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1.
Clinics ; 69(10): 677-682, 10/2014. tab
Article in English | LILACS | ID: lil-730467

ABSTRACT

OBJECTIVES: To determine the serum and tissue levels of markers of impaired oxidative metabolism and correlate these levels with the histopathology and Alvarado score of acute appendicitis patients. METHOD: Sixty-five acute appendicitis patients (mean age, 31.4±12.06 years; male/female, 30/35) and 30 healthy control subjects were studied. The Alvarado score was recorded. Serum samples were obtained before surgery and 12 hours postoperatively to examine the total antioxidant status, total oxidant status, paraoxonase, stimulated paraoxonase, arylesterase, catalase, myeloperoxidase, ceruloplasmin, oxidative stress markers (advanced oxidized protein products and total thiol level) and ischemia-modified albumin. Surgical specimens were also evaluated. RESULTS: The diagnoses were acute appendicitis (n = 37), perforated appendicitis (n = 8), phlegmonous appendicitis (n = 12), perforated+phlegmonous appendicitis (n = 4), or no appendicitis (n = 4). The Alvarado score of the acute appendicitis group was significantly lower than that of the perforated+phlegmonous appendicitis group (p = 0.004). The serum total antioxidant status, total thiol level, advanced oxidized protein products, total oxidant status, catalase, arylesterase, and ischemia-modified albumin levels were significantly different between the acute appendicitis and control groups. There was no correlation between the pathological extent of acute appendicitis and the tissue levels of the markers; additionally, there was no correlation between the tissue and serum levels of any of the parameters. CONCLUSIONS: The imbalance of oxidant/antioxidant systems plays a role in the pathogenesis acute appendicitis. The Alvarado score can successfully predict the presence and extent of acute appendicitis. .


Subject(s)
Adolescent , Adult , Aged , Female , Humans , Male , Middle Aged , Young Adult , Appendicitis/metabolism , Oxidative Stress/physiology , Reactive Oxygen Species/analysis , Acute Disease , Appendectomy , Antioxidants/analysis , Aryldialkylphosphatase/analysis , Biomarkers/analysis , Case-Control Studies , Carboxylic Ester Hydrolases/analysis , Prospective Studies , Peroxidases/analysis , Reference Values , Reactive Oxygen Species/metabolism , Statistics, Nonparametric , Serum Albumin/analysis
2.
Indian J Exp Biol ; 2014 Nov; 52(11): 1128-1137
Article in English | IMSEAR | ID: sea-153803

ABSTRACT

Different explants of fenugreek, T. foenum-graecum L. (Var. RMt-303), were compared for their callus induction and subsequent shoot regeneration capabilities on Murashige and Skoog media supplemented with different phytohormones in varying concentration. The highest percentage of callus induction frequency was observed in 1ppm benzylaminopurine (BAP). Maximum shoots were induced on media supplemented with 0.5ppm BAP using leaf and stem tissues as explants. However, root tissues showed only callusing with no subsequent shooting. Cotyledonary node responded better than hypocotyls in terms of shoot induction on media supplemented with thidiazuron (0.1ppm). The callus was subjected to drought stress as simulated by reduced water potential of growth media due to addition of mannitol. Calli could withstand -2 MPa water potential till 30 days indicating that the drought stress tolerance mechanisms are functional in this variety. Chlorophyll a and b and total chlorophyll, proline and total phenolic contents, total peroxidase and catalase activities increased under stress conditions suggesting the tolerance of callus to drought stress. However, ascorbate peroxidase, guaiacol peroxidase activities were found to decrease slightly. Malondialdehyde and H2O2 contents were found to decrease while only a slight disturbance was found in membrane stability index. These results underline the mechanisms that are crucial for drought stress tolerance in fenugreek.


Subject(s)
Adaptation, Physiological , Catalase/analysis , Chlorophyll/analysis , Culture Media/pharmacology , Dehydration/chemically induced , Dehydration/metabolism , Droughts , Mannitol/toxicity , Organoids/drug effects , Organoids/physiology , Oxidative Stress , Peroxidases/analysis , Phenols/analysis , Phenylurea Compounds/pharmacology , Plant Cells/drug effects , Plant Cells/physiology , Plant Leaves/growth & development , Plant Proteins/analysis , Plant Shoots/growth & development , Plants, Medicinal/physiology , Proline/analysis , Regeneration/drug effects , Regeneration/physiology , Stress, Physiological , Thiadiazoles/pharmacology , Trigonella/physiology
3.
Braz. j. microbiol ; 40(1): 31-39, Jan.-Mar. 2009. ilus, graf, tab
Article in English | LILACS | ID: lil-513112

