Schmidt Elizabeth M S, Escribano Damián, Martinez-Subiela Silvia, Martinez-Miró Silvia, Hernández Fuensanta, Tvarijonaviciute Asta, Cerón José J, Tecles Fernando
Department of Veterinary Clinical Sciences, School of Veterinary Medicine and Animal Science, São Paulo State University (FMVZ - UNESP), campus of Botucatu. Rua Dr. Walter Maurício Correa, s/n, Botucatu, SP, 18618-681, Brazil.
Interdisciplinary Laboratory of Clinical Analysis (Interlab-UMU), Veterinary Clinical Hospital, Campus of Excellence Mare Nostrum, University of Murcia, Espinardo-Murcia, 30100, Spain.
BMC Vet Res. 2016 Oct 28;12(1):242. doi: 10.1186/s12917-016-0871-9.
Leptin has been measured in human in saliva samples. However, the low leptin concentration found in this biological fluid makes necessary the use of high sensitive methods. To the authors' knowledge, leptin has not been measured in porcine saliva. This study aimed to develop and validate a time-resolved immunofluorometric assay (TR-IFMA) for salivary leptin measurements in pigs, using a species-specific antibody, and to evaluate how salivary leptin changes with body weight, food ingestion, and in experimental models of stress and inflammation. Polyclonal antibodies were produced in rabbits immunized with recombinant porcine leptin and used to develop a sandwich TR-IFMA.
The method had intra-assay and inter-assay coefficients of variation lower than 10 and 16 %, respectively. The assay was accurate and the low limit of detection allowed detection of leptin in all analyzed samples. Salivary leptin concentration was positively correlated to body weight (r = 0.58, P = 0.01) and increased after food ingestion (P < 0.001) and after 24 h of applying a model of experimental inflammation by turpentine injection (P < 0.05). However, it did not significantly change after a model of acute stress consisting of a nose snare restraining.
These results indicate that the developed assay can measure leptin in porcine saliva in a reliable way and that leptin in saliva is influenced by body weight, food ingestion and inflammation.
已对人类唾液样本中的瘦素进行了检测。然而,在这种生物体液中发现的瘦素浓度较低,因此需要使用高灵敏度的方法。据作者所知,尚未对猪唾液中的瘦素进行检测。本研究旨在开发并验证一种使用种特异性抗体检测猪唾液中瘦素的时间分辨免疫荧光测定法(TR-IFMA),并评估唾液瘦素如何随体重、食物摄入以及应激和炎症实验模型而变化。用重组猪瘦素免疫兔子制备多克隆抗体,并用于开发夹心TR-IFMA。
该方法的批内和批间变异系数分别低于10%和16%。该测定准确,检测下限允许在所有分析样本中检测到瘦素。唾液瘦素浓度与体重呈正相关(r = 0.58,P = 0.01),食物摄入后(P < 0.001)以及通过松节油注射应用实验性炎症模型24小时后升高(P < 0.05)。然而,在由鼻圈套约束组成的急性应激模型后,它没有显著变化。
这些结果表明,所开发的测定法能够可靠地检测猪唾液中的瘦素,并且唾液中的瘦素受体重、食物摄入和炎症的影响。