RESUMEN

Ferroptosis is a recently recognized process of cell death characterized by accumulation of iron-dependent lipid peroxides. Herein, we demonstrate that peroxisome proliferator-activated receptor δ (PPARδ) inhibits ferroptosis of mouse embryonic fibroblasts (MEFs) derived from cysteine/glutamate transporter (xCT)-knockout mice. Activation of PPARδ by the specific ligand GW501516 led to a dose-dependent decrease in ferroptotic cell death triggered by xCT deficiency, along with decreased levels of intracellular iron accumulation and lipid peroxidation. These effects of GW501516 were abolished by PPARδ-targeting small interfering RNA (siRNA) and the PPARδ inhibitor GSK0660, indicating that PPARδ inhibits xCT deficiency-induced ferroptosis. In addition, GW501516-activated PPARδ time- and dose-dependently upregulated catalase expression at both the mRNA and protein levels. This PPARδ-mediated upregulation of catalase was markedly attenuated in cells treated with PPARδ-targeting siRNA and GSK0660, indicating that expression of catalase is dependent on PPARδ. Consistently, the effects of GW501516 on ferroptosis of xCT-deficient MEFs were counteracted in the presence of 3-amino-1,2,4-triazole, a specific inhibitor of catalase, suggesting that catalase is essential for the effect of PPARδ on ferroptosis triggered by xCT deficiency. GW501516-activated PPARδ stabilized peroxisomes through catalase upregulation by targeting peroxisomal hydrogen peroxide-mediated lysosomal rupture, which led to ferroptosis of xCT-deficient MEFs. Collectively, these results demonstrate that PPARδ modulates ferroptotic signals in xCT-deficient MEFs by regulating catalase expression.

Asunto(s)

Sistema de Transporte de Aminoácidos y+/deficiencia , Ferroptosis , Fibroblastos/metabolismo , PPAR gamma/metabolismo , Peroxisomas/metabolismo , Sistema de Transporte de Aminoácidos y+/genética , Animales , Catalasa/biosíntesis , Catalasa/genética , Células Cultivadas , Inducción Enzimática , Ferroptosis/efectos de los fármacos , Fibroblastos/efectos de los fármacos , Fibroblastos/patología , Peróxido de Hidrógeno/metabolismo , Peroxidación de Lípido , Ratones Noqueados , Estrés Oxidativo , PPAR gamma/agonistas , PPAR gamma/genética , Peroxisomas/efectos de los fármacos , Peroxisomas/genética , Peroxisomas/patología , Transducción de Señal , Tiazoles/farmacología

RESUMEN

Oxidative stress-induced cell damage and death of the retinal pigmented epithelium (RPE), a polarized monolayer that maintains retinal health and homeostasis, lead to the development of age-related macular degeneration (AMD). Several studies show that the naturally occurring antioxidant Lutein (Lut) can protect RPE cells from oxidative stress. However, the poor solubility and low oral bioavailability limit the potential of Lut as a therapeutic agent. In this study, lutein diglutaric acid (Lut-DG), a prodrug of Lut, was synthesized and its ability to protect human ARPE-19 cells from oxidative stress was tested compared to Lut. Both Lut and Lut-DG significantly decreased H2O2-induced reactive oxygen species (ROS) production and protected RPE cells from oxidative stress-induced death. Moreover, the immunoblotting analysis indicated that both drugs exerted their protective effects by modulating phosphorylated MAPKs (p38, ERK1/2 and SAPK/JNK) and downstream molecules Bax, Bcl-2 and Cytochrome c. In addition, the enzymatic antioxidants glutathione peroxidase (GPx) and catalase (CAT) and non-enzymatic antioxidant glutathione (GSH) were enhanced in cells treated with Lut and Lut-DG. In all cases, Lut-DG was more effective than its parent drug against oxidative stress-induced damage to RPE cells. These findings highlight Lut-DG as a more potent compound than Lut with the protective effects against oxidative stress in RPE cells through the modulation of key MAPKs, apoptotic and antioxidant molecular pathways.

Asunto(s)

Antioxidantes/farmacología , Células Epiteliales/efectos de los fármacos , Luteína/análogos & derivados , Estrés Oxidativo/efectos de los fármacos , Profármacos/farmacología , Epitelio Pigmentado de la Retina/efectos de los fármacos , Proteínas Reguladoras de la Apoptosis/biosíntesis , Proteínas Reguladoras de la Apoptosis/genética , Catalasa/biosíntesis , Catalasa/genética , Línea Celular , Citocromos c/biosíntesis , Citocromos c/genética , Evaluación Preclínica de Medicamentos , Células Epiteliales/metabolismo , Regulación de la Expresión Génica/efectos de los fármacos , Glutatión/biosíntesis , Glutatión/genética , Glutatión Peroxidasa/biosíntesis , Glutatión Peroxidasa/genética , Humanos , Peróxido de Hidrógeno/toxicidad , Luteína/química , Luteína/farmacología , Sistema de Señalización de MAP Quinasas/efectos de los fármacos , Degeneración Macular/tratamiento farmacológico , Estructura Molecular , Especies Reactivas de Oxígeno/metabolismo , Epitelio Pigmentado de la Retina/citología

