Cognitive decline is one of the many characteristics of aging. Reduced long-term potentiation (LTP) and long-term depression (LTD) are thought to be responsible for this decline, although the precise mechanisms underlying LTP and LTD dampening in the old remain unclear. We previously showed that aging is accompanied by the loss of cholesterol from the hippocampus, which leads to PI3K/Akt phosphorylation. Given that Akt de-phosphorylation is required for glutamate receptor internalization and LTD, we hypothesized that the decrease in cholesterol in neuronal membranes may contribute to the deficits in LTD typical of aging. Here, we show that cholesterol loss triggers p-Akt accumulation, which in turn perturbs the normal cellular and molecular responses induced by LTD, such as impaired AMPA receptor internalization and its reduced lateral diffusion. Electrophysiology recordings in brain slices of old mice and in anesthetized elderly rats demonstrate that the reduced hippocampal LTD associated with age can be rescued by cholesterol perfusion. Accordingly, cholesterol replenishment in aging animals improves hippocampal-dependent learning and memory in the water maze test.

Small bacteria are strongly buffeted by Brownian forces that make completely straight runs impossible. A model for bacterial motion is formulated in which the effects of fluctuational forces and torques on the run phase are taken into account by using coupled Langevin equations. An integrated description of the motion, including runs and tumbles, is then obtained by the use of convolution and Laplace transforms. The properties of the velocity-velocity correlation function, of the mean displacement, and of the two relevant diffusion coefficients are examined in terms of the bacterial sizes and of the magnitude of the propelling forces. For bacteria smaller than E. coli, the integrated diffusion coefficient crosses over from a jump-dominated to a rotational-diffusion-dominated form.