Targeting PI3K/AKT signaling pathway in obesity.

AKT Alpelisib (PubChem CID: 56649450) Amentoflavone (PubChem CID: 5281600) Astragaloside IV (PubChem CID: 13943297) Betulinic acid (PubChem CID: 64971) Capsaicin (PubChem CID: 1548943) Carbenoxolone (PubChem CID: 636403) Catalpol (PubChem CID: 91520) Celastrol (PubChem CID: 122724) Druggability Epigallocatechin gallate (PubChem CID: 650464) Ginsenoside Rb2 (PubChem CID: 6917976) Glycyrrhetinic acid (PubChem CID: 10114) Isoliquiritigenin (PubChem CID: 638278) Kaempferol (PubChem CID: 5280863) Maackiain (PubChem CID: 91510) Natural compounds Nigelladine A (PubChem CID: 86302612) Nigelladine B (PubChem CID: 86302611) Nigelladine C (PubChem CID: 86302610) Obesity Ononin (PubChem CID: 442813) Orientin (PubChem CID: 5281675) Oxyberberine (PubChem CID: 11066) PI3K Pharmacotherapy

Journal

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
ISSN: 1950-6007
Titre abrégé: Biomed Pharmacother
Pays: France
ID NLM: 8213295

Informations de publication

Date de publication:
Mar 2023
Historique:
received: 30 11 2022
revised: 09 01 2023
accepted: 10 01 2023
pubmed: 14 1 2023
medline: 8 2 2023
entrez: 13 1 2023
Statut: ppublish

Résumé

Obesity is a disorder with an increasing prevalence, which impairs the life quality of patients and intensifies societal health care costs. The development of safe and innovative prevention strategies and therapeutic approaches is thus of great importance. The complex pathophysiology of obesity involves multiple signaling pathways that influence energy metabolism in different tissues. The phosphatidylinositol 3-kinases (PI3K)/protein kinase B (AKT) pathway is critical for the metabolic homeostasis and its function in insulin-sensitive tissues is described in the context of health, obesity and obesity-related complications. The PI3K family participates in the regulation of diverse physiological processes including but not limited to cell growth, survival, differentiation, autophagy, chemotaxis, and metabolism depending on the cellular context. AKT is downstream of PI3K in the insulin signaling pathway, and promotes multiple cellular processes by targeting a plethora of regulatory proteins that control glucose and lipid metabolism. Natural products are essential for prevention and treatment of many human diseases, including obesity. Anti-obesity natural compounds effect multiple pathophysiological mechanisms involved in obesity development. Numerous recent preclinical studies reveal the advances in using plant secondary metabolites to target the PI3K/AKT signaling pathway for obesity management. In this paper the druggability of PI3K as a target for compounds with anti-obesity potential is evaluated. Perspectives on the strategies and limitations for clinical implementation of obesity management using natural compounds modulating the PI3K/AKT pathway are suggested.

Identifiants

pubmed: 36638594
pii: S0753-3322(23)00032-X
doi: 10.1016/j.biopha.2023.114244
pii:
doi:

Substances chimiques

Insulin 0
Phosphatidylinositol 3-Kinase EC 2.7.1.137
Phosphatidylinositol 3-Kinases EC 2.7.1.-
Proto-Oncogene Proteins c-akt EC 2.7.11.1

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

114244

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement The authors declare that the work on this review paper was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Martina S Savova (MS)

Center of Plant Systems Biology and Biotechnology, 4000 Plovdiv, Bulgaria; Laboratory of Metabolomics, Institute of Microbiology, Bulgarian Academy of Sciences, 139 Ruski Blvd., 4000 Plovdiv, Bulgaria.

Liliya V Mihaylova (LV)

Center of Plant Systems Biology and Biotechnology, 4000 Plovdiv, Bulgaria; Laboratory of Metabolomics, Institute of Microbiology, Bulgarian Academy of Sciences, 139 Ruski Blvd., 4000 Plovdiv, Bulgaria.

Daniel Tews (D)

Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, Ulm University Medical Center, 89077 Ulm, Germany.

Martin Wabitsch (M)

Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, Ulm University Medical Center, 89077 Ulm, Germany.

Milen I Georgiev (MI)

Center of Plant Systems Biology and Biotechnology, 4000 Plovdiv, Bulgaria; Laboratory of Metabolomics, Institute of Microbiology, Bulgarian Academy of Sciences, 139 Ruski Blvd., 4000 Plovdiv, Bulgaria. Electronic address: milengeorgiev@gbg.bg.

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Classifications MeSH