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Metformin-phytochemical combination therapy in metabolic dysfunction-associated steatotic liver disease: mechanistic insights and therapeutic potential

Amri J, Karimpour A, Meshkani R

Naunyn-Schmiedeberg's archives of pharmacology, 2026

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a multifactorial metabolic disorder characterized by excessive hepatic lipid accumulation, insulin resistance, oxidative stress, and chronic inflammation. Its pathogenesis spans interconnected metabolic, inflammatory, and fibrotic pathways, limiting the efficacy of single-target therapeutic approaches. Metformin (MET), a first-line antidiabetic agent, improves hepatic lipid metabolism primarily through AMPK activation and enhanced fatty acid oxidation; however, its therapeutic impact on inflammatory and redox pathways remains limited, and its use is frequently associated with gastrointestinal adverse effects. In this context, phytochemicals-diverse plant-derived bioactive compounds with pleiotropic metabolic and antioxidant properties-have emerged as promising adjuncts to MET to achieve broader pathway coverage. For the first time, this comprehensive review evaluates preclinical in vivo evidence on metformin-phytochemical combination therapy in in vivo models of MASLD, with a specific focus on its mechanistic and therapeutic advantages over monotherapy. A comprehensive literature search was conducted using PubMed, Scopus, Web of Science, and Google Scholar. Only original preclinical in vivo studies evaluating the combination of metformin with an isolated phytochemical in animal models of MASLD were included. Data were extracted on compound identity, dosing regimens, experimental models, and metabolic,…

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Evidence Hub reads this as a review, done in animal, not in people. Its evidence level is 5 of 5 (Very low · case / narrative / animal / in vitro / in silico). Case reports, narrative reviews, and animal, cell or computer-model studies give the weakest evidence for human health.

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