TanshinonellA phenanthroimidazole derivative polarizes macrophage to improve metabolic homeostasis

被引:10
作者
Ma, Lei [1 ,2 ]
Luo, Shiya [1 ]
Zhou, Lin [1 ]
Zhao, Zewei [1 ]
Li, Qiao [3 ]
Xu, Lin [4 ]
Gong, Baoyong [5 ]
Qi, Weiwei [1 ,2 ]
Zhou, Ti [1 ,2 ]
Yang, Xia [1 ,2 ]
Gao, Guoquan [1 ,2 ]
Mei, Wenjie [6 ]
Yang, Zhonghan [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Zhongshan Sch Med, Affiliated Guangzhou Women & Childrens Hosp, Program Mol Med, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Zhongshan Sch Med, Dept Biochem, Guangzhou 510080, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Guangzhou 510080, Guangdong, Peoples R China
[4] SUN Yat Sen Univ, Sch Publ Hlth, Guangzhou 510006, Guangdong, Peoples R China
[5] Guangdong Lab Anim Monitoring Inst, Guangdong Prov Key Lab Lab Anim, Guangzhou 510663, Guangdong, Peoples R China
[6] Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Tanshinonell A; Phenanthroimidazole derivative; Macrophage; Metabolic homeostasis; Obesity; Insulin resistance; VASODILATIVE ACTIVITY; IIA; OBESITY; INFLAMMATION; IDENTIFICATION; BINDING;
D O I
10.1016/j.bbrc.2019.05.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophages infiltrated in adipose tissue play a key role in obesity. Some traditional pharmaceutical compounds may shift the polarization of recruited macrophages to improve metabolic homeostasis. TanshinonellA (TAN2A) is a major active component of Salvia miltiorrhiza, a traditional anti-inflammatory cardiovascular medicine. In our study, we firstly constructed a phenanthroimidazole derivative of TAN2A named TAN20 by chemical synthesis, then identified its structure by chromatography and hydrogen spectroscopy, and finally examined its effects on immunometabolic responses. We found that TAN20 significantly induced the alternatively-activated (M2) rather than the classically-activated macrophages (M1), mainly through releasing the type II cytokines. Such effects were more pronounced than that from TAN2A. Compared to TAN2A, TAN20 substantially reduced body weight, decreased serum free fatty acid and HOMA-IR, and increased insulin sensitivity in obesity-induced diabetic mice. These effects of TAN20 were further validated on diabetic cynomolgus monkeys, which are closer to human physiological conditions. Taken together, our findings explicitly showed that TAN20 significantly polarized the macrophage and improved metabolic homeostasis in obesity-induced diabetic models, suggesting that TAN20 may be a potential drug against diabetes and obesity. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:861 / 867
页数:7
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