Licochalcone F alleviates glucose tolerance and chronic inflammation in diet-induced obese mice through Akt and p38 MAPK.
第一作者:
Eun-Jung,Bak
第一单位:
Oral Cancer Research Institute, Yonsei University College of Dentistry, Seoul, South Korea.
作者:
主题词
脂细胞(Adipocytes);脂肪组织(Adipose Tissue);动物(Animals);消炎药(Anti-Inflammatory Agents);血糖(Blood Glucose);体重(Body Weight);查耳酮类(Chalcones);趋化因子CCL2(Chemokine CCL2);慢性病(Chronic Disease);环氧化酶2(Cyclooxygenase 2);减量调节(Down-Regulation);葡糖耐受不良(Glucose Intolerance);炎症(Inflammation);白细胞介素1β(Interleukin-1beta);白细胞介素6(Interleukin-6);巨噬细胞(Macrophages);男(雄)性(Male);小鼠(Mice);小鼠, 近交C57BL(Mice, Inbred C57BL);小鼠, 肥胖(Mice, Obese);NF-κB(NF-kappa B);一氧化氮合酶Ⅱ型(Nitric Oxide Synthase Type II);肥胖症(Obesity);原癌基因蛋白质c-akt(Proto-Oncogene Proteins c-akt);RNA, 信使(RNA, Messenger);信号传导(Signal Transduction);肿瘤坏死因子α(Tumor Necrosis Factor-alpha);p38丝裂原活化蛋白激酶类(p38 Mitogen-Activated Protein Kinases)
DOI
10.1016/j.clnu.2015.03.005
PMID
25823386
发布时间
2022-04-09
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