Exploring the Gut Microbiota–Muscle Axis in Duchenne Muscular Dystrophy
暂无分享,去创建一个
[1] Wen-jun Zhao,et al. Effect of gut microbiota-mediated tryptophan metabolism on inflammaging in frailty and sarcopenia. , 2024, The journals of gerontology. Series A, Biological sciences and medical sciences.
[2] M. Mariadassou,et al. Insight into the role of gut microbiota in Duchenne muscular dystrophy: an age-related study in mdx mice. , 2023, The American journal of pathology.
[3] Han-Jie Li,et al. The impact of microbiota-derived short-chain fatty acids on macrophage activities in disease: Mechanisms and therapeutic potentials. , 2023, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[4] Tianhao Xu,et al. Fndc5/irisin deficiency leads to dysbiosis of gut microbiota contributing to the depressive-like behaviors in mice , 2023, Brain Research.
[5] Liegang Liu,et al. Faecal microbiota transplantation from young rats attenuates age‐related sarcopenia revealed by multiomics analysis , 2023, Journal of cachexia, sarcopenia and muscle.
[6] J. Metzger,et al. Duchenne muscular dystrophy: disease mechanism and therapeutic strategies , 2023, Frontiers in Physiology.
[7] Lisha Li,et al. Immunological mechanisms of inflammatory diseases caused by gut microbiota dysbiosis: A review. , 2023, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[8] K. O'Halloran,et al. Microbes, metabolites and muscle: Is the gut–muscle axis a plausible therapeutic target in Duchenne muscular dystrophy? , 2023, Experimental physiology.
[9] L. Galasso,et al. Polyamines and Physical Activity in Musculoskeletal Diseases: A Potential Therapeutic Challenge , 2023, International journal of molecular sciences.
[10] Tianyu Li,et al. Gut-muscle axis and sepsis-induced myopathy: The potential role of gut microbiota. , 2023, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.
[11] K. Belosludtsev,et al. Ion Channels of the Sarcolemma and Intracellular Organelles in Duchenne Muscular Dystrophy: A Role in the Dysregulation of Ion Homeostasis and a Possible Target for Therapy , 2023, International journal of molecular sciences.
[12] S. Wong,et al. Gut-muscle crosstalk. A perspective on influence of microbes on muscle function , 2023, Frontiers in Medicine.
[13] R. Capasso,et al. Targeting gut dysbiosis against inflammation and impaired autophagy in Duchenne muscular dystrophy , 2023, EMBO molecular medicine.
[14] C. Villa,et al. Microbiota dysbiosis influences immune system and muscle pathophysiology of dystrophin‐deficient mice , 2022, EMBO molecular medicine.
[15] Y. Torrente,et al. Immunoproteasome Inhibition Ameliorates Aged Dystrophic Mouse Muscle Environment , 2022, International journal of molecular sciences.
[16] G. Wu,et al. Gut microbiota-bile acid-skeletal muscle axis. , 2022, Trends in microbiology.
[17] D. Kass,et al. Pharmacological TRPC6 inhibition improves survival and muscle function in mice with Duchenne muscular dystrophy , 2022, JCI insight.
[18] A. Michelucci,et al. Postdevelopmental knockout of Orai1 improves muscle pathology in a mouse model of Duchenne muscular dystrophy , 2022, The Journal of general physiology.
[19] M. Farrar,et al. Incidence of Duchenne muscular dystrophy in the modern era; an Australian study , 2022, European Journal of Human Genetics.
[20] W. MacNaughton,et al. Role of the Endocannabinoid System in the Regulation of Intestinal Homeostasis , 2022, Cellular and molecular gastroenterology and hepatology.
[21] Guangyao Li,et al. Mechanisms Involved in Gut Microbiota Regulation of Skeletal Muscle , 2022, Oxidative medicine and cellular longevity.
[22] D. Dardevet,et al. Gut microbes and muscle function: can probiotics make our muscles stronger? , 2022, Journal of cachexia, sarcopenia and muscle.
[23] Kenta Yamamoto,et al. Patients with low muscle mass have characteristic microbiome with low potential for amino acid synthesis in chronic liver disease , 2022, Scientific Reports.
[24] B. De Paepe,et al. The Role of Taurine in Skeletal Muscle Functioning and Its Potential as a Supportive Treatment for Duchenne Muscular Dystrophy , 2022, Metabolites.
