Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/186638
Título: Effects of Periploca chevalieri Browicz on Postprandial Glycemia and Carbohydrate-Hydrolyzing Enzymes
Autor: Lima, Katelene
Malmir, Maryam
Sabiha, Shabnam
Pinto, Rui
Silva, Isabel Moreira da
Figueira, Maria Eduardo
Rocha, João
Duarte, Maria Paula
Silva, Olga
Palavras-chave: Antiglycation
Diabetes
DPP4
Herbal medicine
Periploca chevalieri
α-amylase
α-glucosidase
Molecular Medicine
Pharmaceutical Science
Drug Discovery
SDG 3 - Good Health and Well-being
Data: 18-Jun-2025
Resumo: Background/Objectives: Periploca chevalieri Browicz (Apocynaceae), an endemic species of the Cabo Verde archipelago, is commonly used in traditional medicine for the treatment of diabetes. The aim of this study was to characterize the chemical profiles of the aqueous and hydroethanolic (70%) extracts of the P. chevalieri dried aerial parts (PcAE and PcEE) and evaluate their potential to modulate postprandial glycemia and inhibit key carbohydrate-hydrolyzing enzymes. Methods: The chemical characterization was performed by LC/UV-DAD-ESI/MS/MS. An in vivo evaluation of postprandial glycemia modulation was conducted on healthy CD1 mice submitted to an oral sucrose tolerance test. In vitro enzymatic inhibition was performed for the α-amylase, α-glucosidase, and DPP4 enzymes. Additionally, antioxidant and antiglycation activities were also assessed. Results: Phenolic acid derivatives, flavanols, proanthocyanidins, and flavonols were the major classes of secondary metabolites identified. PcEE at 170 mg/kg of body weight significantly (p < 0.05) reduced the postprandial glycemia peak in CD1 mice submitted to sucrose overload. Regarding the enzymatic inhibition, both extracts showed concentration-dependent inhibitory potential against the α-amylase, α-glucosidase, and DPP4 enzymes. Both extracts inhibited α-glucosidase more effectively than acarbose. Conclusions: The obtained results supports the traditional use of P. chevalieri and suggest the potential for further pharmacological investigation.
Descrição: Funding Information: This research was funded by the Foundation for Science and Technology (FCT, Portugal) through national funds to iMed.ULisboa (UIDP/04138/2020) and to the Mechanical Engineering and Resource Sustainability Center—MEtRICs unit, which is funded by national funds from FCT/MCTES (UIDB/04077/2020 and UIDP/04077/2020). Publisher Copyright: © 2025 by the authors.
Peer review: yes
URI: http://hdl.handle.net/10362/186638
DOI: https://doi.org/10.3390/ph18060913
ISSN: 1424-8247
Aparece nas colecções:Home collection (FCT)

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