School of Anthropology, University of Arizona, Tucson, AZ 85721, USA; Cognitive Science Program, University of Arizona, Tucson, AZ 85721, USA.
Department of Psychology and Program in Neuroscience, The Florida State University, Tallahassee, FL 32306, USA.
Psychoneuroendocrinology. 2021 Oct;132:105368. doi: 10.1016/j.psyneuen.2021.105368. Epub 2021 Jul 26.
Oxytocin has garnered much interest due to its role in affective states, social behaviors, and diverse physiological functions. However, approaches for measuring endogenous oxytocin concentrations have generated considerable controversy and debate. Common procedures for measuring oxytocin often produce uncorrelated results, and the detected concentrations frequently vary across two orders of magnitude. These findings have led some researchers to argue that immunoassays of plasma oxytocin may be unreliable and nonspecific, particularly when samples are not first processed using an extraction procedure. Here, we assess the specificity of oxytocin immunoassays using plasma samples from wildtype (WT) and oxytocin knockout (KO) mice. Plasma samples from both genotypes were measured using immunoassay and were measured with or without a solid-phase extraction. Using a commercially available kit from Arbor Assays, we demonstrate that both techniques generate a clear contrast between genotypes, with wildtype samples containing high concentrations of oxytocin (unextracted mean = 468 pg/ml; extracted mean = 381 pg/ml), while knockout samples measured below the lower limit of detection. Analytical validations demonstrated good parallelism and spike recovery for both methods. Furthermore, the same wildtype samples measured with both procedures were highly correlated (r = 0.95), although unextracted samples measured at significantly higher concentrations (p = 2.0 ×10, Cohen's d = 2.65). To test the generalizability of these results across immunoassay kits, we performed additional assays with kits from Cayman Chemical and Enzo Life Sciences. The Cayman Chemical kit produced results similar to Arbor Assays with a clean signal differentiating WT and KO plasma, both with and without an extraction step. The Enzo kit also differentiated the genotypes, with correlation between extracted and unextracted samples, but was considerably more susceptible to interference without the extraction, as evidenced by false positive signal in KO plasma samples. The extent to which these results generalize to other species remains unknown and challenging to assess.
由于催产素在情感状态、社会行为和多种生理功能中的作用,它引起了广泛关注。然而,测量内源性催产素浓度的方法引起了相当大的争议和争论。测量催产素的常用方法通常会产生不相关的结果,并且检测到的浓度在两个数量级范围内经常变化。这些发现导致一些研究人员认为,血浆催产素的免疫测定可能不可靠和非特异性,特别是当样品未经提取程序处理时。在这里,我们使用野生型(WT)和催产素敲除(KO)小鼠的血浆样本评估催产素免疫测定的特异性。使用免疫测定法测量两种基因型的血浆样本,并测量是否进行固相萃取。使用 Arbor Assays 公司提供的商业试剂盒,我们证明两种技术都能在基因型之间产生明显的对比,野生型样本含有高浓度的催产素(未提取的平均值为 468 pg/ml;提取的平均值为 381 pg/ml),而 KO 样本的测量值低于检测下限。分析验证表明两种方法都具有良好的平行性和加标回收率。此外,两种方法测量的相同野生型样本高度相关(r=0.95),尽管未提取的样本测量浓度明显更高(p=2.0×10,Cohen's d=2.65)。为了测试这些结果在免疫测定试剂盒中的通用性,我们使用 Cayman Chemical 和 Enzo Life Sciences 的试剂盒进行了额外的测定。Cayman Chemical 试剂盒的结果与 Arbor Assays 相似,具有清晰的信号区分 WT 和 KO 血浆,无论是提取步骤还是不提取步骤。Enzo 试剂盒也区分了基因型,提取和未提取的样本之间存在相关性,但在没有提取的情况下更容易受到干扰,因为 KO 血浆样本中出现了假阳性信号。这些结果在多大程度上适用于其他物种仍然未知,并且难以评估。