Department of Physiology, University of Kentucky, Lexington, KY, USA.
J Biol Rhythms. 2010 Dec;25(6):450-9. doi: 10.1177/0748730410385648.
In rodents, the preovulatory luteinizing hormone (LH) surge is timed by a circadian rhythm. We recently reported that a phenobarbital-induced delay of the estrous cycle in Syrian hamsters is associated with an approximately 2-h phase advance in both the circadian locomotor activity rhythm and the timing of the LH surge. The following study tests the hypothesis that a >2-h nonpharmacological phase advance in the circadian pacemaker that delays the estrous cycle by a day will also phase advance the LH surge by approximately 2 h. Activity rhythms were continuously monitored in regularly cycling hamsters using running wheels or infrared detectors for about 10 days prior to jugular cannulation. The next day, on proestrus, hamsters were transferred to the laboratory for 1 of 3 treatments: transfer to a "new cage" (and wheel) from zeitgeber time (ZT) 4 to 8 (with ZT12 defined as time of lights-off), or exposure to a "novel wheel" at ZT5 or ZT1. All animals were then placed in constant dark (DD). Blood samples were obtained just before onset of DD and hourly for the next 6 h, on that day and the next day for determination of plasma LH concentrations. Running activity was monitored in DD for about 10 more days. Transfer to a novel wheel at either ZT5 or ZT1 delayed the LH surge to day 2 in most hamsters, whereas exposure to a new cage did not. Only the delayed LH surges were phase advanced at least 2.5 h on average in all 3 groups. However, wheel-running activity was similarly phase advanced in all 3 groups regardless of the timing of the LH surge; thus, the phase advances in circadian activity rhythms were not associated with the 1-day delay of the LH surge. Interestingly, the number of wheel revolutions was closely associated with the 1-day delay of LH surges following exposure to a novel wheel at either ZT1 or ZT5. These results suggest that the intensity of wheel running (or an associated stimulus) plays an important role in the circadian timing mechanism for the LH surge.
在啮齿动物中,促黄体生成素(LH)的促排卵激增是由昼夜节律控制的。我们最近报道,苯巴比妥诱导的叙利亚仓鼠发情周期延迟与昼夜节律性运动活动节律和 LH 激增时间的大约 2 小时相位提前有关。以下研究测试了以下假设:通过大约 2 小时的昼夜节律起搏器的非药物性相位提前,将发情周期延迟一天,也将使 LH 激增提前大约 2 小时。在进行颈静脉插管之前,使用跑步轮或红外探测器连续监测大约 10 天的定期循环仓鼠的活动节律。第二天,在发情前期,将仓鼠转移到实验室进行 3 种处理之一:从 Zeitgeber 时间(ZT)4 到 8 转移到“新笼子”(和轮子)(ZT12 定义为熄灯时间),或在 ZT5 或 ZT1 暴露于“新轮子”。所有动物随后均置于持续黑暗(DD)中。在 DD 开始前,当天和第二天的前 6 小时,每隔 1 小时获得一次血液样本,以确定血浆 LH 浓度。在 DD 中,大约再监测 10 天的跑步活动。在 ZT5 或 ZT1 时转移到新轮子会使大多数仓鼠的 LH 激增延迟到第 2 天,而暴露于新笼子则不会。只有延迟的 LH 激增在所有 3 个组中平均至少提前了 2.5 小时。然而,无论 LH 激增的时间如何,所有 3 个组中的跑步活动都同样提前;因此,昼夜节律活动节律的相位提前与 LH 激增的 1 天延迟无关。有趣的是,在 ZT1 或 ZT5 暴露于新轮子后,轮圈旋转的次数与 LH 激增的 1 天延迟密切相关。这些结果表明,轮子旋转的强度(或相关刺激)在 LH 激增的昼夜节律计时机制中起着重要作用。