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1.
Journal of Southern Medical University ; (12): 552-559, 2023.
Article in Chinese | WPRIM | ID: wpr-986961

ABSTRACT

OBJECTIVE@#To evaluate the regulatory effect of berberine on autophagy and apoptosis balance of fibroblast-like synoviocytes (FLSs) from patients with in rheumatoid arthritis (RA) and explore the mechanism.@*METHODS@#The inhibitory effect of 10, 20, 30, 40, 50, 60, 70, and 80 μmol/L berberine on RA-FLS proliferation was assessed using CCK-8 method. Annexin V/PI and JC-1 immunofluorescence staining was used to analyze the effect of berberine (30 μmol/L) on apoptosis of 25 ng/mL TNF-α- induced RA-FLSs, and Western blotting was performed to detect the changes in the expression levels of autophagy- and apoptosis-related proteins. The cells were further treated with the autophagy inducer RAPA and the autophagy inhibitor chloroquine to observe the changes in autophagic flow by laser confocal detection of mCherry-EGFP-LC3B. RA-FLSs were treated with the reactive oxygen species (ROS) mimic H2O2 or the ROS inhibitor NAC, and the effects of berberine on ROS, mTOR and p-mTOR levels were observed.@*RESULTS@#The results of CCK-8 assay showed that berberine significantly inhibited the proliferation of RA-FLSs in a time- and concentration-dependent manner. Flow cytometry and JC-1 staining showed that berberine (30 μmol/L) significantly increased apoptosis rate (P < 0.01) and reduced the mitochondrial membrane potential of RA-FLSs (P < 0.05). Berberine treatment obviously decreased the ratios of Bcl-2/Bax (P < 0.05) and LC3B-II/I (P < 0.01) and increased the expression of p62 protein in the cells (P < 0.05). Detection of mCherry-EGFP-LC3B autophagy flow revealed obvious autophagy flow block in berberine-treated RA-FLSs. Berberine significantly reduced the level of ROS in TNF-α-induced RA-FLSs and upregulated the expression level of autophagy-related protein p-mTOR (P < 0.01); this effect was regulated by ROS level, and the combined use of RAPA significantly reduced the pro-apoptotic effect of berberine in RA-FLSs (P < 0.01).@*CONCLUSION@#Berberine can inhibit autophagy and promote apoptosis of RA-FLSs by regulating the ROS-mTOR pathway.


Subject(s)
Humans , Synoviocytes , Berberine/metabolism , Reactive Oxygen Species/metabolism , Tumor Necrosis Factor-alpha/metabolism , Hydrogen Peroxide/metabolism , Sincalide/metabolism , Cell Proliferation , Arthritis, Rheumatoid/metabolism , Signal Transduction , TOR Serine-Threonine Kinases/metabolism , Apoptosis , Fibroblasts , Autophagy , Cells, Cultured
2.
Chinese Journal of Biotechnology ; (12): 2070-2080, 2023.
Article in Chinese | WPRIM | ID: wpr-981190

ABSTRACT

5-aminovalanoic acid (5AVA) can be used as the precursor of new plastics nylon 5 and nylon 56, and is a promising platform compound for the synthesis of polyimides. At present, the biosynthesis of 5-aminovalanoic acid generally is of low yield, complex synthesis process and high cost, which hampers large-scale industrial production. In order to achieve efficient biosynthesis of 5AVA, we developed a new pathway mediated by 2-keto-6-aminohexanoate. By combinatory expression of L-lysine α-oxidase from Scomber japonicus, α-ketoacid decarcarboxylase from Lactococcus lactis and aldehyde dehydrogenase from Escherichia coli, the synthesis of 5AVA from L-lysine in Escherichia coli was achieved. Under the initial conditions of glucose concentration of 55 g/L and lysine hydrochloride of 40 g/L, the final consumption of 158 g/L glucose and 144 g/L lysine hydrochloride, feeding batch fermentation to produce 57.52 g/L of 5AVA, and the molar yield is 0.62 mol/mol. The new 5AVA biosynthetic pathway does not require ethanol and H2O2, and achieved a higher production efficiency as compared to the previously reported Bio-Chem hybrid pathway mediated by 2-keto-6-aminohexanoate.


Subject(s)
Nylons , Lysine/metabolism , Hydrogen Peroxide/metabolism , Metabolic Engineering , Plastics/metabolism , Fermentation , Escherichia coli/metabolism , Aminocaproates/metabolism
3.
Chinese Journal of Biotechnology ; (12): 4705-4718, 2022.
Article in Chinese | WPRIM | ID: wpr-970342

ABSTRACT

Catalase is widely used in the food, medical, and textile industries. It possesses exceptional properties including high catalytic efficiency, high specificity, and environmental friendliness. Free catalase cannot be recycled and reused in industry, resulting in a costly industrial biotransformation process if catalase is used as a core ingredient. Developing a simple, mild, cost-effective, and environmentally friendly approach to immobilize catalase is anticipated to improve its utilization efficiency and enzymatic performance. In this study, the catalase KatA derived from Bacillus subtilis 168 was expressed in Escherichia coli. Following separation and purification, the purified enzyme was prepared as an immobilized enzyme in the form of enzyme-inorganic hybrid nanoflowers, and the enzymatic properties were investigated. The results indicated that the purified KatA was obtained through a three-step procedure that included ethanol precipitation, DEAE anion exchange chromatography, and hydrophobic chromatography. Then, by optimizing the process parameters, a novel KatA/Ca3(PO4)2 hybrid nanoflower was developed. The optimum reaction temperature of the free KatA was determined to be 35 ℃, the optimum reaction temperature of KatA/Ca3(PO4)2 hybrid nanoflowers was 30-35 ℃, and the optimum reaction pH of both was 11.0. The free KatA and KatA/Ca3(PO4)2 hybrid nanoflowers exhibited excellent stability at pH 4.0-11.0 and 25-50 ℃. The KatA/Ca3(PO4)2 hybrid nanoflowers demonstrated increased storage stability than that of the free KatA, maintaining 82% of the original enzymatic activity after 14 d of storage at 4 ℃, whereas the free KatA has only 50% of the original enzymatic activity. In addition, after 5 catalytic reactions, the nanoflower still maintained 55% of its initial enzymatic activity, indicating that it has good operational stability. The Km of the free KatA to the substrate hydrogen peroxide was (8.80±0.42) mmol/L, and the kcat/Km was (13 151.53± 299.19) L/(mmol·s). The Km of the KatA/Ca3(PO4)2 hybrid nanoflowers was (32.75±2.96) mmol/L, and the kcat/Km was (4 550.67±107.51) L/(mmol·s). Compared to the free KatA, the affinity of KatA/Ca3(PO4)2 hybrid nanoflowers to the substrate hydrogen peroxide was decreased, and the catalytic efficiency was also decreased. In summary, this study developed KatA/Ca3(PO4)2 hybrid nanoflowers using Ca2+ as a self-assembly inducer, which enhanced the enzymatic properties and will facilitate the environmentally friendly preparation and widespread application of immobilized catalase.


