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对照患者和帕金森病患者脑脊液中多巴胺-β-羟化酶的夹心酶免疫测定法

Sandwich enzyme immunoassay of dopamine-?-hydroxylase in cerebrospinal fluid from control and parkinsonian patients.

作者信息

Mogi M, Harada M, Kojima K, Inagaki H, Kondo T, Narabayashi H, Arai T, Teradaira R, Fujita K, Kiuchi K, Nagatsu T

机构信息

Department of Oral Biochemistry, Matsumoto Dental College, Shiojiri 399-07, Japan.

出版信息

Neurochem Int. 1988;12(2):187-91. doi: 10.1016/0197-0186(88)90126-x.

Abstract

A sandwich enzyme immunoassay (EIA) was established by using purified human serum dopamine-?-hydroxylase (DBH) as a standard protein and a monospecific polyclonal antibody raised against human DBH purified from human pheochromocytoma. The EIA was applied to measuring DBH levels in human CSF from Parkinsonian patients and control patients devoid of neurological diseases. The control group had DBH content of 21.1 +/- 3.1 ng/ml CSF and DBH activity of 24.0 +/- 3.7 ? U/ml CSF, and Parkinsonian group 3.3 ? 0.7 ng/ml CSF (16% of control) and 4.6 +/- 0.7 ?U/ml CSF (19% of control) (mean +/- SEM). Thus, both DBH content and DBH activity in CSF were reduced in Parkinsonian patients to less than 20% of the control values (P $ ? 0.005 ). However, the specific activity (units of enzyme activity/mg of DBH protein) in CSF of Parkinsonian patients was similar to that of control patients. These results suggest that the reduced DBH activity in CSF from Parkinsonian patients is caused by a reduction in DBH protein content, and is not due to production of an inactive form of DBH, for example, by combining with endogenous inhibitor(s). These data support our previous findings that DBH activities in the Parkinsonian brain and CSF are decreased.

摘要

通过使用纯化的人血清多巴胺-β-羟化酶(DBH)作为标准蛋白以及针对从人嗜铬细胞瘤中纯化的人DBH产生的单特异性多克隆抗体,建立了一种夹心酶免疫测定法(EIA)。该EIA用于测量帕金森病患者和无神经系统疾病的对照患者脑脊液中的DBH水平。对照组脑脊液中DBH含量为21.1±3.1 ng/ml,DBH活性为24.0±3.7?U/ml脑脊液,帕金森病组为3.3?0.7 ng/ml脑脊液(对照组的16%)和4.6±0.7?U/ml脑脊液(对照组的19%)(平均值±标准误)。因此,帕金森病患者脑脊液中的DBH含量和DBH活性均降至对照值的20%以下(P $?0.005)。然而,帕金森病患者脑脊液中的比活性(酶活性单位/mg DBH蛋白)与对照患者相似。这些结果表明,帕金森病患者脑脊液中DBH活性降低是由DBH蛋白含量降低引起的,而不是由于产生了无活性形式的DBH,例如与内源性抑制剂结合。这些数据支持了我们之前的发现,即帕金森病患者大脑和脑脊液中的DBH活性降低。

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