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      n-3 polyunsaturated fatty acids supplementation enhances hippocampal functionality in aged mice

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          Abstract

          As major components of neuronal membranes, omega-3 polyunsaturated acids (n-3 PUFA) exhibit a wide range of regulatory functions, modulating from synaptic plasticity to neuroinflammation, from oxidative stress to neuroprotection. Recent human and animal studies indicated the n-3 PUFA neuroprotective properties in aging, with a clear negative correlation between n-3 PUFA levels and hippocampal deficits. The present multidimensional study was aimed at associating cognition, hippocampal neurogenesis, volume, neurodegeneration and metabolic correlates to verify n-3 PUFA neuroprotective effects in aging. To this aim 19 month-old mice were given n-3 PUFA mixture, or olive oil or no dietary supplement for 8 weeks during which hippocampal-dependent mnesic functions were tested. At the end of behavioral testing morphological and metabolic correlates were analyzed. n-3 PUFA supplemented aged mice exhibited better object recognition memory, spatial and localizatory memory, and aversive response retention, without modifications in anxiety levels in comparison to controls. These improved hippocampal cognitive functions occurred in the context of an enhanced cellular plasticity and a reduced neurodegeneration. In fact, n-3 PUFA supplementation increased hippocampal neurogenesis and dendritic arborization of newborn neurons, volume, neuronal density and microglial cell number, while it decreased apoptosis, astrocytosis and lipofuscin accumulation in the hippocampus. The increased levels of some metabolic correlates (blood Acetyl-L-Carnitine and brain n-3 PUFA concentrations) found in n-3 PUFA supplemented mice also pointed toward an effective neuroprotection. On the basis of the present results n-3 PUFA supplementation appears to be a useful tool in health promotion and cognitive decline prevention during aging.

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          Neuroplasticity in old age: sustained fivefold induction of hippocampal neurogenesis by long-term environmental enrichment.

          Neurons are continually born from endogenous stem cells and added to the dentate gyrus throughout life, but adult hippocampal neurogenesis declines precipitously with age. Short-term exposure to an enriched environment leads to a striking increase in new neurons, along with a substantial improvement in behavioral performance. Could this plastic response be relevant for explaining the beneficial effects of leading "an active life" on brain function and pathology? Adult hippocampal neurogenesis in mice living in an enriched environment from the age of 10 to 20 months was fivefold higher than in controls. Relatively, the increase in neuronal phenotypes was entirely at the expense of newly generated astrocytes. This cellular plasticity occurred in the context of significant improvements of learning parameters, exploratory behavior, and locomotor activity. Enriched living mice also had a reduced lipofuscin load in the dentate gyrus, indicating decreased nonspecific age-dependent degeneration. Therefore, in mice signs of neuronal aging can be diminished by a sustained active and challenging life, even if this stimulation started only at medium age. Activity exerts not only an acute but also a sustained effect on brain plasticity.
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            Neocortical neuron number in humans: effect of sex and age.

            Modern stereological methods provide precise and reliable estimates of the number of neurons in specific regions of the brain. We decided to estimate the total number of neocortical neurons in the normal human brain and to analyze it with respect to the major macro- and microscopical structural components, to study the internal relationships of these components, and to quantitate the influence of important physiological variables on brain structure. The 94 brains reported represent a consecutive collection of brains from the general Danish population. The average numbers of neocortical neurons were 19 billion in female brains and 23 billion in male brains, a 16% difference. In our study, which covered the age range from 20 years to 90 years, approximately 10% of all neocortical neurons are lost over the life span in both sexes. Sex and age were the main determinants of the total number of neurons in the human neocortex, whereas body size, per se, had no influence on neuron number. Some of the data presented have been analyzed by using new mathematical designs. An equation predicting the total neocortical neuron number in any individual in which sex and age are known is provided.
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              Astrocytes in the aging brain express characteristics of senescence-associated secretory phenotype.

