Molecular mechanisms of Agardhiella subulata attenuates hepatic fibrosis by modulating hepatic stellate cell activation via the reduction of autophagy

• Published in: Journal of functional foods Vol. 96; p. 105226
• Main Authors: Anwar, Choirul, Tsai, Mei-Ling, Chen, Bio-Nain, Hsu, Li-Yun, Lai, Ching-Shu
• Format: Journal Article
• Language: English
• Published: Elsevier Ltd 01.09.2022; Elsevier
• Subjects: Agardhiella subulata; Autophagy; Hepatic fibrosis; Hepatic stellate cell; Lipid droplet; Hepatic fibrosis; Lipid droplet; PLIN; ATGL; Agardhiella subulata; GPT; Autophagy; GOT; ECM; GFAP; SD; α-SMA; ASE; CCl4; HSC; TGF-β1; KCs; Hepatic stellate cell; SMAD; LC3
• ISSN: 1756-4646; 2214-9414
• DOI: 10.1016/j.jff.2022.105226

[Display omitted] •Agardhiella subulata extract (ASE) alleviated hepatic fibrosis in CCl4 treated Sprague–Dawley rats.•ASE reduced hepatocyte apoptosis, macrophage infiltration, and hepatic stellate cells (HSCs) activation.•ASE suppressed HSCs activation through downregulation of TGF-β1/Smad signaling.•ASE attenuated autophagy and lipid droplets degradation in HSCs. In this study, we investigated the effects of Agardhiella subulata extract (ASE) and its underlying mechanisms in vivo and in vitro. Rats induced hepatic fibrosis with CCl4 and transforming growth factor-β1 (TGF-β1) activated rat hepatic stellate cell line (HSC-T6) was used. The results showed that ASE (oral, 10 or 50 mg/kg) effectively attenuated liver fibrogenesis in the rats. This was evidenced by decreases in serum glutamic oxaloacetic transaminase and glutamic pyruvic transaminase levels, histopathological changes, decreased collagen deposition, and extracellular matrix formation. ASE significantly reduced hepatocyte apoptosis, Kupffer cell activation, and the levels of fibrogenic molecules such as alpha-smooth muscle actin and collagen. Furthermore, ASE downregulated the TGF-β1/Smad signaling pathway and concomitantly inhibited the activation of hepatic stellate cells by reducing autophagy and inducing the regeneration of lipid droplets both in vivo and in vitro. Overall, ASE inhibited various mechanisms that are important targets in the prevention of hepatic fibrosis.