Huether G, Zhou D, Schmidt S, Wiltfang J, Rüther E
Department of Psychiatry, University of Göttingen, Germany.
Biol Psychiatry. 1997 Jun 15;41(12):1174-80. doi: 10.1016/s0006-3223(96)00265-x.
The influence of feeding rats only half the amount of their normal daily intake of a complete rat chow on the affinity and the density of serotonin (5-HT) transporters was measured in membrane preparations of the frontal cortex and the midbrain by a [3H]paroxetine binding assay. In young rats (10 weeks), a significant reduction of about 30% of the Bmax values of [3H]paroxetine binding occurred in the frontal cortex after 1 and 2 weeks of restricted food intake. No starvation-induced decline of the density of 5-HT transporters was seen in the midbrain. When older rats (50 weeks) were subjected to the same 50% reduction of daily food intake for 2 weeks, no such down-regulation of the density of cortical 5-HT transporters was observed. The affinity of the 5-HT transporters, as indicated by the unchanged Kd values of [3H]paroxetine binding, was not affected by semistarvation in both regions and at both ages. The observed decline of [3H]paroxetine binding sites in the frontal cortex of young adult rats is the first demonstration of long-term regulatory phenomena of brain 5-HT transporters triggered by a physiologic stimulus.
通过[³H]帕罗西汀结合试验,在额叶皮质和中脑的膜制剂中测量了仅给大鼠喂食其正常每日完整大鼠饲料摄入量一半的量对血清素(5-HT)转运体亲和力和密度的影响。在幼鼠(10周龄)中,限制食物摄入1周和2周后,额叶皮质中[³H]帕罗西汀结合的Bmax值显著降低约30%。中脑中未观察到饥饿诱导的5-HT转运体密度下降。当老年大鼠(50周龄)同样每日食物摄入量减少50%持续2周时,未观察到皮质5-HT转运体密度的这种下调。如[³H]帕罗西汀结合的Kd值未改变所示,5-HT转运体的亲和力在两个区域和两个年龄段均不受半饥饿影响。在年轻成年大鼠额叶皮质中观察到的[³H]帕罗西汀结合位点的下降是由生理刺激触发的脑5-HT转运体长时程调节现象的首次证明。