Hery M, Barrit M C, Faudon M, Hery F
Peptides. 1986 Mar-Apr;7(2):183-8. doi: 10.1016/0196-9781(86)90210-x.
Vasoactive intestinal peptide (VIP) inhibits serotonin (5-HT) uptake in the suprachiasmatic area (SCA) of the rat. The present study investigates the possibility of a functional relationship between 5-HT uptake mechanisms and 5-HT autoreceptor activity in this effect of VIP in the SCA. The hypothesis of a linkage between these two mechanisms of 5-HT regulation has been recently proposed. We investigated the possibility of the presence of 5-HT autoreceptors in the SCA. Using superfusion system, exogenous 5-HT (500 and 50 nM) increased the release of newly synthesized 3H-5-HT. In contrast, 5 nM of exogenous 5-HT inhibited this release. This latter effect was antagonized by methiothepin (10(-7) M). In contrast, the concentration of methiothepin required to inhibit the VIP effect was 10(-6) or 10(-5) M, the same molarity found to decrease the 5-HT uptake. On the other hand, the increase of the 3H-5-HT in the synaptic cleft, induced by VIP, did not modify the inhibition of 3H-5-HT release induced by 5 nM of exogenous 5-HT. We conclude that the effect of VIP on 5-HT metabolism in the SCA is linked to the 5-HT uptake mechanism but not to the activity of 5-HT presynaptic autoreceptors. In our experimental conditions, the activity of 5-HT autoreceptors is independent of the 5-HT uptake processes.
血管活性肠肽(VIP)可抑制大鼠视交叉上区(SCA)对5-羟色胺(5-HT)的摄取。本研究探讨了在SCA中VIP的这一作用下,5-HT摄取机制与5-HT自身受体活性之间功能关系的可能性。最近有人提出了5-HT调节的这两种机制之间存在联系的假说。我们研究了SCA中存在5-HT自身受体的可能性。利用灌流系统,外源性5-HT(500和50 nM)可增加新合成的3H-5-HT的释放。相反,5 nM的外源性5-HT则抑制这种释放。后一种作用可被甲硫噻平(10(-7) M)拮抗。相比之下,抑制VIP作用所需的甲硫噻平浓度为10(-6) 或10(-5) M,这与发现可降低5-HT摄取的摩尔浓度相同。另一方面,VIP诱导的突触间隙中3H-5-HT的增加,并未改变5 nM外源性5-HT诱导的3H-5-HT释放的抑制作用。我们得出结论,VIP对SCA中5-HT代谢的作用与5-HT摄取机制有关,但与5-HT突触前自身受体的活性无关。在我们的实验条件下,5-HT自身受体的活性独立于5-HT摄取过程。