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UPLC-ESI/MSn metabolic profiling of Cedrela odorata L. and Toona ciliata M. Roem and in vitro investigation of their anti-diabetic activity supported with molecular docking studies

Heba A.S. El-Nashar 1
Ayman M. Al-Qaaneh 2, 3
Md. Shimul Bhuia 4, 5
Raihan Chowdhury 4, 5
Mostafa A. Abdel-maksoud 6
Hossam Ebaid 7
Abdul Malik 8
Muhammad Torequl Islam 4, 5, 9
Aufy Mohammed 10
Esraa A Elhawary 1
Publication typeJournal Article
Publication date2024-11-15
scimago Q1
wos Q2
SJR0.830
CiteScore8.4
Impact factor4.2
ISSN22962646
Abstract
Introduction

The genus Cedrela is one of the phytochemically rich genera of the family Meliaceae. In this study, two Cedrela species, namely, Cedrela odorata and Toona ciliata M. Roem (formerly Cedrela toona), were selected for in-depth phytochemical profiling with the aid of UPLC-ESI/MSn analysis followed by evaluation of their anti-diabetic potential through assessment of in vitro α-amylase and α-glucosidase inhibitory effects, alongside the molecular docking studies on these target enzymes.

Materials and methods

UPLC-ESI/MSn technique was applied to tentatively identify the extracts. The anti-diabetic properties were assessed using BioVision α-amylase and α-glucosidase inhibitor screening kits. Further, the molecular docking studies utilized PyRx® and Discovery Studio software.

Results and discussion

The UPLC-ESI/MSn analysis led to the identification and quantification of 55 metabolites with their fragmentation patterns for the first time for these two species. Flavonoids represented the main identified class, followed by phenylpropanoids, terpenes, tannins, and others. The two species showed potent enzyme inhibition, where C. odorata and C. toona significantly inhibited α-amylase (IC50 = 4.83 ± 0.01 and 3.50 ± 0.03 μg/mL) compared to pioglitazone (IC50 = 2.17 ± 0.23 μg/mL), while their α-glycosidase inhibitory properties were also potent with (IC50 = 7.17 ± 0.01 and 6.50 ± 0.69 μg/mL), respectively, compared to acarbose (IC50 = 4.83 ± 1.02 μg/mL). The enzyme inhibitory activities were further confirmed by in silico molecular docking of the main identified components with the respective binding sockets in both α-amylase and α-glycosidase enzymes.

Conclusion

These promising results could pave the way for a novel discovery of natural phytoconstituents with potent anti-diabetic activity.

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El-Nashar H. A. et al. UPLC-ESI/MSn metabolic profiling of Cedrela odorata L. and Toona ciliata M. Roem and in vitro investigation of their anti-diabetic activity supported with molecular docking studies // Frontiers in Chemistry. 2024. Vol. 12.
GOST all authors (up to 50) Copy
El-Nashar H. A., Al-Qaaneh A. M., Bhuia M. S., Chowdhury R., Abdel-maksoud M. A., Ebaid H., Malik A., Torequl Islam M., Mohammed A., Elhawary E. A. UPLC-ESI/MSn metabolic profiling of Cedrela odorata L. and Toona ciliata M. Roem and in vitro investigation of their anti-diabetic activity supported with molecular docking studies // Frontiers in Chemistry. 2024. Vol. 12.
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TY - JOUR
DO - 10.3389/fchem.2024.1462309
UR - https://www.frontiersin.org/articles/10.3389/fchem.2024.1462309/full
TI - UPLC-ESI/MSn metabolic profiling of Cedrela odorata L. and Toona ciliata M. Roem and in vitro investigation of their anti-diabetic activity supported with molecular docking studies
T2 - Frontiers in Chemistry
AU - El-Nashar, Heba A.S.
AU - Al-Qaaneh, Ayman M.
AU - Bhuia, Md. Shimul
AU - Chowdhury, Raihan
AU - Abdel-maksoud, Mostafa A.
AU - Ebaid, Hossam
AU - Malik, Abdul
AU - Torequl Islam, Muhammad
AU - Mohammed, Aufy
AU - Elhawary, Esraa A
PY - 2024
DA - 2024/11/15
PB - Frontiers Media S.A.
VL - 12
PMID - 39618969
SN - 2296-2646
ER -
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@article{2024_El-Nashar,
author = {Heba A.S. El-Nashar and Ayman M. Al-Qaaneh and Md. Shimul Bhuia and Raihan Chowdhury and Mostafa A. Abdel-maksoud and Hossam Ebaid and Abdul Malik and Muhammad Torequl Islam and Aufy Mohammed and Esraa A Elhawary},
title = {UPLC-ESI/MSn metabolic profiling of Cedrela odorata L. and Toona ciliata M. Roem and in vitro investigation of their anti-diabetic activity supported with molecular docking studies},
journal = {Frontiers in Chemistry},
year = {2024},
volume = {12},
publisher = {Frontiers Media S.A.},
month = {nov},
url = {https://www.frontiersin.org/articles/10.3389/fchem.2024.1462309/full},
doi = {10.3389/fchem.2024.1462309}
}