Altered insulin secretion dynamics relate to oxidative stress and inflammasome activation in children with obesity and insulin resistance

dc.contributor.authorGonzález-Domínguez, Álvaro
dc.contributor.authorBelmonte, Thalía
dc.contributor.authorDomínguez-Riscat, Jesús
dc.contributor.authorRuíz-Ocaña, Pablo
dc.contributor.authorMuela-Zarzuela, Inés
dc.contributor.authorSaez-Benito, Ana
dc.contributor.authorMontañez, Raúl
dc.contributor.authorMateos, Rosa María
dc.contributor.authorLechuga-Sancho, Alfonso María
dc.date.accessioned2024-11-26T10:51:54Z
dc.date.available2024-11-26T10:51:54Z
dc.date.issued2023-08-20
dc.departamentoBiología Molecular y Bioquímica
dc.description.abstractBackground: Insulin resistance (IR) is considered the main driver of obesity related metabolic complications, and is related to oxidative stress and inflammation, which in turn promote each other. There is currently no specific definition of IR in children, rather, that for adult population is used by pediatric endocrinologists instead. Altered insulin secretion dynamics are associated with worse metabolic profiles and type 2 diabetes mellitus development, thus we aimed to test whether insulin response relates to oxidative stress and inflammation in children. Methods: We conducted a case-control study, including 132 children classified as follows: 33 children without obesity (Lean); 42 with obesity but no IR according to the American Diabetes Association criteria for adults (OBIR-); 25 with obesity and IR and an early insulin response to an oral glucose tolerance test (OGTT) (EP-OBIR +); 32 with obesity, IR, and a late insulin peak (LP-OBIR +); and studied variables associated with lipid and carbohydrate metabolism, oxidative stress, inflammation and inflammasome activation. Results: The measured parameters of children with obesity, IR, and an early insulin response were similar to those of children with obesity but without IR. It was late responders who presented an impaired antioxidant system and elevated oxidative damage in erythrocytes and plasma, and inflammasome activation at their white blood cells, despite lower classical inflammation markers. Increased uric acid levels seems to be one of the underlying mechanisms for inflammasome activation. Conclusions: It is insulin response to an OGTT that identifies children with obesity suffering oxidative stress and inflammasome activation more specifically. Uric acid could be mediating this pathological inflammatory response by activating NLRP3 in peripheral blood mononuclear cells.es_ES
dc.description.sponsorshipFunding for open access publishing: Universidad de Cádiz/CBUA. The authors would like to express their gratitude to Dr. James Patrick Boylan (PhD), for his English language edition of the final version. Funded by Spanish Government (Sanitary Research Fund (FIS)), code PI18/01316. A.G.-D. is supported by an intramural grant from the Biomedical Research and Innovation Institute of Cádiz (INiBICA), code LII19/16IN-CO24.es_ES
dc.identifier.citationGonzález-Domínguez, Á., Belmonte, T., Domínguez-Riscart, J. et al. Altered insulin secretion dynamics relate to oxidative stress and inflammasome activation in children with obesity and insulin resistance. J Transl Med 21, 559 (2023). https://doi.org/10.1186/s12967-023-04337-7es_ES
dc.identifier.doi10.1186/s12967-023-04337-7
dc.identifier.urihttps://hdl.handle.net/10630/35311
dc.language.isoenges_ES
dc.publisherSpringer Naturees_ES
dc.rights.accessRightsopen accesses_ES
dc.subjectDiabeteses_ES
dc.subject.otherChildhood obesityes_ES
dc.subject.otherInflammasome activationes_ES
dc.subject.otherInsulin resistancees_ES
dc.subject.otherOral glucose tolerance testes_ES
dc.subject.otherOxidative stresses_ES
dc.titleAltered insulin secretion dynamics relate to oxidative stress and inflammasome activation in children with obesity and insulin resistancees_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication

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