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      Central administration of afzelin extracted from Ribes fasciculatum improves cognitive and memory function in a mouse model of dementia

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          Abstract

          Neurodegenerative disorders are characterized by the decline of cognitive function and the progressive loss of memory. The dysfunctions of the cognitive and memory system are closely related to the decreases in brain-derived neurotrophic factor (BDNF) and cAMP response element-binding protein (CREB) signalings. Ribes fasciculatum, a medicinal plant grown in diverse countries, has been reported to pharmacological effects for autoimmune diseases and aging recently. Here we found that afzelin is a major compound in Ribes fasciculatum. To further examine its neuroprotective effect, the afzelin (100 ng/µl, three times a week) was administered into the third ventricle of the hypothalamus of C57BL/6 mice for one month and scopolamine was injected (i.p.) to these mice to impair cognition and memory before each behavior experiment. The electrophysiology to measure long-term potentiation and behavior tests for cognitive and memory functions were performed followed by investigating related molecular signaling pathways. Chronic administration of afzelin into the brain ameliorated synaptic plasticity and cognitive/memory behaviors in mice given scopolamine. Studies of mice’s hippocampi revealed that the response of afzelin was accountable for the restoration of the cholinergic systems and molecular signal transduction via CREB-BDNF pathways. In conclusion, the central administration of afzelin leads to improved neurocognitive and neuroprotective effects on synaptic plasticity and behaviors partly through the increase in CREB-BDNF signaling.

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          Most cited references62

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          Oxidative Stress, Synaptic Dysfunction, and Alzheimer’s Disease

          Alzheimer’s disease (AD) is a devastating neurodegenerative disorder without a cure. Most AD cases are sporadic where age represents the greatest risk factor. Lack of understanding of the disease mechanism hinders the development of efficacious therapeutic approaches. The loss of synapses in the affected brain regions correlates best with cognitive impairment in AD patients and has been considered as the early mechanism that precedes neuronal loss. Oxidative stress has been recognized as a contributing factor in aging and in the progression of multiple neurodegenerative diseases including AD. Increased production of reactive oxygen species (ROS) associated with age- and disease-dependent loss of mitochondrial function, altered metal homeostasis, and reduced antioxidant defense directly affect synaptic activity and neurotransmission in neurons leading to cognitive dysfunction. In addition, molecular targets affected by ROS include nuclear and mitochondrial DNA, lipids, proteins, calcium homeostasis, mitochondrial dynamics and function, cellular architecture, receptor trafficking and endocytosis, and energy homeostasis. Abnormal cellular metabolism in turn could affect the production and accumulation of amyloid-β (Aβ) and hyperphosphorylated Tau protein, which independently could exacerbate mitochondrial dysfunction and ROS production, thereby contributing to a vicious cycle. While mounting evidence implicates ROS in the AD etiology, clinical trials with antioxidant therapies have not produced consistent results. In this review, we will discuss the role of oxidative stress in synaptic dysfunction in AD, innovative therapeutic strategies evolved based on a better understanding of the complexity of molecular mechanisms of AD, and the dual role ROS play in health and disease.
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            Hypothalamic stem cells control aging speed partly through exosomal miRNAs

            SUMMARY Hypothalamic control of aging was recently proposed, but the responsible mechanisms still remain unclear. Here, following the observation that aging of mice started with a substantial loss of hypothalamic stem/progenitor cells that co-express Sox2 and Bmi1, we developed several mouse models with ablation of these hypothalamic cells, each of them consistently displaying an acceleration in aging-like physiological changes or shortening in lifespan. Conversely, aging retardation and lifespan extension were achieved in mid-aged mice when locally implanted with healthy hypothalamic stem/progenitor cells that were genetically engineered to survive from aging-related hypothalamic inflammatory microenvironment. Mechanistically, hypothalamic stem/progenitor cells greatly contributed to exosomal miRNAs in the cerebrospinal fluid which declined over aging, while central treatment with healthy hypothalamic stem/progenitor cells-secreted exosomes led to slowdown of aging. In conclusion, aging speed is controlled significantly by hypothalamic stem cells partially through release of exosomal miRNAs.
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              A Brief History of Long-Term Potentiation.

              Since the discovery of long-term potentiation (LTP) in 1973, thousands of papers have been published on this intriguing phenomenon, which provides a compelling cellular model for learning and memory. Although LTP has suffered considerable growing pains over the years, LTP has finally come of age. Here the rich history of LTP is reviewed. These are exciting times and the pace of discovery is remarkable.

                Author and article information

                Contributors
                cwchoi78@gmail.com
                minsoo.kim@kist.re.kr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                28 April 2021
                28 April 2021
                2021
                : 11
                : 9182
                Affiliations
                [1 ]GRID grid.35541.36, ISNI 0000000121053345, Brain Science Institute, Korea Institute of Science and Technology (KIST), ; Seoul, Republic of Korea
                [2 ]Natural Product Research Team, Gyeonggi Biocenter, Gyeonggido Business and Science Accelerator, Gyeonggi-Do, Republic of Korea
                [3 ]GRID grid.35541.36, ISNI 0000000121053345, Division of Bio-Medical Science & Technology, , University of Science and Technology KIST School, ; Seoul, Republic of Korea
                [4 ]GRID grid.412576.3, ISNI 0000 0001 0719 8994, Department of Food Science and Nutrition, , Pukyong National University, ; Busan, Republic of Korea
                [5 ]GRID grid.484628.4, ISNI 0000 0001 0943 2764, Infectious Disease Research Center, Citizen’s Health Bureau, Seoul Metropolitan Government, ; 110, Sejong-daero, Jung-gu, Seoul, 04524 Republic of Korea
                Article
                88463
                10.1038/s41598-021-88463-6
                8080596
                33911138
                32bb3462-d857-4078-85bd-8966d17551cd
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 14 August 2020
                : 13 April 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003725, National Research Foundation of Korea;
                Award ID: NRF-2020M3A9D8039920
                Funded by: FundRef http://dx.doi.org/10.13039/501100014189, Korea Institute of Planning and Evaluation for Technology in Food, Agriculture and Forestry;
                Award ID: 317042-03-2-HD020
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                biochemistry,drug discovery,neuroscience
                Uncategorized
                biochemistry, drug discovery, neuroscience

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