Miguez J M, Simonneaux V, Pevet P
Neurobiologie des Fonctions Rythmiques et Saisonnières, CNRS-URA 1332, Université Louis Pasteur, Strasbourg, France.
J Pineal Res. 1997 Sep;23(2):63-71. doi: 10.1111/j.1600-079x.1997.tb00337.x.
This study investigated whether the activation of pinealocyte beta-adrenergic receptors is involved in the regulation of serotonin (5-HT) synthesis and release, as it is for melatonin production. In addition, the role of the intra- and extra-cellular 5-HT in modulating the synthesis of melatonin induced by the beta-adrenergic agonist isoproterenol (ISO) was also studied. The incubation of dissociated pinealocytes with 0.1-10 microM ISO resulted in a concentration-dependent increase of melatonin synthesis. 5-HT release and intracellular 5-HT content were increased by 0.1 and 1 microM ISO but they were reduced after ISO 10 microM. Moreover, when incubated with the tryptophan hydroxylase inhibitor p-chlorophenylalanine (PCPA), the secretion of 5-HT as well as the intracellular 5-HT levels were markedly reduced in both ISO-stimulated and unstimulated conditions. Melatonin release was also inhibited by PCPA, although it responded in the expected manner to increasing concentrations of ISO. These data indicate that the release of 5-HT from pinealocytes depends on the availability of cytoplasmic 5-HT, which in turn is highly dependent on the tryptophan hydroxylase activity. In cells stimulated with moderate ISO concentrations, 5-HT release may be an important regulatory process of pineal 5-HT. After a large stimulation of N-acetyltransferase (NAT) activity by ISO, the synthesis of melatonin prevails on 5-HT release, whose decrease is associated to a deficit of intracellular 5-HT. On the other hand, the present study shows that the incubation of pineal cells with high concentrations of 5-HT or with a selective 5-HT2 receptor agonist, alpha-methyl-5-hydroxytryptamine, reverses partially the inhibitory effect of PCPA on the ISO-stimulated melatonin synthesis. In contrast the 5-HT2 antagonist, ketanserin, results in an inhibiton of the release of melatonin following ISO stimulation. These results suggest that released 5-HT may have a role in the full expression of the beta-adrenergically induced NAT activity and, thus, may contribute to the optimal melatonin synthesis at night.
本研究调查了松果体细胞β-肾上腺素能受体的激活是否如在褪黑素产生过程中那样,参与血清素(5-羟色胺,5-HT)合成与释放的调节。此外,还研究了细胞内和细胞外5-HT在调节β-肾上腺素能激动剂异丙肾上腺素(ISO)诱导的褪黑素合成中的作用。将离体的松果体细胞与0.1 - 10微摩尔/升的ISO孵育,导致褪黑素合成呈浓度依赖性增加。0.1和1微摩尔/升的ISO可使5-HT释放及细胞内5-HT含量增加,但10微摩尔/升的ISO作用后二者均降低。此外,当与色氨酸羟化酶抑制剂对氯苯丙氨酸(PCPA)一起孵育时,在ISO刺激和未刺激条件下,5-HT的分泌以及细胞内5-HT水平均显著降低。PCPA也抑制褪黑素释放,尽管它对ISO浓度增加的反应符合预期。这些数据表明,松果体细胞释放5-HT取决于细胞质5-HT的可用性,而细胞质5-HT又高度依赖色氨酸羟化酶活性。在用中等浓度ISO刺激的细胞中,5-HT释放可能是松果体5-HT重要的调节过程。在ISO大量刺激N-乙酰转移酶(NAT)活性后,褪黑素的合成优先于5-HT释放,5-HT释放的减少与细胞内5-HT缺乏有关。另一方面,本研究表明,用高浓度5-HT或选择性5-HT2受体激动剂α-甲基-5-羟色胺孵育松果体细胞,可部分逆转PCPA对ISO刺激的褪黑素合成的抑制作用。相反,5-HT2拮抗剂酮色林可导致ISO刺激后褪黑素释放受到抑制。这些结果表明,释放的5-HT可能在β-肾上腺素能诱导的NAT活性的充分表达中起作用,因此可能有助于夜间最佳褪黑素的合成。