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1.
Reprod Domest Anim ; 57(5): 515-523, 2022 May.
Artículo en Inglés | MEDLINE | ID: mdl-35088462

RESUMEN

The objective was to compare effects of encapsulated or free glutathione (GSH) on the quality of frozen-thawed bull sperm. Ejaculates were collected via artificial vagina from six mature Holstein bulls once weekly for 6 weeks. All ejaculates had motility ≥70%, sperm concentration ≥1.0 × 109 /ml and ≤15% morphologically abnormal sperm. Each week, semen was pooled and diluted with lecithin-based extenders containing various concentrations of encapsulated (E0, E1, E2.5 and E5 mM) or free (F0, F1, F2.5 and F5 mM) GSH, with total glutathione content determined before and after cryopreservation. Total GSH in fresh semen was (mean+SEM) 4.8 ± 0.2 nmol/108 sperm, whereas in frozen-thawed semen of group F0 (control), it decreased to 1.4 ± 0.2 nmol/108 sperm, a 70.8% reduction (p < .05). In addition, total GSH in frozen-thawed semen from groups E2.5, E5 and F5 were 2.4 ± 0.2, 2.8 ± 0.2 and 1.8 ± 0.2 nmol/108 sperm, respectively (E5 versus. F0, p < .05). Compared to group F0, frozen-thawed sperm from group E2.5 had greater (p < .05) percentages of sperm that were viable (Annexin-V) (61.1 ± 1.8 versus. 71.1 ± 1.8) and that had cell membrane integrity (eosin-nigrosin) (64.5 ± 3.1 versus. 80.0 ± 3.1). Furthermore, frozen-thawed sperm from group E2.5 had the numerically highest total and progressive motility (CASA) and cell membrane functionality (HOS) and the lowest percentage of early apoptotic sperm (Annexin-V). However, acrosome membrane integrity (PSA) of E5 had the lowest mean (p < .05), whereas E2.5 caused a small nonsignificant decrease (69.1 ± 1.4%) compared to E0 and F0. In conclusion, 2.5 mM encapsulated GSH in semen extender significantly improved the quality of frozen-thawed bull sperm.


Asunto(s)
Preservación de Semen , Motilidad Espermática , Animales , Anexinas , Bovinos , Criopreservación/veterinaria , Crioprotectores/farmacología , Medios de Cultivo/farmacología , Suplementos Dietéticos , Congelación , Glutatión/farmacología , Masculino , Análisis de Semen/veterinaria , Preservación de Semen/veterinaria , Espermatozoides
2.
Microb Pathog ; 106: 78-84, 2017 May.
Artículo en Inglés | MEDLINE | ID: mdl-28188900

RESUMEN

In the present study, we isolated Lactobacillus sakei strain DGH5 from raw beef meat. This bacterium plays an inhibitory effect against food-spoiling bacteria and food-borne pathogens, including Listeria monocytogenes, a gram-positive and pathogenic bacterium. Lactobacillus sakei strain DGH5 was identified through both phenotypical and biochemical tests accompanied with 16S rRNA sequence analysis. Among all the sources of carbon, nitrogen and phosphorous forms, we selected the most potent compounds to optimize the condition for the highest antagonistic activity. Among the sugars, polygalacturonic acid demonstrated to improve the antagonistic activity. Ammonium nitrate demonstrated to be suitable nitrogen sources. Amongst phosphorous sources, disodium hydrogen phosphate had the greatest antagonistic effect. According to Taguchi's orthogonal array, temperature, disodium hydrogen phosphate and soy Peptone had significant effect on antagonistic activity. Furthermore, mean comparisons showed that the optimum conditions achieved at pH 6.0, 25 °C temperature, 1.5% (w/v) Na2HPO4 and 0.5% (w/v) peptone.


Asunto(s)
Antibiosis , Microbiología de Alimentos , Latilactobacillus sakei/crecimiento & desarrollo , Latilactobacillus sakei/aislamiento & purificación , Latilactobacillus sakei/fisiología , Análisis de Varianza , Animales , Bovinos , Recuento de Colonia Microbiana , ADN Bacteriano , Bacterias Grampositivas/efectos de los fármacos , Bacterias Grampositivas/crecimiento & desarrollo , Concentración de Iones de Hidrógeno , Latilactobacillus sakei/genética , Listeria monocytogenes/efectos de los fármacos , Listeria monocytogenes/crecimiento & desarrollo , Carne/microbiología , Nitratos/metabolismo , Nitrógeno/metabolismo , Pectinas/antagonistas & inhibidores , Peptonas/antagonistas & inhibidores , Fosfatos/antagonistas & inhibidores , Filogenia , ARN Ribosómico 16S/genética , Análisis de Secuencia , Temperatura
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