Prosser R A, Edgar D M, Heller H C, Miller J D
Department of Biological Sciences, Stanford University, CA 94305.
Brain Res. 1994 Apr 18;643(1-2):296-301. doi: 10.1016/0006-8993(94)90036-1.
The primary mammalian circadian clock is located within the suprachiasmatic nuclei (SCN), but the cellular organization of the clock is not yet known. We investigated the potential role of glial cells in the clock mechanism by determining whether disrupting glial activity affects the in vitro circadian rhythm of neuronal activity and the in vivo circadian activity rhythm in rats. We used two agents (octanol and halothane) that block gap junctions, and one (fluorocitrate) that inhibits glial metabolism. All three agents disrupted the circadian pattern of neuronal activity. Octanol flattened the rhythm at the highest concentration (200 microM) and induced a small phase delay at a lower concentration (66 microM). Halothane and fluorocitrate induced ultradian rhythmicity. Fluorocitrate injected into the SCN of an intact rat induced arrhythmicity for about 1 week, after which the rhythm reappeared with a 1.6 h delay. These results suggest that glia play an important role in the SCN circadian clock.
哺乳动物的主要昼夜节律时钟位于视交叉上核(SCN)内,但该时钟的细胞组织尚不清楚。我们通过确定破坏神经胶质细胞活性是否会影响大鼠体外神经元活动的昼夜节律和体内昼夜活动节律,来研究神经胶质细胞在时钟机制中的潜在作用。我们使用了两种阻断缝隙连接的药物(辛醇和氟烷)以及一种抑制神经胶质细胞代谢的药物(氟代柠檬酸)。所有这三种药物都破坏了神经元活动的昼夜模式。辛醇在最高浓度(200微摩尔)时使节律变平,并在较低浓度(66微摩尔)时诱导出小的相位延迟。氟烷和氟代柠檬酸诱导出超日节律。向完整大鼠的SCN注射氟代柠檬酸会诱导约1周的心律失常,之后节律重新出现,延迟1.6小时。这些结果表明,神经胶质细胞在SCN昼夜节律时钟中起重要作用。