Bacon E, Matsokis N, Roujansky P, de Barry J, Gombos G
Centre de Neurochimie du C.N.R.S., U44 INSERM, Strasbourg, France.
Brain Res Dev Brain Res. 1989 Jun 1;47(2):293-7. doi: 10.1016/0165-3806(89)90185-5.
The specific binding of [3H]flunitrazepam was studied to biochemically specify the morphological alterations induced in mouse cerebellum by a single injection of an antimitotic agent, methylazoxymethanol (MAM) performed at the beginning of the postnatal life. The MAM injection causes a general reduction of the benzodiazepine receptors in the adult mice which is particularly severe in mice having been injected the 1st day of postnatal life (so-called MAM0 mice) as compared to animals injected the 5th day (MAM5 mice): in MAM0 mice the benzodiazepine receptor is reduced to half of the control value. The affinity of the benzodiazepine towards its receptor was not affected and the topographic and biochemical action of MAM in the central nervous system was ascertained. Correlations could be made between the biochemical modifications and the morphological alterations otherwise described.
研究了[3H]氟硝西泮的特异性结合,以从生物化学角度明确在出生后早期单次注射抗有丝分裂剂甲基氧化偶氮甲醇(MAM)所诱导的小鼠小脑形态学改变。MAM注射导致成年小鼠中苯二氮䓬受体普遍减少,与出生后第5天注射的动物(所谓的MAM5小鼠)相比,在出生后第1天注射的小鼠(MAM0小鼠)中尤为严重:在MAM0小鼠中,苯二氮䓬受体减少至对照值的一半。苯二氮䓬对其受体的亲和力未受影响,并且确定了MAM在中枢神经系统中的拓扑学和生化作用。可以在生化改变与其他方式描述的形态学改变之间建立相关性。