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1.
Braz. j. med. biol. res ; 45(11): 1002-1010, Nov. 2012. ilus
Article in English | LILACS | ID: lil-650578

ABSTRACT

Ricinus communis L. is of great economic importance due to the oil extracted from its seeds. Castor oil has been used for pharmaceutical and industrial applications, as a lubricant or coating agent, as a component of plastic products, as a fungicide or in the synthesis of biodiesel fuels. After oil extraction, a castor cake with a large amount of protein is obtained. However, this by-product cannot be used as animal feed due to the presence of toxic (ricin) and allergenic (2S albumin) proteins. Here, we propose two processes for detoxification and allergen inactivation of the castor cake. In addition, we establish a biological test to detect ricin and validate these detoxification processes. In this test, Vero cells were treated with ricin, and cell death was assessed by cell counting and measurement of lactate dehydrogenase activity. The limit of detection of the Vero cell assay was 10 ng/mL using a concentration of 1.6 x 10(5) cells/well. Solid-state fermentation (SSF) and treatment with calcium compounds were used as cake detoxification processes. For SSF, Aspergillus niger was grown using a castor cake as a substrate, and this cake was analyzed after 24, 48, 72, and 96 h of SSF. Ricin was eliminated after 24 h of SSF treatment. The cake was treated with 4 or 8% Ca(OH)2 or CaO, and both the toxicity and the allergenic properties were entirely abolished. A by-product free of toxicity and allergens was obtained.


Subject(s)
Animals , Allergens/drug effects , Aspergillus niger/growth & development , Calcium Compounds/pharmacology , Ricinus communis/drug effects , Inactivation, Metabolic , Allergens/toxicity , Aspergillus niger/drug effects , Chlorocebus aethiops , Ricinus communis/toxicity , Cell Death/drug effects , Cell Degranulation/drug effects , Enzyme Activation , Fermentation , L-Lactate Dehydrogenase/metabolism , Mast Cells/drug effects , Ricin/isolation & purification , Ricin/toxicity , Time Factors , Toxicity Tests , /isolation & purification , /toxicity , Vero Cells
2.
Braz. j. med. biol. res ; 39(11): 1435-1444, Nov. 2006. ilus, graf
Article in English | LILACS | ID: lil-437826

ABSTRACT

Evidence based on immunological cross-reactivity and anti-diabetic properties has suggested the presence of insulin-like peptides in plants. The objective of the present study was to investigate the presence of insulin-like proteins in the leaves of Bauhinia variegata ("pata-de-vaca", "mororó"), a plant widely utilized in popular medicine as an anti-diabetic agent. We show that an insulin-like protein was present in the leaves of this plant. A chloroplast protein with a molecular mass similar to that of bovine insulin was extracted from 2-mm thick 15 percent SDS-PAGE gels and fractionated with a 2 x 24 cm Sephadex G-50 column. The activity of this insulin-like protein (0.48 mg/mL) on serum glucose levels of four-week-old Swiss albino (CF1) diabetic mice was similar to that of commercial swine insulin used as control. Further characterization of this molecule by reverse-phase hydrophobic HPLC chromatographic analysis as well as its antidiabetic activity on alloxan-induced mice showed that it has insulin-like properties. Immunolocalization of the insulin-like protein in the leaves of B. variegata was performed by transmission electron microscopy using a polyclonal anti-insulin human antibody. Localization in the leaf blades revealed that the insulin-like protein is present mainly in chloroplasts where it is also found associated with crystals which may be calcium oxalate. The presence of an insulin-like protein in chloroplasts may indicate its involvement in carbohydrate metabolism. This finding has strengthened our previous results and suggests that insulin-signaling pathways have been conserved through evolution.


Subject(s)
Animals , Cattle , Mice , Bauhinia/chemistry , Chloroplasts/chemistry , Diabetes Mellitus, Experimental/drug therapy , Hypoglycemic Agents/isolation & purification , Insulin-Like Growth Factor Binding Proteins/isolation & purification , Plant Leaves/chemistry , Autoantibodies/blood , Bauhinia/cytology , Chromatography, High Pressure Liquid , Chloroplasts/ultrastructure , Electrophoresis, Polyacrylamide Gel , Hypoglycemic Agents/therapeutic use , Immunoglobulin G/blood , Insulin-Like Growth Factor Binding Proteins/therapeutic use , Microscopy, Electron, Transmission , Plant Leaves/cytology
3.
Mem. Inst. Oswaldo Cruz ; 99(6): 559-562, Oct. 2004. tab
Article in English | LILACS | ID: lil-387900

