Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Más filtros

Bases de datos
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
Funct Integr Genomics ; 14(2): 275-83, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24652097

RESUMEN

The centipede Scolopendra subspinipes mutilans is an environmentally beneficial and medically important arthropod species. Although this species is increasingly applied as a reliable source of new antimicrobial peptides, the transcriptome of this species is a prerequisite for more rational selection of antimicrobial peptides. In this report, we isolated total RNA from the whole body of adult centipedes, S. subspinipes mutilans, that were nonimmunized and immunized against Escherichia coli, and we generated a total of 77,063 pooled contigs and singletons using high-throughput sequencing. To screen putative antimicrobial peptides, in silico analyses of the S. subspinipes mutilans transcriptome were performed based on the physicochemical evidence of length, charge, isoelectric point, and in vitro and in vivo aggregation scores together with the existence of continuous antimicrobial peptide stretches. Moreover, we excluded some transcripts that showed similarity with both previously known antimicrobial peptides and the human proteome, had a proteolytic cleavage site, and had downregulated expression compared with the nonimmunized sample. As a result, we selected 17 transcripts and tested their antimicrobial activity with a radial diffusion assay. Among them, ten synthetic peptides experimentally showed antimicrobial activity against microbes and no toxicity to mouse erythrocytes. Our results provide not only a useful set of antimicrobial peptide candidates and an efficient strategy for novel antimicrobial peptide development but also the transcriptome data of a big centipede as a valuable resource.


Asunto(s)
Péptidos Catiónicos Antimicrobianos/farmacología , Proteínas de Artrópodos/farmacología , Artrópodos/genética , Medicamentos Herbarios Chinos/metabolismo , Transcriptoma , Secuencia de Aminoácidos , Animales , Péptidos Catiónicos Antimicrobianos/síntesis química , Péptidos Catiónicos Antimicrobianos/genética , Proteínas de Artrópodos/biosíntesis , Proteínas de Artrópodos/genética , Artrópodos/inmunología , Artrópodos/microbiología , Candida albicans/efectos de los fármacos , Candida albicans/crecimiento & desarrollo , Mapeo Contig , Alcaloides Diterpénicos , Eritrocitos/citología , Eritrocitos/efectos de los fármacos , Escherichia coli/química , Escherichia coli/efectos de los fármacos , Escherichia coli/crecimiento & desarrollo , Hemólisis/efectos de los fármacos , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Inmunización , Ratones , Pruebas de Sensibilidad Microbiana , Datos de Secuencia Molecular , Pseudomonas aeruginosa/efectos de los fármacos , Pseudomonas aeruginosa/crecimiento & desarrollo , Alineación de Secuencia , Técnicas de Síntesis en Fase Sólida , Staphylococcus aureus/efectos de los fármacos , Staphylococcus aureus/crecimiento & desarrollo
2.
Acta Biochim Pol ; 54(3): 641-6, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17717607

RESUMEN

This study compared the ability of daidzein, a soy isoflavone, with that of 17beta-estradiol to prevent bone loss in cadmium (Cd)-exposed ovariectomized (OVX) rats during growth. Four week-old female Wistar rats were randomly assigned to five treatment groups of 9 rats each, either (1) sham-operated (SH); (2) OVX and placed on experimental diets (OVX); (3) OVX fed 50 ppm of CdCl2 (OVX-Cd); (4) OVX fed 50 ppm of CdCl2 and 10 microg of daidzein per kg of body mass (OVX-CD-D); or (5) OVX fed 50 ppm of CdCl2 and 10 microg of estrogen per kg of body mass (OVX-CD-E). All rats were given free access to AIN-76 modified diet and drinking water, with or without Cd, for 8 weeks. The OVX groups gained more (P < 0.05) body mass than the SH group. Femoral mass was increased by feeding daidzein and estradiol, whereas femoral length was not (P > 0.05) significantly different among groups. Femoral breaking force was not significantly different among groups, however, femoral BMD was significantly lower in OVX-Cd than in the SH and OVX groups. Morphologically proliferative cartilage and hypertrophic cells in femur showed normal distribution in OVX-Cd-D and OVX-Cd-E groups unlike those in OVX-Cd group. These findings suggest that Cd-OVX-induced osteopenia or osteoporosis probably results from an increase in bone turnover.


Asunto(s)
Huesos/efectos de los fármacos , Glycine max/química , Isoflavonas/farmacología , Ovariectomía , Animales , Densidad Ósea/efectos de los fármacos , Huesos/metabolismo , Cadmio/toxicidad , Calcio/metabolismo , Estradiol/farmacología , Femenino , Fémur/efectos de los fármacos , Fémur/metabolismo , Ratas , Ratas Wistar
3.
J Med Food ; 11(3): 479-85, 2008 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-18800895

RESUMEN

The biochemical mechanisms of Chlorella vulgaris protection against cadmium (Cd)-induced liver toxicity were investigated in male Sprague-Dawley rats (5 weeks of age, weighing 90-110 g). Forty rats were randomly divided into one control and three groups treated with 10 ppm Cd: one Cd without Chlorella (Cd-0C), one Cd with 5% Chlorella (Cd-5C), and one Cd with 10% Chlorella (Cd-10C) groups. The rats had free access to water and diet for 8 weeks. Body weight gain and relative liver weight were significantly lower in the Cd-0C group than in Cd-5C and Cd-10C groups. Rats in the Cd-0C group had significantly higher hepatic concentrations of Cd and metallothioneins (MTs) than in the Cd-5C or Cd-10C group. The hepatic MT I/II mRNA was expressed in all experimental rats. MT II was more expressed in the Cd-5C and Cd-10C groups than in the Cd-0C group. Morphologically, a higher level of congestion and vacuolation was observed in the livers of the Cd-0C group compared to those of the Cd-5C and Cd-10C groups. Therefore, this study suggests that C. vulgaris has a protective effect against Cd-induced liver damage by reducing Cd accumulation and stimulating the expression of MT II in liver. However, the details of the mechanism of C. vulgaris on liver toxicity remains to be clarified by further studies.


Asunto(s)
Intoxicación por Cadmio/tratamiento farmacológico , Cadmio/metabolismo , Chlorella vulgaris , Hepatopatías/prevención & control , Hígado/fisiopatología , Metalotioneína/genética , Metalotioneína/metabolismo , Animales , Peso Corporal/efectos de los fármacos , Cadmio/toxicidad , Intoxicación por Cadmio/genética , Enfermedad Hepática Inducida por Sustancias y Drogas , Suplementos Dietéticos , Hepatocitos , Hiperemia , Hígado/efectos de los fármacos , Masculino , Tamaño de los Órganos , Polvos , Ratas
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA