Application of natural antioxidants for the formulation of functional meat products

There is growing interest in finding healthier meals that offer more than just nutritional benefits. Meat and meat products are consumed all over the world, so it is possible to use them as matrices to make sure that people get enough bioactive components from their food. Besides extending the meat product's shelf-life and improving its composition (by integrating antioxidant molecules), it could also help people stay healthy by lowering lipid oxidative products. In this review, we look at whether developing and eating functional meat products is a viable method for improving meat composition and stability and reducing the oxidative consequences associated with the consumption of meat intake. The inclusion of plant bioactive compounds and antioxidants in meat products should protect the composition and quality of functional meat and meat products as well as the customers' health status. The key plant components with antioxidant capabilities employed in the composition of functional meat products will be discussed in this review.

DNA damage by oxidized fatty acids detected by DNA/SPE biosensor

Electrochemical DNA/screen-printed electrode biosensor (DNA/SPE biosensor) was tested for the detection of alterations in DNA formed as a consequence of the reaction between DNA and oxidative products of fatty acids. Interaction of DNA with a mixture of products generated during the oxidation of linoleic and oleic acids manifested DNA damage depending on a tested fatty acid and the presence of hydroperoxides and thiobarbituric acid reactive substances (TBARS) determined after the oxidation of fatty acids. A bigger extent of the DNA damage was registered in the case of the interaction with oxidized linoleic acid with the high content of TBARS. The results achieved suggest the possible application of DNA/SPE biosensor in the detection of an interaction between DNA and products of fatty acid oxidation.

The Comparative Metabolism of Some Substituted Phenyl-N-Methylcarbamate Insecticides

<p>1. The metabolism of the N-methylcarbamates of 3-tertbutylphenol; 3,5-ditertbutylphenol; and 2-isopropoxyphenol was investigated in insects and mammals. 2. The major degradative pathway in enzyme systems from insects and mice was oxidative. The major metabolites from tertbutyl substituted phenyl-N-methylcarbamates were N-hydroxymethyl derivatives and tertbutanol derivatives. Baygon yielded N-hydroxymethyl, ring hydroxyl and O-dealkyl derivatives as major metabolites. 3. The rates of oxidation of the three insecticides in each enzyme system were similar. 4. Oxidation was inhibited by piperonyl butoxide and Metopirone, apparent I50 for singly oxidised metabolites was 10-4 M, and for metabolites with two oxidations 10-5M. 5. Enzymic hydrolysis of carbamate insecticides required reduced cofactor in insect and mouse systems. Mouse blood did not effect hydrolysis. 6. A wide variation of oxidising ability was found in live insects. Musca domestica was most active, Tenebrio molitor and Costelytra zealandica were least active. 7. Insecticide synergists reduce insects' ability to oxidise Baygon to acetone. 8. Musca domestica and Lucilia sericata larvae oxidised carbamate insecticides slower than the adult forms. 9. Mice excrete 3-tertbutylphenyl-N-methylcarbamate as phenolic metabolites, with only minor oxidative products. 10. Different rates of metabolism among insects could account for the selective toxicity of aryl-N-methylcarbamates.</p>

The Comparative Metabolism of Some Substituted Phenyl-N-Methylcarbamate Insecticides

<p>1. The metabolism of the N-methylcarbamates of 3-tertbutylphenol; 3,5-ditertbutylphenol; and 2-isopropoxyphenol was investigated in insects and mammals. 2. The major degradative pathway in enzyme systems from insects and mice was oxidative. The major metabolites from tertbutyl substituted phenyl-N-methylcarbamates were N-hydroxymethyl derivatives and tertbutanol derivatives. Baygon yielded N-hydroxymethyl, ring hydroxyl and O-dealkyl derivatives as major metabolites. 3. The rates of oxidation of the three insecticides in each enzyme system were similar. 4. Oxidation was inhibited by piperonyl butoxide and Metopirone, apparent I50 for singly oxidised metabolites was 10-4 M, and for metabolites with two oxidations 10-5M. 5. Enzymic hydrolysis of carbamate insecticides required reduced cofactor in insect and mouse systems. Mouse blood did not effect hydrolysis. 6. A wide variation of oxidising ability was found in live insects. Musca domestica was most active, Tenebrio molitor and Costelytra zealandica were least active. 7. Insecticide synergists reduce insects' ability to oxidise Baygon to acetone. 8. Musca domestica and Lucilia sericata larvae oxidised carbamate insecticides slower than the adult forms. 9. Mice excrete 3-tertbutylphenyl-N-methylcarbamate as phenolic metabolites, with only minor oxidative products. 10. Different rates of metabolism among insects could account for the selective toxicity of aryl-N-methylcarbamates.</p>

Study of Human Neutrophil Elastase Levels and the Correlation with ARDS Severity in Thoracic Trauma Patients

