Background: The source of glutamine for renal ammonium production is ultimately dietary protein in the fed state and body proteins in fasting.
Objective: Our objective was to determine if less NH(+)(4) would be excreted by fasted dogs with chronic metabolic acidosis resulting in conservation of lean body mass.
Methods: Acid-loaded fed and fasted dogs were given 10 mmol NH(4)Cl/kg for 5 days; the fasted group had food withheld on days 4 and 5.
Results: The renal production of NH(+)(4) was not significantly different in both acid-loaded groups, yet the rate of NH(+)(4) excretion was significantly lower in the fasted dogs (8 vs. 21 mmol NH(+)(4)/mmol creatinine). The urine pH was significantly higher (6.0 versus 5.5) while titratable acid and the urine flow rate were significantly lower in these fasted dogs. Despite nearly equal urine flow rates and Na(+) excretion rates after an infusion of saline, the fasted dogs failed to increase the rate of excretion of NH(+)(4) to rates seen in the fed group.
Conclusions: The lower rate of excretion of NH(+)(4) in fasted, acidotic dogs appeared to be due to a lower distal H(+) secretion. This may help preserve lean body mass during fasting.
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http://dx.doi.org/10.1159/000065033 | DOI Listing |
Int J Pharm
November 2024
Department of Bioanalysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, Ghent 9000, Belgium; Clinical Pharmacology and Pharmacometrics, Janssen R&D, Division of Janssen Pharmaceutica NV, Turnhoutseweg 30, Beerse 2340, Belgium.
Oral drug administration is the most convenient route of administration in the pediatric population. However, children are often not fasted when drugs are orally administered, hence potential food-drug interactions might occur. Most of these interactions are extrapolated from studies performed in human adults where a recommended high-fat, high-calorie meal is administered prior to drug dosing.
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January 2025
Novo Nordisk A/S, Global Research Technologies, 2760 Måløv, Denmark.
Oral delivery of peptides requires formulations with high concentrations of permeation enhancer (PE) to promote absorption, and often necessitates fasting time between dosing and food ingestion. Improved formulations promoting a more rapid absorption would increase convenience of use but requires a faster onset of action. We have developed a salcaprozate-based ionic liquid (IL) formulation, namely choline salcaprozate (CHONAC), for oral delivery of a glucagon-like peptide-1 (GLP-1) analogue via gastric absorption.
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January 2025
Small molecule CMC development, Drug Product Development, AbbVie Inc., North Chicago, IL 60064, United States. Electronic address:
A 45 % drug loaded (DL) amorphous nanoparticle (ANP) formulation for a BCS IV drug demonstrated promising pharmacokinetics in dogs (Purohit, et al., J. Pharm.
View Article and Find Full Text PDFVet Radiol Ultrasound
January 2025
AzurVet, Centre de vétérinaires spécialistes, Saint-Laurent-Du-Var, France.
The ultrasonographic appearance of the ileocecocolic junction (ICCJ), comprising the ileocolic junction (ICJ) and the cecocolic junction (CCJ), has not been established in dogs. The purpose of this prospective study was (1) to evaluate the feasibility and technique of systematic ultrasonographic evaluation of the ICJ and CCJ and (2) to describe its ultrasonographic features. Abdominal ultrasound was performed in 102 fasted dogs, free of digestive signs.
View Article and Find Full Text PDFVet J
December 2024
Department of Veterinary Sciences, University of Pisa, Viale delle Piagge, 2, Pisa 56124, Italy; Department of Veterinary Medicine, University of Sassari, Via Vienna, 2, Sassari 07100, Italy. Electronic address:
This study investigates the pharmacokinetics (PK) of imipramine, a tricyclic antidepressant used in human psychiatric disorders and increasingly considered in veterinary medicine. Despite its longstanding use in canines, prior research on imipramine's PK in dogs is lacking. This study aimed to determine the PK of imipramine in dogs in regards to feeding conditions, and to ascertain whether desipramine (active metabolite) is formed or not.
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