Inhibition of pancreatic lipase by environmental xenoestrogens

被引:18
作者
Hu, Qing [1 ]
Guan, Xiao-Qing [1 ]
Song, Li-Lin [2 ]
Wang, Hao-Nan [1 ]
Xiong, Yuan [1 ]
Liu, Jun-Ling [1 ]
Yin, Heng [2 ]
Cao, Yun-Feng [2 ,3 ]
Hou, Jie [4 ]
Yang, Ling [1 ]
Ge, Guang-Bo [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Inst Interdisciplinary Integrat Med Res, Shanghai 201203, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
[3] Dalian Runsheng Kangtai Med Lab Co Ltd, Dalian, Peoples R China
[4] Dalian Med Univ, Coll Basic Med Sci, Dalian 116044, Peoples R China
关键词
Pancreatic lipase (PL); Environmental xenoestrogens; Hexestrol (HEX); Diethylstilbestrol (DES); Dienestrol (DS); ENDOCRINE DISRUPTING CHEMICALS; BISPHENOL-A BPA; SELECTIVE INHIBITORS; RISK-ASSESSMENT; EXPOSURE; WATER; DIETHYLSTILBESTROL; ANALOGS; GROMACS; POTENT;
D O I
10.1016/j.ecoenv.2020.110305
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Environmental xenoestrogens are the most accessible endocrine disrupting chemicals that have been reported with harmful effects on human health. Although the influences of xenoestrogens on the endocrine system have been extensively studied, it remains unclear whether these xenoestrogens can affect the digestive system in mammals. This study aimed to investigate the inhibitory effects and the underlying mechanism of six nonsteroidal synthetic estrogens (including hexestrol, diethylstilbestrol, dienestrol, bisphenol A, bisphenol AF and bisphenol Z) on pancreatic lipase (PL), a key digestive enzyme responsible for lipid digestion and absorption in mammals. The results clearly demonstrated that hexestrol, diethylstilbestrol and dienestrol exhibited strong inhibition on PL, with the IC50 values of less than 1.0 mu M. Further investigations elucidated that these three synthetic estrogens functioned as mixed inhibitors of PL, with the K-i values of less than 1 mu M. Moreover, molecular dynamics simulations showed that diethylstilbestrol and its analogues might block the binding of sub-strate on PL via occupying the portal to the active site of PL and thereby inhibit the hydrolytic activity of this key enzyme. Collectively, these results suggested that diethylstilbestrol and its analogues were potent PL inhibitors, which might play a profound role in lipid absorption and weight gain in mammals.
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页数:8
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