Sesquiterpene Polygodial from Drimys brasiliensis (Winteraceae) Down-Regulates Implant-Induced Inflammation and Fibrogenesis in Mice.
Bruno Antonio FerreiraAnderson Ferraz Norton FilhoSimone Ramos DeconteTatiana Carla TomiossoFernanda ThevenardSilvia Passos AndradeJoão Henrique Ghilardi LagoFernanda de Assis AraújoPublished in: Journal of natural products (2020)
Drimys brasiliensis (Winteraceae) has been investigated in traditional medicine for its anti-inflammatory properties to treat gastric ulcers and allergic and respiratory system diseases as well as for cancer treatment. In this work, we investigate the ability of the sesquiterpene polygodial, isolated from D. brasiliensis stem barks, to modulate the chronic inflammatory response induced by polyester-polyurethane sponge implants in C57BL/6J mice. Daily treatment with polygodial inhibited the macrophage content in the implants as determined by the activity of the N-acetyl-β-d-glucosaminidase enzyme as well as decreased the levels of CXCL1/KC and CCL2/JE/MCP-1 pro-inflammatory chemokines and the presence of mast cells along the formed fibrovascular tissue. Similarly, the deposition of a new extracellular matrix (total collagen and type I and III collagen fibers) as well as the production of the TGF-β1 cytokine were attenuated in implants treated with polygodial, showing for the first time its antifibrogenic capacity. The hemoglobin content, the number of newly formed vessels, and the levels of VEGF cytokine, which were used as parameters for the assessment of the neovascularization of the implants, did not change after treatment with polygodial. The anti-inflammatory and antifibrogenic effects of polygodial over the components of the granulation tissue induced by the sponge implant indicate a therapeutic potential for the treatment of inflammatory diseases associated with the development of fibrovascular tissue.
Keyphrases
- soft tissue
- anti inflammatory
- extracellular matrix
- inflammatory response
- oxidative stress
- physical activity
- vascular endothelial growth factor
- type diabetes
- drug induced
- adipose tissue
- liver injury
- endothelial cells
- metabolic syndrome
- lipopolysaccharide induced
- mass spectrometry
- diabetic retinopathy
- insulin resistance
- liver fibrosis
- wild type
- atopic dermatitis
- optical coherence tomography