Subject(s)
Catalase , Nanostructures/chemistry , Hydrogen Peroxide/metabolism , Enzymes, Immobilized/chemistry , Catalysis
4.
Biol. Res ; 55: 27-27, 2022. ilus, tab, graf
Article in English | LILACS | ID: biblio-1447503

ABSTRACT

BACKGROUND: Cytokinin signal transduction is mediated by a two-component system (TCS). Two-component systems are utilized in plant responses to hormones as well as to biotic and abiotic environmental stimuli. In plants, response regulatory genes (RRs) are one of the main members of the two-component system (TCS). METHOD: From the aspects of gene structure, evolution mode, expression type, regulatory network and gene function, the evolution process and role of RR genes in the evolution of the cotton genome were analyzed. RESULT: A total of 284 RR genes in four cotton species were identified. Including 1049 orthologous/paralogous gene pairs were identified, most of which were whole genome duplication (WGD). The RR genes promoter elements contain phytohormone responses and abiotic or biotic stress-related cis-elements. Expression analysis showed that RR genes family may be negatively regulate and involved in salt stress and drought stress in plants. Protein regulatory network analysis showed that RR family proteins are involved in regulating the DNA-binding transcription factor activity (COG5641) pathway and HP kinase pathways. VIGS analysis showed that the GhRR7 gene may be in the same regulatory pathway as GhAHP5 and GhPHYB, ultimately negatively regulating cotton drought stress by regulating POD, SOD, CAT, H2O2 and other reactive oxygen removal systems. CONCLUSION: This study is the first to gain insight into RR gene members in cotton. Our research lays the foundation for discovering the genes related to drought and salt tolerance and creating new cotton germplasm materials for drought and salt tolerance.


Subject(s)
Plant Proteins/genetics , Plant Proteins/metabolism , Gene Expression Regulation, Plant/genetics , Phylogeny , Stress, Physiological/genetics , Genes, Regulator , Gossypium/genetics , Droughts , Hydrogen Peroxide/metabolism
5.
Biol. Res ; 55: 19-19, 2022. ilus, tab, graf
Article in English | LILACS | ID: biblio-1383921

ABSTRACT

BACKGROUND: Acidophilic microorganisms like Leptospirillum sp. CF 1 thrive in environments with extremely low pH and high concentrations of dissolved heavy metals that can induce the generation of reactive oxygen species (ROS). Several hypothetical genes and proteins from Leptospirillum sp. CF 1 are known to be up regulated under oxidative stress conditions. RESULTS: In the present work, the function of hypothetical gene ABH19_09590 from Leptospirillum sp. CF 1 was studied. Heterologous expression of this gene in Escherichia coli led to an increase in the ability to grow under oxidant conditions with 5 mM K2CrO4 or 5 mM H2O2. Similarly, a significant reduction in ROS production in E. coli transformed with a plasmid carrying ABH19_09590 was observed after exposure to these oxidative stress elicitors for 30 min, compared to a strain complemented with the empty vector. A co transcriptional study using RT PCR showed that ABH19_09590 is contained in an operon, here named the "och" operon, that also contains ABH19_09585, ABH19_09595 and ABH19_09600 genes. The expression of the och operon was significantly up regulated in Leptospirillum sp. CF 1 exposed to 5 mM K2CrO4 for 15 and 30 min. Genes of this operon potentially encode a NADH:ubiquinone oxidoreductase, a CXXC motif containing protein likely involved in thiol/disulfide exchange, a hypothetical protein, and a di hydroxy acid dehydratase. A comparative genomic analysis revealed that the och operon is a characteristic genetic determinant of the Leptospirillum genus that is not present in other acidophiles. CONCLUSIONS: Altogether, these results suggest that the och operon plays a protective role against chromate and hydrogen peroxide and is an important mechanism required to face polyextremophilic conditions in acid environments.


Subject(s)
Chromates/metabolism , Hydrogen Peroxide/metabolism , Hydrogen Peroxide/pharmacology , Operon , Bacteria/genetics , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Reactive Oxygen Species/metabolism , Oxidative Stress/genetics , Escherichia coli
6.
Biol. Res ; 55: 8-8, 2022. ilus
Article in English | LILACS | ID: biblio-1383912

ABSTRACT

BACKGROUND: Salmonella Typhimurium is a Gram negative pathogen that causes a systemic disease in mice resembling typhoid fever. During its infective cycle, S. Typhimurium is phagocytized by macrophages and proliferates inside a Salmonella containing vacuole where Salmonella is exposed and survives oxidative stress induced by H2O2 through modulation of gene expression. After exposure of Salmonella to H2O2, the expression of the porin encoding gene ompX increases, as previously shown by microarray analysis. Expression of ompX mRNA is regulated at a post transcriptional level by MicA and CyaR sRNAs in aerobiosis. In addition, sequence analysis predicts a site for OxyS sRNA in ompX mRNA. RESULTS: In this work we sought to evaluate the transcriptional and post transcriptional regulation of ompX under H2O2 stress. We demonstrate that ompX expression is induced at the transcriptional level in S . Typhimurium under such conditions. Unexpectedly, an increase in ompX gene transcript and promoter activity after challenges with H2O2 does not translate into increased protein levels in the wild type strain, suggesting that ompX mRNA is also regulated at a post transcriptional level, at least under oxidative stress. In silico gene sequence analysis predicted that sRNAs CyaR, MicA, and OxyS could regulate ompX mRNA levels. Using rifampicin to inhibit mRNA expression, we show that the sRNAs (MicA, CyaR and OxyS) and the sRNA:mRNA chaperone Hfq positively modulate ompX mRNA levels under H2O2 induced stress in Salmonella during the exponential growth phase in Lennox broth. CONCLUSIONS: Our results demonstrate that ompX mRNA is regulated in response to H2O2 by the sRNAs CyaR, MicA and OxyS is Salmonella Typhimurium.


