Novel Combinatorial Regimen of Garcinol and Curcuminoids for Non-alcoholic Steatohepatitis (NASH) in Mice.
Muhammed MajeedShaheen MajeedNagabhushanam KalyanamLincy LawrenceLakshmi A MundkurPublished in: Scientific reports (2020)
Non-alcoholic steatohepatitis (NASH) is a progressive form of Non-alcoholic fatty liver disease (NAFLD), a chronic liver disease with a significant unmet clinical need. In this study, we examined the protective effects of Garcinia indica extract standardized to contain 20% w/w of Garcinol (GIE) and 95% Curcuminoids w/w from Curcuma longa (Curcuminoids) in a Stelic animal model (STAM) of NASH. The STAM mice developed steatosis, hepatocyte ballooning, and inflammation, which were significantly reduced by the combination of GIE and Curcuminoids, resulting in a lower NAFLD activity score. The treatment reduced fibrosis as observed by Sirius red staining, liver hydroxyproline content and mRNA levels of TGF- β and collagen in the liver. Immunostaining with alpha-smooth muscle actin (α SMA) revealed a significant reduction in hepatic stellate cells. Intriguingly, the combination regimen markedly decreased the mRNA levels of MCP1 and CRP and both mRNA and protein levels of TNF-α. NF-kB, reduced the hepatic and circulating FGF21 levels and altered the nonenzymatic (glutathione) and enzymatic antioxidant markers (Glutathione peroxidase, and superoxide dismutase). Our results suggest that the combination of GIE and Curcuminoids can reduce the severity of NASH by reducing steatosis, fibrosis, oxidative stress, and inflammation. The results suggest that the combinatorial regimen could be an effective supplement to prevent the progression of liver steatosis to inflammation and fibrosis in NASH.
Keyphrases
- oxidative stress
- induced apoptosis
- high fat diet induced
- smooth muscle
- insulin resistance
- liver fibrosis
- diabetic rats
- high fat diet
- liver injury
- hydrogen peroxide
- ischemia reperfusion injury
- dna damage
- rheumatoid arthritis
- multiple sclerosis
- metabolic syndrome
- type diabetes
- single cell
- drug induced
- immune response
- cell death
- nitric oxide
- signaling pathway
- anti inflammatory
- transforming growth factor
- small molecule
- flow cytometry