Objective: To investigate the effect of dietary fat on the pharmacokinetics and pharmacodynamics of cyclosporine. Me&oak Sixteen stable kidney transplants recipients (mean age, 50.4 years; age range, 19 to 63 years; six women) who were maintained on oral cyclosporine therapy were randomized to recei
The effect of the fat content of food on the pharmacokinetics and pharmacodynamics of SDZ FOX 988, an antidiabetic agent, in the dog
β Scribed by David T.-W. Lau; G. Kalafsky; Renee L. Aun; Francis L. S. Tse
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 538 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0142-2782
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
SDZ FOX 988 (FOX 988) is being developed for the treatment of type II diabetes. The objective of this study was to examine the effect of the fat content of food on the pharmacokinetics and pharmacodynamics of FOX 988 following oral administration in the dog. In a randomized, crossβover design, four dogs received a single 10 mg kg^β1^ dose of ^14^CβFOX 988 suspension concomitantly with food containing 10% fat or 40% fat, or with the 10% fat food at 4 h postβdose. Serial blood, urine, and fecal samples were collected for 96 h and analyzed for total radioactivity. Blod concentrations of 53β450, the active metabolite of FOX 988, were also determined. Serum concentrations of Ξ²βhydroxybutyrate and glucose, pharmacological markers for the antidiabetic effects, were measured serially for 24 h after dosing. The animals receiving the lowβfat meal at dosing and at 4 h postβdose exhibited similar extents of absorption, as shown by similar AUC values and urianry radioactivity recovery. Administration of the highβfat meal at dosing significantly enhanced the absorption of FOX 988 and resulted in high blood concentrations of 53β450. However, no significant differences in the pharmacological activity of the drug were observed among the three treatments.
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The effects of temporary water deprivation for 48 h on the pharmacokinetics and pharmacodynamics of bumetanide were examined after intravenous (i.v.) administration of bumetanide, 8mg kg-' to control and water deprived rats (n=7). The values of AUC, t,,, and MRT increased 79.0, 417, and 633 per cent