Subject(s)
Animals , Mice , Salmonella typhimurium/genetics , Salmonella typhimurium/metabolism , Bacterial Outer Membrane Proteins/genetics , Porins/genetics , Porins/metabolism , RNA, Bacterial/genetics , RNA, Bacterial/metabolism , Gene Expression Regulation, Bacterial , Hydrogen Peroxide/metabolism , Hydrogen Peroxide/pharmacology
7.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 494-505, 2022.
Article in English | WPRIM | ID: wpr-939914

ABSTRACT

Impaired immunomodulatory capacity and oxidative stress are the key factors limiting the effectiveness of mesenchymal stem cell transplantation therapy. The present study was aimed to investigate the effects of jujuboside A (JuA) on the protective effect and immunomodulatory capacity of human umbilical cord mesenchymal stem cells (hUC-MSCs). Hydrogen peroxide was used to establish an oxidative damage model of hUC-MSCs, while PBMCs isolated from rats were used to evaluate the effect of JuA pre-treatment on the immunomodulatory capacity of hUC-MSCs. Furthermore, Hoechst 33258 staining, lactate dehydrogenase test, measurement of malondialdehyde, Western blot, high-performance liquid chromatography; and flow cytometry were performed. Our results indicated that JuA (25 μmol·L-1) promoted the proliferation of hUC-MSCs, but did not affect the differentiating capability of these cells. JuA pre-treatment inhibited apoptosis, prevented oxidative damage, and up-regulated the protein expression of nuclear factor-erythroid factor 2-related factor 2 and heme oxygenase 1 in hUC-MSCs in which oxidative stress was induced with H2O2. In addition, JuA pre-treatment enhanced the inhibitory effect of hUC-MSCs against abnormally activated PBMCs, which was related to stimulation of the expression and activity of indoleamine 2,3-dioxygenase. In conclusion, our results demonstrate that JuA pre-treatment can enhance the survival and immunomodulatory ability through pathways related to oxidative stress, providing a new option for the improvement of hUC-MSCs in the clinical setting.


Subject(s)
Animals , Humans , Rats , Cell Differentiation , Hydrogen Peroxide/metabolism , Mesenchymal Stem Cells , Oxidative Stress , Saponins , Umbilical Cord/metabolism
8.
Electron. j. biotechnol ; 30: 110-117, nov. 2017. graf, tab, ilus
Article in English | LILACS | ID: biblio-1021571

ABSTRACT

Background: Catalase (CAT) is an important enzyme that degrades H2O2 into H2O and O2. To obtain an efficient catalase, in this study, a new strain of high catalase-producing Serratia marcescens, named FZSF01, was screened and its catalase was purified and characterized. Results: After optimization of fermentation conditions, the yield of catalase produced by this strain was as high as 51,468 U/ml. This catalase was further purified using two steps: DEAE-fast flow and Sephedex-G150. The purified catalase showed a specific activity of 197,575 U/mg with a molecular mass of 58 kDa. This catalase exhibited high activity at 20­70°C and pH 5.0­11.0. Km of the catalase was approximately 68 mM, and Vmax was 1886.8 mol/min mg. This catalase was further identified by LC­MS/MS, and the encoding gene was cloned and expressed in Escherichia coli BL21 (DE3) with a production of 17,267 ± 2037 U/ml. Conclusions: To our knowledge, these results represent one of the highest fermentation levels reported among current catalase-producing strains. This FZSF01 catalase may be suitable for several industrial applications that comprise exposure to alkaline conditions and under a wide range of temperatures.


Subject(s)
Serratia marcescens/enzymology , Catalase/metabolism , Recombination, Genetic , Serratia marcescens/genetics , RNA, Ribosomal, 16S , Kinetics , Catalase/isolation & purification , Catalase/genetics , Chromatography, Liquid , Sequence Analysis, DNA , Electrophoresis , Escherichia coli/genetics , Escherichia coli/metabolism , Fermentation , Hydrogen Peroxide/metabolism
9.
Braz. j. microbiol ; 48(3): 537-543, July-Sept. 2017. graf
Article in English | LILACS | ID: biblio-889126

ABSTRACT

Abstract Metallothioneins are a superfamily of low-molecular-weight, cysteine (Cys)-rich proteins that are believed to play important roles in protection against metal toxicity and oxidative stress. The main purpose of this study was to investigate the effect of heterologous expression of a rice metallothionein isoform (OsMTI-1b) on the tolerance of Saccharomyces cerevisiae to Cd2+, H2O2 and ethanol stress. The gene encoding OsMTI-1b was cloned into p426GPD as a yeast expression vector. The new construct was transformed to competent cells of S. cerevisiae. After verification of heterologous expression of OsMTI-1b, the new strain and control were grown under stress conditions. In comparison to control strain, the transformed S. cerevisiae cells expressing OsMTI-1b showed more tolerance to Cd2+ and accumulated more Cd2+ ions when they were grown in the medium containing CdCl2. In addition, the heterologous expression of GST-OsMTI-1b conferred H2O2 and ethanol tolerance to S. cerevisiae cells. The results indicate that heterologous expression of plant MT isoforms can enhance the tolerance of S. cerevisiae to multiple stresses.


Subject(s)
Plant Proteins/genetics , Oryza/genetics , Saccharomyces cerevisiae/metabolism , Cadmium/metabolism , Gene Expression , Ethanol/metabolism , Hydrogen Peroxide/metabolism , Metallothionein/genetics , Plant Proteins/metabolism , Saccharomyces cerevisiae/genetics , Oxidative Stress , Protein Isoforms/genetics , Protein Isoforms/metabolism , Metallothionein/metabolism
10.
Int. j. morphol ; 34(2): 431-435, June 2016. ilus
Article in Spanish | LILACS | ID: lil-787016

ABSTRACT

El estrés oxidativo es definido como un desbalance entre la producción de oxidantes y antioxidantes. La inducción de tolerancia a estrés en los ovocitos conllevaría a un mejor desarrollo embrionario. En bovinos, la incubación de ovocitos maduros con diferentes estresores (térmicos, alta presión hidrostática, oxidativos) incrementaría la tasa de generación de blastocitos. Este estudio evalúa el efecto de la modulación del estado redox incrementando el estrés oxidativo con H2O2 en ovocitos maduros bajo condiciones de cultivo in vitro y su efecto sobre el potencial de desarrollo embrionario. Para ello, ovocitos procedentes de ovarios de matadero fueron madurados en medio TCM-199 suplementado durante 22­23 h, a 38,5 °C, 5 % CO2 y humedad a saturación. Al final de las 22­23 h se incubaron los ovocitos maduros con 0, 50, 100 y 200 µM H2O2. La fecundación in vitro se realizó co-incubando los ovocitos durante 18 h con una concentración final de 1x106 espermatozoides/mL. Los presuntos cigotos fueron denudados y cultivados en medio KSOM-0,4 % BSA a 38,5 °C en atmósfera de baja tensión de O2 (5 % O2, 5 % CO2 y 90 % N2) y humedad a saturación. El estrés oxidativo inducido con H2O2 a una concentración de 50 y 100 µM produce una tasa de división de los embriones similar al control (88,7 %, 83,2 % y 86,4 % respectivamente, p>0,05), disminuyendo significativamente al utilizar una concentración de 200 µM (58,8 %, p<0,05). Asimismo, H2O2 causó un efecto similar en la tasa de blastocitos con 50 µM (20,4 % vs. 25,8 % control, p>0.05) pero disminuyó significativamente con 100 y 200 µM (10,7 % y 3,3 % respectivamente, p<0,05). Es posible, que estos embriones resistentes al estrés oxidativo puedan tener una mayor sobrevida durante los procesos de criopreservación que generan altos niveles de especies reactivas de oxígeno en los embriones.


