Baudry M, Shahi K, Gall C
Center for the Neurobiology of Learning and Memory, University of California, Irvine 92717.
Brain Res. 1988 Dec;464(4):313-8. doi: 10.1016/0169-328x(88)90040-x.
Several factors involved in the regulation of ornithine decarboxylase (ODC) activity in adult rat brain tissue have been identified by using the in vitro hippocampal slice preparation. The same amino acids that have previously been reported to induce ODC in tissue culture, i.e., asparagine and glutamine, were found to produce a concentration- and time-dependent increase in ODC activity that reached a 100 fold the control value after 6 h of incubation. The effect of asparagine was totally blocked by inhibition of either protein or RNA synthesis, suggesting that the inducing amino acids increase ODC activity by stimulating the transcription of genes directly or indirectly regulating ODC activity. The effect of the inducing amino acids was potentiated by a variety of factors which by themselves did not modify ODC activity. In particular, opioid peptides markedly potentiated the effect of asparagine. Although the opiate antagonists naloxone and naltrexone totally blocked the effects of the opioid peptides on ODC induction, they also produced an inhibition of the asparagine-mediated increase in ODC activity. Other factors like dibutyryl cyclic AMP and insulin also potentiated the effects of asparagine on ODC activity. These results provide the first description of ODC induction in an in vitro preparation of adult brain tissue and indicate that the hippocampal slice preparation could be used to study the molecular mechanisms which regulate the expression and activity of ODC in the adult central nervous system. Moreover the data suggest possible mechanisms which may be involved in the induction of ODC in hippocampus by seizure activity.
通过使用体外海马切片制备方法,已确定了成年大鼠脑组织中参与鸟氨酸脱羧酶(ODC)活性调节的几个因素。先前报道在组织培养中诱导ODC的相同氨基酸,即天冬酰胺和谷氨酰胺,被发现会使ODC活性产生浓度和时间依赖性增加,孵育6小时后达到对照值的100倍。天冬酰胺的作用被蛋白质或RNA合成的抑制完全阻断,这表明诱导氨基酸通过直接或间接调节ODC活性的基因转录来增加ODC活性。诱导氨基酸的作用被多种自身不改变ODC活性的因素增强。特别是,阿片肽显著增强了天冬酰胺的作用。虽然阿片拮抗剂纳洛酮和纳曲酮完全阻断了阿片肽对ODC诱导的作用,但它们也抑制了天冬酰胺介导的ODC活性增加。其他因素如二丁酰环磷酸腺苷和胰岛素也增强了天冬酰胺对ODC活性的作用。这些结果首次描述了成年脑组织体外制备中ODC的诱导,并表明海马切片制备可用于研究调节成年中枢神经系统中ODC表达和活性的分子机制。此外,数据表明癫痫活动可能参与海马中ODC诱导的可能机制。