[25] Jiaming Yu,et al. Ileal FXR-FGF15/19 signaling activation improves skeletal muscle loss in aged mice , 2022, Mechanisms of Ageing and Development.
[26] T. Larcher,et al. TRPC3, but not TRPC1, as a good therapeutic target for standalone or complementary treatment of DMD , 2021, Journal of translational medicine.
[27] H. Sakurai,et al. Orai1–STIM1 Regulates Increased Ca2+ Mobilization, Leading to Contractile Duchenne Muscular Dystrophy Phenotypes in Patient-Derived Induced Pluripotent Stem Cells , 2021, Biomedicines.
[28] N. A. Sagar,et al. Polyamines: Functions, Metabolism, and Role in Human Disease Management , 2021, Medical sciences.
[29] C. Goodman,et al. The Regulation of Polyamine Pathway Proteins in Models of Skeletal Muscle Hypertrophy and Atrophy - a potential role for mTORC1. , 2021, American journal of physiology. Cell physiology.
[30] D. Duan,et al. Abnormal Calcium Handling in Duchenne Muscular Dystrophy: Mechanisms and Potential Therapies , 2021, Frontiers in Physiology.
[31] Q. Xiao,et al. FGF19 protects skeletal muscle against obesity‐induced muscle atrophy, metabolic derangement and abnormal irisin levels via the AMPK/SIRT‐1/PGC‐α pathway , 2021, Journal of cellular and molecular medicine.
[32] E. Mercuri,et al. Duchenne muscular dystrophy , 2021, Nature Reviews Disease Primers.
[33] Jiaming Yu,et al. Depletion of gut microbiota induces skeletal muscle atrophy by FXR-FGF15/19 signalling , 2021, Annals of medicine.
[34] C. Romanin,et al. STIM Proteins: An Ever-Expanding Family , 2020, International journal of molecular sciences.
[35] S. Tagliaferri,et al. The Gut-Muscle Axis in Older Subjects with Low Muscle Mass and Performance: A Proof of Concept Study Exploring Fecal Microbiota Composition and Function with Shotgun Metagenomics Sequencing , 2020, International journal of molecular sciences.
[36] W. Wahli,et al. PPARs and Microbiota in Skeletal Muscle Health and Wasting , 2020, International journal of molecular sciences.
[37] D. Song,et al. Improvement in host metabolic homeostasis and alteration in gut microbiota in mice on the high-fat diet: A comparison of calcium supplements. , 2020, Food research international.
[38] K. Mackie,et al. Review of the Endocannabinoid System. , 2020, Biological Psychiatry: Cognitive Neuroscience and Neuroimaging.
[39] Chengmei Sun,et al. Therapeutic Strategies for Duchenne Muscular Dystrophy: An Update , 2020, Genes.
[40] Wei-Dong Chen,et al. The Relationship Between Gut Microbiota and Inflammatory Diseases: The Role of Macrophages , 2020, Frontiers in Microbiology.
[41] P. Rensen,et al. Role of the endocannabinoid system in the regulation of the skeletal muscle response to exercise. , 2020, Current opinion in pharmacology.
[42] T. Lesker,et al. Perturbation of the gut microbiome by Prevotella spp. enhances host susceptibility to mucosal inflammation , 2020, Mucosal Immunology.
[43] Yong Guo,et al. The gut microbiota attenuates muscle wasting by regulating energy metabolism in chemotherapy-induced malnutrition rats , 2020, Cancer Chemotherapy and Pharmacology.
[44] Shijun Hu,et al. The therapeutic potential of mesenchymal stem cells for cardiovascular diseases , 2020, Cell Death & Disease.
[45] D. Mavroudis,et al. The Prognostic Value of the Detection of Microbial Translocation in the Blood of Colorectal Cancer Patients , 2020, Cancers.
[46] M. Shimizu,et al. Low Levels of Serum Tryptophan Underlie Skeletal Muscle Atrophy , 2020, Nutrients.
[47] E. Chambers,et al. Short-chain fatty acids as potential regulators of skeletal muscle metabolism and function , 2020, Nature Metabolism.
[48] G. Lamb,et al. Higher MMP2 abundance and gelatinolytic activity in 28- & 70-d mdx compared with wild-type mice is alleviated in mdx mice with pre-natal taurine supplementation. , 2020, American journal of physiology. Cell physiology.
[49] Bruno A. Cisterna,et al. Active acetylcholine receptors prevent the atrophy of skeletal muscles and favor reinnervation , 2020, Nature Communications.