Oxidative stress is defined as an imbalance between the production of oxidants and antioxidants. The induction of stress tolerance in oocytes leads to a better embryonic development. In cattle incubating mature oocytes with different stressors (thermal, high hydrostatic pressure, oxidative) increase the generation rate of blastocysts. The purpose of this study was to evaluate the effect of modulating the redox state increasing the oxidative stress through H2O2 in mature oocyte under in vitro culture conditions and its effect on the potential of embryonic development. To do this, oocytes from slaughterhouse ovaries were matured in TCM-199 medium supplemented for 22­23 h at 38.5 °C, 5 % CO2 and humidified atmosphere. At the end of 22­23 h, the treatments with 0, 50, 100 and 200 µM H2O2 were applied for 1 h. IVF was performed co-incubating the eggs for 18 h with a final concentration of 1x106 sperm/mL. The presumptive zygotes were denuded and cultured in medium KSOM-0.4 % BSA to 38.5 °C in an atmosphere of low concentration of O2 (5 % O2, 5 % CO2 and 90 % N2) and humidified atmosphere. The results show that the induction of oxidative stress by H2O2 produces a similar effect using a concentration of 50 and 100 mM in the cleavage rate of embryos compared to control (88.7 %, 83.2 % and 86,4 % respectively, p>0.05) and decreasing significantly by using a concentration of 200 mM (58.8 %, p<0.05). Also, H2O2 caused a similar effect on the rate of blastocysts with 50 µM (20.4 % vs. 25.8 control, p>0.05) but decreased significantly with 100 and 200 µM (10.7 % and 3.3 % respectively, p<0.05). It is possible that these embryos resistant to oxidative stress may have a higher survival in the cryopreservation processes that generating high levels of reactive oxygen species.


Subject(s)
Animals , Cattle , Adaptation, Physiological , Embryo, Mammalian/physiology , Hydrogen Peroxide/metabolism , Oxidative Stress , Reactive Oxygen Species/metabolism , Blastocyst/metabolism , Fertilization in Vitro
11.
Biol. Res ; 49: 1-5, 2016. ilus, graf, tab
Article in English | LILACS | ID: biblio-950857

ABSTRACT

BACKGROUND: α-Farnesene is a volatile sesquiterpene synthesized by the plant mevalonate (MVA) pathway through the action of α-farnesene synthase. The α-farnesene synthase 1 (MdAFS1) gene was isolated from apple peel (var. white winterpearmain), and transformed into tobacco (Nicotiana tabacum NC89). The transgenic plants had faster stem elongation during vegetative growth and earlier flowering than wild type (WT). Our studies focused on the transgenic tobacco phenotype. RESULTS: The levels of chlorophyll and soluble protein decreased and a lower seed biomass and reduced net photosynthetic rate (Pn) in transgenic plants. Reactive oxygen species (ROS) such as hydrogen peroxide (H2O2) and superoxide radicals (O2._) had higher levels in transgenics compared to controls. Transgenic plants also had enhanced sensitivity to oxidative stress. The transcriptome of 8-week-old plants was studied to detect molecular changes. Differentially expressed unigene analysis showed that ubiquitin-mediated proteolysis, cell growth, and death unigenes were upregulated. Unigenes related to photosynthesis, antioxidant activity, and nitrogen metabolism were downregulated. Combined with the expression analysis of senescence marker genes, these results indicate that senescence started in the leaves of the transgenic plants at the vegetative growth stage. CONCLUSIONS: The antioxidative defense system was compromised and the accumulation of reactive oxygen species (ROS) played an important role in the premature aging of transgenic plants.


Subject(s)
Tobacco/physiology , Plants, Genetically Modified/physiology , Antioxidants/physiology , Photosynthesis/physiology , Sesquiterpenes/analysis , Sesquiterpenes/metabolism , Time Factors , Tobacco/genetics , Genetic Markers , Gene Expression/physiology , Plants, Genetically Modified/genetics , Reactive Oxygen Species/analysis , Reactive Oxygen Species/metabolism , Superoxides/analysis , Superoxides/metabolism , Plant Leaves/physiology , Oxidative Stress/physiology , Gene Expression Regulation, Plant/physiology , Real-Time Polymerase Chain Reaction , Hydrogen Peroxide/analysis , Hydrogen Peroxide/metabolism
12.
Rev. bras. epidemiol ; 18(1): 194-207, Jan-Mar/2015. tab
Article in Portuguese | LILACS | ID: lil-736436

ABSTRACT

OBJETIVO: Analisar os fatores pessoais associados à prevalência e duração dos benefícios auxílio-doença decorrentes de sinovite e tenossinovite (CID10 M65). MÉTODO: Estudo transversal referente aos benefícios auxílio-doença decorrentes de sinovite e tenossinovite concedidos pelo Instituto Nacional de Seguro Social aos empregados no Brasil em 2008. Dados sobre o ramo de atividade econômica (Classificação Nacional de Atividades Econômicas - CNAE divisão, classe), sexo, idade, espécie e duração dos benefícios foram coletados do Sistema Único de Benefícios. A população corresponde à média mensal dos vínculos empregatícios declarados ao Cadastro Nacional de Informações Sociais. RESULTADOS: Em 2008 foram concedidos 35.601 benefícios auxílio-doença decorrentes de sinovite e tenossinovite, com prevalência de 10,9/10.000 vínculos empregatícios. No conjunto dos benefícios auxílio-doença houve maior razão de prevalência (RP) acidentária (RP 1,2), sendo esta maior em mulheres (RP 3,3), e em trabalhadores com idade acima de 39 anos (RP 1,4). As CNAE 37-Esgoto (55,4) e 60-Atividade de rádio e TV (47,1) apresentaram as maiores prevalências, no entanto, 64-Atividade de serviços financeiros e 6422-Bancos múltiplos caracterizaram mais acidentes de trabalho (RP 3,2 e 3,8, respectivamente) e maior duração (70 e 73 dias, respectivamente). A maior duração de benefício ocorreu entre trabalhadores com idade superior a 39 anos. Tanto a CNAE-divisão 60-Atividade de rádio e TV, quanto a CNAE-classe 6010-Atividade de rádio apresentaram elevadas razões de feminilidade (RP 8,1 e 10,8, respectivamente). CONCLUSÃO: A incapacidade para o trabalho por sinovite e tenossinovite apresenta associação tanto da prevalência quanto da duração com o ramo de atividade, sexo, idade e espécie de benefício (previdenciário/acidentário). .