RESUMEN

Pseudomonas aeruginosa is an opportunistic pathogen that uses malonate among its many carbon sources. We recently reported that, when grown in blood from trauma patients, P. aeruginosa expression of malonate utilization genes was upregulated. In this study, we explored the role of malonate utilization and its contribution to P. aeruginosa virulence. We grew P. aeruginosa strain PA14 in M9 minimal medium containing malonate (MM9) or glycerol (GM9) as a sole carbon source and assessed the effect of the growth on quorum sensing, virulence factors, and antibiotic resistance. Growth of PA14 in MM9, compared to GM9, reduced the production of elastases, rhamnolipids, and pyoverdine; enhanced the production of pyocyanin and catalase; and increased its sensitivity to norfloxacin. Growth in MM9 decreased extracellular levels of N-acylhomoserine lactone autoinducers, an effect likely associated with increased pH of the culture medium; but had little effect on extracellular levels of PQS. At 18 hr of growth in MM9, PA14 formed biofilm-like structures or aggregates that were associated with biomineralization, which was related to increased pH of the culture medium. These results suggest that malonate significantly impacts P. aeruginosa pathogenesis by influencing the quorum sensing systems, the production of virulence factors, biofilm formation, and antibiotic resistance.

Asunto(s)

Biopelículas/crecimiento & desarrollo , Farmacorresistencia Bacteriana/fisiología , Malonatos/metabolismo , Pseudomonas aeruginosa/patogenicidad , Percepción de Quorum/fisiología , Antibacterianos/farmacología , Biomineralización/fisiología , Catalasa/biosíntesis , Decanoatos , Disacáridos/biosíntesis , Glicerol/metabolismo , Norfloxacino/farmacología , Oligopéptidos/biosíntesis , Pseudomonas aeruginosa/efectos de los fármacos , Pseudomonas aeruginosa/metabolismo , Piocianina/biosíntesis , Serina Endopeptidasas/biosíntesis , Virulencia , Factores de Virulencia/metabolismo

RESUMEN

Catalases are a large group of enzymes that decompose hydrogen peroxide to oxygen and hydrogen, and have been applied widely in numerous areas. Bacillus subtilis ATCC 6051a is a well-known host strain for high level secretion of heterologous peptides. However, the application of 6051a was seriously hampered by insufficient transformation efficiency. In this study, D-xylose inducible comK was integrated into the genome of B. subtilis ATCC 6051a, generating 164S, a mutant owns a transformation efficiency of 1 000-fold higher than its parent strain, thus allowing gene replacement by double crossover recombination using linear dsDNAs. The efficiency of the flanking arms for homologous recombination was then analyzed. We found that 400 bp was the minimal length of homologous fragments required to initiate efficient recombination in the 164S strain. In addition, DNA cassettes encoding two mesophilic catalases (Orf 2-62 and Orf 2-63) from B. licheniformis were integrated onto 164S. The catalytic properties of recombinant Orf 2-62 and Orf 2-63 were analyzed, and were found to be predominantly secreted into the fermentation broth, although they obviously lack any known secretory signal peptide. This work demonstrated that B. subtilis 164S is an excellent cell tool, not only for its superior secretion capacity, but also for its convenience in genetic modification.

Asunto(s)

Bacillus subtilis/genética , Bacillus subtilis/metabolismo , Catalasa/biosíntesis , Bacillus licheniformis/genética , Proteínas Bacterianas/genética , Fermentación , Ingeniería Genética , Genoma Bacteriano , Recombinación Homóloga , Microbiología Industrial , Proteínas Recombinantes/biosíntesis , Factores de Transcripción/genética , Transformación Bacteriana , Xilosa/metabolismo

RESUMEN

Novel coronary pneumonia (COVID-19) is a respiratory distress syndrome caused by a new type of coronavirus. Understanding the genetic basis of susceptibility and prognosis to COVID-19 is of great significance to disease prevention, molecular typing, prognosis, and treatment. However, so far, there have been only two genome-wide association studies (GWASs) on the susceptibility of COVID-19. Starting with these reported DNA variants, we found the genes regulated by these variants through cis-eQTL and cis-meQTL acting. We further did a series of bioinformatics analysis on these potential risk genes. The analysis shows that the genetic variants on EHF regulate the expression of its neighbor CAT gene via cis-eQTL. There was significant evidence that CAT and the SARS-CoV-2-related S protein binding protein ACE2 interact with each other. Intracellular localization results showed that CAT and ACE2 proteins both exists in the cell membrane and extracellular area and their interaction could have an impact on the cell invasion ability of S protein. In addition, the expression of these three genes showed a significant positive correlation in the lungs. Based on these results, we propose that CAT plays a crucial intermediary role in binding effectiveness of ACE2, thereby affecting the susceptibility to COVID-19.

Asunto(s)

COVID-19 , Catalasa , Regulación Enzimológica de la Expresión Génica , Predisposición Genética a la Enfermedad , Polimorfismo Genético , SARS-CoV-2/metabolismo , Enzima Convertidora de Angiotensina 2/genética , Enzima Convertidora de Angiotensina 2/metabolismo , COVID-19/genética , COVID-19/metabolismo , Catalasa/biosíntesis , Catalasa/genética , Femenino , Estudio de Asociación del Genoma Completo , Humanos , Masculino , Estudios Retrospectivos , Glicoproteína de la Espiga del Coronavirus/genética , Glicoproteína de la Espiga del Coronavirus/metabolismo , Factores de Transcripción/genética , Factores de Transcripción/metabolismo

RESUMEN

Pigmented bacterial symbionts play major roles in the health of coral holobionts. However, there is scarce knowledge on the diversity of these microbes for several coral species. To gain further insights into holobiont health, pigmented bacterial isolates of Fabibacter pacificus (Bacteroidetes; n = 4), Paracoccus marcusii (Alphaproteobacteria; n = 1), and Pseudoalteromonas shioyasakiensis (Gammaproteobacteria; n = 1) were obtained from the corals Mussismilia braziliensis and Montastraea cavernosa in Abrolhos Bank, Brazil. Cultures of these bacterial symbionts produced strong antioxidant activity (catalase, peroxidase, and oxidase). To explore these bacterial isolates further, we identified their major pigments by HPLC and mass spectrometry. The six phylogenetically diverse symbionts had similar pigment patterns and produced myxol and keto-carotene. In addition, similar carotenoid gene clusters were confirmed in the whole genome sequences of these symbionts, which reinforce their antioxidant potential. This study highlights the possible roles of bacterial symbionts in Montastraea and Mussismilia holobionts.

