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Am J Physiol Endocrinol Metab (December 21, 2004). doi:10.1152/ajpendo.00118.2004
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Submitted on March 10, 2004
Accepted on December 1, 2004

Regulation of adiponectin receptor gene expression in diabetic mice

Kouichi Inukai1*, Youhei Nakashima1, Masaki Watanabe1, Nobuki Takata1, Takahiro Sawa1, Susumu Kurihara1, Takuya Awata1, and Shigehiro Katayama1

1 Division of Endocrinology and Diabetes, Department of Internal Medicine, Saitama Medical School, Saitama, Japan

* To whom correspondence should be addressed. E-mail: inukai{at}saitama-med.ac.jp.

Adiponectin is an adipocyte-derived factor, which plays pivotal roles in lipid and glucose metabolism in muscle and liver. Two adiponectin receptor types were recently identified; AdipoR1 is abundantly expressed in muscle, whereas AdipoR2 is predominantly expressed in the liver. To clarify the regulation of adiponectin receptor gene expression in diabetic states, we examined mRNA levels of AdipoR1 in the muscles of diabetic animals by northern blotting. The level of AdipoR1 mRNA was increased approximately 2.5-fold in muscle of streptozotocin (STZ) diabetic mice, but the normal level was restored by insulin administration, indicating that insulin has an inhibitory effect on AdipoR1 expression. To confirm this inhibitory effect of insulin, we performed in vitro experiments using C2C12 skeletal muscle cells. Insulin treatment for 24 h decreased AdipoR1 expression by approximately 60% in C2C12 cells. In addition, this effect was mediated by the phosphatidylinositol-3 kinase (PI-3 kinase) dependent pathway rather than the mitogen-activated protein kinase (MAPK) pathway. AdipoR1 expression in insulin resistant diabetic mice was also investigated. AdipoR1 expression was decreased by 36% in type 2 diabetic obese db/db mice, as compared to lean mice. In contrast, hepatic AdipoR2 expression was not significantly changed in either STZ mice or genetically obese mice. Our results indicate that regulation of AdipoR1, but not that of AdipoR2, may be involved in glucose and lipid metabolism in diabetic states.




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