Selected article for: "body weight and placebo control"

Title: Research Communications of the 27(th) ECVIM-CA Congress: Intercontinental, Saint Julian's, Malta, 14th to 16th September 2017
  • Document date: 2017_11_7
  • ID: roslkxeq_9
    Snippet: ESCG -O -3 EFFECT OF MIRTAZAPINE ON CANINE GASTRIC EMPTY-ING ASSESSED BY 13C-SODIUM ACETATE BREATH TEST (13C-SABT). N. Schleifenbaum 1 , S. Salavati 2 , R. Neiger 1 . 1 Small Animal Clinic -Justus-Liebig-University Giessen, Giessen, Germany, 2 The Royal (Dick) School of Veterinary Studies and The R, University of Edinburgh, Edinburgh, UK Delayed gastric emptying is suspected to occur in several common conditions in dogs, for example metabolic/ -e.....
    Document: ESCG -O -3 EFFECT OF MIRTAZAPINE ON CANINE GASTRIC EMPTY-ING ASSESSED BY 13C-SODIUM ACETATE BREATH TEST (13C-SABT). N. Schleifenbaum 1 , S. Salavati 2 , R. Neiger 1 . 1 Small Animal Clinic -Justus-Liebig-University Giessen, Giessen, Germany, 2 The Royal (Dick) School of Veterinary Studies and The R, University of Edinburgh, Edinburgh, UK Delayed gastric emptying is suspected to occur in several common conditions in dogs, for example metabolic/ -endocrine disorders or inflammatory bowel disease. It can also be a sequela in critical care patients suffering from sepsis, peritonitis or pancreatitis. Treating the underlying cause is indicated, but additional supportive treatment in the form of prokinetic drugs is scarce, especially as 5-HT4 receptor agonists are not widely available. The antidepressant mirtazapine, routinely used at low dosages for its appetite stimulating properties in small animals, has been reported to accelerate gastric emptying both in people and (at high dosages) in experimental healthy dogs. The effects of mirtazapine on gastric emptying times using a non-invasive test have not been assessed. Hence, assessing the effect of different dosages of this drug on gastric half emptying times (G50%) in healthy dogs using the 13 C-SABT was sought. Six healthy Beagle dogs (3-5 years, 9.7-11 .6 kg body weight) were included. Mirtazapine was used at increasing dosages (0.6 mg/kg = MLo, 2 mg/kg = MMe, 20 mg/kg = MHi). Initially, MLo, placebo and prucalopride (1 mg/kg as a positive control) were administered orally in a cross-over design. Subsequently, MMe and MHi were administered and compared to a second and third placebo treatment. This approach was chosen to enable interim analysis of data, as ethical approval only allowed to progress to a higher mirtazapine dose if no effect was seen with the lower one. On day 4 of each treatment, a test meal consisting of each dog's half daily calorie requirement and 150 mg 13 C-sodium acetate was fed after an overnight fast and a 13 C-SABT was performed. Breath samples were obtained with a facial mask before (0 min) and 30, 60, 120, 180, 240, 300 , and 360 min after test meal ingestion. 12 CO 2 / 13 CO 2 ratio in the breath was measured by nondispersive infrared spectroscopy and delta-over baseline (DOB) values plotted against time. G50% was calculated for each treatment based on cumulative non-linear curve fitting of the DOB values. Median G50% was 78.3 min (range 48.4-93. 3) with MLo, ) with MMed and 106.4 min (range 83. 1-144. 2) with MHi. Median G50% for Prucalopride and for placebo was 61.9 min (43. .0) and 67.1 min (38. 1-146.1) respectively.

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