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精神分裂症患者血清中肌酸激酶BB的放射免疫测定

Radioimmunoassay measurement of creatine kinase BB in the serum of schizophrenic patients.

作者信息

Lerner M H, Friedhoff A J

出版信息

Clin Chim Acta. 1980 Oct 23;107(1-2):121-8. doi: 10.1016/0009-8981(80)90421-0.

Abstract

Brain type creatine kinase (BB) isoenzyme was measured using a highly sensitive and specific radioimmunoassay procedure (limit of detection, 1 microgram/l of sample) in two schizophrenic populations, an acute non-medicated group consisting of 35 subjects and a chronic group of 15 subjects. Since the assay can also measure the B subunit of MB isoenzyme, patients were selected so as to exclude subjects with possible heart, kidney or other ailments which might result in an increased serum creatine kinase B subunit. Both the acute schizophrenics (3.0 +/- 0.23) mean S.E.M. and the chronic schizophrenics (2.9 +/- 0.33) had serum levels of creating kinase BB similar to those of controls (2.8 +/- 0.21) and non-cardiac patients (3.5 +/- 0.58). Patients having myocardial infarction or neurovascular surgery had elevated creatine kinase B subunit. Similar but much less sensitive quantitative results were obtained using agarose multizonal electrophoresis. Despite a recent report that human brain contains the creatine kinase MM isoenzyme, analysis of five human brains using DEAE-Sephadex-A50 for MM isoenzyme fractionation, followed by immunodiffusion analysis of concentrated eluate revealed no detectable MM isoenzyme. The results from these studies suggest that the elevated serum creatine kinase activity of schizophrenic patients is most likely not of brain origin.

摘要

采用高灵敏度和特异性的放射免疫分析方法(检测限为1微克/升样本),对两组精神分裂症患者的脑型肌酸激酶(BB)同工酶进行了测定。一组是由35名受试者组成的急性未用药组,另一组是由15名受试者组成的慢性组。由于该检测方法也能测量MB同工酶的B亚基,因此对患者进行了筛选,以排除可能患有心脏、肾脏或其他疾病而导致血清肌酸激酶B亚基升高的受试者。急性精神分裂症患者(3.0±0.23,均值±标准误)和慢性精神分裂症患者(2.9±0.33)的血清脑型肌酸激酶水平与对照组(2.8±0.21)和非心脏疾病患者(3.5±0.58)相似。患有心肌梗死或接受神经血管手术的患者肌酸激酶B亚基升高。使用琼脂糖多区电泳获得了相似但灵敏度低得多的定量结果。尽管最近有报道称人类大脑含有肌酸激酶MM同工酶,但使用DEAE-葡聚糖A50对五个人脑进行MM同工酶分级分离,随后对浓缩洗脱液进行免疫扩散分析,结果显示未检测到MM同工酶。这些研究结果表明,精神分裂症患者血清肌酸激酶活性升高很可能并非源于大脑。

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