ABSTRACT

Dengue is an infectious disease of viral etiology transmitted by the mosquitoes Aedes aegypti, A. albopictus, and A. scutellaris. It can develop either as a benign form or as a severe hemorrhagic form. Previous work showed an association of the hemorrhagic form with human leukocyte antigens (HLA), suggesting a role of genetic factors in disease susceptibility. Nevertheless, data on HLA association with the classical form of the disease is scarce in literature. Sixty-four patients and 667 normal individuals, living in the state of Paraná, Southern Brazil, were used as test and control group, respectively. The patients developed the disease during a virus 1 dengue outbreak either in Maringá city in 1995 (47) or in Paranavaí city in 1999 (17). The diagnostic was confirmed through serology and/or viral culture. HLA class I and II typing was performed by the classical microlynfocitotoxicity test using monoclonal antisera and fluorobeads. Qui-square statistical analysis confirmed a positive association with HLA-DQ1 (76.6 percent vs 57.7 percent; p = 0.005243; pc = 0.026215). HLA-DR1 also presented an increased frequency in the test group, not statistically significant after p correction though (32.8 percent vs 15.9 percent; p = 0.005729; pc = 0.080206). In conclusion, genetic factors may play a role on the susceptibility to the classical dengue, virus 1, in the Brazilian population. Further independent studies should be performed in the Brazilian population to confirm these preliminary data.


Subject(s)
Humans , Male , Female , Dengue , Dengue Virus , Genetic Predisposition to Disease , HLA Antigens , Brazil , Case-Control Studies , Risk Factors
5.
Braz. j. med. biol. res ; 36(9): 1167-1173, Sept. 2003. ilus, tab, graf
Article in English | LILACS | ID: lil-342857

ABSTRACT

Since the discovery of bovine insulin in plants, much effort has been devoted to the characterization of these proteins and elucidation of their functions. We report here the isolation of a protein with similar molecular mass and same amino acid sequence to bovine insulin from developing fruits of cowpea (Vigna unguiculata) genotype Epace 10. Insulin was measured by ELISA using an anti-human insulin antibody and was detected both in empty pods and seed coats but not in the embryo. The highest concentrations (about 0.5 ng/æg of protein) of the protein were detected in seed coats at 16 and 18 days after pollination, and the values were 1.6 to 4.0 times higher than those found for isolated pods tested on any day. N-terminal amino acid sequencing of insulin was performed on the protein purified by C4-HPLC. The significance of the presence of insulin in these plant tissues is not fully understood but we speculate that it may be involved in the transport of carbohydrate to the fruit


Subject(s)
Animals , Cattle , Insulin , Plant Proteins , Plants , Sequence Homology, Amino Acid , Blotting, Western , Chromatography, High Pressure Liquid , Electrophoresis, Polyacrylamide Gel , Enzyme-Linked Immunosorbent Assay , Insulin , Molecular Weight , Plant Proteins , Plants
6.
Braz. j. med. biol. res ; 33(2): 191-8, Feb. 2000.
Article in English | LILACS | ID: lil-252294

ABSTRACT

The presence of phaseolin (a vicilin-like 7S storage globulin) peptides in the seed coat of the legume Phaseolus lunatus L. (lima bean) was demonstrated by N-terminal amino acid sequencing. Utilizing an artificial seed system assay we showed that phaseolin, isolated from both cotyledon and testa tissues of P. lunatus, is detrimental to the nonhost bruchid Callosobruchus maculatus (F) (cowpea weevil) with ED50 of 1.7 and 3.5 percent, respectively. The level of phaseolin in the seed coat (16.7 percent) was found to be sufficient to deter larval development of this bruchid. The expression of a C. maculatus-detrimental protein in the testa of nonhost seeds suggests that the protein may have played a significant role in the evolutionary adaptation of bruchids to legume seeds


Subject(s)
Animals , Coleoptera/physiology , Fabaceae/chemistry , Plant Proteins/isolation & purification , Seeds/chemistry , Amino Acid Sequence , Plant Diseases/parasitology , Plant Proteins/analysis
7.
Rev. Soc. Argent. Ginecol. Infanto Juvenil ; 6(1): 3-14, 1999. ilus, graf
Article in Spanish | LILACS | ID: lil-243440

