Prosser Rebecca A
University of Tennessee, Department of Biochemistry and Cellular and Molecular Biology, M407 Walter's Life Sciences Building, Knoxville, TN 37996, USA.
Brain Res. 2003 Mar 14;966(1):110-5. doi: 10.1016/s0006-8993(02)04206-3.
The mammalian circadian clock in the suprachiasmatic nucleus (SCN) receives multiple afferent signals that could potentially modulate its phase. One input, the serotonin (5-HT) projection from the raphe nuclei, has been extensively investigated in rats and hamsters, yet its role(s) in modulating circadian clock phase remains controversial. To expand our investigation of 5-HT modulation of the SCN clock, we investigated the phase-shifting effects of 5-HT and its agonist, (+)8-hydroxy-2-(di-n-propylamino)tetralin (DPAT), when applied to mouse SCN brain slices. 5-HT induced 2-3 h phase advances when applied during subjective day, while non-significant phase shifts were seen after 5-HT application at other times. These phase shifts were completely blocked by the 5-HT antagonist, metergoline. DPAT also induced phase shifts when applied during mid-subjective day, and this effect appeared dose-dependent. Together, these results demonstrate that the mouse SCN, like that of the rat, is directly sensitive to in vitro phase-resetting by 5-HT.
哺乳动物视交叉上核(SCN)中的昼夜节律时钟接收多种传入信号,这些信号可能会调节其相位。其中一种输入,即来自中缝核的5-羟色胺(5-HT)投射,已经在大鼠和仓鼠中得到了广泛研究,但其在调节昼夜节律时钟相位中的作用仍存在争议。为了扩展我们对5-HT对SCN时钟调节作用的研究,我们研究了将5-HT及其激动剂(+)8-羟基-2-(二正丙基氨基)四氢萘(DPAT)应用于小鼠SCN脑片时的相位移动效应。在主观白天应用5-HT时会诱导2-3小时的相位提前,而在其他时间应用5-HT后观察到的相位移动不显著。这些相位移动被5-HT拮抗剂麦角林完全阻断。在主观白天中期应用DPAT时也会诱导相位移动,并且这种效应似乎呈剂量依赖性。总之,这些结果表明,小鼠的SCN与大鼠的一样,对5-HT的体外相位重置直接敏感。