Asunto(s)

Antozoos/microbiología , Antioxidantes/metabolismo , Bacteroidetes/metabolismo , Paracoccus/metabolismo , Pigmentos Biológicos/metabolismo , Pseudoalteromonas/metabolismo , Animales , Bacteroidetes/genética , Bacteroidetes/aislamiento & purificación , Brasil , Carotenoides/metabolismo , Catalasa/biosíntesis , ADN Bacteriano/genética , Genoma Bacteriano/genética , Oxidorreductasas/biosíntesis , Paracoccus/genética , Paracoccus/aislamiento & purificación , Peroxidasa/biosíntesis , Pigmentos Biológicos/genética , Pseudoalteromonas/genética , Pseudoalteromonas/aislamiento & purificación , ARN Ribosómico 16S/genética , Análisis de Secuencia de ADN , Simbiosis

RESUMEN

ETHNOPHARMACOLOGICAL RELEVANCE: Si-Wu-Tang (SWT), a prestigious herbal formula from China, has been extensively used for centuries for female-related diseases. It has been documented that SWT has a significant inhibitory effect on non-triple-negative breast cancer (non-TNBC) cells. However, there has been limited comprehensive analysis of the targeted effects of the anticancer components of SWT and its exact biological mechanism. AIM OF THE STUDY: This study aims to uncover the mechanism by which SWT treats non-TNBC by applying a network pharmacological method combined with experimental validation. MATERIALS AND METHODS: First, SWT compounds were collected from the Traditional Chinese Medicines Systems Pharmacology database (TCMSP) and The Encyclopedia of Traditional Chinese Medicine (ETCM), and then the targets related to SWT were obtained from the TCMSP and SwissTarget databases. Second, a target data set of non-TNBC proteins was established by using the Online Mendelian Inheritance in Man (OMIM), GeneCards and Gene Expression Omnibus (GEO) databases. Third, based on the overlap of targets between SWT and non-TNBC, a protein-protein interaction (PPI) network was built to analyse the interactions among these targets, which focused on screening for hub targets by topology. On these hub genes, we conducted a meta-analysis and survival analysis to screen the best match targets, ESR1, PPARG, CAT, and PTGS2, which had a strong correlation with the ingredients of SWT in our verification by molecular docking. In vitro experiments further proved the reliability of the network pharmacology findings. Finally, FunRich software and the ClusterProfiler package were utilized for the enrichment analysis of Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) data. RESULTS: A total of 141 active ingredients and 116 targets of SWT were selected. GO enrichment analysis showed that the biological processes through which SWT acted against non-TNBC (FDR<0.01) mainly involved modulating energy metabolism and apoptosis. According to RT-qPCR and Western blotting, the mRNA and protein expression of ESR1, PPARG and PTGS2 were upregulated (P < 0.01), and the mRNA and protein levels of CAT were downregulated (P < 0.01), suggesting a multi-gene regulatory molecular mechanism of SWT against non-triple-negative breast cancer. CONCLUSIONS: This research explored the multi-gene pharmacological mechanism of action of SWT against non-TNBC through network pharmacology and in vitro experiments. The findings provide new ideas for research on the mechanism of action of Chinese medicine against breast cancer.

Asunto(s)

Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/farmacología , Neoplasias de la Mama/tratamiento farmacológico , Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/farmacología , Apoptosis/efectos de los fármacos , Catalasa/biosíntesis , Catalasa/genética , Ciclooxigenasa 2/genética , Bases de Datos de Compuestos Químicos , Bases de Datos Genéticas , Metabolismo Energético/efectos de los fármacos , Receptor alfa de Estrógeno/biosíntesis , Receptor alfa de Estrógeno/genética , Femenino , Regulación Neoplásica de la Expresión Génica , Redes Reguladoras de Genes , Humanos , Estimación de Kaplan-Meier , Células MCF-7 , Medicina Tradicional China/métodos , Simulación del Acoplamiento Molecular , PPAR gamma/biosíntesis , PPAR gamma/genética , Unión Proteica , Mapas de Interacción de Proteínas

