Petkov V D, Petkov V V, Popova J, Konstantinova E
Acta Physiol Pharmacol Bulg. 1987;13(1):11-9.
The changes in the 5-HT1-binding sites, developing during ageing and under the effect of 10-day administration of L-DOPA and haloperidol, were studied in the cerebral cortex, striatum and hypothalamus of 2-, 10- and 22-month-old rats. The values of Bmax of the 5-HT1-binding sites decreased in all three brain structures studied with the ageing of the experimental animals. Both L-DOPA and haloperidol did not change the general character of the changes in the number of 5-HT1-receptors, developing during ageing, but at the same time L-DOPA reduced their density in the three age periods and in the three cerebral areas studied, while haloperidol increased their number in the 2- and 10-month-old rats. The Kd-values of the 5-HT1-receptors manifested very varied changes, determined both by ageing and by the administration of L-DOPA and haloperidol. The generalized interpretation of these results with the results obtained in earlier studies on the age-determined changes in DA2 and the enkephalin receptors, as well as of the content of biogenic monoamines and MAO-activities, made it possible to see new elements in the adaptive possibilities of the cerebral receptors. On the other hand, the results obtained in the present and earlier studies show that ageing is paralleled by deviations in the equilibrium of the cerebral transmitter systems which seem to play an important role for the development of the behavioural changes connected with ageing.
研究了2个月、10个月和22个月大的大鼠大脑皮层、纹状体和下丘脑5-HT1结合位点在衰老过程中以及在左旋多巴和氟哌啶醇10天给药作用下的变化。随着实验动物的衰老,在所研究的所有三个脑结构中,5-HT1结合位点的Bmax值均降低。左旋多巴和氟哌啶醇均未改变衰老过程中5-HT1受体数量变化的总体特征,但同时左旋多巴在研究的三个年龄段和三个脑区均降低了其密度,而氟哌啶醇在2个月和10个月大的大鼠中增加了其数量。5-HT1受体的Kd值表现出非常多样的变化,这既由衰老决定,也由左旋多巴和氟哌啶醇的给药决定。将这些结果与早期关于DA2和脑啡肽受体的年龄决定变化以及生物源性单胺含量和MAO活性的研究结果进行综合解释,使得有可能在脑受体的适应性可能性中看到新的元素。另一方面,本研究和早期研究获得的结果表明,衰老伴随着脑递质系统平衡的偏差,这似乎对与衰老相关的行为变化的发展起着重要作用。