Tanshinone IIA and Cryptotanshinone Counteract Inflammation by Regulating Gene and miRNA Expression in Human SGBS Adipocytes.
Sara CarpiStefano QuartaStefano DocciniAnella SavianoNoemi MariglianoBeatrice PoliniMarika MassaroMaria Annunziata CarluccioNadia CalabrisoMartin WabitschFilippo Maria SantorelliMarco CecchiniFrancesco MaionePaola NieriEgeria ScodittiPublished in: Biomolecules (2023)
Inflammation of the adipose tissue contributes to the onset and progression of several chronic obesity-related diseases. The two most important lipophilic diterpenoid compounds found in the root of Salvia milthorrhiza Bunge (also called Danshen), tanshinone IIA (TIIA) and cryptotanshinone (CRY), have many favorable pharmacological effects. However, their roles in obesity-associated adipocyte inflammation and related sub-networks have not been fully elucidated. In the present study, we investigated the gene, miRNAs and protein expression profile of prototypical obesity-associated dysfunction markers in inflamed human adipocytes treated with TIIA and CRY. The results showed that TIIA and CRY prevented tumor necrosis factor (TNF)-α induced inflammatory response in adipocytes, by counter-regulating the pattern of secreted cytokines/chemokines associated with adipocyte inflammation (CCL2/MCP-1, CXCL10/IP-10, CCL5/RANTES, CXCL1/GRO-α, IL-6, IL-8, MIF and PAI-1/Serpin E1) via the modulation of gene expression (as demonstrated for CCL2/MCP-1, CXCL10/IP-10, CCL5/RANTES, CXCL1/GRO-α, and IL-8), as well as related miRNA expression (miR-126-3p, miR-223-3p, miR-124-3p, miR-155-5p, and miR-132-3p), and by attenuating monocyte recruitment. This is the first demonstration of a beneficial effect by TIIA and CRY on adipocyte dysfunction associated with obesity development and complications, offering a new outlook for the prevention and/or treatment of metabolic diseases.
Keyphrases
- adipose tissue
- insulin resistance
- high fat diet induced
- oxidative stress
- metabolic syndrome
- high fat diet
- liver injury
- endothelial cells
- drug induced
- gene expression
- weight loss
- type diabetes
- inflammatory response
- liver fibrosis
- skeletal muscle
- diabetic rats
- rheumatoid arthritis
- poor prognosis
- weight gain
- binding protein
- copy number
- high glucose
- dna methylation
- genome wide
- risk factors
- immune response
- small molecule
- physical activity
- lipopolysaccharide induced
- dendritic cells
- genome wide identification