RESUMEN

Accumulation of stress ethylene in plants due to osmotic stress is a major challenge for the achievement of optimum sweet corn crop yield with limited availability of irrigation water. A significant increase in earth's temperature is also making the conditions more crucial regarding the availability of ample quantity of irrigation water for crops production. Plant growth promoting rhizobacteria (PGPR) can play an imperative role in this regard. Inoculation of rhizobacteria can provide resistance and adaptability to crops against osmotic stress. In addition, these rhizobacteria also have potential to solve future food security issues. That's why the current study was planned to examine the efficacious functioning of Pseudomonas fluorescens strains on yields and physiological characteristics of sweet corn (Zea mays L. var saccharata) under different levels of irrigation. Three irrigation levels i.e., 100% (I100 no stress), 80% (I80), and 60% (I60) were used during sweet corn cultivation. However, there were four rhizobacteria strains i.e., P. fluorescens P1, P. fluorescens P3, P. fluorescens P8, P. fluorescens P14 which were used in the experiment. The results showed that severe water stress (60% of plant water requirement) decreased chlorophyll a, chlorophyll b, and total chlorophyll contents, Fv/Fm ratio and nutrients uptake. A significant increase in F0, Fm, proline, total soluble sugars, catalase (CAT) and peroxidase (POX) activity led to less ear yield and canned seed yield. Combination of four strains significantly increased the yield traits of sweet corn i.e., ear and (44%) and canned seed yield (27%) over control. The highest promoting effect was observed in the combination of four strains treatment and followed by P1 strain in reducing the harmful effects of drought stress and improving sweet corn productivity. However, P14 gave minimum improvement in growth and yield indices under limited availability of water. In conclusion, combination of four strains inoculation is an efficacious approach for the achievement of better yield of sweet corn under osmotic stress.

Asunto(s)

Proteínas Bacterianas/biosíntesis , Liasas de Carbono-Carbono/biosíntesis , Etilenos/metabolismo , Reguladores del Crecimiento de las Plantas/metabolismo , Pseudomonas fluorescens/enzimología , Zea mays/microbiología , Riego Agrícola , Proteínas Bacterianas/genética , Biomasa , Liasas de Carbono-Carbono/genética , Catalasa/biosíntesis , Clorofila/biosíntesis , Clorofila A/biosíntesis , Producción de Cultivos/métodos , Productos Agrícolas , Sequías , Peroxidasa/biosíntesis , Prolina/metabolismo , Pseudomonas fluorescens/genética , Rizosfera , Estrés Fisiológico , Simbiosis/fisiología , Zea mays/crecimiento & desarrollo , Zea mays/metabolismo

RESUMEN

Acute ethanol intoxication by excessive drinking is an important cause of alcohol-induced death. Stress exposure has been identified as one risk factor for alcohol abuse. Previous reports indicated that stressors may augment inhibitory effects of alcohol, but the underlying mechanism remains unknown. Here, we reported that chronic unpredictable stress increased the sensitivity to the acute ethanol intoxication in mice via impairing nuclear factor (erythroid-derived 2)-like 2 (Nrf2)-catalase signaling. Nrf2 activity regulates the expression of catalase, a key antioxidant enzyme that mediates ethanol oxidation in the brain. Pharmacological blockade of catalase or Nrf2 activity significantly aggravated acute ethanol intoxication. Sulforaphane, a cruciferous vegetable-derived activator of Nrf2, significantly attenuated acute ethanol intoxication. Furthermore, the stress-induced aggravation of acute alcoholism was rapidly reversed by sulforaphane. Our findings suggest that Nrf2 may function as a novel drug target for the prevention of acute alcoholism, especially in psychiatric patients, by controlling catalase-mediated ethanol oxidation.

Asunto(s)

Alcoholismo/metabolismo , Catalasa/biosíntesis , Etanol/administración & dosificación , Isotiocianatos/uso terapéutico , Factor 2 Relacionado con NF-E2/metabolismo , Estrés Psicológico/metabolismo , Sulfóxidos/uso terapéutico , Alcoholismo/tratamiento farmacológico , Alcoholismo/psicología , Animales , Catalasa/genética , Regulación Enzimológica de la Expresión Génica , Isotiocianatos/farmacología , Masculino , Ratones , Ratones Endogámicos C57BL , Factor 2 Relacionado con NF-E2/antagonistas & inhibidores , Estrés Psicológico/tratamiento farmacológico , Estrés Psicológico/psicología , Sulfóxidos/farmacología

RESUMEN

Context: Satureja khuzistanica Jamzad. (Lamiaceae), is known for its antifungal and antioxidant compounds, especially rosmarinic acid (RA).Objective: The study examines the effect of elicitors on RA production and phytochemical properties of S. khuzistanica.Materials and methods: In vitro plants were treated with methyl jasmonate (MeJA) and multi-walled carbon nanotubes (MWCNTs). In vivo plants were treated with MWCNTs and salicylic acid (SA). RA was measured by HPLC. Catalase (CAT), guaiacol peroxidase (POD) and ascorbate peroxidase (APX) were quantified. DPPH and ß-carotene were assayed in in vivo extracts. The antifungal effects of extracts were evaluated against Fusarium solani K (FsK).Results: The highest RA contents of in vitro plants were 50 mg/L MeJA (140.99 mg/g DW) and 250 mg/L MWCNTs (140.49 mg/g DW). The highest in vivo were 24 h MWCNTs (7.13 mg/g DW) and 72 h SA (9.12 mg/g DW). The maximum POD and APX activities were at 100 mg/L MeJA (5 and 4 mg protein, respectively). CAT had the highest activities at 50 mg/L MeJA (2 mg protein). DPPH and ß-carotene showed 50% and 80% inhibition, respectively. The FsK aggregation was the lowest for in vitro extract in number of conidia [1.82 × 1010], fresh weight (6.51 g) and dry weight (0.21 g) that proved RA inhibitory effects. The callus reduces FsK growth diameter to 2.75 on the 5th day.Discussion and conclusions: Application of MeJA, SA, and MWCNTSs could increase RA in S. khuzistanica and highlighted potential characteristics in pharmaceutical and antifungal effects.

