Pharmaceuticals (May 2024)

Pharmacokinetic–Pharmacodynamic Correlation Analysis of <i>Rhodiola crenulata</i> in Rats with Myocardial Ischemia

  • Zhixin Jia,
  • Guoming Zou,
  • Yongyan Xie,
  • Enning Zhang,
  • Mureziya Yimingjiang,
  • Xianlong Cheng,
  • Cong Fang,
  • Feng Wei

DOI
https://doi.org/10.3390/ph17050595
Journal volume & issue
Vol. 17, no. 5
p. 595

Abstract

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The pharmacokinetics (PK) of Rhodiola crenulata in rats were studied, and pharmacokinetic–pharmacodynamic (PK-PD) correlation analysis was performed to elucidate their time–concentration–effect relationship. The myocardial ischemia model was made with pituitrin. Rats were divided into sham operation, sham operation administration, model, and model administration groups (SG, SDG, MG, and MDG, respectively; n = 6). Blood was collected from the fundus venous plexus at different time points after oral administration. The HPLC-QQQ-MS/MS method was established for the quantification of five components of Rhodiola crenulata. CK, HBDH, SOD, LDH, and AST at different time points were detected via an automatic biochemical analyzer. DAS software was used to analyze PK parameters and PK-PD correlation. The myocardial ischemia model was established successfully. There were significant differences in the PK parameters (AUC0–t, AUC0–∞, Cmax) in MDG when compared with SDG. Two PD indicators, CK and HBDH, conforming to the sigmoid-Emax model, had high correlation with the five components, which indicated a delay in the pharmacological effect relative to the drug concentration in plasma. The difference in the PK parameters between modeled and normal rats was studied, and the time–concentration–effect of composition and effect indicators were investigated. This study can provide reference for the rational clinical application of Rhodiola crenulata and for related studies of other anti-myocardial ischemia drugs.

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