Masubuchi S, Honma S, Abe H, Nakamura W, Honma K
Department of Physiology, Hokkaido University Graduate School of Medicine, N-15, W-7, Kita-ku, Sapporo 060-8638, Japan.
Eur J Neurosci. 2001 Oct;14(7):1177-80. doi: 10.1046/j.0953-816x.2001.01749.x.
It is well established that the Clock gene is essential for expressing circadian activity rhythms in mammals under constant darkness. The Clock gene product is a positive component of a molecular feedback loop which is assumed to generate the circadian rhythm. On the other hand, chronic treatment of methamphetamine (MAP) induces locomotor activity rhythm in a circadian domain, which is independent of the suprachiasmatic nucleus (SCN) and is driven by a pacemaker outside the SCN. However, it is not known whether the pacemaker outside the SCN possesses a similar molecular mechanism to that in the SCN. Here we show that MAP restores locomotor activity rhythm in arrhythmic homozygous Clock mutant (Clock/Clock) mice under constant darkness. This result indicates that the Clock mutation does not affect the MAP-induced locomotor rhythm.
众所周知,在持续黑暗条件下,Clock基因对于哺乳动物表达昼夜活动节律至关重要。Clock基因产物是一个分子反馈环的正向组成部分,该反馈环被认为可产生昼夜节律。另一方面,长期给予甲基苯丙胺(MAP)可在昼夜节律范围内诱导运动活动节律,这种节律独立于视交叉上核(SCN),由SCN外的一个起搏器驱动。然而,尚不清楚SCN外的起搏器是否具有与SCN中类似的分子机制。在此我们表明,在持续黑暗条件下,MAP可恢复无节律的纯合Clock突变体(Clock/Clock)小鼠的运动活动节律。这一结果表明,Clock突变并不影响MAP诱导的运动节律。