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DOI 10.1159/000369737

Медицинская библиотека · Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2015

Pioglitazone lowers serum retinol binding protein 4 by suppressing its expression in adipose tissue of obese rats.

Zhu Chaoyu, Xiao Yuanyuan, Liu Xiaohua, Han Junfeng, Zhang Jianmei, Wei Li, Jia Weiping

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND/AIMS: Pioglitazone, a peroxisome proliferator-activated receptor γ activator, is clinically used to treat insulin resistance. However, the underlying mechanism of pioglitazone's action remains unclear. We investigated whether, and how, pioglitazone modulates serum level of retinol binding protein 4 (RBP4), an adipocytokine associated with obesity and insulin resistance.

METHODS

Insulin sensitivity was determined by oral glucose tolerance test, and RBP4 expression was detected by RT-PCR and Western blotting.

RESULTS

Pioglitazone treatment significantly decreased serum RBP4 levels in obese rats, which was correlated with reduced body weight and increased insulin sensitivity. Moreover, pioglitazone greatly decreased RBP4 mRNA and protein levels in adipose tissue but not in the liver. Consistently, pioglitazone treatment significantly reduced RBP4 protein expression in 3T3-L1 adipocytes but not in HepG2 cells.

CONCLUSION

These results demonstrate that pioglitazone inhibits the level of serum RPB4 by suppressing RBP4 expression in adipose tissue of obese rats, suggesting that inhibiting RBP4 expression in adipocytes may provide a mechanism by which pioglitazone improves insulin sensitivity in insulin-resistant subjects.

Для цитирования: Zhu Chaoyu, Xiao Yuanyuan, Liu Xiaohua, Han Junfeng, Zhang Jianmei, Wei Li, Jia Weiping. Pioglitazone lowers serum retinol binding protein 4 by suppressing its expression in adipose tissue of obese rats.. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology. 2015. DOI: 10.1159/000369737.

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