OBJECTIVE: To analyse the personal and occupational factors associated with the prevalence and duration of sickness benefit claims due to synovitis and tenosynovitis (CID10 M65). METHODS: Cross-sectional study regarding sickness benefit claims due to synovitis and tenosynovitis granted to employees by National Institute of Social Security in Brazil in 2008. Data on economic activity (Economic Activities National Classification - CNAE division, class), sex, age, type and duration of benefits were collected from the Unified Benefit System. The study's population consists of the average monthly employment contracts declared to the National Register of Social Information. RESULTS: In 2008, 35,601 employees were granted sickness benefits due to synovitis and tenosynovitis, with a prevalence of 10.9/10,000 employments. Sickness benefits showed higher prevalence rates (PR) for work-related claims (PR 1,2), mostly made by females (PR 3.3) and by workers older than 39 years (PR 1,4). The CNAE 37-Sewage (55.4) and 60-Broadcasting Activity (47.1) had the highest overall prevalence. However, the 64-Financial service activities, except insurance and pension funding and 6422-Multiple banks with commercial service had the highest rates of work-related claims (RP 3.2 and 3.8, respectively), and the longer duration (70 and 73 days, respectively). Workers older than 39 years had the highest durations of work disability claims. Both the CNAE-division 60-Broadcasting Activity, and the CNAE-class 6010-Radio showed a high activity ratio of females (PR 8.1 and 10.8, respectively). CONCLUSION: The work disability due to synovitis and tenosynovitis presents prevalence and duration associated with economic activity, sex, age and kind of benefit (non work-related and work-related claims). .


Subject(s)
Humans , Globins/chemistry , Hydrogen Peroxide/chemistry , Nerve Tissue Proteins/chemistry , Nitrites/chemistry , Amino Acid Sequence , Binding Sites , Catalysis , Cysteine/chemistry , Cysteine/metabolism , Disulfides/chemistry , Disulfides/metabolism , Globins/metabolism , Hydrogen Peroxide/metabolism , Kinetics , Models, Molecular , Molecular Sequence Data , Myoglobin/chemistry , Myoglobin/metabolism , Nerve Tissue Proteins/metabolism , Nitrites/metabolism , Oxidation-Reduction , Protein Conformation , Phenol/chemistry , Phenols/chemistry , Phenylacetates/chemistry , Tandem Mass Spectrometry
13.
Bauru; s.n; 2015. 119 p. ilus, graf.
Thesis in Portuguese | LILACS, BBO | ID: biblio-867426

ABSTRACT

Os mastócitos (MCs) estão presentes tanto no periodonto normal quanto inflamado, em diferentes quantidades e em vários locais. Nos últimos anos, a eficácia e a contribuição dos MCs em eliminar bactérias, através de sua atividade microbicida intracelular, estão se tornando cada vez mais reconhecidas. Assim, a partir de MCs murinos desafiados in vitro com o periodontopatógeno Aggregatibacter actinomycetemcomitans (ATCC 29523) por 3, 5, 10 e 24 horas, o presente estudo teve como objetivo investigar a capacidade microbicida intracelular de MCs, e comparar com a capacidade microbicida de macrófagos peritoneais murinos (MPs), considerados fagócitos profissionais, por meio da contagem das unidades formadoras de colônias. Além disso, avaliou-se a produção e liberação de mediadores microbicidas, óxido nítrico (NO) e peróxido de hidrogênio (H2O2), por meio do método colorimétrico de Griess e pela degradação de substratos fluorescentes, respectivamente. Para a análise estatística, foram utilizados os testes estatísticos ANOVA Fatorial seguido do teste de Tukey e teste de correlação de Pearson (p<0.05). Nossos resultados revelaram que os MCs foram capazes de eliminar eficientemente o periodontopatógeno, principalmente após 10h de desafio intracelular. Comparando-se a atividade microbicida dos dois tipos celulares, verificou-se, nos períodos de 3h e 5h de desafio, um menor percentual de colônias viáveis no interior de MPs, em comparação aos MCs. Inversamente, nos períodos de 10h e 24h, observaram-se menores valores percentuais de colônias intracelulares nos MCs em relação aos MPs. Além disso, a produção/liberação de NO bem como, em menor proporção, de H2O2 pelos MCs foram concordantes com a sua capacidade microbicida. Este é o primeiro estudo que demonstra a eficiente ação microbicida intracelular de MCs murinos contra Aggregatibacter actinomycetemcomitans, com produção e liberação de substâncias potencialmente bactericidas, e de forma mais eficaz que os macrófagos...


Mast cells (MCs) are present in both normal and inflamed periodontal tissues, in varying amounts and locations. Recently, MCs contribution in eliminating bacteria and its effectiveness, through its intracellular microbicidal activity, have been increasingly recognized. Thus, this study aimed to investigate the intracellular microbicide capacity of MCs, and compare it with the microbicide capacity of murine peritoneal macrophages (MPs), considered professional phagocytes, by counting the colony forming units. Both cell types were challenged in vitro with periodontopathogen Aggregatibacter actinomycetemcomitans (ATCC 29523) by 3, 5, 10 and 24 hours. Additionally, the production and release of microbicidal agents, nitric oxide (NO) and hydrogen peroxide (H2O2) were evaluated by means of colorimetric Griess method and by the degradation of fluorescent substrates, respectively. Statistical analysis was performed by ANOVA Factorial test followed by Tukey and Pearson's correlation test (p <0.05). Our results revealed that MCs are able to efficiently eliminate periodontopathogen, mainly after 10 hours of intracellular challenge. The microbicidal activity of both cell types, in 3 and 5 hours of challenge showed a lower percentage of viable colonies inside MPs, compared to MCs. Contradictorily, in 10 and 24 hours a lower percentage of intracellular colonies in MCs was observed in relation to MPs. Moreover, the production/release of NO and, in minor proportion, of H2O2 by MCs was in agreement with its microbicidal capacity. Therefore, this is the first report to describe the intracellular microicidal activity of murine MCs against Aggregatibacter actinomycetemcomitans, concerning production and release of potentially bactericidal substances, which is more effective than macrophages. These results suggest the importance of these cells in pathogenesis and defense mechanisms of biofilm-associated periodontal disease.


