A. D. J. Watson

EFFECTS OF PROLIGESTONE AND MEGESTROL ON PLASMA ADRENOCORTICOTROPHIC HORMONE, INSULIN AND INSULIN-LIKE GROWTH FACTOR-1 CONCENTRATIONS IN CATS

This paper reports changes in adrenocorticotrophic hormone (ACTH), insulin and insulin-like growth factor-1 (IGF-1) concentrations in cats from a previously published study. The cats were given oral megestrol acetate (MA, 5 mg once daily for 14 days), subcutaneous proligestone (PRG, 100 mg on two occasions one week apart) or subcutaneous saline (1 ml as for PRG). In the cats given saline (n = 6), basal ACTH, insulin and IGF-1 did not change significantly throughout the following seven weeks. The cats given MA (n = 7) developed significant suppression of plasma ACTH concentrations and hyperinsulinaemia during treatment and for two to four weeks after MA dosage ceased. In the cats given PRG (n = 7), plasma ACTH concentrations were not significantly altered although three cats had markedly suppressed values for some time after PRG treatment had ceased. Serum insulin concentrations were not significantly altered in the PRG-treated cats. The results suggest PRG may be a preferable alternative to MA in some situations.

Plasma-cortisol concentrations in dogs given cortisone or placebo by mouth

Fasted normal dogs (n = 8) were given fixed doses of cortisone acetate orally as 5 mg and 25 mg tablets; plasma cortisol concentrations were determined, and Cmax, tmax and area under the curve of plasma cortisol concentration plotted against time from zero to 12 hours were compared for the two preparations. In addition, these variables were compared when 25 mg tablets were administered with and without food. No significant difference in cortisol availability was noted for the two preparations and feeding did not apparently affect cortisone absorption. The findings in two hypoadrenocorticoid dogs were similar. Plasma cortisol concentrations in placebo-treated dogs similarly sampled showed minor fluctuations and were generally within accepted reference limits for normal dogs.

EFFECT OF INGESTA AND OF TABLETS OF DIFFERENT STRENGTHS ON THE SYSTEMIC AVAILABILITY OF DIGOXIN IN NORMAL DOGS

The plasma concentrations of digoxin were measured in eight normal dogs given digoxin on four occasions, using three different feeding regimens and tablets of two strengths. Although ingesta tended to slow the absorption of digoxin, the systemic availability of the drug, based on measurements of Cmax, tmax and AUC did not differ when digoxin tablets were given with canned food, with dry food, or without food. However, some of the pharmacokinetic characteristics and smaller individual variations with the dry food regimen would be considered advantageous for maintenance therapy. Tablets containing 62.5 micrograms or 250 micrograms of digoxin had a similar relative bioavailability. The peak plasma digoxin concentrations were higher in female dogs, and the trends in other data also suggested that the systemic availability of digoxin was better in female dogs.