              Cellular stress increases progressively with aging in mammalian tissues. Chronic stress triggers several signaling cascades that can induce a condition called cellular senescence. Recent studies have demonstrated that senescent cells express a senescence-associated secretory phenotype (SASP). Emerging evidence indicates that the number of cells expressing biomarkers of cellular senescence increases in tissues with aging, which implies that cellular senescence is an important player in organismal aging. In the brain, the aging process is associated with degenerative changes, e.g. synaptic loss and white matter atrophy, which lead to progressive cognitive impairment. There is substantial evidence for the presence of oxidative, proteotoxic and metabolic stresses in aging brain. A low-level, chronic inflammatory process is also present in brain during aging. Astrocytes demonstrate age-related changes that resemble those of the SASP: (i) increased level of intermediate glial fibrillary acidic protein and vimentin filaments, (ii) increased expression of several cytokines and (iii) increased accumulation of proteotoxic aggregates. In addition, in vitro stress evokes a typical senescent phenotype in cultured astrocytes and, moreover, isolated astrocytes from aged brain display the proinflammatory phenotype. All of these observations indicate that astrocytes are capable of triggering the SASP and the astrocytes in aging brain display typical characteristics of cellular senescence. Bearing in mind the many functions of astrocytes, it is evident that the age-related senescence of astrocytes enhances the decline in functional capacity of the brain. We will review the astroglial changes occurring during aging and emphasize that senescent astrocytes can have an important role in age-related neuroinflammation and neuronal degeneration. © 2011 The Authors. European Journal of Neuroscience © 2011 Federation of European Neuroscience Societies and Blackwell Publishing Ltd.
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                Author and article information

                Contributors
                Journal
                Front Aging Neurosci
                Front Aging Neurosci
                Front. Aging Neurosci.
                Frontiers in Aging Neuroscience
                Frontiers Media S.A.
                1663-4365
                25 August 2014
                2014
                : 6
                : 220
                Affiliations
                [1] 1Department of Psychology, University Sapienza of Rome Rome, Italy
                [2] 2Lab of Experimental and Behavioral Neurophysiology, Santa Lucia Foundation Rome, Italy
                [3] 3Department of Experimental and Clinical Sciences, University “G. D'Annunzio” Chieti, Pescara, Italy
                [4] 4Division of Information Technology, Engineering and the Environment, Mawson Institute, University of South Australia Mawson Lakes, SA, Australia
                [5] 5Lab of Proteomic and metabonomic, Santa Lucia Foundation Rome, Italy
                [6] 6Department of Experimental Medicine and Surgery, University Tor Vergata of Rome Rome, Italy
                [7] 7Lab of Clinical and Behavioral Neurology, Santa Lucia Foundation Rome, Italy
                [8] 8Department of Neuroscience, University Tor Vergata of Rome Rome, Italy
                [9] 9Institute of Cell Biology and Neurobiology, National Research Council, Santa Lucia Foundation Rome, Italy
                Author notes

                Edited by: P. Hemachandra Reddy, Oregen Health and Science University, USA

                Reviewed by: Juan Manuel Encinas, Ikerbasque, The Basque Foundation for Science/University of the Basque Country (UPV/EHU), Spain; Gemma Calamandrei, Istituto Superiore di Sanità - National Health Institute, Italy

                *Correspondence: Debora Cutuli, Lab of Experimental and Behavioral Neurophysiology, Santa Lucia Foundation, Via del Fosso di Fiorano 64, 00143 Rome, Italy; Department of Psychology, University Sapienza of Rome, Via dei Marsi 78, 00185 Rome, Italy e-mail: debora.cutuli@ 123456uniroma1.it

                This article was submitted to the journal Frontiers in Aging Neuroscience.

                †Stefano Farioli-Vecchioli and Laura Petrosini contributed equally to this work.

                Article
                10.3389/fnagi.2014.00220
                4142709
                25202271
                826542a8-3cc5-4410-9ff6-86660c26742c
                Copyright © 2014 Cutuli, De Bartolo, Caporali, Laricchiuta, Foti, Ronci, Rossi, Neri, Spalletta, Caltagirone, Farioli-Vecchioli and Petrosini.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 20 June 2014
                : 05 August 2014
                Page count
                Figures: 7, Tables: 2, Equations: 0, References: 84, Pages: 17, Words: 12658
                Categories
                Neuroscience
                Original Research Article

                Neurosciences
                aging,omega-3 fatty acids,cognitive decline,hippocampus,neuroprotection
                Neurosciences
                aging, omega-3 fatty acids, cognitive decline, hippocampus, neuroprotection

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