Subject(s)
Animals , Male , Female , Mice , Aggregatibacter actinomycetemcomitans/growth & development , Bone Marrow Cells/physiology , Mast Cells/physiology , Colony Count, Microbial , Periodontal Diseases/pathology , Nitric Oxide/biosynthesis , Hydrogen Peroxide/metabolism , Time Factors
14.
Bauru; s.n; 2015. 119 p. ilus, graf.
Thesis in Portuguese | LILACS | ID: lil-794221

ABSTRACT

Os mastócitos (MCs) estão presentes tanto no periodonto normal quanto inflamado, em diferentes quantidades e em vários locais. Nos últimos anos, a eficácia e a contribuição dos MCs em eliminar bactérias, através de sua atividade microbicida intracelular, estão se tornando cada vez mais reconhecidas. Assim, a partir de MCs murinos desafiados in vitro com o periodontopatógeno Aggregatibacter actinomycetemcomitans (ATCC 29523) por 3, 5, 10 e 24 horas, o presente estudo teve como objetivo investigar a capacidade microbicida intracelular de MCs, e comparar com a capacidade microbicida de macrófagos peritoneais murinos (MPs), considerados fagócitos profissionais, por meio da contagem das unidades formadoras de colônias. Além disso, avaliou-se a produção e liberação de mediadores microbicidas, óxido nítrico (NO) e peróxido de hidrogênio (H2O2), por meio do método colorimétrico de Griess e pela degradação de substratos fluorescentes, respectivamente. Para a análise estatística, foram utilizados os testes estatísticos ANOVA Fatorial seguido do teste de Tukey e teste de correlação de Pearson (p<0.05). Nossos resultados revelaram que os MCs foram capazes de eliminar eficientemente o periodontopatógeno, principalmente após 10h de desafio intracelular. Comparando-se a atividade microbicida dos dois tipos celulares, verificou-se, nos períodos de 3h e 5h de desafio, um menor percentual de colônias viáveis no interior de MPs, em comparação aos MCs. Inversamente, nos períodos de 10h e 24h, observaram-se menores valores percentuais de colônias intracelulares nos MCs em relação aos MPs. Além disso, a produção/liberação de NO bem como, em menor proporção, de H2O2 pelos MCs foram concordantes com a sua capacidade microbicida. Este é o primeiro estudo que demonstra a eficiente ação microbicida intracelular de MCs murinos contra Aggregatibacter actinomycetemcomitans, com produção e liberação de substâncias potencialmente bactericidas, e de forma mais eficaz que os macrófagos...


Mast cells (MCs) are present in both normal and inflamed periodontal tissues, in varying amounts and locations. Recently, MCs contribution in eliminating bacteria and its effectiveness, through its intracellular microbicidal activity, have been increasingly recognized. Thus, this study aimed to investigate the intracellular microbicide capacity of MCs, and compare it with the microbicide capacity of murine peritoneal macrophages (MPs), considered professional phagocytes, by counting the colony forming units. Both cell types were challenged in vitro with periodontopathogen Aggregatibacter actinomycetemcomitans (ATCC 29523) by 3, 5, 10 and 24 hours. Additionally, the production and release of microbicidal agents, nitric oxide (NO) and hydrogen peroxide (H2O2) were evaluated by means of colorimetric Griess method and by the degradation of fluorescent substrates, respectively. Statistical analysis was performed by ANOVA Factorial test followed by Tukey and Pearson's correlation test (p <0.05). Our results revealed that MCs are able to efficiently eliminate periodontopathogen, mainly after 10 hours of intracellular challenge. The microbicidal activity of both cell types, in 3 and 5 hours of challenge showed a lower percentage of viable colonies inside MPs, compared to MCs. Contradictorily, in 10 and 24 hours a lower percentage of intracellular colonies in MCs was observed in relation to MPs. Moreover, the production/release of NO and, in minor proportion, of H2O2 by MCs was in agreement with its microbicidal capacity. Therefore, this is the first report to describe the intracellular microicidal activity of murine MCs against Aggregatibacter actinomycetemcomitans, concerning production and release of potentially bactericidal substances, which is more effective than macrophages. These results suggest the importance of these cells in pathogenesis and defense mechanisms of biofilm-associated periodontal disease...


Subject(s)
Animals , Male , Female , Mice , Aggregatibacter actinomycetemcomitans/growth & development , Bone Marrow Cells/physiology , Mast Cells/physiology , Colony Count, Microbial , Periodontal Diseases/pathology , Nitric Oxide/biosynthesis , Hydrogen Peroxide/metabolism , Time Factors
15.
Indian J Biochem Biophys ; 2014 Oct; 51(5): 407-415
Article in English | IMSEAR | ID: sea-154272

ABSTRACT

The involvement of 1, 1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging activity and contents of H2O2, malondialdehyde (MDA) and proline was investigated in determining salinity tolerance among seedlings of thirty chickpea (Cicer arietinum L.) genotypes having different pedigrees. Chickpea genotypes, including cultivars and advanced lines were grown for 7 days under control and salt stress (50 mM NaCl) conditions. The genotypes showed differential response to salt stress in terms of growth, DPPH radical scavenging activity and contents of H2O2, MDA and proline in seedlings. On the basis of seedling growth, the genotypes having better performance under stress conditions had reduced levels of H2O2 and MDA contents, but increased levels of proline and DPPH radical scavenging activity. Stress tolerance index for these parameters was also determined. Agglomerative hierarchal clustering by Pearson correlation coefficient grouped the genotypes into two major clusters — MC I and MC II. MC II and A1-1 sub-cluster of MC-I comprised mainly of genotypes that showed higher stress resistance levels for the respective parameters in comparison to genotypes in other sub-clusters. Thus, it is possible to identify salt-tolerant genotypes on the basis of above parameters without a field trial.


Subject(s)
Biphenyl Compounds/metabolism , Cicer/physiology , Free Radical Scavengers/metabolism , Hydrogen Peroxide/metabolism , Malondialdehyde/metabolism , Oxidative Stress/physiology , Picrates/metabolism , Proline/metabolism , Reactive Oxygen Species/metabolism , Salinity , Salt Tolerance/physiology , Seedlings/physiology
16.
J. bras. med ; 102(4)julho - agosto 2014. graf, ilus
Article in Portuguese | LILACS | ID: lil-725926

ABSTRACT

Os pacientes com diabetes mellitus (DM) apresentam maior prevalência de doenças tireoidianas que a população geral. A autoimunidade certamente é um fator-chave na relação entre essas disfunções endócrinas. Entretanto, outros mecanismos, como redução da captação de iodeto, da atividade tireoperoxidase e aumento do estresse oxidativo na glândula tireoide, também parecem contribuir para este fato. O presente trabalho visa rever aspectos importantes na relação entre DM e doenças tireoidianas, com especial ênfase nos mecanismos envolvidos no aumento do estresse oxidativo na glândula tireoide decorrente do DM...


