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      Towards a Unified Understanding of Lithium Action in Basic Biology and its Significance for Applied Biology

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          Abstract

          Lithium has literally been everywhere forever, since it is one of the three elements created in the Big Bang. Lithium concentration in rocks, soil, and fresh water is highly variable from place to place, and has varied widely in specific regions over evolutionary and geologic time. The biological effects of lithium are many and varied. Based on experiments in which animals are deprived of lithium, lithium is an essential nutrient. At the other extreme, at lithium ingestion sufficient to raise blood concentration significantly over 1 mM/, lithium is acutely toxic. There is no consensus regarding optimum levels of lithium intake for populations or individuals—with the single exception that lithium is a generally accepted first-line therapy for bipolar disorder, and specific dosage guidelines for sufferers of that condition are generally agreed on. Epidemiological evidence correlating various markers of social dysfunction and disease vs. lithium level in drinking water suggest benefits of moderately elevated lithium compared to average levels of lithium intake. In contrast to other biologically significant ions, lithium is unusual in not having its concentration in fluids of multicellular animals closely regulated. For hydrogen ions, sodium ions, potassium ions, calcium ions, chloride ions, and magnesium ions, blood and extracellular fluid concentrations are closely and necessarily regulated by systems of highly selective channels, and primary and secondary active transporters. Lithium, while having strong biological activity, is tolerated over body fluid concentrations ranging over many orders of magnitude. The lack of biological regulation of lithium appears due to lack of lithium-specific binding sites and selectivity filters. Rather lithium exerts its myriad physiological and biochemical effects by competing for macromolecular sites that are relatively specific for other cations, most especially for sodium and magnesium. This review will consider what is known about the nature of this competition and suggest using and extending this knowledge towards the goal of a unified understanding of lithium in biology and the application of that understanding in medicine and nutrition.

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          Most cited references126

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          Distribution of the Elements in Some Major Units of the Earth's Crust

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            Essential role of BDNF in the mesolimbic dopamine pathway in social defeat stress.

            Mice experiencing repeated aggression develop a long-lasting aversion to social contact, which can be normalized by chronic, but not acute, administration of antidepressant. Using viral-mediated, mesolimbic dopamine pathway-specific knockdown of brain-derived neurotrophic factor (BDNF), we showed that BDNF is required for the development of this experience-dependent social aversion. Gene profiling in the nucleus accumbens indicates that local knockdown of BDNF obliterates most of the effects of repeated aggression on gene expression within this circuit, with similar effects being produced by chronic treatment with antidepressant. These results establish an essential role for BDNF in mediating long-term neural and behavioral plasticity in response to aversive social experiences.
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              Adult hippocampal neurogenesis buffers stress responses and depressive behavior

              Summary Glucocorticoids are released in response to stressful experiences and serve many beneficial homeostatic functions. However, dysregulation of glucocorticoids is associated with cognitive impairments and depressive illness 1, 2 . In the hippocampus, a brain region densely populated with receptors for stress hormones, stress and glucocorticoids strongly inhibit adult neurogenesis 3 . Decreased neurogenesis has been implicated in the pathogenesis of anxiety and depression, but direct evidence for this role is lacking 4, 5 . Here we show that adult-born hippocampal neurons are required for normal expression of the endocrine and behavioral components of the stress response. Using transgenic and radiation methods to specifically inhibit adult neurogenesis, we find that glucocorticoid levels are slower to recover after moderate stress and are less suppressed by dexamethasone in neurogenesis-deficient mice compared with intact mice, consistent with a role for the hippocampus in regulation of the hypothalamic-pituitary-adrenal (HPA) axis 6, 7 . Relative to controls, neurogenesis-deficient mice showed increased food avoidance in a novel environment after acute stress, increased behavioral despair in the forced swim test, and decreased sucrose preference, a measure of anhedonia. These findings identify a small subset of neurons within the dentate gyrus that are critical for hippocampal negative control of the HPA axis and support a direct role for adult neurogenesis in depressive illness.
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                Author and article information

                Contributors
                jake@illinois.edu
                Journal
                J Membr Biol
                J. Membr. Biol
                The Journal of Membrane Biology
                Springer US (New York )
                0022-2631
                1432-1424
                10 November 2017
                10 November 2017
                2017
                : 250
                : 6
                : 587-604
                Affiliations
                [1 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                [2 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Center for Biophysics and Computational Biology, University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                [3 ]ISNI 0000 0000 9284 9490, GRID grid.418920.6, Department of Biosciences, , COMSATS Institute of Information Technology, ; Islamabad, Pakistan
                [4 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Department of Animal Sciences, , University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                [5 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                [6 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Neuroscience Program, , University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                [7 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, National Center for Supercomputing Applications, University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                [8 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Department of Molecular and Integrative Physiology, , University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                [9 ]ISNI 0000 0000 9482 7121, GRID grid.267313.2, Department of Cell Biology, , UT Southwestern Medical Center, ; Dallas, TX USA
                [10 ]ISNI 0000 0001 2353 285X, GRID grid.170693.a, Department of Physics, , University of South Florida, ; Tampa, FL USA
                [11 ]ISNI 0000 0004 1936 9991, GRID grid.35403.31, Illinois Informatics Institute, , University of Illinois at Urbana-Champaign, ; Urbana, IL USA
                [12 ]ISNI 0000 0004 1936 9676, GRID grid.133342.4, Present Address: Department of Psychological and Brain Sciences, , University of California at Santa Barbara, ; Santa Barbara, CA USA
                Author information
                http://orcid.org/0000-0002-7892-5295
                Article
                9998
                10.1007/s00232-017-9998-2
                5696506
                29127487
                25fec82c-a662-42e3-a472-700276ea62c3
                © The Author(s) 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 22 July 2017
                : 21 October 2017
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                © Springer Science+Business Media, LLC, part of Springer Nature 2017

                Molecular biology
                ion channels and transporters,magnesium-dependent enzymes,physical properties of biological membranes

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