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dc.contributor.editorVázquez-Carrera, Manuel
dc.contributor.editorWahli, Walter
dc.date.accessioned2022-06-21T09:06:55Z
dc.date.available2022-06-21T09:06:55Z
dc.date.issued2022
dc.identifierONIX_20220621_9783036541921_14
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/84580
dc.description.abstractMounting evidence suggests a bidirectional relationship between metabolism and inflammation. Molecular crosstalk between these processes occurs at different levels with the participation of nuclear receptors, including peroxisome proliferator-activated receptors (PPARs). There are three PPAR isotypes, α, β/δ, and γ, which modulate metabolic and inflammatory pathways, making them key for the control of cellular, organ, and systemic processes. PPAR activity is governed by fatty acids and fatty acid derivatives, and by drugs used in clinics (glitazones and fibrates). The study of PPAR action, also modulated by post-translational modifications, has enabled extraordinary advances in the understanding of the multifaceted roles of these receptors in metabolism, energy homeostasis, and inflammation both in health and disease. This Special Issue of IJMS includes a broad range of basic and translational article, both original research and reviews, focused on the latest developments in the regulation of metabolic and/or inflammatory processes by PPARs in all organs and the microbiomes of different vertebrate species.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: generalen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PS Biology, life sciencesen_US
dc.subject.classificationthema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSB Biochemistryen_US
dc.subject.othernuclear receptor
dc.subject.othergene transcription
dc.subject.otherinflammation
dc.subject.othermolecular docking
dc.subject.otherPPARβ/δ
dc.subject.otherlung
dc.subject.otherpulmonary artery
dc.subject.otherGW0742
dc.subject.otherGSK3787
dc.subject.otherdocking
dc.subject.otherlipopolysaccharide (LPS)
dc.subject.otherPPARγ ligand
dc.subject.othercoumarin
dc.subject.otherfluorescent ligand
dc.subject.otherscreening
dc.subject.othercrystal structure
dc.subject.otherPPAR
dc.subject.otheratopic dermatitis
dc.subject.otherpsoriasis
dc.subject.othermetabolic reprograming
dc.subject.otherglucose
dc.subject.otherfatty acids
dc.subject.othermycobacteria
dc.subject.otherM. tuberculosis
dc.subject.otherM. leprae
dc.subject.otherPPARs
dc.subject.otherlipid droplets
dc.subject.othermetabolic alterations
dc.subject.otherhepatic damage
dc.subject.othernuclear factors
dc.subject.otherpharmacological targets
dc.subject.otherAMPK
dc.subject.otherGDF15
dc.subject.otherinsulin resistance
dc.subject.othertype 2 diabetes mellitus
dc.subject.otherperoxisome proliferator-activated receptor gamma (PPARγ)
dc.subject.otherreal-time PCR
dc.subject.otherELISA
dc.subject.otherimmunohistochemistry
dc.subject.othersignaling pathway
dc.subject.otherPPAR gamma
dc.subject.otherbrain
dc.subject.otherneural stem cells
dc.subject.otherinfection
dc.subject.otherneuroinflammation
dc.subject.otherHIV
dc.subject.otherZika
dc.subject.othercytomegalovirus
dc.subject.otherneurogenesis
dc.subject.othermicroglia
dc.subject.otherliver damage
dc.subject.othertoll-like receptor 4
dc.subject.otherP2Y2 receptor
dc.subject.othermetabolic syndrome
dc.subject.otherresveratrol
dc.subject.otherquercetin
dc.subject.otherPPARα
dc.subject.otherperoxisome
dc.subject.otherβ-oxidation
dc.subject.otherPPRE
dc.subject.otherligand
dc.subject.othercoregulator
dc.subject.othermicronutrients
dc.subject.otherPPARα knockout
dc.subject.otheradipose tissue
dc.subject.otherbrowning
dc.subject.otherlipid metabolism
dc.subject.otherdepression
dc.subject.otherPPARg
dc.subject.otherneuropathology
dc.subject.othercorticotropin releasing hormone
dc.subject.othernorepinephrine
dc.subject.othersubgenual prefrontal cortex
dc.subject.otheramygdala
dc.subject.othernucleus accumbens
dc.subject.othercommon carotid artery occlusion
dc.subject.otherelectroretinography
dc.subject.otherfibroblast growth factor 21
dc.subject.otherpemafibrate
dc.subject.otherperoxisome proliferator-activated receptor alpha
dc.subject.otherretinal ischemia
dc.subject.otherskeletal muscle
dc.subject.othersubstrate metabolism
dc.subject.othernonalcoholic fatty liver disease (NAFLD)
dc.subject.othersex dimorphism
dc.subject.otherlipidomics
dc.subject.otherhepatic sex-biased gene expression
dc.subject.otherPPARγ
dc.subject.otherpulmonary arterial hypertension
dc.subject.otherTGFβ
dc.subject.othervascular injury
dc.subject.otherproliferation
dc.subject.otherkidney fibrosis
dc.subject.otherpattern-recognition receptors
dc.subject.otherphagocytosis
dc.subject.othernitric oxide synthase
dc.subject.otherfenofibrate
dc.subject.otheroleoylethanolamide
dc.subject.otherpalmitoylethanolamide
dc.subject.othercancer
dc.subject.otherimmunity
dc.subject.otherobesity
dc.subject.otherdiabetes
dc.subject.othermiRNA
dc.subject.otherDNA methylation
dc.subject.otherhistone modification
dc.subject.otherperoxisome-proliferator-activated receptor
dc.subject.otherfatty acid oxidation
dc.subject.otherdoping control
dc.subject.otherregulatory T cells
dc.subject.otherexercise
dc.subject.othernuclear receptors
dc.subject.othernutrigenomics
dc.subject.otherenergy homeostasis
dc.subject.otherdairy animals
dc.subject.othernon-alcoholic fatty liver disease (NAFLD)
dc.subject.othernon-alcoholic steatohepatitis (NASH)
dc.subject.otherperoxisome proliferator-activated receptors (PPAR)
dc.subject.otherbezafibrate
dc.subject.otherfenofibric acid
dc.subject.otherperoxisome proliferator-activated receptor
dc.subject.otherdual/pan agonist
dc.subject.otherX-ray crystallography
dc.subject.othern/a
dc.titlePPARs as Key Mediators of Metabolic and Inflammatory Regulation
dc.typebook
oapen.identifier.doi10.3390/books978-3-0365-4191-4
oapen.relation.isPublishedBy46cabcaa-dd94-4bfe-87b4-55023c1b36d0
oapen.relation.isbn9783036541921
oapen.relation.isbn9783036541914
oapen.pages456


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