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Inhibition of α-Glucosidase and Pancreatic Lipase Properties of Mitragyna speciosa (Korth.) Havil. (Kratom) Leaves

Kratom (Mitragyna speciosa (Korth.) Havil.) has been used to reduce blood sugar and lipid profiles in traditional medicine, and mitragynine is a major constituent in kratom leaves. Previous data on the blood sugar and lipid-altering effects of kratom are limited. In this study, phytochemical analyse...

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Autores principales: Limcharoen, Thanchanok, Pouyfung, Phisit, Ngamdokmai, Ngamrayu, Prasopthum, Aruna, Ahmad, Aktsar Roskiana, Wisdawati, Wisdawati, Prugsakij, Woraanong, Warinhomhoun, Sakan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9572452/
https://www.ncbi.nlm.nih.gov/pubmed/36235558
http://dx.doi.org/10.3390/nu14193909
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author Limcharoen, Thanchanok
Pouyfung, Phisit
Ngamdokmai, Ngamrayu
Prasopthum, Aruna
Ahmad, Aktsar Roskiana
Wisdawati, Wisdawati
Prugsakij, Woraanong
Warinhomhoun, Sakan
author_facet Limcharoen, Thanchanok
Pouyfung, Phisit
Ngamdokmai, Ngamrayu
Prasopthum, Aruna
Ahmad, Aktsar Roskiana
Wisdawati, Wisdawati
Prugsakij, Woraanong
Warinhomhoun, Sakan
author_sort Limcharoen, Thanchanok
collection PubMed
description Kratom (Mitragyna speciosa (Korth.) Havil.) has been used to reduce blood sugar and lipid profiles in traditional medicine, and mitragynine is a major constituent in kratom leaves. Previous data on the blood sugar and lipid-altering effects of kratom are limited. In this study, phytochemical analyses of mitragynine, 7-hydroxymitragynine, quercetin, and rutin were performed in kratom extracts. The effects on α-glucosidase and pancreatic lipase activities were investigated in kratom extracts and mitragynine. The LC-MS/MS analysis showed that the mitragynine, quercetin, and rutin contents from kratom extracts were different. The ethanol extract exhibited the highest total phenolic content (TPC), total flavonoid content (TFC), and total alkaloid content (TAC). Additionally, compared to methanol and aqueous extracts, the ethanol extract showed the strongest inhibition activity against α-glucosidase and pancreatic lipase. Compared with the anti-diabetic agent acarbose, mitragynine showed the most potent α-glucosidase inhibition, with less potent activity of pancreatic lipase inhibition. Analysis of α-glucosidase and pancreatic lipase kinetics revealed that mitragynine inhibited noncompetitive and competitive effects, respectively. Combining mitragynine with acarbose resulted in a synergistic interaction with α-glucosidase inhibition. These results have established the potential of mitragynine from kratom as a herbal supplement for the treatment and prevention of diabetes mellitus.
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spelling pubmed-95724522022-10-17 Inhibition of α-Glucosidase and Pancreatic Lipase Properties of Mitragyna speciosa (Korth.) Havil. (Kratom) Leaves Limcharoen, Thanchanok Pouyfung, Phisit Ngamdokmai, Ngamrayu Prasopthum, Aruna Ahmad, Aktsar Roskiana Wisdawati, Wisdawati Prugsakij, Woraanong Warinhomhoun, Sakan Nutrients Article Kratom (Mitragyna speciosa (Korth.) Havil.) has been used to reduce blood sugar and lipid profiles in traditional medicine, and mitragynine is a major constituent in kratom leaves. Previous data on the blood sugar and lipid-altering effects of kratom are limited. In this study, phytochemical analyses of mitragynine, 7-hydroxymitragynine, quercetin, and rutin were performed in kratom extracts. The effects on α-glucosidase and pancreatic lipase activities were investigated in kratom extracts and mitragynine. The LC-MS/MS analysis showed that the mitragynine, quercetin, and rutin contents from kratom extracts were different. The ethanol extract exhibited the highest total phenolic content (TPC), total flavonoid content (TFC), and total alkaloid content (TAC). Additionally, compared to methanol and aqueous extracts, the ethanol extract showed the strongest inhibition activity against α-glucosidase and pancreatic lipase. Compared with the anti-diabetic agent acarbose, mitragynine showed the most potent α-glucosidase inhibition, with less potent activity of pancreatic lipase inhibition. Analysis of α-glucosidase and pancreatic lipase kinetics revealed that mitragynine inhibited noncompetitive and competitive effects, respectively. Combining mitragynine with acarbose resulted in a synergistic interaction with α-glucosidase inhibition. These results have established the potential of mitragynine from kratom as a herbal supplement for the treatment and prevention of diabetes mellitus. MDPI 2022-09-21 /pmc/articles/PMC9572452/ /pubmed/36235558 http://dx.doi.org/10.3390/nu14193909 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Limcharoen, Thanchanok
Pouyfung, Phisit
Ngamdokmai, Ngamrayu
Prasopthum, Aruna
Ahmad, Aktsar Roskiana
Wisdawati, Wisdawati
Prugsakij, Woraanong
Warinhomhoun, Sakan
Inhibition of α-Glucosidase and Pancreatic Lipase Properties of Mitragyna speciosa (Korth.) Havil. (Kratom) Leaves
title Inhibition of α-Glucosidase and Pancreatic Lipase Properties of Mitragyna speciosa (Korth.) Havil. (Kratom) Leaves
title_full Inhibition of α-Glucosidase and Pancreatic Lipase Properties of Mitragyna speciosa (Korth.) Havil. (Kratom) Leaves
title_fullStr Inhibition of α-Glucosidase and Pancreatic Lipase Properties of Mitragyna speciosa (Korth.) Havil. (Kratom) Leaves
title_full_unstemmed Inhibition of α-Glucosidase and Pancreatic Lipase Properties of Mitragyna speciosa (Korth.) Havil. (Kratom) Leaves
title_short Inhibition of α-Glucosidase and Pancreatic Lipase Properties of Mitragyna speciosa (Korth.) Havil. (Kratom) Leaves
title_sort inhibition of α-glucosidase and pancreatic lipase properties of mitragyna speciosa (korth.) havil. (kratom) leaves
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9572452/
https://www.ncbi.nlm.nih.gov/pubmed/36235558
http://dx.doi.org/10.3390/nu14193909
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