Asunto(s)

Cinamatos/análisis , Cinamatos/farmacología , Depsidos/análisis , Depsidos/farmacología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Reguladores del Crecimiento de las Plantas/farmacología , Satureja/química , Satureja/metabolismo , Acetatos/farmacología , Antifúngicos/análisis , Antifúngicos/farmacología , Antioxidantes/análisis , Antioxidantes/farmacología , Ascorbato Peroxidasas/biosíntesis , Ascorbato Peroxidasas/metabolismo , Catalasa/biosíntesis , Catalasa/metabolismo , Ciclopentanos/farmacología , Fusarium/crecimiento & desarrollo , Nanotubos de Carbono , Oxilipinas/farmacología , Peroxidasa/biosíntesis , Peroxidasa/metabolismo , Fitoquímicos , Ácido Salicílico/farmacología , Ácido Rosmarínico

RESUMEN

To remedy carotid artery stenosis and prevent stroke surgical intervention is commonly used, and the gold standard being carotid endarterectomy (CEA). During CEA cerebrovascular hemoglobin oxygen saturation decreases and when this decrease reaches critical levels it leads to cerebral hypoxia that causes neuronal damage. One of the proposed mechanism that affects changes during CEA and contribute to acute brain ischemia (ABI) is oxidative stress. The increased production of reactive oxygen species and reactive nitrogen species during ABI may cause an unregulated inflammatory response and further lead to structural and functional injury of neurons. Antioxidant activity are involved in the protection against neuronal damage after cerebral ischemia. We hypothesized that neuronal injury and poor outcomes in patients undergoing CEA may be results of oxidative stress that disturbed function of antioxidant enzymes and contributed to the DNA damage in lymphocytes.

Asunto(s)

Isquemia Encefálica/enzimología , Catalasa/biosíntesis , Endarterectomía Carotidea/efectos adversos , Hipoxia Encefálica/enzimología , Complicaciones Intraoperatorias/enzimología , Linfocitos/enzimología , Superóxido Dismutasa-1/biosíntesis , Superóxido Dismutasa/biosíntesis , Isquemia Encefálica/etiología , Estenosis Carotídea/enzimología , Estenosis Carotídea/cirugía , Catalasa/sangre , Catalasa/genética , Daño del ADN , Radicales Libres , Regulación Enzimológica de la Expresión Génica , Humanos , Hipoxia Encefálica/etiología , Complicaciones Intraoperatorias/etiología , Mitocondrias/metabolismo , Modelos Biológicos , Estrés Oxidativo , Daño por Reperfusión/enzimología , Daño por Reperfusión/etiología , Superóxido Dismutasa/sangre , Superóxido Dismutasa/genética , Superóxido Dismutasa-1/sangre , Superóxido Dismutasa-1/genética

RESUMEN

The effects of glucose and sucrose on the gene expression of nitric oxide synthase (NOS) in Staphylococcus vitulinus and colour formation in dry sausages were investigated. The results showed that sucrose addition promoted nitric oxide (NO) production in media when compared with glucose. In addition, sucrose could up-regulate nos (encoding NOS) and katA (encoding catalase KatA) gene expression by enhancing oxidative stress levels. In the sausages inoculated with S. vitulinus, a*-values (indicating redness) of the sausages with added sucrose were higher than those of samples with added glucose (P < 0.05) but did not differ from those in the nitrite treatment group (P > 0.05). The UV-vis spectra results showed that nitrosylmyoglobin (NO-Mb) was formed in the sausages with either S. vitulinus or nitrite added. In the S. vitulinus-inoculated sausages, sucrose addition led to a higher NO-Mb content than that after glucose addition, which was attributed to up-regulation of the nos gene. This study provides a potential method to enhance NO yield in S. vitulinus and colour formation in dry sausages without nitrite addition.

Asunto(s)

Catalasa/biosíntesis , Glucosa/metabolismo , Óxido Nítrico Sintasa/biosíntesis , Staphylococcus/metabolismo , Sacarosa/metabolismo , Animales , Catalasa/genética , Color , Productos de la Carne/análisis , Mioglobina/biosíntesis , Óxido Nítrico/biosíntesis , Óxido Nítrico Sintasa/genética , Nitritos/metabolismo , Oxidación-Reducción , Estrés Oxidativo/efectos de los fármacos , Staphylococcus/enzimología , Staphylococcus/genética , Activación Transcripcional , Regulación hacia Arriba

RESUMEN

Oxidative stress is an unavoidable consequence of interactions with various reactive oxygen species (ROS)-inducing agents that would damage cells or even cause cell death. Bacteria have developed defensive systems, including induction of stress-sensing proteins and detoxification enzymes, to handle oxidative stress. Cyclic diguanylate (c-di-GMP) is a ubiquitous intracellular bacterial second messenger that coordinates diverse aspects of bacterial growth and behavior. In this study, we revealed a mechanism by which c-di-GMP regulated bacterial oxidative stress resistance in Pseudomonas putida KT2440. High c-di-GMP level was found to enhance bacterial resistance towards hydrogen peroxide. Transcription assay showed that expression of two oxidative stress resistance genes, fpr-1 and katE, was promoted under high c-di-GMP level. Deletion of fpr-1 and katE both decreased bacterial tolerance to hydrogen peroxide and weakened the effect of c-di-GMP on oxidative stress resistance. The promoted expression of fpr-1 under high c-di-GMP level was caused by increased cellular ROS via a transcriptional regulator FinR. We further demonstrated that the influence of high c-di-GMP on cellular ROS depend on the existence of FleQ, a transcriptional regulatory c-di-GMP effector. Besides, the regulation of katE by c-di-GMP was also FleQ dependent in an indirect way. Our results proved a connection between c-di-GMP and oxidative stress resistance and revealed a mechanism by which c-di-GMP regulated expression of fpr-1 and katE in P. putida KT2440.

