4.5 Article

Acetyl-11-Keto-Beta-Boswellic Acid Has Therapeutic Benefits for NAFLD Rat Models That Were Given a High Fructose Diet by Ameliorating Hepatic Inflammation and Lipid Metabolism

Journal

INFLAMMATION
Volume -, Issue -, Pages -

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10753-023-01853-y

Keywords

Non-alcoholic fatty liver disease (NAFLD); Acetyl-11-keto-beta-boswellic acid (AKBA); AMP-activated protein kinase (AMPK); Inflammasome; Peroxisome proliferator-activated receptor gamma (PPAR-gamma)

Ask authors/readers for more resources

This study investigates the potential of Acetyl-11-keto-beta-boswellic acid (AKBA), an anti-inflammatory compound from Boswellia species, in preventing and treating non-alcoholic fatty liver disease (NAFLD). The results demonstrate that AKBA improves NAFLD-related serum parameters and inflammatory markers, preserves lipid metabolism, improves hepatic steatosis, and suppresses liver inflammation, thus preventing the progression of NAFLD.
Acetyl-11-keto-beta-boswellic acid (AKBA), a potent anti-inflammatory compound purified from Boswellia species, was investigated in a preclinical study for its potential in preventing and treating non-alcoholic fatty liver disease (NAFLD), the most common chronic inflammatory liver disorder. The study involved thirty-six male Wistar rats, equally divided into prevention and treatment groups. In the prevention group, rats were given a high fructose diet (HFrD) and treated with AKBA for 6 weeks, while in the treatment group, rats were fed HFrD for 6 weeks and then given a normal diet with AKBA for 2 weeks. At the end of the study, various parameters were analyzed including liver tissues and serum levels of insulin, leptin, adiponectin, monocyte chemoattractant protein-1 (MCP-1), transforming growth factor beta (TGF-ss), interferon gamma (INF-gamma), interleukin-6 (IL-6), and tumor necrosis factor alpha (TNF-alpha). Additionally, the expression levels of genes related to the inflammasome complex and peroxisome proliferator-activated receptor gamma (PPAR-gamma), as well as the levels of phosphorylated and non-phosphorylated AMP-activated protein kinase alpha-1 (AMPK-alpha 1) protein, were measured. The results showed that AKBA improved NAFLD-related serum parameters and inflammatory markers and suppressed PPAR-gamma and inflammasome complex-related genes involved in hepatic steatosis in both groups. Additionally, AKBA prevented the reduction of the active and inactive forms of AMPK-alpha 1 in the prevention group, which is a cellular energy regulator that helps suppress NAFLD progression. In conclusion, AKBA has a beneficial effect on preventing and avoiding the progression of NAFLD by preserving lipid metabolism, improving hepatic steatosis, and suppressing liver inflammation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available