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六星期癸二酸补充可改善 db/db 小鼠的空腹血糖、HbA1c 和葡萄糖耐量。

Six weeks' sebacic acid supplementation improves fasting plasma glucose, HbA1c and glucose tolerance in db/db mice.

机构信息

Nestlé Research Center, Route du Jorat, Lausanne, Switzerland.

出版信息

Diabetes Obes Metab. 2010 Dec;12(12):1120-6. doi: 10.1111/j.1463-1326.2010.01308.x.

Abstract

AIM

To investigate the impact of chronic ingestion of sebacic acid (SA), a 10-carbon medium-chain dicarboxylic acid, on glycaemic control in a mouse model of type 2 diabetes (T2D).

METHODS

Three groups of 15 db/db mice were fed for 6 weeks either a chow diet (Ctrl) or a chow diet supplemented with 1.5 or 15% (SA(1.5%) and SA(15%) , respectively) energy from SA. Fasting glycaemia was measured once a week and HbA1c before and after supplementation. An oral glucose tolerance test (OGTT) was performed at the end of the supplementation. Gene expression was determined by transcriptomic analysis on the liver of the Ctrl and SA(15%) groups.

RESULTS

After 42 days of supplementation, fasting glycaemia and HbA1c were ∼70 and 25% lower in the SA(15%) group compared with the other groups showing a beneficial effect of SA on hyperglycaemia. During OGTT, plasma glucose area under the curve was reduced after SA(15%) compared with the other groups. This effect was associated with a tendency for an improved insulin response. In the liver, Pck1 and FBP mRNA were statistically decreased in the SA(15%) compared with Ctrl suggesting a reduced hepatic glucose output induced by SA.

CONCLUSION

Dietary supplementation of SA largely improves glycaemic control in a mouse model of T2D. This beneficial effect may be due to (i) an improved glucose-induced insulin secretion and (ii) a reduced hepatic glucose output.

摘要

目的

研究中链二元羧酸癸二酸(SA)的慢性摄入对 2 型糖尿病(T2D)小鼠模型血糖控制的影响。

方法

15 只 db/db 小鼠分为 3 组,分别喂食标准饲料(Ctrl)或标准饲料添加 1.5%或 15%(SA(1.5%)和 SA(15%))能量的 SA,持续 6 周。每周测量一次空腹血糖,补充前后测量 HbA1c。补充结束时进行口服葡萄糖耐量试验(OGTT)。通过对 Ctrl 和 SA(15%)组肝脏的转录组分析来确定基因表达。

结果

补充 42 天后,SA(15%)组的空腹血糖和 HbA1c 分别比其他组低约 70%和 25%,表明 SA 对高血糖有益。在 OGTT 期间,与其他组相比,SA(15%)组的血浆葡萄糖曲线下面积降低。这种作用与胰岛素反应的改善有关。在肝脏中,与 Ctrl 相比,SA(15%)组的 Pck1 和 FBP mRNA 统计学上降低,表明 SA 可减少肝葡萄糖输出。

结论

SA 的饮食补充可显著改善 T2D 小鼠的血糖控制。这种有益作用可能是由于(i)改善了葡萄糖诱导的胰岛素分泌,和(ii)减少了肝葡萄糖输出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f93/2997326/9dc18af5cf7d/dom0012-1120-f1.jpg

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