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Meta-analysis shows salidroside improves metabolic markers in rodent NAFLD models

Meta-analysis shows salidroside improves metabolic markers in rodent NAFLD models
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Key Takeaway
Meta-analysis of animal models suggests salidroside improves NAFLD markers, but clinical verification is needed.

This meta-analysis evaluates the effects of salidroside in rodent models of nonalcoholic fatty liver disease (NAFLD). The synthesis includes 12 eligible animal studies, though specific sample sizes and follow-up durations were not reported. The analysis covers a wide range of secondary outcomes, including hepatic triglycerides, total cholesterol, nonalcoholic steatohepatitis (NAS) scores, body weight, liver weight, liver index, and various serum biomarkers.

Key metabolic and inflammatory outcomes demonstrated significant changes. Hepatic triglycerides showed a standardized mean difference (SMD) of -3.88, while hepatic total cholesterol decreased with an SMD of -4.15. The NAS score decreased with an SMD of -4.79. Other lipid parameters, including serum triglycerides (SMD = -2.92), serum total cholesterol (SMD = -2.11), LDL-C (SMD = -2.82), and liver index (SMD = -2.24), also decreased. Conversely, HDL-C increased with an SMD of 2.34, and GSH increased with an SMD of 3.51. Antioxidant markers SOD and GSH showed substantial increases (SMD = 3.96 and 3.51, respectively), while inflammatory cytokines IL-6, IL-1β, and MCP-1 decreased.

Body weight decreased with an SMD of -0.75, and liver weight decreased with an SMD of -1.12. Glucose metabolism markers, including fasting blood glucose (SMD = -1.74) and HOMA-IR (SMD = -2.54), improved. Liver injury markers ALT and AST decreased with SMDs of -3.26 and -2.80, respectively. However, the authors note that publication bias was present and pathological characteristics differ between animal models and humans. Safety data, adverse events, and tolerability were not reported. The authors conclude that clinical efficacy and safety still need to be further verified by high-quality clinical studies.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
ObjectiveThe purpose of this study was to systematically evaluate the therapeutic effect of salidroside on rodent NAFLD models through a meta-analysis of multiple animal experiments, and to explore its potential mechanism of anti-oxidative stress and anti-inflammation, to provide a theoretical basis for the clinical treatment of salidroside in NAFLD.MethodsA total of 12 eligible animal studies were identified by searching eight databases of Web of Science, PubMed, Embase, Cochrane Library, CNKI, Wanfang, VIP, and CBM (up to June 2025). The SYRCLE bias risk assessment tool was used to evaluate the quality of the included literature. The review used Manager 5.4 and Stata 18 software to perform a meta-analysis of the outcome indicators included in the study.ResultsMeta-analysis showed salidroside significantly improved multiple outcomes: for the main outcome indicators: hepatic TG (SMD = −3.88), hepatic TC (SMD = −4.15), the NAS score (SMD = −4.79) were significantly decreased. And basic indicators, body weight (SMD = −0.75), liver weight (SMD = −1.12), and liver index (SMD = −2.24) all decreased; for lipid metabolism indicators, serum TG (SMD = −2.92), serum TC (SMD = −2.11), and LDL-C (SMD = −2.82) decreased while HDL-C (SMD = 2.34) increased, notably with dose-dependent improvements in hepatic TG and serum TC (better effect at ≥100 mg/kg/d) and rats being more sensitive to serum TG improvement; for liver function indicators, serum ALT (SMD = −3.26) and AST (SMD = −2.80) decreased, with a more pronounced effect when treatment duration was ≤4 weeks; the NAS score decreased, with a better therapeutic effect in rats than in mice; and for secondary indicators, FBG (SMD = −1.74), FSI (SMD = −1.88), HOMA-IR (SMD = −2.54), and MDA (SMD = −3.24) decreased, GSH (SMD = 3.51) and SOD (SMD = 3.96) increased, and IL-6 (SMD = −2.28), IL-1β (SMD = −1.31), and MCP-1 (SMD = −1.71) decreased. Sensitivity analysis and funnel plots indicated that the results were robust; however, a certain degree of publication bias was present.ConclusionIn rodent NAFLD models, salidroside can significantly improve the pathological state dominated by oxidative stress/inflammation. The treatment effect is affected by the treatment time, dose, type, and other factors. Its mechanism of action is mainly anti-oxidative stress and anti-inflammatory effects. Due to the differences in pathological characteristics between animal models and humans in this study, the clinical efficacy and safety of salidroside still need to be further verified by high-quality clinical studies.Systematic Review RegistrationIdentifier, CRD420251083205.
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