Asunto(s)

Proteínas Bacterianas/biosíntesis , Catalasa/biosíntesis , GMP Cíclico/análogos & derivados , Peróxido de Hidrógeno/toxicidad , Péptidos y Proteínas de Señalización Intracelular/biosíntesis , Pseudomonas putida/metabolismo , GMP Cíclico/metabolismo , Regulación Bacteriana de la Expresión Génica/genética , Peróxido de Hidrógeno/metabolismo , Estrés Oxidativo/fisiología , Pseudomonas putida/genética

RESUMEN

Hyperthyroidism is an endocrine disorder characterized by excessive secretion of thyroid hormones T3 and T4. Thyroid hormones exert pleiotropic actions on numerous tissues and induce an overall increase in metabolism, with an increase in energy demand and oxygen consumption. Therefore, the purpose of this study was to investigate the effects of hyperthyroidism on the production of reactive oxygen species (ROS) in lymph node and spleen cells of euthyroid and hyperthyroid mice, analyzing antioxidant mechanisms involved in the restitution of the cellular redox state. For this, thirty female Balb/c (H-2d) mice were randomly divided into two groups: euthyroid (by treatment with placebo) and hyperthyroid (by treatment with 12 mg/l of T4 in drinking water for 30 days). We found a significant increase in ROS and an increase in the genomic and protein expression of the antioxidant enzymes catalase (CAT) and glutathione peroxidase-1 (GPx-1) in lymph node and spleen cells of hyperthyroid mice. In vitro treatment with H2O2 (250 µM) of the lymphoid cells of euthyroid mice increased the expression levels of CAT and GPx-1. The hyperthyroidism increased the phosphorylation levels of Nrf2 (nuclear factor erythroid 2-related factor) and the kinase activity of protein kinase C (PKC) and extracellular signal-regulated kinase (ERK). Additionally, we found an increase in the expression of the classic isoenzymes of PKCα, ß and γ. In conclusion, these results indicated that the increase in ROS found in the hyperthyroid state induces the antioxidant enzyme transcription through the activation of the Nrf-2 factor in lymphoid tissues. This shows the influence of hyperthyroidism on the regulation of the cellular antioxidant system.

Asunto(s)

Catalasa/genética , Glutatión Peroxidasa/genética , Hipertiroidismo/metabolismo , Factor 2 Relacionado con NF-E2/metabolismo , Estrés Oxidativo/fisiología , Superóxido Dismutasa-1/genética , Animales , Catalasa/biosíntesis , Quinasas MAP Reguladas por Señal Extracelular/metabolismo , Femenino , Glutatión Peroxidasa/biosíntesis , Hipertiroidismo/sangre , Hipertiroidismo/enzimología , Hipertiroidismo/genética , Tejido Linfoide/metabolismo , Ratones , Ratones Endogámicos BALB C , Factor 2 Relacionado con NF-E2/genética , Proteína Quinasa C/metabolismo , Especies Reactivas de Oxígeno/metabolismo , Superóxido Dismutasa-1/biosíntesis , Tirotropina/sangre , Tiroxina/administración & dosificación , Tiroxina/sangre , Activación Transcripcional , Triyodotironina/sangre , Glutatión Peroxidasa GPX1

RESUMEN

Epigenetic agents, such as neonatal isolation during neurodevelopmental period of life, can change various regions of the brain. It may further induce psychological disorders such as autistic-like phenomena. This study indicated the role of chronic increased anterior cingulate cortex (ACC) output on alteration of caudate putamen (CPu) as a main behavior regulator region of the brain in adult maternal deprived (MD) rats. For making an animal model, neonates were isolated from their mothers in postnatal days (PND 1-10, 3 h/day). Subsequently, they bilaterally received pLenti-CaMKIIa-hChR2 (H134R)-mCherry-WPRE virus in ACC area via stereotaxic surgery in PND50. After 22 days, these regions were exposed to blue laser (473 nm) for six consecutive days (15 min/day). Then, behavioral deficits were tested and were compared with control group in the following day. Animals were immediately killed and their brains were prepared for tissue processing. Results showed that neonatal isolation induces autistic-like behaviors and leads to overexpression of NMDAR1 and Nox2-gp91phox proteins and elevation of catalase activity in the CPu regions of the adult offspring compared with control group. Chronic optogenetic stimulation of ACC neurons containing (ChR2+) led to significant reduction in the appearance of stereotypical behavior and alien-phobia in MD rats. The amount of NMDAR1 and Nox2-gp91phox expression and the catalase activity in CPu were reduced after this treatment. Therefore, autistic-like behavior seems to be related with elevation of NMDAR1 and Nox2-gp91phox protein levels that enhance the effect of glutamatergic projection on CPu regions. Optogenetic treatment also could ameliorate behavioral deficits by modulating these protein densities.