Diabetes mellitus (DM) patients show a greater prevalence of thyroid disorders than general population. Autoimmunity is a key factor in the relation between these endocrine diseases. However, additional mechanisms, such as reduction of iodide uptake and thyroperoxidase activity, besides increased oxidative stress in the thyroid gland seem to contribute for this fact. The present work aims to review important aspects in the relation between DM and thyroid disease, with special emphasis in the mechanisms involved in the increased oxidative stress in the thyroid gland due to DM...


Subject(s)
Humans , Male , Female , Diabetes Mellitus, Type 1/complications , Diabetes Mellitus, Type 1/metabolism , Thyroid Diseases , Autoimmunity , Diabetes Complications/metabolism , Cardiovascular Diseases/etiology , Hyperthyroidism/complications , Thyroid Hormones/biosynthesis , Thyroid Hormones/metabolism , NADPH Oxidases/analysis , NADPH Oxidases/metabolism , Oxidative Stress , Hydrogen Peroxide/metabolism
17.
Biol. Res ; 47: 1-10, 2014. graf, tab
Article in English | LILACS | ID: biblio-950772

ABSTRACT

BACKGROUND: Based on the ethnomedicinal uses and the effective outcomes of natural products in various diseases, this study was designed to evaluate Isodon rugosus as possible remedy in oxidative stress, alzheimer's and other neurodegenerative diseases. Acetylecholinestrase (AChE) and butyrylcholinesterase (BChE) inhibitory activities of crude methanolic extract (Ir.Cr), resultant fractions (n-hexane (Ir.Hex), chloroform (Ir.Cf), ethyl acetate (Ir.EtAc), aqueous (Ir.Aq)), flavonoids (Ir.Flv) and crude saponins (Ir.Sp) of I. rugosus were investigated using Ellman's spectrophotometric method. Antioxidant potential of I. rugosus was determined using DPPH, H2O2 and ABTS free radicals scavenging assays. Total phenolic and flavonoids contents of plant extracts were determined and expressed in mg GAE/g dry weight and mg RTE/g of dry sample respectively. RESULTS: Among different fractions Ir.Flv and Ir.Cf exhibited highest inhibitory activity against AChE (87.44 ± 0.51, 83.73 ± 0.64%) and BChE (82.53 ± 0.71, 88.55 ± 0.77%) enzymes at 1 mg/ml with IC50 values of 45, 50 for AChE and 40, 70 µg/ml for BChE respectively. Activity of these fractions were comparable to galanthamine causing 96.00 ± 0.30 and 88.61 ± 0.43% inhibition of AChE and BChE at 1 mg/ml concentration with IC50 values of 20 and 47 µg/ml respectively. In antioxidant assays, Ir.Flv, Ir.Cf, and Ir.EtAc demonstrated highest radicals scavenging activities in DPPH and H2O2 assays which were comparable to ascorbic acid. Ir.Flv was found most potent with IC50 of 19 and 24 µg/ml against DPPH and H2O2 radicals respectively. Whereas antioxidant activates of plant samples against ABTS free radicals was moderate. Ir.Cf, Ir.EtAc and Ir.Cr showed high phenolic and flavonoid contents and concentrations of these compounds in different fractions correlated well to their antioxidant and anticholinestrase activities. CONCLUSION: It may be inferred from the current investigations that the Ir.Sp, Ir.Flv and various fractions of I. rugosus are good sources of anticholinesterase and antioxidant compounds. Different fractions can be subjected to activity guided isolation of bioactive compounds effective in neurological disorders.


Subject(s)
Saponins/analysis , Flavonoids/analysis , Plant Extracts/chemistry , Cholinesterase Inhibitors/analysis , Isodon/chemistry , Antioxidants/analysis , Picrates/metabolism , Acetylcholinesterase/drug effects , Saponins/isolation & purification , Spectrophotometry/methods , Sulfonic Acids/metabolism , Flavonoids/isolation & purification , Biphenyl Compounds/metabolism , Butyrylcholinesterase/drug effects , Chloroform , Free Radical Scavengers/metabolism , Oxidative Stress/drug effects , Inhibitory Concentration 50 , Isodon/classification , Isodon/enzymology , Plant Components, Aerial/chemistry , Complex Mixtures , Methanol , Benzothiazoles/metabolism , Free Radicals/analysis , Hexanes , Hydrogen Peroxide/metabolism , Medicine, Traditional , Acetates
18.
Journal of Korean Medical Science ; : 230-237, 2014.
Article in English | WPRIM | ID: wpr-35685

ABSTRACT

This study investigated whether tempol, an anti-oxidant, protects against renal injury by modulating phosphatidylinositol 3-kinase (PI3K)-Akt-Forkhead homeobox O (FoxO) signaling. Mice received unilateral ureteral obstruction (UUO) surgery with or without administration of tempol. We evaluated renal damage, oxidative stress and the expression of PI3K, Akt, FoxO3a and their target molecules including manganese superoxide dismutase (MnSOD), catalase, Bax, and Bcl-2 on day 3 and day 7 after UUO. Tubulointerstitial fibrosis, collagen deposition, alpha-smooth muscle actin-positive area, and F4/80-positive macrophage infiltration were significantly lower in tempol-treated mice compared with control mice. The expression of PI3K, phosphorylated Akt, and phosphorylated FoxO3a markedly decreased in tempol-treated mice compared with control mice. Tempol prominently increased the expressions of MnSOD and catalase, and decreased the production of hydrogen peroxide and lipid peroxidation in the obstructed kidneys. Significantly less apoptosis, a lower ratio of Bax to Bcl-2 expression and fewer apoptotic cells in TUNEL staining, and decreased expression of transforming growth factor-beta1 were observed in the obstructed kidneys from tempol-treated mice compared with those from control mice. Tempol attenuates oxidative stress, inflammation, and fibrosis in the obstructed kidneys of UUO mice, and the modulation of PI3K-Akt-FoxO3a signaling may be involved in this pathogenesis.


