Related Experiment Video
Updated: Jun 27, 2025

Polymalic Acid-based Nano Biopolymers for Targeting of Multiple Tumor Markers: An Opportunity for Personalized Medicine?
Published on: June 13, 2014
Onion Polyphenols as Multi-Target-Directed Ligands in MASLD: A Preliminary Molecular Docking Study
Maria Rosaria Paravati1, Anna Caterina Procopio1, Maja Milanović2
1Department of Health Sciences, University "Magna Graecia", 88100 Catanzaro, Italy.
Abstract:
A sedentary lifestyle associated with unregulated diets rich in high-calorie foods have contributed to the great prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD) latterly, with up to 60% in the high-risk population and 25% in the general population. The absence of specific pharmacological strategies for this syndrome represents one of the major problems in the management of MASLD patients. Lifestyle interventions and adherence to a healthy diet are the main cornerstones of current therapies. The identification of nutraceuticals useful in the treatment of MASLD appears to be one of the most promising strategies for the development of new effective and safe treatments for this disease. The onion, one of the most widely studied foods in the field of nutraceuticals, serves as an inexhaustible reservoir of potent compounds with various beneficial effects. The following preliminary study analyzes, mediating in silico studies, the iteration of a library of typical onion compounds with 3-hydroxy-3-methylglutaryl-coenzyme A reductase, liver receptors X α and β, as well as peroxisome proliferator-activated receptors α and γ. In this study, for the first time promising smart molecules from the onion that could have a beneficial action in MASLD patients were identified.
Insights
Onions contain compounds that may help treat metabolic dysfunction-associated steatotic liver disease (MASLD). This study identified potential therapeutic molecules from onions targeting key pathways involved in MASLD.
Area of Science:
- Nutraceutical research
- Hepatology
- Computational chemistry
Background:
- Metabolic dysfunction-associated steatotic liver disease (MASLD) is increasingly prevalent, affecting up to 60% in high-risk groups.
- Current MASLD management relies on lifestyle changes, lacking specific pharmacological treatments.
- Nutraceuticals offer a promising avenue for developing safe and effective MASLD therapies.
Purpose of the Study:
- To identify potential therapeutic compounds from onions for MASLD treatment.
- To investigate the interaction of onion compounds with key molecular targets in MASLD.
Main Methods:
- In silico analysis of a library of onion compounds.
- Computational screening against HMG-CoA reductase, liver X receptors (α and β), and PPARs (α and γ).
Main Results:
- Identification of novel, promising molecules from onions with potential therapeutic effects on MASLD.
- Demonstration of potential interactions between specific onion compounds and key MASLD-related targets.
Conclusions:
- Onion-derived compounds show potential as a novel therapeutic strategy for MASLD.
- Further research into these identified molecules could lead to new MASLD treatments.
More Related Videos
07:14Author Spotlight: Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers
Published on: May 12, 2023
11:44Cellular Membrane Affinity Chromatography Columns to Identify Specialized Plant Metabolites Interacting with Immobilized Tropomyosin Kinase Receptor B
Published on: January 19, 2022
Related Concept Videos
Ligand Binding and Linkage
Ligand Binding Sites
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
Complexometric Titration: Ligands
Targeted Cancer Therapies
There are several types of targeted therapies against...
Targets for Drug Action: Overview
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...