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Bio-Guided Isolation of Two New Hypoglycemic Triterpenoid Saponins from Polygonum capitatum

PURPOSE: Diabetes is a common disease caused by a combination of genetic and environmental factors, which was the top three diseases threatening human health. Therefore, it is necessary to seek more efficient hypoglycemic drugs. The main objective of this study was to investigate the potential hypog...

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Autores principales: Huang, Doudou, Du, Zenan, Chen, Yanhong, Dong, Zhiying, Wang, Xiujuan, Li, Mengshuang, Zhang, Feng, Chen, Wansheng, Sun, Lianna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8689516/
https://www.ncbi.nlm.nih.gov/pubmed/34949913
http://dx.doi.org/10.2147/DDDT.S341354
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author Huang, Doudou
Du, Zenan
Chen, Yanhong
Dong, Zhiying
Wang, Xiujuan
Li, Mengshuang
Zhang, Feng
Chen, Wansheng
Sun, Lianna
author_facet Huang, Doudou
Du, Zenan
Chen, Yanhong
Dong, Zhiying
Wang, Xiujuan
Li, Mengshuang
Zhang, Feng
Chen, Wansheng
Sun, Lianna
author_sort Huang, Doudou
collection PubMed
description PURPOSE: Diabetes is a common disease caused by a combination of genetic and environmental factors, which was the top three diseases threatening human health. Therefore, it is necessary to seek more efficient hypoglycemic drugs. The main objective of this study was to investigate the potential hypoglycemic effects of compounds from Polygonum capitatum. MATERIALS AND METHODS: Our experiments were divided into three steps: (1) α-amylase test and oral starch tolerance test (OSTT) for screening the biological extract part of P. capitatum; (2) chemical isolation and identification using various separation techniques, and spectrum methods; and (3) evaluation of α-amylase inhibitory activity of isolates and in silico analysis for mechanism investigation. RESULTS: The n-butanol fractioned part of P. capitatum was confirmed to be the biological part according to α-amylase test. Then, two new triterpenoid saponins were isolated from the n-butanol part, which were also the first isolated triterpenoid saponins from P. capitatum. The activities of compounds 1 and 2 against α-amylase were 51.9±2.8% and 38.1±2.2%, respectively, which was consistent with the molecular docking analysis. In which, 1 and 2 showed the binding affinity energy for α-amylase was −9.4 kcal/mol and −7.8 kcal/mol, respectively. CONCLUSION: Two new triterpenoid saponins were firstly isolated from P. capitatum, and displays potency as a hypoglycemic agent through blocking α-amylase.
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spelling pubmed-86895162021-12-22 Bio-Guided Isolation of Two New Hypoglycemic Triterpenoid Saponins from Polygonum capitatum Huang, Doudou Du, Zenan Chen, Yanhong Dong, Zhiying Wang, Xiujuan Li, Mengshuang Zhang, Feng Chen, Wansheng Sun, Lianna Drug Des Devel Ther Original Research PURPOSE: Diabetes is a common disease caused by a combination of genetic and environmental factors, which was the top three diseases threatening human health. Therefore, it is necessary to seek more efficient hypoglycemic drugs. The main objective of this study was to investigate the potential hypoglycemic effects of compounds from Polygonum capitatum. MATERIALS AND METHODS: Our experiments were divided into three steps: (1) α-amylase test and oral starch tolerance test (OSTT) for screening the biological extract part of P. capitatum; (2) chemical isolation and identification using various separation techniques, and spectrum methods; and (3) evaluation of α-amylase inhibitory activity of isolates and in silico analysis for mechanism investigation. RESULTS: The n-butanol fractioned part of P. capitatum was confirmed to be the biological part according to α-amylase test. Then, two new triterpenoid saponins were isolated from the n-butanol part, which were also the first isolated triterpenoid saponins from P. capitatum. The activities of compounds 1 and 2 against α-amylase were 51.9±2.8% and 38.1±2.2%, respectively, which was consistent with the molecular docking analysis. In which, 1 and 2 showed the binding affinity energy for α-amylase was −9.4 kcal/mol and −7.8 kcal/mol, respectively. CONCLUSION: Two new triterpenoid saponins were firstly isolated from P. capitatum, and displays potency as a hypoglycemic agent through blocking α-amylase. Dove 2021-12-14 /pmc/articles/PMC8689516/ /pubmed/34949913 http://dx.doi.org/10.2147/DDDT.S341354 Text en © 2021 Huang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Huang, Doudou
Du, Zenan
Chen, Yanhong
Dong, Zhiying
Wang, Xiujuan
Li, Mengshuang
Zhang, Feng
Chen, Wansheng
Sun, Lianna
Bio-Guided Isolation of Two New Hypoglycemic Triterpenoid Saponins from Polygonum capitatum
title Bio-Guided Isolation of Two New Hypoglycemic Triterpenoid Saponins from Polygonum capitatum
title_full Bio-Guided Isolation of Two New Hypoglycemic Triterpenoid Saponins from Polygonum capitatum
title_fullStr Bio-Guided Isolation of Two New Hypoglycemic Triterpenoid Saponins from Polygonum capitatum
title_full_unstemmed Bio-Guided Isolation of Two New Hypoglycemic Triterpenoid Saponins from Polygonum capitatum
title_short Bio-Guided Isolation of Two New Hypoglycemic Triterpenoid Saponins from Polygonum capitatum
title_sort bio-guided isolation of two new hypoglycemic triterpenoid saponins from polygonum capitatum
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8689516/
https://www.ncbi.nlm.nih.gov/pubmed/34949913
http://dx.doi.org/10.2147/DDDT.S341354
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