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Adiponectin protects against development of metabolic disturbances in a PCOS mouse model
Högskolan i Skövde, Institutionen för hälsa och lärande. Högskolan i Skövde, Forskningsspecialiseringen Hälsa och Lärande. Department of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. (Translationell medicin (TRIM), Translational Medicine)ORCID-id: 0000-0003-4616-6789
Department of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
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2017 (Engelska)Ingår i: Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, E-ISSN 1091-6490, Vol. 114, nr 34, s. E7187-E7196, artikel-id 201708854Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Adiponectin, together with adipocyte size, is the strongest factor associated with insulin resistance in women with polycystic ovary syndrome (PCOS). This study investigates the causal relationship between adiponectin levels and metabolic and reproductive functions in PCOS. Prepubertal mice overexpressing adiponectin from adipose tissue (APNtg), adiponectin knockouts (APNko), and their wild-type (WT) littermate mice were continuously exposed to placebo or dihydrotestosterone (DHT) to induce PCOS-like traits. As expected, DHT exposure led to reproductive dysfunction, as judged by continuous anestrus, smaller ovaries with a decreased number of corpus luteum, and an increased number of cystic/atretic follicles. A two-way between-groups analysis showed that there was a significant main effect for DHT exposure, but not for genotype, indicating adiponectin does not influence follicle development. Adiponectin had, however, some protective effects on ovarian function. Similar to in many women with PCOS, DHT exposure led to reduced adiponectin levels, larger adipocyte size, and reduced insulin sensitivity in WTs. APNtg mice remained metabolically healthy despite DHT exposure, while APNko-DHT mice were even more insulin resistant than their DHT-exposed littermate WTs. DHT exposure also reduced the mRNA expression of genes involved in metabolic pathways in gonadal adipose tissue of WT and APNko, but this effect of DHT was not observed in APNtg mice. Moreover, APNtg-DHT mice displayed increased pancreatic mRNA levels of insulin receptors, Pdx1 and Igf1R, suggesting adiponectin stimulates beta cell viability/hyperplasia in the context of PCOS. In conclusion, adiponectin improves metabolic health but has only minor effects on reproductive functions in this PCOS-like mouse model.

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National Academy of Sciences , 2017. Vol. 114, nr 34, s. E7187-E7196, artikel-id 201708854
Nyckelord [en]
adipose tissue, insulin resistance, polycystic ovary syndrome
Nationell ämneskategori
Fysiologi Medicinska och farmaceutiska grundvetenskaper Medicin och hälsovetenskap
Forskningsämne
Translationell medicin TRIM
Identifikatorer
URN: urn:nbn:se:his:diva-13977DOI: 10.1073/pnas.1708854114ISI: 000408095300019PubMedID: 2-s2.0-85027848679Scopus ID: 000408095300019OAI: oai:DiVA.org:his-13977DiVA, id: diva2:1130822
Tillgänglig från: 2017-08-11 Skapad: 2017-08-11 Senast uppdaterad: 2019-11-20Bibliografiskt granskad

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Proceedings of the National Academy of Sciences of the United States of America
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