[50] R. Hajjar,et al. Single SERCA2a Therapy Ameliorated Dilated Cardiomyopathy for 18 Months in a Mouse Model of Duchenne Muscular Dystrophy. , 2020, Molecular therapy : the journal of the American Society of Gene Therapy.
[51] Anne Fernandez,et al. Interactions between gut microbiota and skeletal muscle , 2020, Nutrition and metabolic insights.
[52] A. Gasbarrini,et al. Gut Microbial, Inflammatory and Metabolic Signatures in Older People with Physical Frailty and Sarcopenia: Results from the BIOSPHERE Study , 2019, Nutrients.
[53] M. Lustgarten. The Role of the Gut Microbiome on Skeletal Muscle Mass and Physical Function: 2019 Update , 2019, Front. Physiol..
[54] Patrice D Cani,et al. Germ-free mice exhibit profound gut microbiota-dependent alterations of intestinal endocannabinoidome signaling[S] , 2019, Journal of Lipid Research.
[55] Z. Fu,et al. Lactobacillus and Bifidobacterium Improved Physiological Function and Cognitive Ability in Aged Mice by the Regulation of Gut Microbiota. , 2019, Molecular nutrition & food research.
[56] Musarrat Maisha Reza,et al. The gut microbiota influences skeletal muscle mass and function in mice , 2019, Science Translational Medicine.
[57] P. Brambilla,et al. Preliminary Evidences of Safety and Efficacy of Flavonoids- and Omega 3-Based Compound for Muscular Dystrophies Treatment: A Randomized Double-Blind Placebo Controlled Pilot Clinical Trial , 2019, Front. Neurol..
[58] M. Mariadassou,et al. Gut bacteria are critical for optimal muscle function:a potential link with glucose homeostasis. , 2019, American journal of physiology. Endocrinology and metabolism.
[59] B. Dhindsa,et al. Gigantic Stomach: A Rare Manifestation of Duchenne Muscular Dystrophy , 2019, Cureus.
[60] M. Watt,et al. Choline administration attenuates aspects of the dystrophic pathology in mdx mice , 2019, Clinical Nutrition Experimental.
[61] E. Conte,et al. A long‐term treatment with taurine prevents cardiac dysfunction in mdx mice , 2019, Translational research : the journal of laboratory and clinical medicine.
[62] Wen-Ching Huang,et al. The Beneficial Effects of Lactobacillus plantarum PS128 on High-Intensity, Exercise-Induced Oxidative Stress, Inflammation, and Performance in Triathletes , 2019, Nutrients.
[63] Guoyao Wu,et al. Protective effects of ghrelin on fasting-induced muscle atrophy in aging mice. , 2018, The journals of gerontology. Series A, Biological sciences and medical sciences.
[64] G. D’Antona,et al. Supplementation with a selective amino acid formula ameliorates muscular dystrophy in mdx mice , 2018, Scientific Reports.
[65] W. Wahli,et al. Metronidazole Causes Skeletal Muscle Atrophy and Modulates Muscle Chronometabolism , 2018, International journal of molecular sciences.
[66] E. Hyatt,et al. Increased polyamines as protective disease modifiers in congenital muscular dystrophy , 2018, Human molecular genetics.
[67] N. Câmara,et al. Chronic inflammation in skeletal muscle impairs satellite cells function during regeneration: can physical exercise restore the satellite cell niche? , 2018, The FEBS journal.
[68] K. Mori,et al. The exercise-inducible bile acid receptor Tgr5 improves skeletal muscle function in mice , 2018, The Journal of Biological Chemistry.
[69] M. Zarei,et al. PPARβ/δ: A Key Therapeutic Target in Metabolic Disorders , 2018, International journal of molecular sciences.
[70] Wei-Dong Chen,et al. Gut Microbiota: An Integral Moderator in Health and Disease , 2018, Front. Microbiol..
[71] J. McArdle,et al. Reducing sarcolipin expression mitigates Duchenne muscular dystrophy and associated cardiomyopathy in mice , 2017, Nature Communications.
[72] S. Ghosh,et al. Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System. , 2017, Cell metabolism.
[73] D. Freyssenet,et al. Fibroblast growth factor 19 regulates skeletal muscle mass and ameliorates muscle wasting in mice , 2017, Nature Medicine.
