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再生大鼠肝脏肝细胞中丙酮酸激酶同工酶转换缺乏证据。

Lack of evidence for a pyruvate kinase isozyme shift in hepatocytes of the regenerating rat liver.

作者信息

Miyanaga O, Ishibashi H, Kurokawa S, Shirahama M, Tsuchiya Y

机构信息

First Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Int J Biochem. 1988;20(11):1219-25. doi: 10.1016/0020-711x(88)90222-4.

Abstract
  1. Pyruvate kinase isozyme shift in a regenerating rat liver was studied. Rats were subjected to a 70% hepatectomy and the liver homogenate or hepatocyte preparations were obtained from the regenerating liver. 2. Using thin layer polyacrylamide gel electrophoresis, liver homogenates from an intact normal rat appeared to contain the L-type isozyme in the greatest number and M2-type to a lesser extent. 3. The ratio of the M2- to L-type increased in the preparations obtained from the regenerating liver. 4. In the hepatocyte preparations prepared from a regenerating rat liver by the conventional method, a small amount of M2-type isozyme was detected. 5. However, the M2-type isozyme was hardly detected in the highly purified hepatocyte preparations prepared using Percoll. 6. Similar results were obtained by separation of the enzyme by DEAE cellulose column chromatography. 7. These results suggest that there is no pyruvate kinase isozyme shift from L- to M2-type in hepatocytes in the course of regeneration. 8. The increased M2-type isozyme in the regenerating rat liver is considered to originate from nonparenchymal cells.
摘要
  1. 对再生大鼠肝脏中的丙酮酸激酶同工酶转变进行了研究。将大鼠进行70%肝切除术,然后从再生肝脏中获取肝脏匀浆或肝细胞制剂。2. 使用薄层聚丙烯酰胺凝胶电泳,完整正常大鼠的肝脏匀浆似乎含有数量最多的L型同工酶,M2型同工酶的含量较少。3. 从再生肝脏获得的制剂中,M2型与L型的比例增加。4. 在通过传统方法从再生大鼠肝脏制备的肝细胞制剂中,检测到少量M2型同工酶。5. 然而,在使用Percoll制备的高度纯化的肝细胞制剂中几乎检测不到M2型同工酶。6. 通过DEAE纤维素柱色谱法分离该酶也得到了类似的结果。7. 这些结果表明,在再生过程中,肝细胞中不存在丙酮酸激酶同工酶从L型向M2型的转变。8. 再生大鼠肝脏中M2型同工酶的增加被认为起源于非实质细胞。

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