Araki T, Kato H, Shuto K, Fujiwara T, Itoyama Y
Department of Neurology, Tohoku University School of Medicine, Aoba-ku, Sendai, Japan.
J Neurol Sci. 1997 May 29;148(2):131-7. doi: 10.1016/s0022-510x(96)05343-9.
We studied the age-related alterations of dopaminergic receptors in the brain of Fisher 344 rats with various age (3 weeks and 6, 12, 18 and 24 months) using in vitro receptor autoradiography. [3H]SCH 23390, [3H]spiperone and [3H]nemonapride, and [3H]mazindol were used to label dopamine D1 receptors, dopamine D2 receptors and dopamine uptake sites, respectively. In immature rats (3 weeks old), [3H]SCH 23390 binding showed a significant increase in most brain regions compared to adult animals (6 months old), whereas [3H]spiperone and [3H]nemonapride bindings showed no significant alteration in any brain areas. In contrast, [3H]mazindol binding showed a significant decline in most brain regions. On the other hand, the age-related alterations in [3H]SCH 23390 binding were not observed in any brain regions. [3H]Spiperone and [3H]nemonapride bindings also showed no significant alteration in the brain during aging, except for a transient alteration in [3H]spiperone binding in the nucleus accumbens and hippocampus of 12 months old rats. However, [3H]mazindol binding showed a significant reduction in most brain areas of 12 months old rats. Thereafter, the age-related reduction in [3H]mazindol binding was observed in most brain regions of 18 and 24 months old rats. The results demonstrate that dopamine uptake sites are more susceptible to the aging process than both dopamine D1 and D2 receptors. Furthermore, our results suggest that dopaminergic receptors and dopamine uptake sites may develop with different patterns and speeds after birth. Our studies may provide valuable information concerning the effect of aging on dopaminergic systems.
我们使用体外受体放射自显影技术,研究了不同年龄(3周龄以及6、12、18和24月龄)的Fisher 344大鼠大脑中多巴胺能受体随年龄的变化。分别使用[3H]SCH 23390、[3H]螺哌隆、[3H]奈莫必利和[3H]吗茚酮来标记多巴胺D1受体、多巴胺D2受体和多巴胺摄取位点。在未成熟大鼠(3周龄)中,与成年动物(6月龄)相比,[3H]SCH 23390结合在大多数脑区显著增加,而[3H]螺哌隆和[3H]奈莫必利结合在任何脑区均未显示出显著变化。相反,[3H]吗茚酮结合在大多数脑区显著下降。另一方面,未观察到[3H]SCH 23390结合在任何脑区有与年龄相关的变化。[3H]螺哌隆和[3H]奈莫必利结合在衰老过程中在大脑中也未显示出显著变化,除了12月龄大鼠伏隔核和海马体中[3H]螺哌隆结合有短暂变化。然而,[3H]吗茚酮结合在12月龄大鼠的大多数脑区显著降低。此后,在18和24月龄大鼠的大多数脑区观察到[3H]吗茚酮结合随年龄的降低。结果表明,多巴胺摄取位点比多巴胺D1和D2受体更容易受到衰老过程的影响。此外,我们的结果表明,多巴胺能受体和多巴胺摄取位点在出生后可能以不同的模式和速度发育。我们的研究可能为衰老对多巴胺能系统的影响提供有价值的信息。