Asunto(s)

Trastorno Autístico , Núcleo Caudado , Giro del Cíngulo , Privación Materna , Optogenética , Putamen , Animales , Femenino , Masculino , Ratas , Animales Recién Nacidos , Trastorno Autístico/fisiopatología , Trastorno Autístico/terapia , Catalasa/biosíntesis , Catalasa/genética , Núcleo Caudado/fisiopatología , Modelos Animales de Enfermedad , Genes Reporteros , Vectores Genéticos/administración & dosificación , Giro del Cíngulo/fisiopatología , Proteínas Luminiscentes/análisis , Proteínas Luminiscentes/genética , Microinyecciones , NADPH Oxidasa 2/biosíntesis , NADPH Oxidasa 2/genética , Proteínas del Tejido Nervioso/biosíntesis , Proteínas del Tejido Nervioso/genética , Fobia Social , Putamen/fisiopatología , Distribución Aleatoria , Receptores de N-Metil-D-Aspartato/biosíntesis , Receptores de N-Metil-D-Aspartato/genética , Conducta Social , Estrés Psicológico , Proteína Fluorescente Roja

RESUMEN

BACKGROUND: Parkinson's disease is the most common neurodegenerative disorder, characterized by loss of dopaminergic neurons in substantia nigra and depletion of dopamine in striatum due to excitotoxicity, oxidative stress and many other factors may contribute to MPTP- and PD-related neurodegeneration. The present study deals with the neuroprotective effect of Naringenin (NGN), a bioflavonoid against MPTP-induced Parkinson's disease in the mouse model. METHODS: Healthy male C57BL/6J mice (18-22 g b wt) were pretreated with NGN [25, 50, 100 mg/kg/b.wt, p.o] once daily for 5 days. Thereafter, 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP) (80 mg/kg b.wt, i.p) was given in two divided doses (2 × 40 mg/kg at 16 h interval). The animals were observed for motor functions 48 h after the first MPTP injection. After completion of behaviour tasks, all animals were euthanized to dissect out the brain and used for biochemical, molecular and histopathological investigations. RESULTS: Pretreatment of NGN significantly reversed the toxic effects of MPTP by reducing LPO levels and increasing the activities of glutathione reductase and catalase along with improved behavioural performance. Interestingly, pre-treatment with NGN down-regulated iNOS expression level in MPTP intoxicated mice brain. In addition, the histopathological evaluation revealed that NGN decreased the nuclear pigmentation and cytoplasmic vacuolation in the substantia nigra and striatal regions when compared to MPTP-intoxicated mice brain. DISCUSSION: The present study showed that NGN exerts neuroprotection by suppressing oxidative stress via antioxidant mechanisms. The above finding suggests that NGN may act as a potential target in the management of PD.

Asunto(s)

1-Metil-4-fenil-1,2,3,6-Tetrahidropiridina , Flavanonas/farmacología , Peroxidación de Lípido/efectos de los fármacos , Fármacos Neuroprotectores/farmacología , Estrés Oxidativo/efectos de los fármacos , Enfermedad de Parkinson Secundaria/prevención & control , Animales , Catalasa/biosíntesis , Cuerpo Estriado/patología , Relación Dosis-Respuesta a Droga , Glutatión Reductasa/biosíntesis , Masculino , Ratones , Óxido Nítrico Sintasa de Tipo II/biosíntesis , Enfermedad de Parkinson Secundaria/inducido químicamente , Enfermedad de Parkinson Secundaria/metabolismo , Enfermedad de Parkinson Secundaria/patología , Sustancia Negra/patología

RESUMEN

A novel method involving ethanol-induced increase in the heterologous recombinant protein expression in E. coli cells was commonly used in recent studies. However, the detailed mechanism of this method is still to be revealed. This work used comparative transcriptomic analysis and numerous experiments to uncover the mechanism of ethanol effects on the expression of heterologous catalase in the recombinant strain E. coli BL21 (pET26b-katA). The key regulatory genes malK and prpD were found to have the most significant effects on the expression of heterologous catalase. Thus, the maltose ABC transporter and carbon metabolism from propanoate metabolism to citrate cycle were found to be the main regulatory pathways activated by ethanol to enhance the synthesis of heterologous proteins. Based on these mechanisms, a universally applicable E. coli expression host strain for improving the expression of heterologous proteins might be constructed.

Asunto(s)

Transportadoras de Casetes de Unión a ATP/metabolismo , Catalasa/biosíntesis , Proteínas de Escherichia coli/metabolismo , Escherichia coli/efectos de los fármacos , Hidroliasas/metabolismo , Transportadoras de Casetes de Unión a ATP/genética , Reactores Biológicos/microbiología , Catalasa/genética , Escherichia coli/genética , Escherichia coli/metabolismo , Proteínas de Escherichia coli/genética , Perfilación de la Expresión Génica , Hidroliasas/genética , Estrés Oxidativo/fisiología , Proteínas Recombinantes/biosíntesis

RESUMEN

Lead (Pb) is a developmental neurotoxicant. We have demonstrated that perinatally Pb-exposed rats consume more ethanol than their control counterparts, a response that seems to be mediated by catalase (CAT) and centrally-formed acetaldehyde, ethanol's first metabolite with attributed reinforcing effects in the brain. The present study sought to disrupt ethanol intake (2-10% ethanol v/v) in rats exposed to 220 ppm Pb or filtered water during gestation and lactation. Thus, to block brain CAT expression, a lentiviral vector coding for a shRNA against CAT (LV-antiCAT vector) was microinfused in the posterior ventral tegmental area (pVTA) either at the onset or towards the end of a chronic voluntary ethanol consumption test. At the end of the study, rats were euthanized and pVTA dissected to measure CAT expression by Western blot. The LV-antiCAT vector administration not only reversed, but also prevented the emergence of the elevated ethanol intake reported in the perinatally Pb-exposed animals, changes that were supported by a significant reduction in CAT expression in the pVTA. These results provide further evidence of the crucial role of this enzyme in the reinforcing properties of ethanol and in the impact of the perinatal Pb programming to challenging events later in life.

