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Updated: May 7, 2026

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Optimized Analysis of In Vivo and In Vitro Hepatic Steatosis
Published on: March 11, 2017
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COMPARATIVE ASSESSMENT OF THE EFFECT OF SILYMARIN, FENOFIBRATE, BETAINE AND ADEMETIONINE ON THE DEVELOPMENT OF
A Zozulya1, V Teslevich1, P Abkhazava1
1North-Western State Medical University named after I.I. Mechnikov, Saint Petersburg, Russia.
Georgian Medical News
|November 28, 2025
Summary
Fenofibrate effectively reduced liver fat and enzyme levels in rats with fructose-induced metabolic dysfunction-associated steatotic liver disease (MASLD). Other agents showed varied effects, with fenofibrate demonstrating the most significant improvements in MASLD markers.
Area of Science:
- Hepatology
- Metabolic Diseases
- Pharmacology
Background:
- Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly NAFLD/MAFLD, is a growing health concern.
- High-fructose diets in animal models reliably induce MASLD, characterized by hepatic steatosis and liver injury.
- Understanding therapeutic interventions for MASLD is crucial for managing liver health.
Purpose of the Study:
- To compare the efficacy of silymarin, fenofibrate, betaine, and ademetionine in treating diet-induced MASLD.
- To assess the impact of these agents on key biochemical markers of liver injury.
- To evaluate morphological changes associated with MASLD and treatment responses.
Main Methods:
- Male Wistar rats were fed a high-fructose diet for five weeks to induce MASLD.
- Animals were treated with silymarin, fenofibrate, betaine, or ademetionine.
- Serum ALT, AST, and hepatic triglyceride levels were measured to assess treatment efficacy.
Main Results:
- Fenofibrate significantly reduced hepatic triglycerides by approximately 60% and lowered ALT/AST levels by 40%.
- Silymarin and betaine demonstrated intermediate improvements in MASLD markers.
- Ademetionine effectively reduced transaminases but had minimal impact on hepatic triglyceride accumulation.
Conclusions:
- Fenofibrate emerged as the most potent agent against fructose-induced hepatic steatosis and elevated transaminases.
- The study suggests fenofibrate's efficacy is linked to PPAR-α activation, promoting fatty acid oxidation and reducing fat synthesis.
- These findings highlight fenofibrate as a promising therapeutic candidate for MASLD.

