Venom Peptides, Polyphenols and Alkaloids: ...
Type de document :
Article dans une revue scientifique: Article de synthèse/Review paper
DOI :
PMID :
Titre :
Venom Peptides, Polyphenols and Alkaloids: Are They the Next Antidiabetics That Will Preserve β-Cell Mass and Function in Type 2 Diabetes?
Auteur(s) :
Lodato, Michele [Auteur]
Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 [IEMN]
Plaisance, Valérie [Auteur]
NanoBioInterfaces - IEMN [NBI - IEMN]
Pawlowski, Valérie [Auteur]
NanoBioInterfaces - IEMN [NBI - IEMN]
Kwapich, Maxime [Auteur]
Hôpital Alexandra Lepève – Centre Hospitalier de Dunkerque [HAL – CH Dunkerque]
Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 [IEMN]
Barras, Alexandre [Auteur]
NanoBioInterfaces - IEMN [NBI - IEMN]
Buissart, Emeline [Auteur]
Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 [IEMN]
Dalle, Stéphane [Auteur]
Institut de Génomique Fonctionnelle [IGF]
Szunerits, Sabine [Auteur]
NanoBioInterfaces - IEMN [NBI - IEMN]
Vicogne, Jérôme [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Boukherroub, Rabah [Auteur]
Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 [IEMN]
Abderrahmani, Amar [Auteur]
NanoBioInterfaces - IEMN [NBI - IEMN]
Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 [IEMN]
Plaisance, Valérie [Auteur]
NanoBioInterfaces - IEMN [NBI - IEMN]
Pawlowski, Valérie [Auteur]
NanoBioInterfaces - IEMN [NBI - IEMN]
Kwapich, Maxime [Auteur]

Hôpital Alexandra Lepève – Centre Hospitalier de Dunkerque [HAL – CH Dunkerque]
Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 [IEMN]
Barras, Alexandre [Auteur]

NanoBioInterfaces - IEMN [NBI - IEMN]
Buissart, Emeline [Auteur]
Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 [IEMN]
Dalle, Stéphane [Auteur]
Institut de Génomique Fonctionnelle [IGF]
Szunerits, Sabine [Auteur]

NanoBioInterfaces - IEMN [NBI - IEMN]
Vicogne, Jérôme [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Boukherroub, Rabah [Auteur]

Institut d’Électronique, de Microélectronique et de Nanotechnologie - UMR 8520 [IEMN]
Abderrahmani, Amar [Auteur]

NanoBioInterfaces - IEMN [NBI - IEMN]
Titre de la revue :
Cells
Pagination :
940
Éditeur :
MDPI
Date de publication :
2023-03
ISSN :
2073-4409
Mot(s)-clé(s) en anglais :
diabetes
insulin secretagogues
pancreatic beta cell
venom
polyphenols
alkaloids
peptides
insulin secretagogues
pancreatic beta cell
venom
polyphenols
alkaloids
peptides
Discipline(s) HAL :
Chimie/Chimie thérapeutique
Sciences du Vivant [q-bio]/Médecine humaine et pathologie/Endocrinologie et métabolisme
Sciences du Vivant [q-bio]/Médecine humaine et pathologie/Endocrinologie et métabolisme
Résumé en anglais : [en]
Improvement of insulin secretion by pancreatic β-cells and preservation of their mass are the current challenges that future antidiabetic drugs should meet for achieving efficient and long-term glycemic control in patients ...
Lire la suite >Improvement of insulin secretion by pancreatic β-cells and preservation of their mass are the current challenges that future antidiabetic drugs should meet for achieving efficient and long-term glycemic control in patients with type 2 diabetes (T2D). The successful development of glucagon-like peptide 1 (GLP-1) analogues, derived from the saliva of a lizard from the Helodermatidae family, has provided the proof of concept that antidiabetic drugs directly targeting pancreatic β-cells can emerge from venomous animals. The literature reporting on the antidiabetic effects of medicinal plants suggests that they contain some promising active substances such as polyphenols and alkaloids, which could be active as insulin secretagogues and β-cell protectors. In this review, we discuss the potential of several polyphenols, alkaloids and venom peptides from snake, frogs, scorpions and cone snails. These molecules could contribute to the development of new efficient antidiabetic medicines targeting β-cells, which would tackle the progression of the disease.Lire moins >
Lire la suite >Improvement of insulin secretion by pancreatic β-cells and preservation of their mass are the current challenges that future antidiabetic drugs should meet for achieving efficient and long-term glycemic control in patients with type 2 diabetes (T2D). The successful development of glucagon-like peptide 1 (GLP-1) analogues, derived from the saliva of a lizard from the Helodermatidae family, has provided the proof of concept that antidiabetic drugs directly targeting pancreatic β-cells can emerge from venomous animals. The literature reporting on the antidiabetic effects of medicinal plants suggests that they contain some promising active substances such as polyphenols and alkaloids, which could be active as insulin secretagogues and β-cell protectors. In this review, we discuss the potential of several polyphenols, alkaloids and venom peptides from snake, frogs, scorpions and cone snails. These molecules could contribute to the development of new efficient antidiabetic medicines targeting β-cells, which would tackle the progression of the disease.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Source :
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