Orlino E N, Olmstead C E, Lazareff J A, Peacock W J, Fisher R S, Fluharty A L
Department of Psychiatry and Biobehavioral Science, University of California, School of Medicine, Los Angeles 90095, USA.
Biochem Mol Med. 1997 Jun;61(1):41-6. doi: 10.1006/bmme.1997.2595.
A direct (as opposed to competitive) enzyme immunoassay (EIA) was developed to detect neuron-specific enolase (NSE) in cerebrospinal fluid (CSF). Most common methods of evaluating NSE levels have utilized radioimmunoassay. These are highly sensitive, but cannot be employed in laboratories not equipped or licensed for the use of radioisotopes. The EIA developed here shows sensitivity within the physiological range of values for CSF-NSE (> I ng/ml) and can be used in laboratories with appropriate densitometric scanning capabilities. The assay was applied to CSF samples obtained from patients with a variety of diagnoses at the time of surgical intervention for their respective disorders. While there were no diagnostically significant differences between the level of NSE in CSF from patients with different neurological disorders utilized in the development of this procedure, we were able to differentiate between marginally different levels of NSE. We conclude that we have developed a safe, fast, reliable, and sensitive assay for NSE in the CSF that can be used to study NSE levels in a variety of neurological cases.
为检测脑脊液(CSF)中的神经元特异性烯醇化酶(NSE),开发了一种直接(而非竞争性)酶免疫测定法(EIA)。评估NSE水平的最常用方法是放射免疫测定法。这些方法高度灵敏,但未配备或未获放射性同位素使用许可的实验室无法采用。此处开发的EIA在CSF - NSE的生理值范围内(>1 ng/ml)显示出敏感性,并且可在具有适当光密度扫描能力的实验室中使用。该测定法应用于在各自疾病的手术干预时从患有各种诊断的患者获得的CSF样本。虽然在此程序开发中使用的不同神经疾病患者的CSF中NSE水平之间没有诊断上的显著差异,但我们能够区分略有不同的NSE水平。我们得出结论,我们已经开发出一种用于CSF中NSE的安全、快速、可靠且灵敏的测定法,可用于研究各种神经病例中的NSE水平。