SIRT3 activator Honokiol attenuates β-Amyloid by modulating amyloidogenic pathway
暂无分享,去创建一个
Timothy Moore | Rajesh Amin | Vishnu Suppiramaniam | Muralikrishnan Dhanasekaran | Manoj Govindarajulu | R. Amin | S. Ramesh | V. Suppiramaniam | Ellery Jones | Sindhu Ramesh | Manoj Govindarajulu | Tyler Lynd | Gwyneth Briggs | Danielle Adamek | Ellery Jones | Jake Heiner | Mohammed Majrashi | Mohammed Majrashi | Timothy Moore | M. Dhanasekaran | Tyler Lynd | G. Briggs | D. Adamek | Jake Heiner | Tyler O Lynd | Mohammed A Majrashi | M. Majrashi
[1] M. Buabeid,et al. Immunological alteration & toxic molecular inductions leading to cognitive impairment & neurotoxicity in transgenic mouse model of Alzheimer's disease , 2017, Life sciences.
[2] Nazanin Mirzaei,et al. PPARγ-coactivator-1α gene transfer reduces neuronal loss and amyloid-β generation by reducing β-secretase in an Alzheimer’s disease model , 2016, Proceedings of the National Academy of Sciences.
[3] Zhi-xiu Lin,et al. Neuroprotective effects of honokiol against beta-amyloid-induced neurotoxicity via GSK-3β and β-catenin signaling pathway in PC12 cells , 2016, Neurochemistry International.
[4] T. Lai,et al. Amyloid-β suppresses AMP-activated protein kinase (AMPK) signaling and contributes to α-synuclein-induced cytotoxicity , 2016, Experimental Neurology.
[5] Y. Chen,et al. Glucose regulates amyloid β production via AMPK , 2015, Journal of Neural Transmission.
[6] D. Holtzman,et al. Three dimensions of the amyloid hypothesis: time, space and 'wingmen' , 2015, Nature Neuroscience.
[7] S. Tangvarasittichai. Oxidative stress, insulin resistance, dyslipidemia and type 2 diabetes mellitus. , 2015, World journal of diabetes.
[8] Anil Kumar,et al. A review on Alzheimer’s disease pathophysiology and its management: an update , 2015, Pharmacological reports : PR.
[9] Dean P. Jones,et al. Honokiol blocks and reverses cardiac hypertrophy in mice by activating mitochondrial SIRT3 , 2015, Nature Communications.
[10] Y. Fukuyama,et al. Nonpeptide neurotrophic agents useful in the treatment of neurodegenerative diseases such as Alzheimer's disease. , 2015, Journal of pharmacological sciences.
[11] C. Arias,et al. Cellular and metabolic alterations in the hippocampus caused by insulin signalling dysfunction and its association with cognitive impairment during aging and Alzheimer's disease: studies in animal models , 2015, Diabetes/metabolism research and reviews.
[12] N. Turner,et al. Mitochondrial dysfunction and insulin resistance: an update , 2014, Endocrine connections.
[13] T. Denney,et al. The role of frataxin in doxorubicin‐mediated cardiac hypertrophy (648.6) , 2014, American journal of physiology. Heart and circulatory physiology.
[14] J. Silberring,et al. Metabolism of Cryptic Peptides Derived from Neuropeptide FF Precursors: The Involvement of Insulin-Degrading Enzyme , 2014, International journal of molecular sciences.
[15] P. Picone,et al. Mitochondrial Dysfunction: Different Routes to Alzheimer's Disease Therapy , 2014, Oxidative medicine and cellular longevity.
[16] R. Swerdlow,et al. The Alzheimer's disease mitochondrial cascade hypothesis: progress and perspectives. , 2014, Biochimica et biophysica acta.
[17] S. M. de la Monte,et al. Brain metabolic dysfunction at the core of Alzheimer's disease. , 2014, Biochemical pharmacology.
[18] Hoau Yan Wang,et al. The nature, significance, and glucagon-like peptide-1 analog treatment of brain insulin resistance in Alzheimer's disease , 2014, Alzheimer's & Dementia.
[19] S. Noha,et al. Honokiol: A non-adipogenic PPARγ agonist from nature☆ , 2013, Biochimica et biophysica acta.
[20] Zhichun Chen,et al. Decoding Alzheimer's disease from perturbed cerebral glucose metabolism: Implications for diagnostic and therapeutic strategies , 2013, Progress in Neurobiology.