ABSTRACT

Wood rotting Basidiomycetes collected in the ôEstação Ecológica do Noroeste Paulistaõ, São José do Rio Preto, São Paulo State, Brazil, concerning Aphyllophorales order and identified as Coriolopsis byrsina SXS16, Lentinus strigellus SXS355, Lentinus sp SXS48, Picnoporus sanguineus SXS 43 and Phellinus rimosus SXS47 were tested for ligninases production by solid state fermentation (SSF) using wheat branor rice straw as culture media. C. byrsina produced the highest laccase (200 U mL-1) and Lentinus sp produced the highest activities of manganese peroxidase (MnP) and lignin peroxidase (LiP) (7 and 8 U mL-1, respectively), when cultivated on wheat bran. The effect of N addition on enzyme production was studied in medium containing rice straw and the data showed an increase of 3 up to 4-fold in the laccase production compared to that obtained in SSF on wheat bran. The laccases presented optimum pH at 3.0-3.5 and were stable at neutral pH values. Optimum pH for MnP and LiP activities was at 3.5 and between 4.5 and 6.0, respectively. All the strains produced laccase with optimum activities between 55-60ºC while the peroxidases presented maximum activity at temperatures of 30 to 55ºC. The crude enzymes promoted decolorization of chemically different dyes with around 70% of decolorization of RBBR and cybacron blue 3GA in 6h oftreatment. The data indicated that enzymes from these basidiomycetes strains are able to decolorize synthetic dyes.


Fungos decompositores de madeira, do grupo Basidiomicetes, coletados na ôEstação Ecológica do NoroestePaulistaõ, São José do Rio Preto, São Paulo, Brasil, pertencentes a ordem Aphyllophorales e identificados como Coriolopsis byrsina SXS16, Lentinus strigellus SXS355, Lentinus sp. SXS48,Picnoporus sanguineus SXS 43 e Phellinus rimosus SXS47 foram estudados para a produção de ligninases por FES (fermentação em estado sólido) usando farelo de trigo ou palha de arroz como meio de cultura. A espécie C. byrsina produziu a maior quantidade de lacase (200 U mL-1) enquanto que Lentinus sp. foi o melhor produtor de manganês peroxidase (MnP) e lignina peroxidase (LiP) (7 e 8 U mL-1, respectivamente), quando cultivados em meio composto por farelo de trigo. A avaliação do efeito da suplementação de nitrogênio do substrato sólido lignocelulósico (palha de arroz) indicou um aumento de 3 a 4 vezes na produção de lacase. A caracterização das enzimasmostrou que as lacases apresentaram atividade ótima em pH 3,0-3,5 e foram estáveis em pH de neutro a alcalino. O pH ótimo para atividade de MnP e LiP foi de 3,5 e entre 4,5 e 6,0, respectivamente. Todas as linhagens produziram lacase com atividade ótima a 55-60ºC, enquanto as peroxidases apresentaram atividades máximas entre temperaturas de 30 e 55ºC. A aplicaçãodas soluções enzimáticas brutas, obtidas pelo cultivo das linhagens em meio de farelo de trigo, em testes de descoloração de corantes sintéticos de diferentes grupos químicos levou amais 70% de perda de cor dos corantes RBBR e de cybacron blue 3GA, em 6h de tratamento. Os dados obtidos indicaramque as soluções enzimáticas contendo ligninases produzidas pelas linhagens de basidiomicetos estudadas promoveram adescoloração de corantes sintéticos.


Subject(s)
Coloring Agents/analysis , Basidiomycota/enzymology , Basidiomycota/isolation & purification , Fermentation , Laccase/analysis , Laccase/isolation & purification , Manganese/analysis , Manganese/isolation & purification , Peroxidases/analysis , Peroxidases/isolation & purification , Methods , Methods , Wood
4.
Braz. j. med. biol. res ; 40(8): 1095-1099, Aug. 2007. tab
Article in English | LILACS | ID: lil-456805

ABSTRACT

The aim of the present study was to evaluate the effect of Ginkgo biloba treatment (EGb 761, 200 mg kg-1 day-1) administered from day 0 to 20 of pregnancy on maternal reproductive performance and on the maternal and fetal liver antioxidant systems of streptozotocin-induced diabetic Wistar rats. On day 21 of pregnancy, the adult rats (weighing approximately 250 ± 50 g, minimum number = 13/group) were anesthetized to obtain maternal and fetal liver samples for superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), and total glutathione (GSH-t) determinations. The uterus was weighed with its contents. The diabetic (G3) and treated diabetic (G4) groups of rats presented significant maternal hyperglycemia, reduced term pregnancy rate, impaired maternal reproductive outcome and fetal-placental development, decreased GSH-Px (G3 = G4 = 0.6 ± 0.2) and SOD (G3 = 223.0 ± 84.7; G4 = 146.1 ± 40.8), and decreased fetal CAT activity (G3 = 22.4 ± 10.6; G4 = 34.4 ± 14.1) and GSH-t (G3 = G4 = 0.3 ± 0.2), compared to the non-diabetic groups (G1, untreated control; G2, treated). For G1, maternal GSH-Px = 0.9 ± 0.2 and SOD = 274.1 ± 80.3; fetal CAT = 92.6 ± 82.7 and GSH-t = 0.6 ± 0.5. For G2, G. biloba treatment caused no toxicity and did not modify maternal or fetal-placental data. EGb 761 at the nontoxic dose used (200 mg kg-1 day-1), failed to modify the diabetes-associated increase in maternal glycemia, decrease in pregnancy rate, decrease in antioxidant enzymes, and impaired fetal development when the rats were treated throughout pregnancy (21 days).


