Ying S W, Rusak B
Department of Psychology, Dalhousie University, Halifax, NS, Canada.
Brain Res. 1994 Jul 18;651(1-2):37-46. doi: 10.1016/0006-8993(94)90678-5.
Serotonergic neurons from the midbrain raphe nuclei innervate the suprachiasmatic nucleus (SCN) of the hypothalamus, which functions as the dominant pacemaker for mammalian circadian rhythms. We investigated the effects of serotonin (5-HT) on firing rates of light-activated SCN cells in urethane-anesthetized hamsters. Micro-iontophoretic application of 5-HT or 5-HT1A agonists (8-OH-DPAT and 5-CT) caused a dose-dependent inhibition of spontaneous activity and photic responses in the majority of SCN cells tested. Application of metergoline alone, a non-selective 5-HT antagonist, slightly increased firing rates during darkness and light exposure, suggesting a tonic serotonergic suppression of SCN activity. Metergoline also effectively attenuated suppression induced by the three 5-HT agonists. In addition, the effects of 8-OH-DPAT were blocked by a 5-HT1A antagonist, SDZ 216-525. However, other putative 5-HT antagonists were weak (propranolol and NAN-190) or ineffective (ketanserin) in blocking the action of 8-OH-DPAT. These results indicate that serotonin has a potent role in reducing photic effects on retinally activated SCN cells in hamsters, and that these effects are mediated by a receptor with properties similar to those of the 5-HT1A subtype.
来自中脑缝核的血清素能神经元支配下丘脑的视交叉上核(SCN),该核作为哺乳动物昼夜节律的主要起搏器。我们研究了血清素(5-羟色胺,5-HT)对氨基甲酸乙酯麻醉的仓鼠中光激活的SCN细胞放电率的影响。微量离子电泳施加5-HT或5-HT1A激动剂(8-羟基二丙胺基四氢萘,8-OH-DPAT和5-羧色胺,5-CT)导致在大多数测试的SCN细胞中自发活动和光反应受到剂量依赖性抑制。单独应用麦角林,一种非选择性5-HT拮抗剂,在黑暗和光照期间略微增加放电率,表明血清素能对SCN活动有紧张性抑制作用。麦角林也有效减弱了三种5-HT激动剂诱导的抑制作用。此外,8-OH-DPAT的作用被5-HT1A拮抗剂SDZ 216-525阻断。然而,其他假定的5-HT拮抗剂在阻断8-OH-DPAT的作用方面较弱(普萘洛尔和NAN-190)或无效(酮色林)。这些结果表明血清素在减少对仓鼠视网膜激活的SCN细胞的光效应方面有重要作用,并且这些效应是由一种性质类似于5-HT1A亚型的受体介导的。