Agell N, Pujol M J, Rius E, Bachs O
Departamento de Biología Celular, Universidad de Barcelona, Spain.
Biochem Biophys Res Commun. 1991 Jun 28;177(3):973-8. doi: 10.1016/0006-291x(91)90633-i.
The administration of the alpha 1-adrenergic antagonist prazosin to hepatectomized rats inhibited DNA synthesis induced in the remaining hepatocytes. This inhibitory effect could be reversed by the simultaneous injection of the agonist phenylephrine. In order to establish how the alpha 1-adrenergic receptors can regulate DNA replication, the effect of prazosin administration on DNA polymerase alpha was examined. At 24 h after partial hepatectomy, the activity of DNA polymerase alpha increased 5, 7 and 9 fold in the homogenates, nuclei and nuclear matrix, respectively. This increase was inhibited by 70%-80% when prazosin was injected at 1, 8 or 11 h after surgery. Kinetic studies revealed that the Km for DNA was 2 fold lower in hepatectomized than in control animals. The administration of prazosin to hepatectomized rats increased the Km to the control values. These results indicate that the alpha 1-adrenergic receptors are involved in the regulation of DNA synthesis through the activation of DNA polymerase alpha and that this activation could be produced by increasing its affinity for DNA.
给肝切除大鼠注射α1 - 肾上腺素能拮抗剂哌唑嗪可抑制剩余肝细胞中诱导的DNA合成。这种抑制作用可通过同时注射激动剂去氧肾上腺素来逆转。为了确定α1 - 肾上腺素能受体如何调节DNA复制,研究了哌唑嗪给药对DNA聚合酶α的影响。部分肝切除术后24小时,DNA聚合酶α的活性在匀浆、细胞核和核基质中分别增加了5倍、7倍和9倍。当在手术后1小时、8小时或11小时注射哌唑嗪时,这种增加被抑制了70% - 80%。动力学研究表明,肝切除大鼠中DNA的Km值比对照动物低2倍。给肝切除大鼠注射哌唑嗪可使Km值增加到对照值。这些结果表明,α1 - 肾上腺素能受体通过激活DNA聚合酶α参与DNA合成的调节,并且这种激活可能是通过增加其对DNA的亲和力产生的。