Subject(s)
Animals , Female , Male , Pregnancy , Rats , Diabetes Mellitus, Experimental/metabolism , Ginkgo biloba/chemistry , Liver/drug effects , Oxidative Stress/drug effects , Peroxidases/analysis , Pregnancy in Diabetics/metabolism , Biomarkers/analysis , Liver/enzymology , Pregnancy Outcome , Pregnancy Rate , Plant Extracts/pharmacology , Rats, Wistar , Streptozocin
5.
Indian J Biochem Biophys ; 1999 Feb; 36(1): 39-43
Article in English | IMSEAR | ID: sea-28152

ABSTRACT

The steady state kinetics of ligninperoxidase catalysed reaction using n-propanol as the organic substrate and monitoring the formation of propanaldehyde at lambda = 300 nm spectrophotometerically as functions of different reaction parameters has been studied. It has been concluded that n-propanol can be used as a substrate for analysing the activity of ligninperoxidase. The turnover number of ligninperoxidase of Phanerochaete chrysosporium using n-propanol as substrate has been found to be higher approximately by a factor of 10(3) as compared to that using veratryl alcohol as the substrate. The method works in assaying the activity of ligninperoxidase produced by Aspergillus fumigatus indicating that it can be used for assaying the ligninperoxidase activities produced by other microorganisms also and is not limited to assaying the ligninase activity produced by Phanerochaete chrysosporium alone. Under identical experimental conditions, horseradish peroxidase does not show peroxidase activity using n-propanol as substrate indicating that the method does not interfere with the activities of other peroxidases.


Subject(s)
1-Propanol , Aspergillus fumigatus/enzymology , Benzyl Alcohols , Hydrogen-Ion Concentration , Kinetics , Peroxidases/analysis , Phanerochaete/enzymology , Substrate Specificity
6.
Acta bioquím. clín. latinoam ; 25(1): 93-9, mar. 1991. tab, ilus
Article in Spanish | LILACS | ID: lil-100840

ABSTRACT

Espermatozoides humanos fueron lavados con PBS y tratados com n-dodecil sarcosinato de sodio (Sarkosyl). El insoluble remanente estaba compuesto por cabezas, cuyas colas fueron cortadas a la altura del cuello o del segmento intermedio y cuyas membranas no sufrieron mayores danos, estando el acrosoma intacto y por pequenos corpusculos que podrian ser acrosomas aislados. Los resultados indican que la accion del detergente es de dos tipos claramente diferenciados: a)diseccion del espermatozoide con separacion de la cola y b)disolucion del mismo dejando el acrosoma intacto. El residuo conserva actividad inmunologica e inmunobiologica


Subject(s)
Humans , Male , Animals , Cell Membrane/drug effects , Detergents , Electrophoresis, Polyacrylamide Gel , Solubility , Spermatozoa/drug effects , Acrosome/drug effects , Acrosome/ultrastructure , Amino Acids/analysis , Carbohydrates/analysis , Cell Membrane/analysis , Cell Membrane/immunology , Electrophoresis, Polyacrylamide Gel , Glycoproteins/analysis , Immune Sera , Peroxidases/analysis , Spermatozoa/analysis , Spermatozoa/enzymology
8.
Yonsei Medical Journal ; : 95-100, 1981.
Article in English | WPRIM | ID: wpr-225822

ABSTRACT

An experiment was conducted in order to investigate the effect of p-dimethylaminoazobenzene (DAB) and 2(3)-tert-butyl-4-hydroxyanisole (BHA) on the lipid peroxidation and peroxide-destroying enzyme system in the rat liver. Dietary supplementation of DAB (0.06%) for three weeks caused the elevation of glutathione-S-transferase activity by 60% and glutathione reductase by 50%, but it decreased glutathione peroxidase and catalase activities significantly. Dietary supplementation of BHA (0.75%) also increased glutatione-S-transferase activity in the liver by 2 folds, and it counteracts DAB effect on the glutathione peroxidase and catalase activities. There was a marked increase in malon-dialdehyde content in the postnuclear fraction of liver by the treatment of DAB, but the addition of BHA lowered the malondialdehyde content to almost the control level. The protective effect of BHA on the lipid peroxidation induced by DAB administration at the enzyme level seems to be due to the induction of glutathione-S-transferase and the protection of glutathione peroxidase and catalase activities from being lowered by DAB administration.


Subject(s)
Male , Rats , Animals , Anisoles/pharmacology , Butylated Hydroxyanisole/pharmacology , Glutathione Peroxidase/analysis , Glutathione Reductase/analysis , Glutathione Transferase/analysis , Lipid Peroxides/metabolism , Liver/drug effects , Liver/metabolism , Peroxidases/analysis , p-Dimethylaminoazobenzene/pharmacology
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