Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/108
DC FieldValueLanguage
dc.contributor.authorMirjana Bećarevićen_US
dc.contributor.authorBožana Nikolićen_US
dc.contributor.authorSvetlana Ignjatovićen_US
dc.date.accessioned2019-09-23T10:03:54Z-
dc.date.available2019-09-23T10:03:54Z-
dc.date.issued2019-09-01-
dc.identifier.issn1728172en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/108-
dc.description.abstract© 2019, Springer-Verlag GmbH Germany, part of Springer Nature. The antiphospholipid syndrome (APS) is an autoimmune disease characterized by the presence of the IgG and/or IgM isotypes of the antiphospholipid antibodies, thrombosis and/or recurrent pregnancy losses. Various markers of inflammation are associated with clinical and/or laboratory features of APS. Adiponectin (Ad) is a member of the adipocytokines that exert its roles by binding to its receptors (AdR). Peroxisome proliferator-activated receptor gamma (PPAR-gamma) agonists induced Ad production. The aged Pparg null-mice represented the first animal model that spontaneously develops APS and this model emphasized the importance of PPAR-gamma signaling in the development of APS. Recombinant Ad (rAd) application was beneficial for the improvement of glucose, insulin and lipid levels in mice. Orally active AdR agonist exerted similar effects to Ad in mice. Due to the re-occurrence of thrombotic episodes in APS patients (despite life-long anticoagulation), administration of PPAR-gamma agonists, rAd, or AdR agonists should be further tested in experimental models of APS, which eventually, will provide more data for novel therapeutic strategies that will ameliorate clinical manifestations of the APS.en_US
dc.language.isoenen_US
dc.relation.ispartofRheumatology Internationalen_US
dc.subjectAdiponectinen_US
dc.subjectAntiphospholipid antibodiesen_US
dc.subjectAntiphospholipid syndromeen_US
dc.subjectInflammationen_US
dc.subjectPPAR-gamma agonisten_US
dc.titleAdiponectin: a therapeutic target in the antiphospholipid syndrome?en_US
dc.typeOtheren_US
dc.identifier.doi10.1007/s00296-019-04349-x-
dc.identifier.pmid39-
dc.identifier.scopus2-s2.0-85067645374-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85067645374-
dc.description.versionPublisheden_US
dc.relation.lastpage1525en_US
dc.relation.firstpage1519en_US
dc.relation.issue9en_US
dc.relation.volume39en_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptKatedra za farmaciju-
crisitem.author.deptKatedra za farmaciju-
crisitem.author.orcid0000-0003-2114-8621-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
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