.01 and 0.1 g/100 g oil) and two different temperatures (accelerated aging temperature, 60 °C; deep frying temperature, 180 °C) were considered. The influence of carnosic acid and heating time on the stability of the oils was studied by experimental design. The results obtained at 60 °C showed a dose dependent inhibition in the formation of primary and secondary oxidation products and a dose dependent enhancement of radical scavenging activity, which was only less significantly influenced by heating time. On the contrary, at 180 °C no protective effect against lipid oxidation was observed and the radical scavenging activity was practically zeroed by heating, probably as a consequence of a fast decomposition of carnosic acid.     

Physical and oxidative stability of whey protein oil-in-water emulsions produced by conventional and ultra high-pressure homogenization: Effects of pressure and protein concentration on emulsion characteristics

Oil-in-water pre-emulsions (15% sunflower + 5% olive oils) obtained by colloid mill homogenization (CM) at 5000 rpm using whey protein isolate at different levels (1, 2 and 4%) were stabilized by ultra high-pressure homogenization (UHPH, 100 and 200 MPa) and by conventional homogenization (CH, 15 MPa). Emulsions were characterized for their physical properties (droplet size distribution, microstructure, surface protein concentration, emulsifying stability against creaming and coalescence, and viscosity) and oxidative stability (hydroperoxide content and thiobarbituric acid reactive substances, TBARs) under light (2000 lux/m² for 10 days). UHPH produced emulsions with lipid droplets of small size in the sub-micron range (100–200 nm) and low surface protein with unimodal distribution when produced at 4% whey proteins and 200 MPa. All emulsions exhibited Newtonian behavior (n ≈ 1). Long term physical stability against creaming and coalescence was observed in UHPH-emulsions, compared to those obtained by CM and CH. However, CH emulsions were highly stable against creaming (days) in comparison to the CM emulsions (hours). UHPH resulted in emulsions highly stable to oxidation compared to CM and CH treatments, especially when 100 MPa treatment was applied.Industrial relevanceIn the food, cosmetic and pharmaceutical sectors, industrial operators are currently interested in developing encapsulating systems to delivery bioactive compounds, which are generally hydrophobic, unstable and sensitive to light, temperature or/and oxygen. Ultra high-pressure homogenization is capable of producing stable submicron emulsions (< 1 μm) with a narrow size distribution, inducing more significant changes in the interfacial protein layer thus preventing droplet coalescence and also inhibit lipid oxidation. The present study suggests that emulsions produced by whey protein (4%) treated by ultra high-pressure homogenization have a good physical stability to flocculation, coalescence and creaming and also high stability to lipid oxidation, opening a wide range of opportunities in the formulation of emulsions containing bioactive components with lipid nature.     

Angiotensin I-converting enzyme inhibitory activity of chickpea and pea protein hydrolysates

ACE inhibitory activity was studied for different hydrolysates obtained from protein concentrates of chickpea (kabuli and desi) and yellow pea (Golden) using in vitro gastrointestinal simulation, alcalase/flavourzyme, and papain. Protein/peptide profiles studied by SDS–PAGE and SE-HPLC, showed a rich composition of the hydrolysates in small peptides having MWs under 4 kDa. Papain hydrolysed yellow pea proteins showed the highest ACE inhibitory activity. In addition, chickpea desi proteins hydrolysed by in vitro gastrointestinal simulation showed higher ACE inhibition (IC₅₀ of 140 ± 1 μg/ml) compared to its digests obtained by alcalase/flavourzyme (IC₅₀ of 228 ± 3 μg/ml) or papain (IC₅₀ of 180 ± 1 μg/ml) and to chickpea kabuli hydrolysed by gastrointestinal simulation (IC₅₀ of 229 ± 1 μg/ml). The results demonstrate that enzymatic hydrolysates of chickpea and pea proteins contain bioactive ACE inhibitory peptides; furthermore, the type of enzyme used for hydrolysis affects the ACE inhibitory activity.     