ABSTRACT

Objetivos: Valorar indicadores psicológicos, sociales y físicos así como hallazgos génito-anales y Enfermedades Sexualmente Transmisibles (EST) en 70 casos certeros de Abuso Sexual (AS). Resultados: Hallazgos génito-anales: * Grupo IA Normal 8,70 por ciento. * Grupo IB Inespecíficos 13,04 por ciento. * Grupo II Sugestivo Abuso Sexual (SAS) 42,03 por ciento. * Grupo III Concluyente Abuso Sexual (ConAS) 34,78 por ciento. * Grupo IV Certeza Abuso Sexual (CerAS) 1,45 por ciento. Hallazgos microbiológicos: Grupo I (Inespecífico): Flora endógena 58,62 por ciento, Patógenos Respiratorios 6,90 por ciento o Intestinales 6,90 por ciento. Grupo II (SAS): G. vaginalis 6,90 por ciento, U. urealyticum 3,45 por ciento, HSV, HPV. Grupo III (ConAS): G. trachomatis > 4 años 31,82 por ciento; T. vaginales > 1 año 3,45 por ciento. Grupo IV (CerAS): N. gonorrhoeae; Sífilis; HIV. Conclusiones: 1. Relato de la niña en 87,14 por ciento; 2. AS intrafamiliar 68,57 por ciento, AS extrafamiliar 24,28 por ciento y no supo en 7,14 por ciento; 3. De los casos intrafamiliares, en 43,75 por ciento el abusador fue el padre; 4. Hallazgos genito-anales SAS 42,03 por ciento y ConAS 34,78 por ciento. Estos índices se modifican a 33,33 por ciento y 46,37 por ciento, al incorporar EST en el criterio diagnóstico; 5. Si bien la vulvovaginitis es un signo inespecífico, el hallazgo de EST en 31,03 por ciento obliga a cultivar las niñas con flujo persistente y/o intermitente; 6. Violencia familiar 45,71 por ciento y alcoholismo y otras drogas 27,14 por ciento; 7. Antecedentes AS en madre o padre 27,14 por ciento; 8. Trastornos escolares 46,15 por ciento; 9. Pareja parental oroginal ya no existía en 70 por ciento


Subject(s)
Humans , Female , Child, Preschool , Child Abuse, Sexual/diagnosis , Rape/diagnosis , Child Abuse, Sexual/psychology , Child Abuse, Sexual/statistics & numerical data , Child Abuse/diagnosis , Sanitary Surveys, Water Supply , Sex Offenses/statistics & numerical data , Socioeconomic Factors , Rape/statistics & numerical data , Rape/psychology
8.
Braz. j. med. biol. res ; 26(2): 163-6, Feb. 1993. graf
Article in English | LILACS | ID: lil-148681

ABSTRACT

Snake venoms usually contain multiple molecular forms of phospholipase A2 enzymes (phosphatide acyl hydrolase, E.C. 3.1.1.4; PLA2). Phospholipases A2 induce a wide range of pharmacological effects which may depend or not on the hydrolysis of phospholipids. In this study, a PLA2 from Bothrops jararaca venom was purified to homogeneity by gel filtration on a Sephacryl S-200 column, followed by FPLC reverse-phase chromatography on a Pep-RPC HR 5/5 column (yield 1.63 per cent of venom protein). The PLA2 activity of the fractions was determined by indirect hemolysis using hen's egg yolk lecithin as substrate. The enzyme is an acidic protein with PI 4.5 and an apparent molecular weight of 14,200, as estimated by gel filtration on a Superose 12 FPLC column. Similar properties have been described for PLA2 from other snake venoms. The N-terminal-sequence of the purified protein was NLMQFETMIMXXAGQ. These partial sequence data show a high degree of homology between the B. jararaca PLA2 and the enzymes from other snake venoms as well as bovine pancreatic PLA2


Subject(s)
Animals , Phospholipases A/isolation & purification , Crotalid Venoms/chemistry , Amino Acid Sequence , Bothrops , Chromatography , Chromatography, Gel , Molecular Sequence Data , Sequence Alignment , Sequence Homology, Amino Acid , Crotalid Venoms/isolation & purification
9.
Braz. j. med. biol. res ; 25(6): 567-82, 1992. ilus
Article in English | LILACS | ID: lil-109071

ABSTRACT

A 1.9s albumin having allergenic activity and denoted Ric c III was isolated from an alcohol extract of defatted Ricinus communis seeds CB-1A, as a homogeneous protein by ion -exchange chromatography on SP-Sephadex, gel filtration on Sephadex G-75 and preparative polyacrylamide gel electrophoresis (6 mg Ric cIII/g CB-1A). The protein contained approximately 98 amino acid residues distributed in 2 chains of 67 anmd 34 residues, a molecular weight of 11.239 based on amino acid composition and pI=4.9 Ric c III can be aligned, on the basis of amino acid composition and partial amino acid sequence data, with residues 18 to 50 (51) and 66 to 130 of the 2S albumin precursor predicted by the cDNA data of S. D. Irwin, J. N. Ken, J. B. C. Findlary and J. M. Lord (Molecular and General Genetics, 222:400-408, 1990). The present data identify Ric c III as the second allergenic 2S storage albumin coded by this DNA


