Graduate School of Natural Science and Technology, Okayama University, Okayama, Japan.
J Biol Rhythms. 2012 Dec;27(6):423-32. doi: 10.1177/0748730412462206.
Most animals show rest/activity rhythms that are regulated by an endogenous timing mechanism, the so-called circadian system. The rhythm becomes weaker with age, but the mechanism underlying the age-associated rhythm change remains to be elucidated. Here we employed Drosophila melanogaster as a model organism to study the aging effects on the rhythm. We first investigated activity rhythms under light-dark (LD) cycles and constant darkness (DD) in young (1-day-old) and middle-aged (30-, 40-, and 50-day-old) wild-type male flies. The middle-aged flies showed a reduced activity level in comparison with young flies. Additionally, the free-running period significantly lengthened in DD, and the rhythm strength was diminished. Immunohistochemistry against pigment-dispersing factor (PDF), a principal neurotransmitter of the Drosophila clock, revealed that PDF levels declined with age. We also found an attenuation of TIMELESS (TIM) oscillation in the cerebral clock neurons in elder flies. Intriguingly, overexpression of PDF suppressed age-associated changes not only in the period and strength of free-running locomotor rhythms but also in the amplitude of TIM oscillations in many pacemaker neurons in the elder flies, suggesting that the age-dependent PDF decline is responsible for the rhythm attenuation. These results suggest that the age-associated reduction of PDF may cause attenuation of intercellular communication in the circadian neuronal network and of TIM cycling, which may result in the age-related rhythm decay.
大多数动物表现出由内源性计时机制(即所谓的生物钟系统)调节的休息/活动节律。随着年龄的增长,这种节律会减弱,但与年龄相关的节律变化背后的机制仍有待阐明。在这里,我们使用黑腹果蝇作为模型生物来研究衰老对节律的影响。我们首先在年轻(1 天大)和中年(30、40 和 50 天大)野生型雄性果蝇的明暗(LD)循环和持续黑暗(DD)条件下研究了活动节律。与年轻果蝇相比,中年果蝇的活动水平降低。此外,在 DD 中自由运行周期明显延长,节律强度减弱。针对黑色素分散因子(PDF)的免疫组织化学染色——果蝇生物钟的主要神经递质,显示 PDF 水平随年龄增长而下降。我们还发现老年果蝇脑中时钟神经元中的 TIMES (TIM)振荡减弱。有趣的是,PDF 的过表达不仅抑制了自由运行运动节律的周期和强度,而且抑制了老年果蝇中许多起搏器神经元中 TIM 振荡的幅度的与年龄相关的变化,这表明与年龄相关的 PDF 下降是导致节律减弱的原因。这些结果表明,与年龄相关的 PDF 减少可能导致生物钟神经元网络中细胞间通讯和 TIM 循环的减弱,这可能导致与年龄相关的节律衰减。