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Anti-hyperlipidemia on rats in vivo and new compounds from the seeds of Psoralea corylifolia.
Zhao, Yi-Ming; Xiu, Meng-Xue; Song, Jian; Zhang, Yue; Shao, Xiao-Jing; Wang, Xue-Hui; Lee, Hyun-Sun; Cui, Long.
Afiliación
  • Zhao YM; College of Pharmacy, Beihua University, Jilin Province 132013, People's Republic of China.
  • Xiu MX; College of Pharmacy, Baicheng Medical College, Jilin Province 137000, People's Republic of China.
  • Song J; College of Pharmacy, Beihua University, Jilin Province 132013, People's Republic of China.
  • Zhang Y; College of Pharmacy, Beihua University, Jilin Province 132013, People's Republic of China.
  • Shao XJ; College of Pharmacy, Beihua University, Jilin Province 132013, People's Republic of China.
  • Wang XH; College of Pharmacy, Beihua University, Jilin Province 132013, People's Republic of China.
  • Lee HS; Molecular Cancer Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 685-1 Yangcheongri, Ochangeup, Cheongwongun, Chungbuk 363-883, Republic of Korea.
  • Cui L; College of Pharmacy, Beihua University, Jilin Province 132013, People's Republic of China. Electronic address: cuilong71@beihua.edu.cn.
Fitoterapia ; 163: 105343, 2022 Nov.
Article en En | MEDLINE | ID: mdl-36328169
ABSTRACT
In this study, it was confirmed at first time that the crude extracts of Psoralea corylifolia seeds (PCE34) can reduce serum lipids (AST, ALT, TG, TC, LDL, ALP, ACP and LDH), body weight and serum sugar, increase HDL and serum insulin in hyperlipidemic wistar rat induced by high-fat diet in vivo. Furthermore, eight new chalcones 1-8, one new flavanone 12, one new coumarin 14, three new meroterpenes 15-17 and one new bakuchiol 20 together with seven known compounds (9-11, 13, 18-19 and 21) were isolated from the PCE34. Their structures were elucidated based on analyses of their spectroscopic (UV, CD, NMR and HREIMS) data. All the isolates were evaluated for in vitro inhibitory activity against DGAT1/2, PTP1B and α-Glucosidase. Among them, compounds 1-3, 8-11, 14-17, 19 and 20 were found to exhibit selective inhibitory activity on DGAT1 with IC50 values ranging from 66.7 ± 1.2 to 87.2 ± 1.3 µM; 1, 8-12, 14 and 20 has the best inhibit active on PTP1B with IC50 values ranging from 13.8 ± 1.1 to 19.1 ± 1.6 µM; 1-12 and 14 displayed the significant inhibitory activities on α-Glucosidase with IC50 values ranging from 29.1 ± 1.2 to 79.4 ± 1.2 µM.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Psoralea Idioma: En Revista: Fitoterapia Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Psoralea Idioma: En Revista: Fitoterapia Año: 2022 Tipo del documento: Article