[21] Ling Wei,et al. Neuro-Modulating Effects of Honokiol: A Review , 2013, Front. Neurol..
[22] Dan-shen Zhang,et al. Oxidative stress, mitochondrial damage and neurodegenerative diseases , 2013, Neural regeneration research.
[23] Julie St-Pierre,et al. PGC1&agr; and mitochondrial metabolism – emerging concepts and relevance in ageing and neurodegenerative disorders , 2012, Journal of Cell Science.
[24] C. Sutherland,et al. Insulin resistance in the brain: an old-age or new-age problem? , 2012, Biochemical pharmacology.
[25] M. Mattson,et al. Soluble amyloid precursor protein-α modulates β-secretase activity and amyloid-β generation , 2012, Nature Communications.
[26] S. Weggen,et al. Autoreactive‐Aβ antibodies promote APP β‐secretase processing , 2012, Journal of neurochemistry.
[27] S. Monte. Brain Insulin Resistance and Deficiency as Therapeutic Targets in Alzheimer's Disease , 2012 .
[28] S. Monte. Contributions of Brain Insulin Resistance and Deficiency in Amyloid-Related Neurodegeneration in Alzheimer’s Disease , 2012, Drugs.
[29] H. Soininen,et al. Midlife vascular risk factors and Alzheimer's disease: evidence from epidemiological studies. , 2012, Journal of Alzheimer's disease : JAD.
[30] M. Chaves,et al. Mechanisms of Brain Aging Regulation by Insulin: Implications for Neurodegeneration in Late-Onset Alzheimer's Disease , 2011, ISRN neurology.
[31] Hui Zheng,et al. Biology and pathophysiology of the amyloid precursor protein , 2011, Molecular Neurodegeneration.
[32] S. H. Kim,et al. Neuronal Sirt3 Protects against Excitotoxic Injury in Mouse Cortical Neuron Culture , 2011, PloS one.
[33] S. Weggen,et al. Presenilin‐1 but not amyloid precursor protein mutations present in mouse models of Alzheimer’s disease attenuate the response of cultured cells to γ‐secretase modulators regardless of their potency and structure , 2011, Journal of neurochemistry.
[34] Y. Yun,et al. 4-O-methylhonokiol attenuated memory impairment through modulation of oxidative damage of enzymes involving amyloid-β generation and accumulation in a mouse model of Alzheimer's disease. , 2011, Journal of Alzheimer's disease : JAD.
[35] N. Bogdanovic,et al. PPARγ co-activator-1α (PGC-1α) reduces amyloid-β generation through a PPARγ-dependent mechanism. , 2011, Journal of Alzheimer's disease : JAD.
[36] Huaxi Xu,et al. APP processing in Alzheimer's disease , 2011, Molecular Brain.
[37] Danica Chen,et al. Calorie restriction reduces oxidative stress by SIRT3-mediated SOD2 activation. , 2010, Cell metabolism.
[38] A. Hofman,et al. Insulin metabolism and the risk of Alzheimer disease , 2010, Neurology.
[39] Wei Yu,et al. Sirt3 Mediates Reduction of Oxidative Damage and Prevention of Age-Related Hearing Loss under Caloric Restriction , 2010, Cell.
[40] S. Jo,et al. Swedish mutation within amyloid precursor protein modulates global gene expression towards the pathogenesis of Alzheimer's disease. , 2010, BMB reports.
[41] A. Chow,et al. Neuroprotective effect of honokiol and magnolol, compounds from Magnolia officinalis, on beta‐amyloid‐induced toxicity in PC12 cells , 2010, Phytotherapy research : PTR.
[42] Huabing Zhang,et al. Sirtuin 3, a New Target of PGC-1α, Plays an Important Role in the Suppression of ROS and Mitochondrial Biogenesis , 2010, PloS one.
[43] J. Orgogozo,et al. Improved Mitochondrial Function in Brain Aging and Alzheimer Disease – the New Mechanism of Action of the Old Metabolic Enhancer Piracetam , 2010, Front. Neurosci..
[44] J. Simon,et al. AMP-activated Protein Kinase Signaling Activation by Resveratrol Modulates Amyloid-β Peptide Metabolism* , 2010, The Journal of Biological Chemistry.
[45] George Perry,et al. Mitochondrial dysfunction is a trigger of Alzheimer's disease pathophysiology. , 2010, Biochimica et biophysica acta.
[46] Robert V Farese,et al. SIRT 3 regulates mitochondrial fatty-acid oxidation by reversible enzyme deacetylation , 2010 .