Subject(s)
Albumins , Allergens/pharmacology , Ricinus/isolation & purification , Plant Proteins, Dietary
10.
Braz. j. med. biol. res ; 24(2): 141-3, 1991. tab
Article in English | LILACS | ID: lil-99447

ABSTRACT

Antigen 5.1 was isolated from the most acidic fraction of castor bean allergens (CB-1A) by gel filtration on Sephadex G-75 followed by polyacrylamide gel electrophoresis (PAGE) (yield: 6.2 mg antigen 5.1/g CB-1A). This antigen was homogeneous by the criteria of PAGE, isoelectric focusing, SDS-PAGE, immunoelectrophoresis and gel filtration. The antigen has an apparent molecular mass of 12 ñ 2 kDa and an isoelectric point of pH 5.1. Antigen 5.1 lacks proline, phenylalanine, threonine and tryptophan. It was immunochemically identical to one of the three immunoprecipitation lines presented by CB-1A by the Ouchterlony technique, and was positive when tested (250 *g) by IgE-mediated passive cutaneous anaphylaxis in LOU.M rats


Subject(s)
Antigens/isolation & purification , Seeds , Ricinus communis/immunology , Allergens/analysis , Amino Acids/analysis , Chromatography, Gel
11.
J. bras. med ; 59(4): 22-4, out. 1990. ilus, tab
Article in Portuguese | LILACS | ID: lil-206718

ABSTRACT

Os autores relatam o caso de um paciente de 35 anos, pardo, pedreiro, portador de adenomas sebáceos na face diagnosticados por biópsia, com poucos sintomas respiratórios, cuja radiografia de tórax revelou infiltrado interticial de base e a prova funcional respiratória, padräo restritivo leve. A seguir, tecem comentários sobre a esclerose tuberosa em suas formas completa e incompleta e o envolvimento pulmonar nesta doença correlacionando com o quadro em questäo.


Subject(s)
Humans , Male , Adult , Adenoma/etiology , Lung Neoplasms/etiology , Tuberous Sclerosis/complications , Tuberous Sclerosis/pathology
12.
An. acad. bras. ciênc ; 62(1): 17-24, mar. 1990. tab
Article in English | LILACS | ID: lil-92236

ABSTRACT

A glycoprotein, RC-13, isolated from Ricinus communis seeds was reduced, S-alkylated and cleaved by trypsin. The tryptic digest was fractionated by ion-exchange chromatography and a glycopeptide was isolated and purified by high-voltage paper electrophoresis. When submitted to amino acid and carbohydrate analyses this major glycopeptide showed the following chemical composition: Lys1, Asp1, Thr2, Ser4, Glu1, Pro2, Gly2, Ala2, Val2, GlcN6, Man6 and Gal8. Hydrazynolysis positioned Ser as the C-terminal residue. It is postulated that this glycopeptide belongs to the C-terminal region of the allergen


Subject(s)
Allergens/isolation & purification , Amino Acids/analysis , Ricinus communis/analysis , Glycopeptides/isolation & purification , Seeds/analysis , Peptide Mapping
14.
Rev. argent. anestesiol ; 44(3): 219-23, jul.-sept. 1986. tab
Article in Spanish | LILACS | ID: lil-38666

ABSTRACT

Está planteada la controversia entre el uso de la ventilación mecánica "profiláctica" y la extubación precoz de los pacientes sometidos a cirugía cardiovascular. En este trabajo analizamos morbilidad, mortalidad e incidencia de reintubación en 130 pacientes pediátricos operados en nuestro centro, en los cuales aplicamos parámetros definidos para decidir o no la extubación precoz al término de la operación. En los 93 pacientes extubados precozmente solo fueron reintubados 4 (4.3%), por complicaciones. La mortalidad de este grupo fue del 0%. En los 37 pacientes no extubados 27 (73%) presentaron complicaciones y la mortalidad fue 8 casos (21.6%). Concluimos que los parámetros de extubación precoz son confiables y que la ventilación mecánica no debe utilizarse en forma rutinaria e indiscriminada


Subject(s)
Infant , Child, Preschool , Cardiovascular Surgical Procedures , Intubation, Intratracheal , Pediatrics , Respiration, Artificial/methods
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