Effects of Compound Kushen Injection on the Pharmacokinetics of Fluoxetine in Rats
Min Tao1, Qing Chen2, Guoxin Hu2
1Department of Paediatrics, Ruian People's Hospital,The Third Affiliated Hospital of Wenzhou Medical University, Zhejiang, China.
None:
In clinical treatment, compound kushen injection (CKI) is often used in combination with fluoxetine (FLX) to enhance the therapeutic effect on tumor-related depression in patients with tumors. To systematically investigate the pharmacokinetic interaction between CKI and FLX in plasma through UPLC-MS/MS analysis. Healthy male Sprague-Dawley rats were allocated to experimental or control groups; the experimental group received an injection of CKI (2 mg/kg) for 7 days, whereas the control group received an equivalent volume of saline. On Day 7, both groups received a single oral dose of FLX (10 mg/kg). Blood samples were subsequently collected from the tail vein at 15 time points over 72 h, after which the plasma concentrations of FLX were quantified using a validated UPLC-MS/MS method. The key pharmacokinetic parameters of FLX differed significantly (p < 0.05) between the two groups. Compared with those in the control group, the AUC(0-∞), Cmax, and T1/2z of FLX in the experimental group increased by 457.06%, 248.25%, and 90.62%, respectively, while CL/F, Vz/F, and Tmax decreased by 74.14%, 60.49%, and 41.11%, respectively. These findings demonstrate that CKI coadministration markedly alters FLX pharmacokinetics, potentially impacting treatment efficacy and safety.
More Related Videos
08:15Network Pharmacology and Validation of the Antidepressant Mechanisms of Qiangzhifang in a Chronic Restraint Stress-induced Depression Rat Model
Published on: June 6, 2025
11:27The Use of Pharmacological-challenge fMRI in Pre-clinical Research: Application to the 5-HT System
Published on: April 25, 2012
Related Concept Videos
Nonlinear Pharmacokinetics: Dependence of Elimination Half-Life and Dose Clearance
A study on guinea pigs examined the...
Pharmacokinetics: Drug–Food and Drug–Viral Interactions
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment
Time Course of Drug Effect
Drug Accumulation During Multiple Dosing: Repetitive IV Injections
Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion
