Furosemide Pharmacokinetics in Adult Rats become Abnormal with an Adverse Intrauterine Environment and Modulated by a Post-Weaning High-Fat Diet
Autor: | Kent L. Thornburg, Barent N. DuBois, Ganesh Cherala, Jacob Pearson, Tahir Mahmood |
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Rok vydání: | 2015 |
Předmět: |
Male
0301 basic medicine medicine.medical_specialty Offspring Intrauterine growth restriction Weaning Urine Organic Anion Transporters Sodium-Independent Biology Diet High-Fat Kidney Toxicology 03 medical and health sciences Organic Anion Transport Protein 1 Sex Factors Sodium Potassium Chloride Symporter Inhibitors Pharmacokinetics Furosemide Pregnancy Internal medicine Diet Protein-Restricted medicine Animals Humans Solute Carrier Family 12 Member 1 Pharmacology Volume of distribution Fetal Growth Retardation Body Weight General Medicine medicine.disease Rats 030104 developmental biology Endocrinology Prenatal Exposure Delayed Effects Body Composition Female medicine.drug |
Zdroj: | Basic & Clinical Pharmacology & Toxicology. 118:432-439 |
ISSN: | 1742-7835 |
DOI: | 10.1111/bcpt.12523 |
Popis: | Adult individuals born with intrauterine growth restriction (IUGR) have physiological maladaptations that significantly increase risk of chronic disease. We suggested that such abnormalities in organ function would alter pharmacokinetics throughout life, exacerbated by environmental mismatch. Pregnant and lactating rats were fed either a purified control diet (18% protein) or low-protein diet (9% protein) to produce IUGR offspring. Offspring were weaned onto either laboratory chow (11% fat) or high-fat diet (45% fat). Adult offspring (5 months old) were dosed with furosemide (10 mg/kg i.p.) and serum and urine collected. The overall exposure profile in IUGR males was significantly reduced due to a ~35% increase in both clearance and volume of distribution. Females appeared resistant to the IUGR phenotype. The effects of the high-fat diet trended in the opposite direction to that of IUGR, with increased drug exposure due to decreases in both clearance (31% males, 46% females) and volume of distribution (24% males, 44% females), with a 10% longer half-life in both genders. The alterations in furosemide pharmacokinetics and pharmacodynamics were explained by changes in the expression of renal organic anion transporters 1 and 3, and sodium-potassium-chloride cotransporter-2. In summary, this study suggests that IUGR and diet interact to produce subpopulations with similar body-weights but dissimilar pharmacokinetic profiles; this underlines the limitation of one-size-fits-all dosing which does not account for physiological differences in body composition resulting from IUGR and diet. |
Databáze: | OpenAIRE |
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