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Pharmacodynamics and Safety Evaluation of Shengxian Decoction in Treating Chronic Heart Failure
Received date: 2025-12-10
Revised date: 2026-02-13
Accepted date: 2026-04-20
Online published: 2026-06-29
Objective: To determine the efficacy of Shengxian decoction on chronic heart failure (CHF) and assess its safety.Methods: For efficacy evaluation, the rat model of CHF following acute myocardial ischemia was established by ligating the left anterior descending coronary artery. The rats were divided into five groups (n=7 per group): sham group, model group, Shengxian decoction low-dose group (4 g·kg-1), Shengxian decoction high-dose group (16 g·kg-1), and positive drug group. The corresponding medicine or saline were administered via gavage for 35 consecutive days. The rat body weight was recorded, and echocardiographic, serum biochemical, and histopathological assessments were performed at the end of the experiment. For the safety evaluation, a one-month repeated-dose study was conducted in rats. The rats were divided into four groups (n=30 per group, half male and half female): control group, Shengxian decoction low-dose group (8 g·kg-1), Shengxian decoction medium-dose group (16 g·kg-1), and Shengxian decoction high-dose group (32 g·kg-1). Medicine or purified water (control) were administered daily via gavage for 28 days. The general physiological observations were recorded. At the end of the dosing period, the indicators such as hematology, coagulation, serum biochemistry, urinalysis, and organ coefficients of rats were detected. Histopathological examination was performed on key organs of rats in the high-dose group.Results: The pharmacodynamic study demonstrated that Shengxian decoction significantly ameliorated body weight loss, increased left ventricular ejection fraction (EF) and left ventricular fractional shortening (FS), reduced serum levels of creatine kinase (CK) and lactate dehydrogenase (LDH), and reduced pathological lesions in CHF rats. The toxicology study indicated that Shengxian decoction had no toxicologically relevant effects on body weight, food consumption, hematology, coagulation, serum biochemistry, urinalysis, or histopathology up to the highest tested dose. The no-observed-adverse-effect level (NOAEL) was determined to be >32 g (crude drug)/kg, which is equivalent to 50 times of the clinical human dose.Conclusion: Shengxian decoction exerts a significant protective effect against CHF induced by left anterior descending coronary artery ligation in rats and demonstrates a favorable safety profile.
Chao Wang
,
Tao Pang
,
Liyuan Yang
,
Xia Tao
,
Feng Zhang
,
Wansheng Chen
.
Pharmacodynamics and Safety Evaluation of
Shengxian Decoction in Treating Chronic Heart Failure
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