Pharmacokinetics and haematological parameters of recombinant human erythropoietin after subcutaneous administrations in horses.
Abstract: The pharmacokinetics of recombinant human Epo (rHuEpo) were investigated after subcutaneous administration to horses. Four horses received a single 30IU kg-1 dose of rHuEpo. One horse received three repeated doses of 120 IU kg-1 at 48 h intervals. Plasma erythropoietin (Epo) was measured by radioimmunoassay. In both cases pharmacokinetic parameters were evaluated using a one-compartment open model and first-order input and output rates. The mean values (+/-SD) for elimination half-life, CL/F, and Vd/F after a single dose were 12.9 +/- 3.34 h, 11.8 +/- 4.96 L h-1, and 233 +/- 126 L, respectively. After repeated doses, elimination half-life, CL/F, and Vdss/F were 11.3 h, 8.94 L h-1, and 145.6 L, respectively. No significant differences were observed between the haematological parameters after a single 30 IU kg-1 administration compared to baseline values. Multiple and high doses of rHuEpo modified red blood cells, haemoglobin, and hematocrit. According to our results, plasma Epo assay can help, during an antidoping control procedure, to support a positive result only up to 72 h after the last rHuEpo.
Publication Date: 1996-12-01 PubMed ID: 8968532DOI: 10.1002/(SICI)1099-081X(199612)17:9<805::AID-BDD995>3.0.CO;2-HGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.
The research investigates how the drug, recombinant human erythropoietin (rHuEpo), interacts with the bodies of horses after being administered subcutaneously. Findings showed some changes in red blood cells, haemoglobin, and hematocrit after multiple and high doses.
Research Methodology
- The study involved pharmacokinetic analysis of the drug, rHuEpo, on horses. Pharmacokinetics is a branch of pharmacology dedicated to determining the fate of substances administered externally to a living organism.
- Four horses were administered a single dose of 30IU kg-1 of rHuEpo. One horse received a triple dose of 120 IU kg-1 every 48 hours. The difference in dosage allowed for a comparative analysis of the effects of the drug.
- Erythropoietin (Epo), a hormone produced by the kidney to promote the formation of red blood cells by the bone marrow, was measured in plasma using radioimmunoassay, which is a method to measure concentrations of antigens.
- The research applied a one-compartment open model to evaluate the pharmacokinetic parameters. This model assumes that the body is a single, homogeneously perfused compartment in terms of drug distribution. Input and output of the drug were assumed to follow first-order kinetics (rate of reaction is directly proportional to the concentration of the unconverted reactants).
Findings
- Parameters measured include elimination half-life (the time it takes for the body to reduce the amount of drug in plasma or total body content by one-half), CL/F (the clearance of the drug from the body when administered via extravascular route), and Vd/F (the total amount of drug in the body divided by the drug concentration in the plasma).
- The values of these parameters varied after a single dose and multiple doses, providing evidence of different pharmacokinetics under different administration circumstances.
- Haematological parameters (related to blood) remained relatively unchanged after a single, low dose administration compared to base values. However, multiple and high doses influenced red blood cells, haemoglobin (transports oxygen in the blood), and haematocrit (proportion of blood volume that is red blood cells).
- The plasma Epo assay proved useful in supporting a positive result up to 72 hours after the last rHuEpo administration. This could be vital in anti-doping control procedures.
Cite This Article
APA
Souillard A, Audran M, Bressolle F, Jaussaud P, Gareau R.
(1996).
Pharmacokinetics and haematological parameters of recombinant human erythropoietin after subcutaneous administrations in horses.
Biopharm Drug Dispos, 17(9), 805-815.
https://doi.org/10.1002/(SICI)1099-081X(199612)17:9<805::AID-BDD995>3.0.CO;2-H Publication
Researcher Affiliations
- Département de Biophysique, Faculté de Pharmacie, Université de Montpellier I, France.
MeSH Terms
- Animals
- Chromatography, High Pressure Liquid
- Erythrocyte Count / drug effects
- Erythropoietin / administration & dosage
- Erythropoietin / blood
- Erythropoietin / pharmacokinetics
- Erythropoietin / pharmacology
- Female
- Half-Life
- Hematocrit
- Hemoglobins / drug effects
- Hemoglobins / metabolism
- Horses
- Humans
- Injections, Subcutaneous
- Male
- Recombinant Proteins / administration & dosage
- Recombinant Proteins / blood
- Recombinant Proteins / pharmacokinetics
- Recombinant Proteins / pharmacology
Citations
This article has been cited 1 times.- Dahlgren AR, Knych HK, Arthur RM, Durbin-Johnson BP, Finno CJ. Transcriptomic Markers of Recombinant Human Erythropoietin Micro-Dosing in Thoroughbred Horses.. Genes (Basel) 2021 Nov 24;12(12).
Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists