In vitro α-glucosidase inhibitory activity of Tamarix nilotica shoot extracts and fractions.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 05 10 2021
accepted: 19 02 2022
entrez: 14 3 2022
pubmed: 15 3 2022
medline: 28 4 2022
Statut: epublish

Résumé

α-glucosidase inhibitors represent an important class of type 2 antidiabetic drugs and they act by lowering postprandial hyperglycemia. Today, only three synthetic inhibitors exist on the market, and there is a need for novel, natural and more efficient molecules exhibiting this activity. In this study, we investigated the ability of Tamarix nilotica ethanolic and aqueous shoot extracts, as well as methanolic fractions prepared from aqueous crude extracts to inhibit α-glucosidase. Both, 50% ethanol and aqueous extracts inhibited α-glucosidase in a concentration-dependent manner, with IC50 values of 12.5 μg/mL and 24.8 μg/mL, respectively. Importantly, α-glucosidase inhibitory activity observed in the T. nilotica crude extracts was considerably higher than pure acarbose (IC50 = 151.1 μg/mL), the most highly prescribed α-glucosidase inhibitor on the market. When T. nilotica crude extracts were fractionated using methanol, enhanced α-glucosidase inhibitory activity was observed in general, with the highest observed α-glucosidase inhibitory activity in the 30% methanol fraction (IC50 = 5.21 μg/mL). Kinetic studies further revealed a competitive reversible mechanism of inhibition by the plant extract. The phytochemical profiles of 50% ethanol extracts, aqueous extracts, and the methanolic fractions were investigated and compared using a metabolomics approach. Statistical analysis revealed significant differences in the contents of the crude extracts and fractions and potentially identified the molecules that were most responsible for these observed variations. Higher α-glucosidase inhibitory activity was associated with an enrichment of terpenoids, fatty acids, and flavonoids. Among the identified molecules, active compounds with known α-glucosidase inhibitory activity were detected, including unsaturated fatty acids, triterpenoids, and flavonoid glycosides. These results put forward T. nilotica as a therapeutic plant for type 2 diabetes and a source of α-glucosidase inhibitors.

Identifiants

pubmed: 35286313
doi: 10.1371/journal.pone.0264969
pii: PONE-D-21-31780
pmc: PMC8920278
doi:

Substances chimiques

Flavonoids 0
Glycoside Hydrolase Inhibitors 0
Plant Extracts 0
Ethanol 3K9958V90M
alpha-Glucosidases EC 3.2.1.20
Methanol Y4S76JWI15

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0264969

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Mariane Daou (M)

Department of Biology, Khalifa University, Abu Dhabi, United Arab Emirates.

Nancy A Elnaker (NA)

Department of Chemistry, Khalifa University, Abu Dhabi, United Arab Emirates.

Michael A Ochsenkühn (MA)

Biology Program, New York University in Abu Dhabi, Abu Dhabi, United Arab Emirates.

Shady A Amin (SA)

Biology Program, New York University in Abu Dhabi, Abu Dhabi, United Arab Emirates.

Ahmed F Yousef (AF)

Department of Biology, Khalifa University, Abu Dhabi, United Arab Emirates.
Center for Membranes and Advances Water Technology (CMAT), Khalifa University, Abu Dhabi, United Arab Emirates.

Lina F Yousef (LF)

Department of Chemistry, Khalifa University, Abu Dhabi, United Arab Emirates.

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