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Salivary and urinary metabolome analysis for pre-puberty-related biomarkers identification in porcine

机译:唾液和尿液代谢组分析可鉴定猪青春期前的生物标志物

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摘要

Estrus synchronization is important for optimal management of gilt reproduction in pig farms. Hormonal treatments, such as synthetic progestogens, are used on a routine basis, but there is a growing demand for non-hormonal alternative breeding tools. Before puberty, gilts exhibit a ‘waiting period,’ related to the ovarian development and gonadotrophin secretions, during which external stimulations, such as boar exposure, could induce and synchronize first ovulation. Practical non-invasive tools for identification of this period in farms are lacking. During this period, urinary oestrone levels are high, but urine sampling is difficult in group-housed females. The aim of this work was to search for specific biomarkers of the ‘waiting period’ in saliva and urine. In total, nine 144- to 147-day-old Large White gilts were subjected to trans-abdominal ultrasonography three times a week for 5 weeks until puberty detection (week –5 to week –1 before puberty). Urine and saliva samples were collected for oestrone assay to detect the ‘waiting period’ and for metabolome analysis using 1H-nuclear magnetic resonance spectroscopy to detect potential biomarkers of the ‘waiting period.’ Gilts were slaughtered 7 days after puberty detection for puberty confirmation. Results were consistent with ultrasonography data for six gilts. Urine and saliva samples from these six gilts were analyzed. Urinary estrone concentration significantly increased 2 weeks before puberty detection. Metabolome analysis of urine samples allowed the identification of 78 spectral bins, among them, 42 low-molecular-weight metabolites were identified. Metabolome analysis of salivary samples allowed the identification of 59 spectral bins, among them, 23 low-molecular-weight metabolites were detected and 17 were identified. No potential biomarker was identified in urinary samples. In saliva, butyrate and 2HOvalerate, 5.79 ppm (putatively uridine), formate, malonate and propionate could be biomarker candidates to ascertain the pre-puberty period in gilt reproduction. These results confirm that non-invasive salivary samples could allow the identification of the physiological status of the gilts and presumably the optimal time for application of the boar effect. This could contribute to synchronize puberty onset and hence to develop non-hormonal breeding tools.
机译:发情同步对于猪场优化后备母猪繁殖非常重要。激素治疗,例如合成孕激素,是常规使用,但对非激素替代育种工具的需求正在增长。在青春期之前,后备母猪表现出一个“等待期”,与卵巢发育和促性腺激素分泌有关,在此期间,外部刺激(如公猪暴露)可以诱导并同步首次排卵。缺乏在农场中识别这一时期的实用无创工具。在此期间,尿雌酮水平很高,但在成群饲养的女性中很难进行尿液采样。这项工作的目的是寻找唾液和尿液中“等待期”的特定生物标记。总共对9具144至147天的大白小母猪每周进行3次经腹超声检查,共5周,直到青春期被检测到(青春期前第5-1周至第-1周)。收集尿液和唾液样本进行雌激素测定,以检测“等待期”,并使用 1 H核磁共振波谱分析代谢组,以检测“等待期”的潜在生物标志物。将Gil猪屠宰7检测青春期后的天数以确认青春期。结果与六个小母猪的超声检查数据一致。分析了这六个后备母猪的尿液和唾液样本。青春期前2周尿雌酮浓度显着增加。尿液样品的代谢组学分析可以鉴定78个光谱区,其中鉴定出42种低分子量代谢物。唾液样品的代谢组学分析可鉴定出59个光谱区,其中检测出23种低分子量代谢物,鉴定出17种。在尿液样本中未发现潜在的生物标志物。在唾液中,丁酸盐和2HO戊酸盐中,5.79 ppm(可能是尿苷),甲酸盐,丙二酸盐和丙酸盐可作为生物标志物的候选物,以确定青春期后备母猪繁殖。这些结果证实,非侵入性唾液样品可以鉴定后备母猪的生理状态,并可能是应用公猪效应的最佳时间。这可能有助于同步青春期发作,从而开发非激素育种工具。

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