[47] M. Jendrach,et al. Mitochondrial dysfunction: An early event in Alzheimer pathology accumulates with age in AD transgenic mice , 2009, Neurobiology of Aging.
[48] Q. Tong,et al. Diet and exercise signals regulate SIRT3 and activate AMPK and PGC-1α in skeletal muscle , 2009, Aging.
[49] J. Buxbaum,et al. PGC-1alpha expression decreases in the Alzheimer disease brain as a function of dementia. , 2009, Archives of neurology.
[50] V. Suppiramaniam,et al. Neurotoxic Effects of Methamphetamine , 2009, Neurochemical Research.
[51] Shiwei Song,et al. A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis , 2008, Proceedings of the National Academy of Sciences.
[52] S. Heales,et al. Oxidative stress and mitochondrial dysfunction in neurodegeneration; cardiolipin a critical target? , 2008, Biochimica et biophysica acta.
[53] H. Fukui,et al. The mitochondrial impairment, oxidative stress and neurodegeneration connection: reality or just an attractive hypothesis? , 2008, Trends in Neurosciences.
[54] W. C. Hallows,et al. Where in the cell is SIRT3?--functional localization of an NAD+-dependent protein deacetylase. , 2008, The Biochemical journal.
[55] M. Mattson,et al. Oxidative stress activates a positive feedback between the γ‐ and β‐secretase cleavages of the β‐amyloid precursor protein , 2007 .
[56] B. Spiegelman,et al. AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1α , 2007, Proceedings of the National Academy of Sciences.
[57] P. Bickford,et al. Oxidative Stress and the Aging Brain: From Theory to Prevention , 2007 .
[58] D. Leibfritz,et al. Free radicals and antioxidants in normal physiological functions and human disease. , 2007, The international journal of biochemistry & cell biology.
[59] S. Craft. Insulin Resistance Syndrome and Alzheimer Disease: Pathophysiologic Mechanisms and Therapeutic Implications , 2006, Alzheimer disease and associated disorders.
[60] J. Quinn,et al. Mitochondria are a direct site of A beta accumulation in Alzheimer's disease neurons: implications for free radical generation and oxidative damage in disease progression. , 2006, Human molecular genetics.
[61] M. Folstein,et al. Insulin, insulin-degrading enzyme and amyloid-β peptide in Alzheimer's disease: review and hypothesis , 2006, Neurobiology of Aging.
[62] P. Reddy,et al. Can herbs provide a new generation of drugs for treating Alzheimer's disease? , 2005, Brain Research Reviews.
[63] Izumi Horikawa,et al. Evolutionarily conserved and nonconserved cellular localizations and functions of human SIRT proteins. , 2005, Molecular biology of the cell.
[64] A. Artola,et al. Insulin modulates hippocampal activity‐dependent synaptic plasticity in a N‐methyl‐d‐aspartate receptor and phosphatidyl‐inositol‐3‐kinase‐dependent manner , 2005, Journal of neurochemistry.
[65] Q. Tong,et al. SIRT3, a Mitochondrial Sirtuin Deacetylase, Regulates Mitochondrial Function and Thermogenesis in Brown Adipocytes* , 2005, Journal of Biological Chemistry.
[66] J. Wands,et al. Impaired insulin and insulin-like growth factor expression and signaling mechanisms in Alzheimer's disease--is this type 3 diabetes? , 2005, Journal of Alzheimer's disease : JAD.
[67] J. Gee,et al. Autophagy, proteasomes, lipofuscin, and oxidative stress in the aging brain. , 2004, The international journal of biochemistry & cell biology.
[68] R. Mayeux,et al. Hyperinsulinemia and risk of Alzheimer disease , 2004, Neurology.
[69] D. Alkon,et al. Insulin and the insulin receptor in experimental models of learning and memory. , 2004, European journal of pharmacology.
[70] H. Cai,et al. Amyloid β peptide load is correlated with increased β-secretase activity in sporadic Alzheimer's disease patients , 2004 .
[71] C. Peers,et al. Hypoxic remodelling of Ca2+ mobilization in type I cortical astrocytes: involvement of ROS and pro‐amyloidogenic APP processing , 2003, Journal of neurochemistry.
[72] H. Cai,et al. Amyloid beta peptide load is correlated with increased beta-secretase activity in sporadic Alzheimer's disease patients. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[73] K. Morgan,et al. Amyloid precursor protein (APP) and the biology of proteolytic processing: relevance to Alzheimer's disease. , 2003, The international journal of biochemistry & cell biology.
