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Diabetes Publish Ahead of Print published online ahead of print January 3, 2008
DOI: 10.2337/db07-0990

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Original Research

Omentin-1, a Novel Adipokine, is decreased in Overweight Insulin Resistant Women with the Polycystic Ovary Syndrome: ex vivo and in vivo Regulation of Omentin-1 by Insulin and Glucose

Bee K Tan, MBBS1, Raghu Adya, MBBS, MSc1, S Farhatullah, MSc1, Kris C Lewandowski, MRCP, MD1,,2, Paul O'Hare, FRCP, MD1, Hendrik Lehnert, FRCP, MD1,,3, and Harpal S Randeva, FRCP, MD, PhD1

1Endocrinology & Metabolism Group, Clinical Sciences Research Institute,Warwick Medical School, University of Warwick, Coventry CV4 7AL, UK
2Department of Endocrinology and Metabolic Diseases, The Medical University of Lodz and Polish Mother's Memorial Research Institute, Lodz, Poland
31st Medical Department, University of Lübeck Medical School, Luebeck, Germany

Polycystic ovary syndrome (PCOS) is associated with insulin resistance and obesity. Recent studies have shown that plasma omentin-1 levels decrease with obesity. Currently, no data exists on the relative expression and regulation of omentin-1 in adipose tissue (AT) of PCOS women.

Objective: To assess mRNA and protein levels of omentin-1 in omental (om) AT of PCOS women and matched controls, including circulating omentin-1. Ex vivo and in vivo regulation of AT omentin-1 was also studied.

Research Design and Methods: Real-time RT-PCR and western blotting were used to assess mRNA and protein expression of omentin-1. Plasma Omentin-1 was measured by ELISA. The effects of D-glucose, insulin, gonadal and adrenal steroids on AT omentin-1 were analysed ex vivo. The in vivo effects of insulin (hyperinsulinemia) on omentin-1 levels were also assessed by a prolonged insulin-glucose infusion.

Results: In addition to decreased plasma omentin-1 levels in PCOS women (P < 0.05), compared to controls, there was significantly lower levels of omentin-1 mRNA (P < 0.01) and protein (P < 0.05) in om AT of PCOS women (P < 0.01). Furthermore, in om AT explants, insulin and glucose significantly dose-dependently decreased omentin-1 mRNA expression, protein levels and secretion into conditioned media (P < 0.05, P < 0.01). Also, hyperinsulinemic induction in healthy subjects significantly reduced plasma omentin-1 levels (P < 0.01).

Conclusions: Our novel findings reveal that omentin-1 is down regulated by insulin and glucose. These may in part explain the decreased omentin-1 levels observed in our overweight PCOS women.


Correspondence: Harpal.Randeva{at}warwick.ac.uk

Key Words: Omentin-1 • PCOS • adipose tissue • adipocyte • adipokine • insulin resistance • metabolic syndrome • insulin • glucose


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