Key result
Compound Fufangteng Oral Liquid improves cardiac function and lowers NT-proBNP in CHF animal models.
Why the study?
Current therapies for chronic heart failure remain limited, and the multi-target effects of Compound Fufangteng Oral Liquid across different CHF models remain unclear.
Does Compound Fufangteng Oral Liquid improve cardiac function and reduce myocardial damage in rat/mouse models of chronic heart failure?
Does Compound Fufangteng Oral Liquid improve cardiac function and reduce myocardial damage in rat/mouse models of chronic heart failure?
Compound Fufangteng Oral Liquid demonstrates cardioprotective effects and improves cardiac function across multiple preclinical models of chronic heart failure.
Answers are grounded in this paper and cite their sources.
Preclinical data support CFFOL efficacy in rodent CHF models; hypothesis-generating, clinical trials required before any human use.
Introduction: CHF is a complex syndrome involving neurohormonal overactivation, inflammation, and myocardial injury. Current therapies remain limited. Compound Fufangteng Oral Liquid (CFFOL) shows multi-target potential, but its effects across different CHF models remain unclear. The study aims to investigate CFFOL's therapeutic effects in three CHF models (qi deficiency, cardiac overload, myocardial injury) and clarify its dose-response relationship. Methods: Three CHF models were established in rats/mice. Animals were randomized into blank control, model, captopril, and CFFOL groups. Cardiac function (EF, FS) was assessed by echocardiography. Serum NT-proBNP, TNF-α, and myocardial enzymes (CK, LDH, α-HBDH) were measured by ELISA. Heart tissues were collected for H&E staining. Results: CFFOL significantly improved cardiac function (EF, FS), reduced serum NT-proBNP, CK, LDH, α-HBDH, and TNF-α levels, and alleviated myocardial pathological changes (vacuolization, fiber disorganization, nuclear condensation, fibrosis). Discussion: Our findings demonstrate that CFFOL exerts cardioprotective effects across multiple CHF models by reducing myocardial damage and attenuating inflammation, consistent with known activities of ginsenosides and astragaloside IV. However, mechanistic claims (JAK/STAT, TGF-β/Smad, IL-17) remain speculative, as molecular assays were not performed. Limitations include lack of blinding, male-only animals, and no pharmacokinetic data. Future studies should incorporate blinded designs, both sexes, and pathway-specific molecular validation. Conclusion: CFFOL shows potential for heart failure treatment, particularly in qi deficiency syndrome. Further clinical studies are needed.
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Lu et al. (2026) studied Chronic Heart Failure. Compound Fufangteng Oral Liquid (CFFOL) vs. Blank control, model, captopril was evaluated on Cardiac function (EF, FS), serum NT-proBNP, TNF-α, and myocardial enzymes. Compound Fufangteng Oral Liquid significantly improved cardiac function, reduced serum NT-proBNP and inflammatory markers, and alleviated myocardial pathological changes in CHF animal models.
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