Horm Metab Res 2004; 36(7): 465-469
DOI: 10.1055/s-2004-825726
Original Basic
© Georg Thieme Verlag Stuttgart · New York

Adiponectin mRNA Levels in Parametrial Adipose Tissue and Serum Adiponectin Levels are Reduced in Mice During Late Pregnancy

E.  Kondo1 , T.  Sugiyama1 , H.  Kusaka1 , N.  Toyoda1
  • 1Department of Obstetrics and Gynecology, Mie University School of Medicine, 2-174 Edobashi, Tsu, Mie, Japan
Further Information

Publication History

Received 22 October 2003

Acceped after Revision 28 January 2004

Publication Date:
11 August 2004 (online)

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Abstract

Adiponectin, a fat-derived factor, is downregulated in insulin resistance and obesity; insulin resistance has been demonstrated during late pregnancy in both humans and in rodents. The present study examines the physiological change of adiponectin gene expression as well as the circulating levels of adiponectin during pregnancy. We examined the relative quantity of adiponectin mRNA produced in the adipose tissues of pregnant compared to virgin mice. We also measured serum adiponectin levels and parametrial adipocyte size in mice throughout pregnancy. Adiponectin mRNA was significantly reduced by 74 ± 8 % and 63 ± 4 % at days 15 and 18 of pregnancy, respectively, compared to virgin mice. Serum adiponectin concentration decreased on days 15 (30.7 ± 8.5 µg/ml) and 18 (27.9 ± 8.7 µg/ml) of pregnancy, and the values were significantly lower than that of virgin mice (56.8 ± 6.6 µg/ml). Parametrial adipocytes from mice on days 15 and 18 of pregnancy were significantly larger than in virgin mice or during early pregnancy. Fat-cell size was closely correlated to degradation of adiponectin gene expression and serum adiponectin levels. These results suggest that changes of adiponectin expression affect metabolic status in pregnant mice.

References

T. Sugiyama, M. D., Ph. D.

Department of Obsterics and Gynecology · School of Medicine · Mie University

2-174 Edobashi · Tsu · Mie 514-8507 · Japan

Phone: + 81/59/231-5023 ·

Fax: + 81/59/231-5202 ·

Email: tak-s@clin.medic.mie-u.ac.jp