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Lactiplantibacillus plantarum strain 84-3 and Staphylococcus aureus phages alleviate type 2-diabetes-induced S.aureus and BCAAs increases by PI3K/AKT/GLUT4 signaling pathway
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作者 Tingting Liang Qihui Gu +6 位作者 Zhuang Liang Tong Jiang Ya Chen Tong Chen Bo Dong Bing Gu Qingping Wu 《Food Science and Human Wellness》 2025年第10期4246-4261,共16页
Epidemiological studies have indicated that branched-chain amino acids(BCAAs)increased and gut microbiota disordered in type 2 diabetes mellitus(T2DM).This study aimed to investigate the mechanism of Lactiplantibacill... Epidemiological studies have indicated that branched-chain amino acids(BCAAs)increased and gut microbiota disordered in type 2 diabetes mellitus(T2DM).This study aimed to investigate the mechanism of Lactiplantibacillus plantarum strain 84-3(Lp84-3)combined with Staphylococcus aureus bacteriophage on ameliorating T2DM.Here we perform a case-control study and identify that Staphylococcus_phage was inversely correlated with fasting blood glucose(FBG).It revealed that Lp84-3 could inhibit the growth of S.aureus,and Lp84-3 contains BCAAs degradation enzymes in its genome.Furthermore,Lp84-3 alone or combined with S.aureus bacteriophage interventions can improve blood glucose,insulin resistance,triglycerides,interleukin-1β,tumor necrosis factor-α(TNF-α),BCAAs,and acetyllactate synthase(ALS)in db/db mice.Lp84-3 and S.aureus bacteriophage decreased S.aureus,Malacoplasma iowae,and Oscillibacter sp.,and increased some beneficial such as L.plantarum and Muribaculaceae bacterium.Transcriptomic analyses revealed that Lp84-3 and S.aureus bacteriophage activated the PI3K/AKT/GLUT4 signaling pathway and upregulated key genes of Il22,Hgf,Col6a1,Gh,Itga10,Fgf23,and Prl involved in glucose metabolism in hypothalamus.Collectively,Lp84-3 and S.aureus bacteriophage alleviate T2DM by modulating gut microbiota and enhancing glucose metabolism in hypothalamus,supporting its potential use as a promising functional compound microecological agent for alleviating T2DM. 展开更多
关键词 Lactiplantibacillus plantarum Staphylococcus aureus phage Branched-chain amino acids Type 2 diabetes mellitus Gut microbiota PI3K/akt/glut4 signaling pathway
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耐力运动增强小鼠骨骼肌葡萄糖摄取能力的作用及白细胞介素15的调控机制
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作者 王哲 王谦 +4 位作者 吴华朵 胡永强 彭子富 郭项英 姜宁 《中国应用生理学杂志》 CAS CSCD 北大核心 2022年第6期696-700,共5页
目的:探讨耐力运动对小鼠骨骼肌葡萄糖摄取能力的影响及白细胞介素(IL-15)的作用机制。方法:将32只C57BL/6J小鼠随机分为安静对照组(Control,C)、耐力训练组(Exercise,E)、PBS注射组(PBS injected,PI)、IL-15注射组(IL-15 injected,II)... 目的:探讨耐力运动对小鼠骨骼肌葡萄糖摄取能力的影响及白细胞介素(IL-15)的作用机制。方法:将32只C57BL/6J小鼠随机分为安静对照组(Control,C)、耐力训练组(Exercise,E)、PBS注射组(PBS injected,PI)、IL-15注射组(IL-15 injected,II)。每组8只,C组小鼠正常饲养8周,E组小鼠进行8周中等强度耐力训练,II组小鼠一次性腹腔注射300μl IL-15复合剂溶液(1.5μg IL-15和7μg IL-15Rα),PI组一次性腹腔注射与II组等量的PBS。其中C组和E组在饲养第7周时,PI组和II组在一次性注射后,各组小鼠禁食12 h,随后进行葡萄糖耐量试验(IPGTT)检测并记录血糖水平。采用Western blot检测小鼠骨骼肌GLUT4、IL-15、AKT、pAKT、AMPK、pAMPK、AS160、pAS160的蛋白表达水平。结果:与C组相比,E组小鼠骨骼肌IL-15、GLUT4、pAMPK、pAKT、pAS160蛋白表达明显升高(P<0.05)。与PI组相比,II组小鼠骨骼肌IL-15、GLUT4、pAMPK、pAS160蛋白表达明显升高(P<0.05)。结论:8周耐力运动和腹腔注射IL-15复合剂均可提升小鼠骨骼肌葡萄糖的摄取能力,但单独增加IL-15可能是通过激活AMPK/AS160/GLUT4通路提升对于葡萄糖的转运能力,这一过程不依赖AKT/AS160/GLUT4通路的激活。 展开更多
关键词 运动 IL-15 小鼠 骨骼肌 akt/as160/glut4通路 AMPK/as160/glut4通路
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