Subject(s)
Animals , Male , Mice , Antioxidants/pharmacology , Collagen/metabolism , Cyclic N-Oxides/pharmacology , Fibrosis , Forkhead Transcription Factors/metabolism , Hydrogen Peroxide/metabolism , Kidney Diseases/drug therapy , Lipid Peroxidation , Mice, Inbred C57BL , Oxidative Stress/drug effects , Phosphatidylinositol 3-Kinases/metabolism , Phosphorylation/drug effects , Proto-Oncogene Proteins c-akt/metabolism , Severity of Illness Index , Signal Transduction/drug effects , Spin Labels , Superoxide Dismutase/metabolism , Ureteral Obstruction/complications
19.
Arq. bras. endocrinol. metab ; 57(8): 594-602, Nov. 2013. graf, tab
Article in English | LILACS | ID: lil-696898

ABSTRACT

OBJECTIVE: This study investigated the effect of interval training on blood biochemistry and immune parameters in type 1 diabetic rats. MATERIALS AND METHODS: Male Wistar rats were divided into four groups: sedentary (SE, n = 15), interval training (IT, n = 17), diabetic sedentary (DSE, n = 17), diabetic interval training (DIT, n = 17). Diabetes was induced by i.v. injection of streptozotocin (60 mg/kg). Swimming Interval Training consisted of 30-s exercise with 30-s rest, for 30 minutes, during 6 weeks, four times a week, with an overload of 15% of body mass. Plasma glucose, lactate, triacylglycerol and total cholesterol concentrations, phagocytic capacity, cationic vesicle content, and superoxide anion and hydrogen peroxide production by blood neutrophils and peritoneal macrophages were evaluated. Proliferation of mesenteric lymphocytes was also estimated. RESULTS: Interval training resulted in attenuation of the resting hyperglycemic state and decreased blood lipids in the DIT group. Diabetes increased the functionality of blood neutrophils and peritoneal macrophages in the DSE group. Interval training increased all functionality parameters of peritoneal macrophages in the IT group. Interval training also led to a twofold increase in the proliferation of mesenteric lymphocytes after 6 weeks of exercise in the DIT group. CONCLUSION: Low-volume high-intensity physical exercise attenuates hyperglycemia and dislipidemia induced by type 1 diabetes, and induces changes in the functionality of innate and acquired immunity.


OBJETIVO: Este estudo investigou os efeitos do treinamento intervalado sobre parâmetros bioquímicos e imunológicos em ratos diabéticos do tipo 1. MATERIAIS E MÉTODOS: Ratos Wistar machos foram divididos em quatro grupos: sedentário (SE, n = 15), treinamento intervalado (TI, n = 17), sedentário diabético (SED, n = 17) e treinamento intervalado diabético (TID, n = 17). O diabetes foi induzido por uma injeção intravenosa de estreptozotocina (60 mg/kg). O treinamento intervalado de natação consistiu de 30s de exercício com 30s de recuperação, 30 minutos, durante 6 semanas, 4 vezes por semana, com sobrecarga de 15% da massa corporal. Foram avaliados glicemia, lactato sanguíneo, concentração de triacilglicerol e colesterol total, capacidade fagocítica, conteúdo de vesículas catiô­nicas, produção de ânion superóxido e peróxido de hidrogênio por neutrófilos sanguíneos e macrófagos peritoneais. A proliferação de linfócitos mesentéricos também foi avaliada. RESULTADOS: O treinamento intervalado resultou em atenuação do estado hiperglicêmico e diminuiu os lipídeos sanguíneos no grupo TID. O diabetes aumentou a funcionalidade dos neutrófilos sanguíneos e macrófagos peritoneais do grupo SED. O treinamento intervalado aumentou todos os parâmetros funcionais dos macrófagos peritoneais do grupo TI. O treinamento intervalado também aumentou duas vezes a proliferação dos linfócitos mesentéricos após seis semanas de exercício do grupo TID. CONCLUSÃO: O treinamento intervalado atenua a hiperglicemia e a dislipidemia induzida pelo diabetes do tipo 1 e induz mudanças na funcionalidade da imunidade inata e adquirida.


Subject(s)
Animals , Male , Diabetes Mellitus, Experimental/chemically induced , Diabetes Mellitus, Experimental/metabolism , Diabetes Mellitus, Type 1/metabolism , Dyslipidemias/etiology , Hyperglycemia/etiology , Physical Conditioning, Animal/methods , Biomarkers , Blood Glucose/metabolism , Cell Proliferation , Disease Models, Animal , Diabetes Mellitus, Type 1/complications , Hydrogen Peroxide/metabolism , Neutrophils/metabolism , Phagocytosis/physiology , Rats, Wistar , Sedentary Behavior , Streptozocin/pharmacology , Superoxides/metabolism
20.
Article in English | IMSEAR | ID: sea-162942

ABSTRACT

Aim: To correlate H2O2 production of Lactobacillus species with the Nugent scores of young Nigerian women in order to assess their vaginal health. Study Design: Cross-sectional study. Place and Duration of Study: Departments of Medical Microbiology & Parasitology, Biochemistry and Obstetrics and Gynaecology, College of Medicine of the University of Lagos, between May and august 2009. Methodology: Ninety- seven isolates of Lactobacillus from eighty-two women without Bacterial vaginosis (BV) and fifteen women with BV were used for the study. BV was diagnosed using Nugent scoring method. Lactobacilli were isolated using MRS agar and categorized into facultative anaerobes and strict anaerobes. Hydrogen peroxide was detected and measured by titration using dilute sulphuric acid and reaction stopped with potassium permanganate. Results: Out of 97 isolates studied, 76 (78%) were facultative anaerobes, while 21 (22%) were strict anaerobes. The facultative anaerobes were obtained from 11 of 15 women with BV and 65 of 82 women without BV. Forty- nine (50.51%) of the 97 isolates produced H2O2. Forty- four of the H2O2 producers were from women without BV while five were from women with BV. Majority (67%) of the strains obtained from women with BV were non-hydrogen peroxide producing. Proportion of H2O2 producing Lactobacillus by Nugent score were 70%, 43% and 33% in negative, intermediate and BV Nugent scores respectively. There was no significant difference between the mean concentrations of H2O2 production in the various Nugent scores. Conclusion: The overall rate of hydrogen peroxide production was low. While the rates of hydrogen peroxide production correlated with Nugent scores, being highest in negative Nugent scores and lowest with BV scores, the concentration of hydrogen peroxide produced had no association with Nugent scores. The Nigerian women studied might have a relatively high susceptibility rate to vaginal infections.


Subject(s)
Adult , Female , Humans , Hydrogen Peroxide/metabolism , Lactobacillus/metabolism , Lactobacillus/physiology , Nigeria , Research Design/methods , Vaginosis, Bacterial/metabolism , Young Adult
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