Mokuno K, Kato K, Kawai K, Matsuoka Y, Yanagi T, Sobue I
J Neurol Sci. 1983 Aug-Sep;60(3):443-51. doi: 10.1016/0022-510x(83)90155-7.
Neuron-specific enolase (NSE) and S-100 protein (S-100) levels in cerebrospinal fluid (CSF) were determined in 129 patients with various neurological diseases. The chronological changes of these nervous system-specific proteins in CSF were also examined in 3 patients with acute disorders. NSE and S-100 levels were elevated in many cases with acute conditions. These specific proteins did not increase simultaneously but independently. These results suggested that NSE and S-100 in CSF would be useful markers for damage of the nervous system and that measurement of both NSE and S-100 might positively indicate whether the damage was neuronal, glial or mixed in origin. Moreover, from the serial determination of these substances, they would be better markers than cell counts and total protein in CSF for the active injury for the nervous tissues.
测定了129例患有各种神经系统疾病患者脑脊液(CSF)中神经元特异性烯醇化酶(NSE)和S-100蛋白(S-100)的水平。还对3例急性疾病患者脑脊液中这些神经系统特异性蛋白的时间变化进行了检查。在许多急性病症中,NSE和S-100水平升高。这些特异性蛋白并非同时升高,而是各自独立升高。这些结果表明,脑脊液中的NSE和S-100可能是神经系统损伤的有用标志物,同时检测NSE和S-100可能有助于明确损伤是神经元性、胶质细胞性还是混合性起源。此外,通过对这些物质的连续测定,相较于脑脊液中的细胞计数和总蛋白,它们可能是神经组织活动性损伤更好的标志物。