Influence of environmental stresses on the physicochemical stability of orange oil bilayer emulsions coated by lactoferrin–soybean soluble polysaccharides and lactoferrin–beet pectin

Based on layer-by-layer electrostatic deposition, orange oil bilayer emulsions stabilized with lactoferrin (LF)–soybean soluble polysaccharides (SSPS) and lactoferrin (LF)–beet pectin (BP) were prepared. The effect of environmental stresses (ionic strength, pH, freeze–thaw and light) on the physicochemical stability of primary and secondary emulsions was investigated. In the absence of anionic polysaccharides, orange oil emulsion was highly unstable and aggregated at pH 7–9 and NaCl of 0.1–0.5 M. The droplets in LF–SSPS coated emulsion were stable against aggregation at pH range of 3–10 and NaCl concentration less than 0.3 M, while the droplets in LF–BP coated emulsion were stable against aggregation at pH 4–9 and NaCl concentrations of 0–0.5 M. All the primary and secondary emulsions showed the instability after the freeze–thaw treatment and the stability could be improved in the presence of maltodextrin. During the light exposure (0.35 W/m², 45 °C) for 8 h, the bilayer emulsions could protect key volatile compounds (decanal, octanal and geranial) from the oxidation compared with the primary emulsions. These results suggested that the layer-by-layer electrostatic deposition could improve the stability of LF-coated emulsion to environmental stresses.     

Consumption of baru seeds [Dipteryx alata Vog.], a Brazilian savanna nut,prevents iron-induced oxidative stress in rats

The protective effect of plant-based foods in human health has been attributed to the presence of bioactive compounds in all parts of the plants. A previous study found a high level of minerals, tannins and phytic acid in the baru nut (Dipteryx alata Vog.), which is a native fruit of the Brazilian savanna. This study investigated the antioxidant activity (AA) of the aqueous and ethyl acetate extracts of the baru nut and the effect of the consumption of this nut on the oxidative status of rats supplemented orally with iron. The AA was evaluated in vitro using the ferric reducing antioxidant power (FRAP), β-carotene/linoleic acid system and free-radical scavenging (DPPH) assays. The total polyphenol concentration was determined spectrophotometrically using the Folin–Ciocalteu reagent. The in vivo study was conducted in male Wistar rats that were fed an AIN-93M diet with or without 10% baru nut or 1% phytic acid and supplemented daily with iron or saline by gavages for 17 days. The liver, heart and spleen were collected for the determination of the malondialdehyde (MDA), carbonyl protein and iron concentrations. The specific activities of catalase, glutathione reductase, glutathione peroxidase and glutathione S-transferase were also determined in these tissues. A T test was used to compare the results among the rats groups and between the different baru nut extracts (p < 0.05). The aqueous extract of the baru nut contained a higher level of phenolic compounds and a higher antioxidant activity, as measured by FRAP and the β-carotene/linoleic system, relative to the EtOAc extract. The iron supplementation reduced the body weight gain, increased the levels of iron and MDA in the liver and the spleen and increased the carbonyl levels in all three tissues. Consumption of the baru nut reduced the carbonyl levels in the liver, heart and spleen of the iron-supplemented rats (p = 0.002, 0.012 and 0.036, respectively) relative to the heart carbonyl level of rats that were fed the control diet (p = 0.000); it also marginally reduced the iron-induced lipid oxidation in the liver (p = 0.117) and the spleen (p = 0.074). Phytic acid reduced the carbonyl level in the spleen (p = 0.020) and marginally reduced the carbonyl level in the liver (p = 0.098) of iron-supplemented rats. These results demonstrated that the consumption of the baru nut protects tissues against iron-induced oxidative stress, and the phytic acid from the baru nut may be partially responsible for this protective effect; however, other compounds such as phenols may also be involved.     

A novel approach to monitor the oxidation process of different types of heated oils by using chemometric tools

The oxidative stability of seven oils with different fatty acid profiles was assessed. Oxidation at 0, 2 and 4 h at 180 °C was monitored by measuring the absorbance of thiobarbituric acid reactive substances (TBARS) along the absorption spectrum (300–600 nm), the volatile aldehydes (HS-SPME–GC–MS) and the fatty acid profile (FID-GC).TBARS absorption spectrum behavior depended on the lipid composition of heated oils. Higher absorbance increments during heating were noticed at 390 nm compared to 532 nm (from 2 to 21 fold higher depending on the oil), pointing to its better sensitivity to detect oxidation. Furthermore, a close relationship between ABS₃₉₀, the loss of polyunsaturated fatty acids and their corresponding oxidation compounds (volatile aldehydes) was revealed by Principal Component Analysis.Multiparametric equations allowed predicting the formation of volatile aldehydes of heated oils by measuring only two parameters: TBARS₃₉₀ during their heating, and the lipid profile in unheated oils (MUFA, ω-3 and ω-6). Results pointed out the interest of choosing ABS₃₉₀ when the oxidative evolution of vegetable oils under heating is assessed by the TBARS test.     

