| Literature DB >> 35885378 |
Daniel Jamrozik1, Weronika Borymska1, Ilona Kaczmarczyk-Żebrowska1.
Abstract
Diabetes is currently a global health problem that is already reported as an epidemic. This metabolic disease, characterized by a disturbance in the carbohydrate, protein, and lipid metabolism, is often accompanied by disorders of several organs. Its treatment is expensive and often difficult to control. Therefore, it seems necessary to search for new drugs and solutions to facilitate therapy and reduce treatment costs. Herbal medicines are becoming more and more popular. Hibiscus sabdariffa (roselle) is a plant that grows wild in a tropical climate. It has been used in folk medicine for thousands of years. Thanks to the numerous active compounds, including polyphenols, polysaccharides, organic acids, or pectins, it is reported to exhibit hypoglycemic, antioxidant, hypotensive, and anti-lipidemic activities and numerous indirect effects that are related to them. The aim of this review was to update the knowledge about the therapeutic effects of roselle in diabetes and its comorbidities based on in vitro, animal, and human studies. After a careful analysis of the scientific literature, it can be stated that roselle is a promising product that can be used either on its own or as an addition to the conventional treatment regimens to prevent or treat diabetes and its accompanying diseases.Entities:
Keywords: Hibiscus sabdariffa; animals; antilipidemic; antioxidant; diabetes; extracts; hypoglycemic; in vitro; patients
Year: 2022 PMID: 35885378 PMCID: PMC9319339 DOI: 10.3390/foods11142134
Source DB: PubMed Journal: Foods ISSN: 2304-8158
Active chemical compounds in Hibiscus sabdariffa.
| Chemical Groups | Active Compounds | References |
|---|---|---|
| Anthocyanins 1 | delphinidin-3-sambubioside cyanidin-3-sambubioside | [ |
| Flavonoids 1 | quercetin, hibiscetin (hibiscetin-3-glucoside), sabdaritrin, gossypitrin, and other gossypetin glycosides, luteolin | [ |
| Phenolic acids 1 | chlorogenic acid, protocatechuic acid, caffeic acid | [ |
| Tannins 1 | no specific name indicated | [ |
| Non-phenolic organic acids | hibiscus acid, hydroxy citric acid, malic acid, ascorbic acid, oxalic acid, succinic acid, tartaric acid, arachidic acid, citric acid | [ |
| Triterpenoids | α-amyrin, lupeol | [ |
| Polysaccharides (Sugars) | galactose, galacturonic acid, rhamnose, arabinose, glucose, mannose, xylose, pectins | [ |
| Others | calcium, magnesium, iron, trace elements, and vitamins | [ |
1 Polyphenols.
Figure 1Molecular mechanisms of roselle action in multiple diabetes-related conditions. Mechanisms described in oval shapes were examined in vitro or in vivo in diabetic models/conditions, while those presented in rectangular boxes were explored in other models/conditions but are putative also for diabetes. ACC—acetyl-CoA Carboxylase; ACE—angiotensin converting enzyme; ACOX—peroxisomal acyl-coenzyme A oxidase; AGEs—advanced glycation end-products; p-Akt—phospho-protein kinase B; pAMPK—phospho-AMP-activated protein kinase; AT-1—angiotensin II receptor; p-Bad—phospho-BCL2-associated agonist of cell death; CD31—cluster of differentiation 31; C/EBPα—CATT/enhancer binding protein-α; C/EBPβ—CATT/enhancer binding protein-β; CPT1—carnitine palmitoyltransferase1; CTGF—connective tissue growth factor; CYP7A1—cytochrome P450 7A1; DPP-4—type 4 dipeptidyl peptidase; EMT—mesenchymal epithelial transition; eNOS—endothelial NO synthase; FASN—fatty acid synthase; FATP—fatty acid transporter protein; GLP-1—glucagon-like peptide 1; GLPR—glucagon-like peptide receptor; GLUT4—glucose transporter type 4; HMGCR—3-hydroxy-3-methylglutaryl-CoA reductase; iNOS—inducible NO synthase; pIRS-1—phospho-insulin receptor substrate 1; MMP-2—migration–matrix metalloproteinase 2; NF-κB—nuclear factor kappa-light-chain-enhancer of activated B cells; PCNA—proliferating cell nuclear antigen; p-PI3K—phospho-phosphatidylinositol 3-kinase; PPARα—proximal proliferator-activated receptor-α; PPARγ—proximal proliferator-activated receptor-γ; PPARδ—proximal proliferator-activated receptor-δ; RAGE—receptor of advanced glycation end product; SGLT-1—sodium-glucose co-transporter-1; SREBP-1c—sterol regulatory element-binding protein-1 c; TGF-β—transforming growth factor β1; TLR4—toll-like receptor 4; TNF-α—tumor necrosis factor α; VSMC—vascular smooth muscle cells.
Figure 2Beneficial effects of different parts of roselle in diabetes and its complications.