[74] E. Ravussin,et al. Calorie restriction and aging: review of the literature and implications for studies in humans. , 2003, The American journal of clinical nutrition.
[75] Matthew P. Frosch,et al. Insulin-degrading enzyme regulates the levels of insulin, amyloid β-protein, and the β-amyloid precursor protein intracellular domain in vivo , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[76] P. Puigserver,et al. Peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC-1 alpha): transcriptional coactivator and metabolic regulator. , 2003, Endocrine reviews.
[77] B. Spiegelman. Peroxisome Proliferator-Activated Receptor-Coactivator 1 ( PGC-1 ) : Transcriptional Coactivator and Metabolic Regulator , 2003 .
[78] P. Wong,et al. Elevated β-secretase expression and enzymatic activity detected in sporadic Alzheimer disease , 2003, Nature Medicine.
[79] George Perry,et al. Role of mitochondrial dysfunction in Alzheimer's disease , 2002, Journal of neuroscience research.
[80] J. Wands,et al. Chronic gestational exposure to ethanol impairs insulin-stimulated survival and mitochondrial function in cerebellar neurons , 2002, Cellular and Molecular Life Sciences CMLS.
[81] C. Arias,et al. β‐Amyloid peptide induces ultrastructural changes in synaptosomes and potentiates mitochondrial dysfunction in the presence of ryanodine , 2002, Journal of neuroscience research.
[82] A. Nunomura,et al. Oxidative Damage Is the Earliest Event in Alzheimer Disease , 2001, Journal of neuropathology and experimental neurology.
[83] S. Hoyer,et al. Inhibition of the Neuronal Insulin Receptor An in Vivo Model for Sporadic Alzheimer Disease? , 2000, Annals of the New York Academy of Sciences.
[84] S. Hoyer,et al. Inhibition of the Neuronal Insulin Receptor Causes Alzheimer‐like Disturbances in Oxidative/Energy Brain Metabolism and in Behavior in Adult Rats , 1999, Annals of the New York Academy of Sciences.
[85] J. Treanor,et al. Beta-secretase cleavage of Alzheimer's amyloid precursor protein by the transmembrane aspartic protease BACE. , 1999, Science.
[86] L. Hersh,et al. Insulin-degrading Enzyme Regulates Extracellular Levels of Amyloid β-Protein by Degradation* , 1998, The Journal of Biological Chemistry.
[87] K. Mohanakumar,et al. Neuroprotection by bromocriptine against 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine‐induced neurotoxicity in mice1 , 1998, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[88] M. Smith,et al. Evidence of oxidative stress and in vivo neurotoxicity of beta-amyloid in a transgenic mouse model of Alzheimer's disease: a chronic oxidative paradigm for testing antioxidant therapies in vivo. , 1998, The American journal of pathology.
[89] M. Williams,et al. Development of Insulin Resistance in 3T3-L1 Adipocytes* , 1997, The Journal of Biological Chemistry.
[90] J. Hardy,et al. Increased amyloid-β42(43) in brains of mice expressing mutant presenilin 1 , 1996, Nature.
[91] A. Schapira,et al. Oxidative stress and mitochondrial dysfunction in neurodegeneration , 1996, Current opinion in neurology.
[92] D. Selkoe,et al. The Swedish mutation causes early-onset Alzheimer's disease by β-secretase cleavage within the secretory pathway , 1995, Nature Medicine.
[93] R. Ramsay,et al. Inhibition of mitochondrial NADH dehydrogenase by pyridine derivatives and its possible relation to experimental and idiopathic parkinsonism. , 1986, Biochemical and biophysical research communications.
[94] R. Burk,et al. Glutathione peroxidase activity in selenium-deficient rat liver. , 1976, Biochemical and biophysical research communications.
[95] S. Marklund,et al. Involvement of the superoxide anion radical in the autoxidation of pyrogallol and a convenient assay for superoxide dismutase. , 1974, European journal of biochemistry.
[96] A. Tzagoloff,et al. [45] Cytochrome oxidase from beef heart mitochondria , 1967 .
[97] E. Wills,et al. MECHANISMS OF LIPID PEROXIDE FORMATION IN TISSUES. ROLE OF METALS AND HAEMATIN PROTEINS IN THE CATALYSIS OF THE OXIDATION UNSATURATED FATTY ACIDS. , 1965, Biochimica et biophysica acta.
[98] I W SIZER,et al. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. , 1952, The Journal of biological chemistry.