Asunto(s)

Consumo de Bebidas Alcohólicas/prevención & control , Encéfalo/enzimología , Catalasa/biosíntesis , Etanol/toxicidad , Plomo/toxicidad , Efectos Tardíos de la Exposición Prenatal/enzimología , Consumo de Bebidas Alcohólicas/efectos adversos , Animales , Encéfalo/efectos de los fármacos , Catalasa/antagonistas & inhibidores , Catalasa/genética , Etanol/administración & dosificación , Femenino , Regulación Enzimológica de la Expresión Génica , Plomo/administración & dosificación , Masculino , Embarazo , Efectos Tardíos de la Exposición Prenatal/inducido químicamente , Efectos Tardíos de la Exposición Prenatal/prevención & control , Ratas , Ratas Wistar

RESUMEN

The relapsing fever spirochete Borrelia turicatae possesses a complex life cycle in its soft-bodied tick vector, Ornithodoros turicata. Spirochetes enter the tick midgut during a blood meal, and, during the following weeks, spirochetes disseminate throughout O. turicata. A population persists in the salivary glands allowing for rapid transmission to the mammalian hosts during tick feeding. Little is known about the physiological environment within the salivary glands acini in which B. turicatae persists. In this study, we examined the salivary gland transcriptome of O. turicata ticks and detected the expression of 57 genes involved in oxidant metabolism or antioxidant defences. We confirmed the expression of five of the most highly expressed genes, including glutathione peroxidase (gpx), thioredoxin peroxidase (tpx), manganese superoxide dismutase (sod-1), copper-zinc superoxide dismutase (sod-2), and catalase (cat) by reverse-transcriptase droplet digital polymerase chain reaction (RT-ddPCR). We also found distinct differences in the expression of these genes when comparing the salivary glands and midguts of unfed O. turicata ticks. Our results indicate that the salivary glands of unfed O. turicata nymphs are highly oxidative environments where reactive oxygen species (ROS) predominate, whereas midgut tissues comprise a primarily nitrosative environment where nitric oxide synthase is highly expressed. Additionally, B. turicatae was found to be hyperresistant to ROS compared with the Lyme disease spirochete Borrelia burgdorferi, suggesting it is uniquely adapted to the highly oxidative environment of O. turicata salivary gland acini.

Asunto(s)

Borrelia/crecimiento & desarrollo , Borrelia/fisiología , Ornithodoros/microbiología , Fiebre Recurrente/transmisión , Glándulas Salivales/metabolismo , Animales , Catalasa/biosíntesis , Catalasa/genética , Regulación de la Expresión Génica/genética , Glutatión Peroxidasa/biosíntesis , Glutatión Peroxidasa/genética , Estrés Oxidativo/fisiología , Peroxirredoxinas/biosíntesis , Peroxirredoxinas/genética , Especies Reactivas de Oxígeno/metabolismo , Fiebre Recurrente/microbiología , Glándulas Salivales/microbiología , Superóxido Dismutasa-1/biosíntesis , Superóxido Dismutasa-1/genética

RESUMEN

Visfatin is an adipokine which has an endocrine effect on reproductive functions and regulates ovarian steroidogenesis. There is scant information about the expression, regulation, and functions of visfatin in the mammalian uterus. The present study examined expression and localization of visfatin in the mouse uterus at various stages of the natural estrous cycle, effects of estrogen and progesterone on localization and expression of visfatin in the ovariectomised mouse uterus and effect of visfatin inhibition by a specific inhibitor, FK866 on proliferation and apoptosis in the uterus. Western blot analysis of visfatin showed high expression in proestrus and metestrus while it declined in estrus and diestrus. Immulocalization study also showed strong immunostaining in the cells of endometrium, myometrium, luminal and glandular epithelium during proestrus and metestrus that estrus and diestrus. The uterine visfatin expression closely related to the increased estrogen levels in proestrus and suppressed when progesterone rose to a high level in diestrus. The treatment with estrogen to ovariectomised mice up-regulates visfatin, PCNA, and active caspase3 whereas progesterone up-regulates PCNA and down-regulates visfatin and active caspase3 expression in mouse uterus. The co-treatment with estrogen and progesterone up-regulates visfatin and down-regulates PCNA and active caspase3. In vitro study showed endogenous visfatin inhibition by FK866 increased expression of PCNA and BCL2 increased catalase activity while FK866 treatment decreased expression of active caspase3 and BAX with decreased SOD and GPx activity. BrdU labeling showed that inhibition of visfatin modulates the uterine proliferation. This study showed that expression of visfatin protein is steroid dependent in mouse uterus which is involved in the regulation of proliferation and apoptosis via modulating antioxidant system in the uterus of mice during the reproductive cycle.

Asunto(s)

Apoptosis/fisiología , Proliferación Celular/fisiología , Endometrio/metabolismo , Estrógenos/metabolismo , Ciclo Estral/metabolismo , Miometrio/metabolismo , Nicotinamida Fosforribosiltransferasa/biosíntesis , Progesterona/metabolismo , Acrilamidas/farmacología , Animales , Caspasa 3/biosíntesis , Catalasa/biosíntesis , Diestro/metabolismo , Estro/metabolismo , Femenino , Glutatión Peroxidasa/biosíntesis , Ratones , Nicotinamida Fosforribosiltransferasa/antagonistas & inhibidores , Piperidinas/farmacología , Proestro/metabolismo , Antígeno Nuclear de Célula en Proliferación/biosíntesis , Superóxido Dismutasa/biosíntesis , Proteína X Asociada a bcl-2/biosíntesis