[74] Y. Takei,et al. The Associations between Circulating Bile Acids and the Muscle Volume in Patients with Non-alcoholic Fatty Liver Disease (NAFLD) , 2017, Internal medicine.
[75] Elaine Holmes,et al. The microbiome of professional athletes differs from that of more sedentary subjects in composition and particularly at the functional metabolic level , 2017, Gut.
[76] M. Oray,et al. Long-term side effects of glucocorticoids , 2016, Expert opinion on drug safety.
[77] Patrice D Cani,et al. Endocannabinoids — at the crossroads between the gut microbiota and host metabolism , 2015, Nature Reviews Endocrinology.
[78] M. Grounds,et al. Taurine deficiency, synthesis and transport in the mdx mouse model for Duchenne Muscular Dystrophy. , 2015, The international journal of biochemistry & cell biology.
[79] T. Horiba,et al. Dietary obacunone supplementation stimulates muscle hypertrophy, and suppresses hyperglycemia and obesity through the TGR5 and PPARγ pathway. , 2015, Biochemical and biophysical research communications.
[80] G. Comi,et al. Improvement of Endurance of DMD Animal Model Using Natural Polyphenols , 2014, BioMed research international.
[81] Takashi Ito,et al. Tissue Depletion of Taurine Accelerates Skeletal Muscle Senescence and Leads to Early Death in Mice , 2014, PloS one.
[82] E. Murphy,et al. Exercise and associated dietary extremes impact on gut microbial diversity , 2014, Gut.
[83] F. Bäckhed,et al. Gut microbiota regulates bile acid metabolism by reducing the levels of tauro-beta-muricholic acid, a naturally occurring FXR antagonist. , 2013, Cell metabolism.
[84] F. Gamelin,et al. The role of the endocannabinoid system in skeletal muscle and metabolic adaptations to exercise: potential implications for the treatment of obesity , 2012, Obesity reviews : an official journal of the International Association for the Study of Obesity.
[85] M. Zatz,et al. Combined Effect of AMPK/PPAR Agonists and Exercise Training in mdx Mice Functional Performance , 2012, PloS one.
[86] J. Verrax,et al. Restoring Specific Lactobacilli Levels Decreases Inflammation and Muscle Atrophy Markers in an Acute Leukemia Mouse Model , 2012, PloS one.
[87] D. Douek,et al. Microbial translocation across the GI tract. , 2012, Annual review of immunology.
[88] J. Clemente,et al. The Impact of the Gut Microbiota on Human Health: An Integrative View , 2012, Cell.
[89] V. Marzo,et al. Peripheral effects of the endocannabinoid system in energy homeostasis: Adipose tissue, liver and skeletal muscle , 2011, Reviews in Endocrine and Metabolic Disorders.
[90] R. Hébert,et al. Pharmacological activation of PPARbeta/delta stimulates utrophin A expression in skeletal muscle fibers and restores sarcolemmal integrity in mature mdx mice. , 2009, Human molecular genetics.
[91] B. Aronow,et al. Calcium influx is sufficient to induce muscular dystrophy through a TRPC-dependent mechanism , 2009, Proceedings of the National Academy of Sciences.
[92] H. Harmsen,et al. Fecal Microbiota Composition and Frailty , 2005, Applied and Environmental Microbiology.
[93] M. Badea,et al. Elevated serum creatine phosphokinase in choline-deficient humans: mechanistic studies in C2C12 mouse myoblasts. , 2004, The American journal of clinical nutrition.
[94] A. Emery,et al. The muscular dystrophies , 2002, The Lancet.
[95] W. Bubb,et al. Abnormalities in brain biochemistry associated with lack of dystrophin: studies of the mdx mouse , 2002, Neuromuscular Disorders.
[96] C. Glass,et al. Signaling by nuclear receptors. , 2001, Cold Spring Harbor perspectives in biology.
[97] J. Blusztajn,et al. Generation of choline for acetylcholine synthesis by phospholipase D isoforms , 2001, BMC Neuroscience.
[98] G. Radda,et al. Brain biochemistry in Duchenne muscular dystrophy: A 1H magnetic resonance and neuropsychological study , 1998, Journal of the Neurological Sciences.
[99] V. Bucci,et al. The nursing home elder microbiome stability and associations with age, frailty, nutrition and physical location , 2018, Journal of medical microbiology.
[100] D. Allen,et al. Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. , 2016, Physiological reviews.
[101] J. Berger,et al. The mechanisms of action of PPARs. , 2002, Annual review of medicine.