Metabolomics-Based Profiling via a Chemometric Approach to Investigate the Antidiabetic Property of Different Parts and Origins of Pistacia lentiscus L.

Author:

Sehaki Chabha12,Molinie Roland1ORCID,Mathiron David3ORCID,Fontaine Jean-Xavier1ORCID,Jullian Nathalie1,Ayati Fadila2,Fernane Farida2ORCID,Gontier Eric1ORCID

Affiliation:

1. BIOPI-UPJV Laboratory UMRT BioEcoAgro INRAE1158, SFR Condorcet FR CNRS 3417, UFR of Sciences, University of Picardie Jules Verne, 33 Rue Saint Leu, 80000 Amiens, France

2. Laboratory of Natural Resources, University Mouloud Mammeri of Tizi-Ouzou, Tizi-Ouzou 15000, Algeria

3. Analytical Platform, UFR of Sciences, University of Picardie Jules Verne, 33 Rue Saint Leu, 80000 Amiens, France

Abstract

Pistacia lentiscus L. is a medicinal plant that grows spontaneously throughout the Mediterranean basin and is traditionally used to treat diseases, including diabetes. The aim of this work consists of the evaluation of the α-glucosidase inhibitory effect (i.e., antidiabetic activity in vitro) of different extracts from the leaves, stem barks and fruits of P. lentiscus harvested on mountains and the littoral of Tizi-Ouzou in Algeria. Metabolomic profiling combined with a chemometric approach highlighted the variation of the antidiabetic properties of P. lentiscus according to the plant’s part and origin. A multiblock OPLS analysis showed that the metabolites most involved in α-glucosidase inhibition activity were mainly found in the stem bark extracts. The highest inhibitory activity was found for the stem bark extracts, with averaged inhibition percentage values of 84.7% and 69.9% for the harvested samples from the littoral and mountain, respectively. On the other hand, the fruit extracts showed a lower effect (13.6%) at both locations. The UHPLC-ESI-HRMS characterization of the metabolites most likely responsible for the α-glucosidase-inhibitory activity allowed the identification of six compounds: epigallocatechin(4a>8)epigallocatechin (two isomers), (epi)gallocatechin-3′-O-galloyl-(epi)gallocatechin (two isomers), 3,5-O-digalloylquinic acid and dihydroxy benzoic acid pentoside.

Funder

the French Ministry of Foreign Affairs through Campus France

the “Conseil Régional de Picardie” through the MTV (Métabo-Typage Végétal) project

the University of Picardie Jules Verne through the French Ministry of Higher Education and Research

the region “Hauts de France”

the European FEDER fund

Algerian authorities

the Tizi-Ouzou UMMTO University

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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