Critical review on anti-obesity effects of phytochemicals through Wnt/β-catenin signaling pathway. (October 2022)
- Record Type:
- Journal Article
- Title:
- Critical review on anti-obesity effects of phytochemicals through Wnt/β-catenin signaling pathway. (October 2022)
- Main Title:
- Critical review on anti-obesity effects of phytochemicals through Wnt/β-catenin signaling pathway
- Authors:
- Luo, Jinhai
Yu, Zhiling
Tovar, Juscelino
Nilsson, Anne
Xu, Baojun - Abstract:
- Abstract: Phytochemicals have been used as one of the sources for the development of anti-obesity drugs. Plants are rich in a variety of bioactive compounds including polyphenols, saponins and terpenes. Phytochemicals inhibit adipocyte differentiation by inhibiting the transcription and translation of adipogenesis transcription factors such as C/EBPα and PPARγ. It has been proved that phytochemicals inhibit the genes and proteins associated with adipogenesis and lipid accumulation by activating Wnt/β-catenin signaling pathway. The activation of Wnt/β-catenin signaling pathway by phytochemicals is multi-target regulation, including the regulation of pathway critical factor β-catenin and its target gene, the downregulation of destruction complex, and the up-regulation of Wnt ligands, its cell surface receptor and Wnt antagonist. In this review, the literature on the anti-obesity effect of phytochemicals through Wnt/β-catenin signaling pathway is collected from Google Scholar, Scopus, PubMed, and Web of Science, and summarizes the regulation mechanism of phytochemicals in this pathway. As one of the alternative methods of weight loss drugs, Phytochemicals inhibit adipogenesis through Wnt/β-catenin signaling pathway. More progress in relevant fields may pose phytochemicals as the main source of anti-obesity treatment. Graphical Abstract: ga1 Highlights: Phytochemicals exhibits anti-obesity effect by Wnt/β-catenin signaling pathway. Multiple compound molecules contribute toAbstract: Phytochemicals have been used as one of the sources for the development of anti-obesity drugs. Plants are rich in a variety of bioactive compounds including polyphenols, saponins and terpenes. Phytochemicals inhibit adipocyte differentiation by inhibiting the transcription and translation of adipogenesis transcription factors such as C/EBPα and PPARγ. It has been proved that phytochemicals inhibit the genes and proteins associated with adipogenesis and lipid accumulation by activating Wnt/β-catenin signaling pathway. The activation of Wnt/β-catenin signaling pathway by phytochemicals is multi-target regulation, including the regulation of pathway critical factor β-catenin and its target gene, the downregulation of destruction complex, and the up-regulation of Wnt ligands, its cell surface receptor and Wnt antagonist. In this review, the literature on the anti-obesity effect of phytochemicals through Wnt/β-catenin signaling pathway is collected from Google Scholar, Scopus, PubMed, and Web of Science, and summarizes the regulation mechanism of phytochemicals in this pathway. As one of the alternative methods of weight loss drugs, Phytochemicals inhibit adipogenesis through Wnt/β-catenin signaling pathway. More progress in relevant fields may pose phytochemicals as the main source of anti-obesity treatment. Graphical Abstract: ga1 Highlights: Phytochemicals exhibits anti-obesity effect by Wnt/β-catenin signaling pathway. Multiple compound molecules contribute to anti-obesity effect of phytochemicals. Phytochemicals achieve anti-obesity effect by multi-target in signaling pathway. Phytochemicals make natural products alternative traditional weight-loss drugs. Future research may use more data from animal studies and clinical experiments. … (more)
- Is Part Of:
- Pharmacological research. Volume 184(2022)
- Journal:
- Pharmacological research
- Issue:
- Volume 184(2022)
- Issue Display:
- Volume 184, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 184
- Issue:
- 2022
- Issue Sort Value:
- 2022-0184-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-10
- Subjects:
- Acc1 Acetyl-CoA carboxylase 1 -- Acox1 acyl-Coenzyme A oxidase 1 -- Akt/PKB protein kinase B -- APC adenomatous polyposis coli -- aP2 adipocyte protein 2 -- AMPK AMP-activated protein kinase -- AXIN axis inhibition -- CCND1 cyclin D1 -- C/EBPα CCAAT/Enhancer-Binding Proteins α -- CK1α casein kinase 1α -- CRD cysteine rich domain -- DKK Dickkopf -- DSH/DVL Dishevelled -- FABP4 fatty acid binding protein 4 -- FASN fatty acid synthase -- FZD Frizzled -- GSK3β glycogen synthase kinase 3β -- TCF T-cell factor -- LEF lymphoid-enhancing factor -- LPL lipoprotein lipase -- LRP5 low-density lipoprotein receptor-related protein 5 -- LRP6 low-density lipoprotein receptor-related protein 6 -- pKA protein kinase A -- PPARγ Peroxisome Proliferator-Activated Receptor γ -- PPARδ Peroxisome Proliferator-Activated Receptor δ -- Pref1 Preadipocyte factor -- RXRα Retinoid X receptorα -- Scd1 Stearoyl-CoA desaturase 1 -- SFRP secreted frizzled-related protein -- Srebp Sterol-regulatory element binding protein -- Wnt Wingless
Phytochemicals -- Anti-obesity -- Wnt/β-catenin signaling pathway -- C/EBPα -- PPARγ -- β-catenin
Pharmacology -- Periodicals
Pharmacology -- Periodicals
Research -- Periodicals
Médicaments -- Recherche -- Périodiques
Pharmacologie -- Périodiques
615.105 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10436618 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.phrs.2022.106461 ↗
- Languages:
- English
- ISSNs:
- 1043-6618
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6446.550000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24055.xml