Brensilver H L, Kaplan M M
Gastroenterology. 1975 Jun;68(6):1556-62.
The serum alkaline phosphatase was fractionated by polyacrylamide gel electrophoresis in 317 patients with elevated serum alkaline phosphatase activity. In 253 patients the source of the elevation was the isoenzyme of presumed liver origin, band L. In 87 of these patients, there was either no obvious liver disease or the alkaline phosphatase elevation was inappropriately high. In 19 of the 87, liver disease was further excluded by liver biopsy or by laparotomy. Because of this, biochemical studies were done to verify the hepatic origin of band L. Band L and alkaline phosphatase extracted from human liver migrated together on polyacrylamide gel electrophoresis before and after digestion with Vibrio cholerae neuraminidase. They had identical pH optima, sedimentation coefficients, Michaelis constants, and rates of inactivation at 55.5 degrees C. They had different rates of inactivation in 3 M urea. Over-all, the data indicate that band L is of liver origin, and that elevation of the hepatic alkaline phosphatase isoenzyme may be a nonspecific finding in certain patients.
对317例血清碱性磷酸酶活性升高的患者,采用聚丙烯酰胺凝胶电泳对血清碱性磷酸酶进行了分离。在253例患者中,升高的来源是推测为肝脏来源的同工酶,即L带。在这些患者中的87例,要么没有明显的肝脏疾病,要么碱性磷酸酶升高程度异常高。在这87例中的19例,通过肝活检或剖腹手术进一步排除了肝脏疾病。因此,进行了生化研究以证实L带的肝脏来源。在经霍乱弧菌神经氨酸酶消化前后,从人肝脏提取的L带和碱性磷酸酶在聚丙烯酰胺凝胶电泳上迁移情况相同。它们具有相同的最适pH、沉降系数、米氏常数以及在55.5℃下的失活速率。它们在3M尿素中的失活速率不同。总体而言,数据表明L带来源于肝脏,并且肝脏碱性磷酸酶同工酶的升高在某些患者中可能是一个非特异性发现。