Author/Authors :
Muto، نويسنده , , Gen and Satoh، نويسنده , , Jo and Muto، نويسنده , , Yoshiko and Takahashi، نويسنده , , Kazuma and Nakazawa، نويسنده , , Tetsuya and Sagara، نويسنده , , Mikio and Miyaguchi، نويسنده , , Shuichi and Fukuzawa، نويسنده , , Masamitsu and Qiang، نويسنده , , Xiaoling and Sakata، نويسنده , , Yoshiyuki and Takizawa، نويسنده , , Yumiko and Li، نويسنده , , Yan and Bando، نويسنده , , Shin-ichiro and Ho، نويسنده ,
Abstract :
We reported that administration of complete Freundʹs adjuvant (CFA) improved glucose tolerance test (GTT) results in obese diabetic KK-Ay mice. In this study, we investigated its mechanism. An injection with CFA remarkably improved GTT for more than a week in KK-Ay mice, although insulin response was not changed compared with saline controls. The hypoglycemic effect of insulin was significantly, but partially, potentiated in the CFA-treated mice compared with the controls, suggesting that CFA stimulated insulin-mediated and non-insulin-mediated glucose disposal. Improvement in the GTT with CFA was partially transferable to nontreated mice by peritoneal exudative cells, but not spleen or lymph node cells. Pretreatment with anti-interleukin (IL)-1α and -1β antibodies or anti-tumor necrosis factor (TNF)-α antibody significantly abrogated the improvement in the GTT with CFA. The results indicate that CFA-induced improvement in glucose intolerance in KK-Ay mice was mediated at least by IL-1 and TNF-α.
Keywords :
Type 2 diabetes , KK-Ay mice , Complete Freundיs adjuvant , IL-1 , TNF-? , Insulin resistance , cytokines