Introduction: Thoracic trauma is trauma that hits the thoracic wall or intra-thoracic organs, either due to blunt trauma or due to sharp trauma. In thoracic trauma often causes impaired ventilation perfusion due to damage to the lung parenchyma. This results in impaired tissue oxygenation, which is one of the causes of Acute respiratory distress Syndrome (ARDS). These changes are caused by the release of pro-inflammatory mediators, plasmatic proteins and proteases into the alveolar space associated with ongoing edema, as well as oxidative products that ultimately result in severe inhibition of the surfactant system. Method: This study will examine the relationship between plasma elastase levels as a predictor of the incidence of ARDS in thoracic trauma patients in Malang. This study is an observational cohort study. The research subjects were thoracic trauma patients who fit the criteria. Result: I t can be concluded that there is a significant relationship between elastase levels and BGA-3. The elastase level is below the value of 11.65 ±1.85, the patient is likely not to experience ARDS in the future. If the value of elastase levels is limited to 23.79 ±3.95, the patient will experience mild type ARDS. Meanwhile, if the value of elastase levels is limited to 57.68 ±18.55, in the future the patient will experience moderate type of ARDS. Meanwhile, if the elastase level is between 107.85 ± 5.04, the patient will likely experience severe ARDS. Conclusion: Based on the characteristic test of the sample characteristics, diagnosis and action, there are significant differences in the causes of ARDS. Neutophil elastase levels correlate with the degree of ARDS incidence.

Amelioration of hemodialysis-induced oxidative stress and fatigue with a hemodialysis system employing electrolyzed water containing molecular hydrogen

Background A novel hemodialysis (HD) system employing electrolyzed water containing molecular hydrogen (E-HD) has been developed to improve the bio-compatibility of HD. This study examined the impact of E-HD on changes in redox state during HD and HD-related fatigue. Method This single-arm, prospective observational study examined 63 patients on chronic HD (41 males; mean age, 72 ± 9 years; median duration of HD, 7 years). Redox parameters (serum myeloperoxidase [MPO], malondialdehyde-protein adduct [MDA-a], thioredoxin 1 [TRX]) during HD were compared between control HD (C-HD) and E-HD after 8 weeks. Fatigue was evaluated using a numerical rating scale (NRS) during the 8-week course. Results In C-HD, an increase in serum MPO accompanied increases in both oxidative products (MDA-a) and anti-oxidant molecules (TRX). In E-HD, although increases in MPO were accentuated during HD, changes in MDA-a and TRX were ameliorated as compared with C-HD. In patients who showed HD-related fatigue (47%) during C-HD, change in MDA-a by HD was a risk factor for the presence of fatigue. During the 8 weeks of observation on E-HD, those patients displayed significant decreases in fatigue scores. Conclusion E-HD ameliorates oxidative stress and supports anti-oxidation during HD, suggesting improved bio-compatibility of the HD system. E-HD may benefit patients with HD-related fatigue, but the mechanisms underlying changes to oxidative stress have yet to be clarified.

Oxidative stability of breast meat from broilers fed diets supplemented with synbiotic and organic acids

The purpose of this study was to investigate the effect of synbiotic and organic acids on oxidative stability of breast broiler meat. The experiment consists on 120, 2 days old Ross 308 chicks, housed in metabolic cages (6 chicks/cage). A 2 x 2 factorial arrangement was considered with 4 treatments and 5 replicates (30 animals per group). Two different levels of synbiotic (0 and 10 g/kg) and two different levels of organic acids (0 and 1.5 g/kg) were added to the standard diets in order to constitute the four experimental diets. For further analysis, breast meat from 6 animals per group were collected in 42nd experimental day. No significant differences were noticed for any oxidative parameter measured in breast samples except TBARS (significant decreased values for OA supplemented groups), at the end of experiment. After 4 days of refrigeration (4°C), the secondary oxidative products (panisidine, TBARS) were significant smaller for E groups, compared to C. After 7 days of refrigeration (4°C), the OA groups had significant smaller values for primary (CD) and secondary oxidation products. Synbiotic and organic acids supplements presented positive effect on meat quality by increasing oxidative stability of breast meat during storage.

Stress-Sensitive Protein Rac1 and Its Involvement in Neurodevelopmental Disorders

Ras-related C3 botulinum toxin substrate 1 (Rac1) is a small GTPase that is well known for its sensitivity to the environmental stress of a cell or an organism. It senses the external signals which are transmitted from membrane-bound receptors and induces downstream signaling cascades to exert its physiological functions. Rac1 is an important regulator of a variety of cellular processes, such as cytoskeletal organization, generation of oxidative products, and gene expression. In particular, Rac1 has a significant influence on certain brain functions like neuronal migration, synaptic plasticity, and memory formation via regulation of actin dynamics in neurons. Abnormal Rac1 expression and activity have been observed in multiple neurological diseases. Here, we review recent findings to delineate the role of Rac1 signaling in neurodevelopmental disorders associated with abnormal spine morphology, synaptogenesis, and synaptic plasticity. Moreover, certain novel inhibitors of Rac1 and related pathways are discussed as potential avenues toward future treatment for these diseases.