Cell and Molecular Biology Program, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Aging Cell. 2012 Jun;11(3):428-38. doi: 10.1111/j.1474-9726.2012.00800.x. Epub 2012 Feb 24.
Sleep-wake cycles break down with age, but the causes of this degeneration are not clear. Using a Drosophila model, we addressed the contribution of circadian mechanisms to this age-induced deterioration. We found that in old flies, free-running circadian rhythms (behavioral rhythms assayed in constant darkness) have a longer period and an unstable phase before they eventually degenerate. Surprisingly, rhythms are weaker in light-dark cycles and the circadian-regulated morning peak of activity is diminished under these conditions. On a molecular level, aging results in reduced amplitude of circadian clock gene expression in peripheral tissues. However, oscillations of the clock protein PERIOD (PER) are robust and synchronized among different clock neurons, even in very old, arrhythmic flies. To improve rhythms in old flies, we manipulated environmental conditions, which can have direct effects on behavior, and also tested a role for molecules that act downstream of the clock. Coupling temperature cycles with a light-dark schedule or reducing expression of protein kinase A (PKA) improved behavioral rhythms and consolidated sleep. Our data demonstrate that a robust molecular timekeeping mechanism persists in the central pacemaker of aged flies, and reducing PKA can strengthen behavioral rhythms.
睡眠-觉醒周期随着年龄的增长而紊乱,但这种退化的原因尚不清楚。我们使用果蝇模型来研究昼夜节律机制对这种年龄诱导的恶化的贡献。我们发现,在老年果蝇中,自由运行的昼夜节律(在持续黑暗中测定的行为节律)在最终退化之前具有更长的周期和不稳定的相位。令人惊讶的是,在光暗循环中,节律较弱,并且在这些条件下,昼夜节律调节的早晨活动高峰减弱。在分子水平上,衰老导致外周组织中生物钟基因表达的振幅降低。然而,时钟蛋白 PERIOD(PER)的振荡在不同的时钟神经元中仍然强大且同步,即使在非常年老、无节律的果蝇中也是如此。为了改善老年果蝇的节律,我们操纵了环境条件,这些条件可以直接影响行为,并且还测试了作用于时钟下游的分子的作用。将温度循环与光暗时间表耦合或降低蛋白激酶 A(PKA)的表达可以改善行为节律并巩固睡眠。我们的数据表明,在老年果蝇的中央起搏器中存在一种强大的分子计时机制,并且降低 PKA 可以增强行为节律。