Hepatoprotective effect of peptic hydrolysate from salmon pectoral fin protein byproducts on ethanol-induced oxidative stress in Sprague–Dawley rats

Bioactive peptides were generated by pepsin hydrolysis from salmon pectoral fin protein byproduct, and the hepatoprotective effect of the peptic hydrolysate (PH) on ethanol-induced oxidative stress was investigated in Sprague–Dawley rats. Administration of ethanol for 4 weeks significantly (p < 0.05) increased serum markers of liver damage, such as alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, and lactate dehydrogenase; however, these activities decreased significantly (p < 0.05) after PH administration. Elevated thiobarbituric acid reactive substance levels in liver tissue and serum decreased significantly (p < 0.05) following administration of PH. Ethanol exposure significantly (p < 0.05) decreased glutathione contents in liver and serum, and hepatic antioxidant enzyme activities such as superoxide dismutase and glutathione peroxidase, while the PH treatment significantly (p < 0.05) increased these altered parameters. These results indicate that the PH had a protective effect against ethanol-induced hepatotoxicity that was comparable to that of silymarin, which was supported by evaluating liver histopathology in the rats.     

Influence of pH and NaCl on monolaurin inactivation of Streptococcus iniae

Streptococcus iniae, a Gram-positive bacterium, has been recognized as a cause of human and fish streptococcosis. Aquacultured fish are susceptible to infection and have been epidemiologically linked with wound infections of fish handlers. Therefore, there is a need to develop methods of prevention and/or control of this pathogen. This study determined the minimum inhibitory concentration of monolaurin (glycerol monolaurate) against S. iniae strains PW and BU and utilized gradient plates at 37°C to determine the combined influence of pH and NaCl on monolaurin inactivation of S. iniae. The minimum inhibitory concentration of monolaurin against strain PW was 12.4±0.3 μg ml⁻¹ and against strain BU was 12.1±0 μg ml⁻¹. Compared to growth in the absence of monolaurin, the incorporation of 6 μg ml⁻¹ monolaurin into the salt (1.12–6.95%)–pH (4.26–8.88) gradient plates prevented growth of strain PW at pH values <6.00 and strain BU at pH values <6.20, regardless of the salt concentration. The combination of monolaurin with environmental variables such as pH and salt proved to be an effective tool for in vitro control of S. iniae.     

Use of microwave processing to reduce the initial contamination by Alicyclobacillus acidoterrestris in a cream of asparagus and effect of the treatment on the lipid fraction

The effects of a short-time microwave (MW) treatments on the survival of Alicyclobacillus acidoterrestris spores (10⁵ spores/g) inoculated in a cream of asparagus, along with the oxidation of the fat component (olive oil), were investigated.The samples were MW-treated at 60–100% of power (2450 MHz) for 3–7 min; power and processing time changed according to a Central Composite Design at two variables/five levels. The combinations resulting in a 2-fold reduction in the number of alicyclobacilli spores (100% of power–5 min; 80%–6 min; 80%–7 min) were stored at different temperatures and times (25 °C/27 days, 37 °C/18 days and 50 °C/9 days), to determine the decay of the qualitative characteristics of the lipid fraction. Peroxide value, K₂₃₂, K₂₇₀ and Rancimat test (induction time) were chosen as indexes of primary and secondary oxidation. MW-effect on the spores depended upon both the power and the treatment time; moreover the interaction [power] × [time] was the most significant variable. As regards the effect of MW on the lipid fraction, the results suggested that MW affected slightly induction time, peroxide values and spectrophotometric determinations, especially at low powers.Industrial relevanceSince the middle of 1990s, MW-processing has been regarded as a convenient approach for the stabilization of vegetable preserves. In Southern Italy, olive oil is an essential ingredient for this kind of food; however, it is well known that a strong thermal processing as well as not-correct storage could affect it significantly and increase the art of oxidation.This research provides some useful information on the effects of MW for a new product, an asparagus cream, focusing on the influence of this approach on olive oil oxidation, thus suggesting that MW could be a convenient preservation technique.