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Screening of Potential α-Glucosidase Inhibitors from the Roots and Rhizomes of Panax Ginseng by Affinity Ultrafiltration Screening Coupled with UPLC-ESI-Orbitrap-MS Method.
Wang, Hong-Ping; Fan, Chun-Lan; Lin, Zhao-Zhou; Yin, Qiong; Zhao, Chen; Peng, Ping; Zhang, Run; Wang, Zi-Jian; Du, Jing; Wang, Zhi-Bin.
Afiliación
  • Wang HP; Scientific Research Institute of Beijing Tongrentang Co., Ltd., Beijing 100011, China.
  • Fan CL; Beijing Tongrentang Technology Development Co., Ltd., Beijing 100079, China.
  • Lin ZZ; Beijing Tongrentang Technology Development Co., Ltd., Beijing 100079, China.
  • Yin Q; Scientific Research Institute of Beijing Tongrentang Co., Ltd., Beijing 100011, China.
  • Zhao C; Scientific Research Institute of Beijing Tongrentang Co., Ltd., Beijing 100011, China.
  • Peng P; Scientific Research Institute of Beijing Tongrentang Co., Ltd., Beijing 100011, China.
  • Zhang R; Beijing Zhongyan Tongrentang Pharmaceutical R & D Co., Ltd., Beijing 100000, China.
  • Wang ZJ; Scientific Research Institute of Beijing Tongrentang Co., Ltd., Beijing 100011, China.
  • Du J; Scientific Research Institute of Beijing Tongrentang Co., Ltd., Beijing 100011, China.
  • Wang ZB; Scientific Research Institute of Beijing Tongrentang Co., Ltd., Beijing 100011, China.
Molecules ; 28(5)2023 Feb 22.
Article en En | MEDLINE | ID: mdl-36903317
Panax ginseng was a traditional Chinese medicine with various pharmacological activities and one of its important activities was hypoglycemic activity; therefore, panax ginseng has been used in China as an adjuvant in the treatment of diabetes mellitus. In vivo and in vitro tests have revealed that ginsenosides, which are derived from the roots and rhizomes of panax ginseng have anti-diabetic effects and produce different hypoglycemic mechanisms by acting on some specific molecular targets, such as SGLT1, GLP-1, GLUTs, AMPK, and FOXO1. α-Glucosidase is another important hypoglycemic molecular target, and its inhibitors can inhibit the activity of α-Glucosidase so as to delay the absorption of dietary carbohydrates and finally reduce postprandial blood sugar. However, whether ginsenosides have the hypoglycemic mechanism of inhibiting α-Glucosidase activity, and which ginsenosides exactly attribute to the inhibitory effect as well as the inhibition degree are not clear, which needs to be addressed and systematically studied. To solve this problem, affinity ultrafiltration screening coupled with UPLC-ESI-Orbitrap-MS technology was used to systematically select α-Glucosidase inhibitors from panax ginseng. The ligands were selected through our established effective data process workflow based on systematically analyzing all compounds in the sample and control specimens. As a result, a total of 24 α-Glucosidase inhibitors were selected from panax ginseng, and it was the first time that ginsenosides were systematically studied for the inhibition of α-Glucosidase. Meanwhile, our study revealed that inhibiting α-Glucosidase activity probably was another important mechanism for ginsenosides treating diabetes mellitus. In addition, our established data process workflow can be used to select the active ligands from other natural products using affinity ultrafiltration screening.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ginsenósidos / Panax Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Ginsenósidos / Panax Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China
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