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低频电针对肥胖型糖尿病小鼠骨骼肌中 SIRT1/PGC-1α 的激活作用改善胰岛素敏感性。

Low-Frequency Electroacupuncture Improves Insulin Sensitivity in Obese Diabetic Mice through Activation of SIRT1/PGC-1α in Skeletal Muscle.

机构信息

Department of Acupuncture and Moxibustion, Hubei University of Chinese Medicine, Wuhan 430061, China.

出版信息

Evid Based Complement Alternat Med. 2011;2011:735297. doi: 10.1155/2011/735297. Epub 2010 Oct 26.

Abstract

Electroacupuncture (EA) has been observed to reduce insulin resistance in obesity and diabetes. However, the biochemical mechanism underlying this effect remains unclear. This study investigated the effects of low-frequency EA on metabolic action in genetically obese and type 2 diabetic db/db mice. Nine-week-old db/m and db/db mice were randomly divided into four groups, namely, db/m, db/m + EA, db/db, and db/db + EA. db/m + EA and db/db + EA mice received 3-Hz electroacupuncture five times weekly for eight consecutive weeks. In db/db mice, EA tempered the increase in fasting blood glucose, food intake, and body mass and maintained insulin levels. In EA-treated db/db mice, improved insulin sensitivity was established through intraperitoneal insulin tolerance test. EA was likewise observed to decrease free fatty acid levels in db/db mice; it increased protein expression in skeletal muscle Sirtuin 1 (SIRT1) and induced gene expression of peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α), nuclear respiratory factor 1 (NRF1), and acyl-CoA oxidase (ACOX). These results indicated that EA offers a beneficial effect on insulin resistance in obese and diabetic db/db mice, at least partly, via stimulation of SIRT1/PGC-1α, thus resulting in improved insulin signal.

摘要

电针(EA)已被观察到可降低肥胖和糖尿病患者的胰岛素抵抗。然而,这种作用的生化机制尚不清楚。本研究探讨了低频 EA 对遗传性肥胖和 2 型糖尿病 db/db 小鼠代谢作用的影响。9 周龄 db/m 和 db/db 小鼠被随机分为 4 组,即 db/m、db/m+EA、db/db 和 db/db+EA。db/m+EA 和 db/db+EA 小鼠每周接受 3-Hz 电针 5 次,连续 8 周。在 db/db 小鼠中,EA 减轻了空腹血糖、摄食量和体重的增加,并维持了胰岛素水平。在接受 EA 治疗的 db/db 小鼠中,通过腹腔内胰岛素耐量试验建立了改善的胰岛素敏感性。同样观察到 EA 降低了 db/db 小鼠的游离脂肪酸水平;它增加了骨骼肌中的 Sirtuin 1(SIRT1)的蛋白表达,并诱导过氧化物酶体增殖物激活受体γ共激活因子 1α(PGC-1α)、核呼吸因子 1(NRF1)和酰基辅酶 A 氧化酶(ACOX)的基因表达。这些结果表明,EA 通过刺激 SIRT1/PGC-1α,对肥胖和糖尿病 db/db 小鼠的胰岛素抵抗产生有益影响,从而改善胰岛素信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0308/2964507/d23181279be0/ECAM2011-735297.001.jpg

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