Suppr超能文献

亮氨酸可促进大鼠骨骼肌对葡萄糖的摄取。

Leucine promotes glucose uptake in skeletal muscles of rats.

作者信息

Nishitani Shinobu, Matsumura Tsuyoshi, Fujitani Shoji, Sonaka Ichiro, Miura Yutaka, Yagasaki Kazumi

机构信息

Pharmaceutical Research Laboratories, Ajinomoto Co., Inc., 1-1, Suzuki-cho, Kawasaki-ku, Kawasaki-shi, Kanagawa 210-8681, Japan.

出版信息

Biochem Biophys Res Commun. 2002 Dec 20;299(5):693-6. doi: 10.1016/s0006-291x(02)02717-1.

Abstract

Soleus muscles isolated from normal rats were incubated to evaluate whether or not leucine promotes glucose uptake under insulin-free conditions, using a labeled 2-deoxyglucose uptake assay. Glucose uptake was promoted by 2mM leucine. A metabolite of leucine, alpha-ketoisocaproic acid (alpha-KIC), also exhibited a similar stimulatory effect, although this was not as potent as leucine. Stimulation of glucose uptake by leucine was completely canceled by pre-treatment with either 10 microM LY294002, a specific inhibitor of phosphatidylinositol 3-kinase (PI3-kinase), or 6 microM GF109203X, a specific inhibitor of protein kinase C (PKC). No significant change was observed by pre-treatment with 1 microM rapamycin, a specific inhibitor of mammalian target of rapamycin (mTOR). These results suggest that leucine stimulates glucose transport in skeletal muscle via PI3-kinase and PKC pathways independently of the mammalian target of mTOR. They also suggest that leucine stimulates glucose transport by an insulin-independent mechanism.

摘要

从正常大鼠分离出比目鱼肌,使用标记的2-脱氧葡萄糖摄取试验进行孵育,以评估在无胰岛素条件下亮氨酸是否促进葡萄糖摄取。2mM亮氨酸可促进葡萄糖摄取。亮氨酸的一种代谢产物α-酮异己酸(α-KIC)也表现出类似的刺激作用,尽管其效力不如亮氨酸。用磷脂酰肌醇3-激酶(PI3-激酶)的特异性抑制剂10μM LY294002或蛋白激酶C(PKC)的特异性抑制剂6μM GF109203X预处理,可完全消除亮氨酸对葡萄糖摄取的刺激作用。用雷帕霉素的特异性抑制剂1μM雷帕霉素预处理未观察到显著变化,雷帕霉素是哺乳动物雷帕霉素靶蛋白(mTOR)的特异性抑制剂。这些结果表明,亮氨酸通过PI3-激酶和PKC途径刺激骨骼肌中的葡萄糖转运,独立于哺乳动物雷帕霉素靶蛋白(mTOR)。它们还表明亮氨酸通过胰岛素非依赖机制刺激葡萄糖转运。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验