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Sorghum extract exerts an anti-diabetic effect by improving insulin sensitivity via PPAR-${gamma}$ in mice fed a high-fat diet
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  • Sorghum extract exerts an anti-diabetic effect by improving insulin sensitivity via PPAR-${gamma}$ in mice fed a high-fat diet
  • Sorghum extract exerts an anti-diabetic effect by improving insulin sensitivity via PPAR-${gamma}$ in mice fed a high-fat diet
저자명
Park. Ji-Heon,Lee. Sun-Hee,Chung. Ill-Min,Park. Yong-Soon
간행물명
Nutrition research and practice
권/호정보
2012년|6권 4호|pp.322-327 (6 pages)
발행정보
한국영양학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

This study investigated the hypothesis that a sorghum extract exerts anti-diabetic effects through a mechanism that improves insulin sensitivity via peroxisome proliferator-activated receptor gamma (PPAR-${gamma}$) from adipose tissue. Seven C57BL/6 mice were fed an AIN-93M diet with fat consisting of 10% of total energy intake (LF) for 14 weeks, and 21 mice were fed a high-fat AIN diet with 60% of calories derived from fat (HF). From week 8, the HF diet-fed mice were orally administered either saline (HF group), 0.5% (0.5% SE group), or 1% sorghum extract (1% SE group) for 6 weeks (n = 7/group). Perirenal fat content was significantly lower in the 0.5% SE and 1% SE groups than that in the HF mice. Levels of total and low-density lipoprotein cholesterol, triglycerides, glucose, and the area under the curve for glucose were significantly lower in mice administered 0.5% SE and 1% SE than those in HF mice. Serum insulin level was significantly lower in mice administered 1% SE than that in HF mice or those given 0.5% SE. PPAR-${gamma}$ expression was significantly higher, whereas the expression of tumor necrosis factor-${alpha}$ was significantly lower in mice given 1% SE compared to those in the HF mice. Adiponectin expression was also significantly higher in mice given 0.5% SE and 1% SE than that in the HF mice. These results suggest that the hypoglycemic effect of SE may be related with the regulation of PPAR-${gamma}$-mediated metabolism in this mouse model.