Ageing or NOT, clock genes are important for memory processes: an interesting hypothesis raising many questions

and retrieval are temporally regulated events. An intrinsic circadian (circa: about; dies: day) timing system influencing the dynamics in memory processing has been detected in animal models, ranging from invertebrates to mammalian species. Several recent investigations, addressing the molecular mechanism behind the circadian modulation of mnemonic processes shed light onto pathways known to be essential in memory processing, such as the cAMP-CREB-MAPK-pathway, which by itself is regulated by the circadian system. Notable, an important role for rhythmic clock gene expressions in the hippocampus and in hippocampus-dependent memory processes has been recently detected. However, the link between the circadian gating of memory processes and its importance for daily life remain highly elusive. In the here presented work [1], Kondratova and co-workers approached the possible effects of ageing on cognitive performances, with the experimental design taking the known parallel decline in functional integrity of the circadian system and cognitive performance into account. For this purpose, the authors used 3-4 months old mice that are deficient for central clock genes, and thus, no longer exhibit circadian rhythms. Importantly, among the mice used, was the Bmal1-deficient mouse News strain, known for its accelerated ageing phenotype. Kondratova and co-workers observed that behaviors, such as habituation to a novel environment were altered in mice with deficiencies/mutations of core clock genes. Habituation to a novel environment can be considered a form of non-associative learning, and is dependent on (a) hippocampus-dependent working memory, a form of short-term memory with regards to intra-session habituation and (b) long-term memory for inter-session habituation. Bmal1-and Clock-knockout mice showed deficiencies in both types of habituation in contrast to Cry1/2-deficient mice that demonstrated facilitated habituation. The authors also proved by using an open field test that elevated anxiety, which often correlates with high locomotor activity and rearing, and deficits in contextual habituation does not attribute to deficits in behavioral learning in the here used clock-gene-knockout mice: Cry1,2-knockout mice showed facilitated habituation in parallel to elevated levels of anxiety, while Bmal1-knockout mice showed deficits in contextual habituation at significantly lower anxiety levels. The presented results confirm that a disruption of circadian clockwork impairs or facilitates in parallel the intra-and inter-session contextual habituation of mice. Commentary on: Kondratova et al. Circadian clock proteins control adaptation to novel environment and memory formation Aging. 2010: this issue