Related Experiment Videos
Gentamicin pharmacokinetics in diabetic dogs
S A Brown1, R W Nelson, C Scott-Moncrieff
1Department of Veterinary Physiology and Pharmacology, College of Veterinary Medicine, Texas A&M University, College Station 77843.
Journal of Veterinary Pharmacology and Therapeutics
|March 1, 1991
Summary
Diabetes mellitus significantly shortens the elimination phase of gentamicin, impacting drug clearance and volume of distribution in dogs. This effect was observed in both induced and naturally occurring diabetes models.
Area of Science:
- Pharmacology
- Endocrinology
- Veterinary Medicine
Background:
- The terminal elimination phase of gentamicin, an antibiotic, is typically prolonged.
- Diabetes mellitus is a metabolic disorder that can affect drug pharmacokinetics.
Purpose of the Study:
- To investigate the impact of diabetes mellitus on gentamicin's elimination phase in dogs.
- To determine if diabetes mellitus alters gentamicin pharmacokinetics, irrespective of the diabetes model.
Main Methods:
- Compared gentamicin pharmacokinetics in normal dogs versus dogs with alloxan-induced or naturally occurring diabetes mellitus.
- Administered a standard dose of gentamicin intravenously to all study groups.
- Analyzed serum gentamicin concentrations over 7 days using non-compartmental pharmacokinetic methods.
Main Results:
- Gentamicin pharmacokinetics during the initial 8 hours were similar between normal and diabetic dogs.
- Diabetic dogs exhibited a significantly shorter mean residence time (MRT) for gentamicin compared to normal dogs.
- Clearance (Cls) was significantly greater, and volume of distribution at steady state (Vd(ss)) was significantly smaller in diabetic dogs.
- Serum gentamicin concentrations fell below 0.020 microgram/ml within 2 days in diabetic dogs, versus 0.048 microgram/ml at 7 days in normal dogs.
Conclusions:
- Diabetes mellitus, regardless of its cause (alloxan-induced or natural), abolishes the terminal elimination phase of gentamicin in dogs.
- This suggests that diabetes significantly alters gentamicin disposition, leading to faster clearance and reduced distribution.