Tam Shu K E, Hasan Sibah, Hughes Steven, Hankins Mark W, Foster Russell G, Bannerman David M, Peirson Stuart N
Sleep and Circadian Neuroscience Institute (Nuffield Department of Clinical Neurosciences), Oxford Molecular Pathology Institute, Sir William Dunn School of Pathology, South Parks Road, Oxford OX1 3RE, UK.
Department of Experimental Psychology, Oxford University, Tinbergen Building, 9 South Parks Road, Oxford OX1 3UD, UK.
Proc Biol Sci. 2016 Dec 28;283(1845). doi: 10.1098/rspb.2016.2275.
Acute light exposure exerts various effects on physiology and behaviour. Although the effects of light on brain network activity in humans are well demonstrated, the effects of light on cognitive performance are inconclusive, with the size, as well as direction, of the effect depending on the nature of the task. Similarly, in nocturnal rodents, bright light can either facilitate or disrupt performance depending on the type of task employed. Crucially, it is unclear whether the effects of light on behavioural performance are mediated via the classical image-forming rods and cones or the melanopsin-expressing photosensitive retinal ganglion cells. Here, we investigate the modulatory effects of light on memory performance in mice using the spontaneous object recognition task. Importantly, we examine which photoreceptors are required to mediate the effects of light on memory performance. By using a cross-over design, we show that object recognition memory is disrupted when the test phase is conducted under a bright light (350 lux), regardless of the light level in the sample phase (10 or 350 lux), demonstrating that exposure to a bright light at the time of test, rather than at the time of encoding, impairs performance. Strikingly, the modulatory effect of light on memory performance is completely abolished in both melanopsin-deficient and rodless-coneless mice. Our findings provide direct evidence that melanopsin-driven and rod/cone-driven photoresponses are integrated in order to mediate the effect of light on memory performance.
急性光照对生理和行为会产生多种影响。尽管光照对人类大脑网络活动的影响已得到充分证实,但光照对认知表现的影响尚无定论,其影响的大小和方向取决于任务的性质。同样,在夜行性啮齿动物中,强光对表现的影响取决于所采用任务的类型,既可能促进也可能干扰表现。至关重要的是,尚不清楚光照对行为表现的影响是通过经典的成像视杆细胞和视锥细胞介导,还是通过表达黑视蛋白的光敏感视网膜神经节细胞介导。在此,我们使用自发物体识别任务研究光照对小鼠记忆表现的调节作用。重要的是,我们研究介导光照对记忆表现影响所需的光感受器。通过采用交叉设计,我们发现当测试阶段在强光(350勒克斯)下进行时,物体识别记忆会受到干扰,无论样本阶段的光照水平如何(10或350勒克斯),这表明在测试时而非编码时暴露于强光会损害表现。令人惊讶的是,在缺乏黑视蛋白的小鼠和既无视杆细胞又无视锥细胞的小鼠中,光照对记忆表现的调节作用完全消失。我们的研究结果提供了直接证据,表明黑视蛋白驱动和视杆/视锥细胞驱动的光反应相互整合,以介导光照对记忆表现的影响。