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Updated: Aug 14, 2026

Assessment of Kidney Function in Mouse Models of Glomerular Disease
Published on: June 30, 2018
Ontogeny of renal P-glycoprotein expression in mice: correlation with digoxin renal clearance
Natasha Pinto1, Naomi Halachmi, Zulfikarali Verjee
1Division of Clinical Pharmacology, The Hospital for Sick Children, and Department of Pharmacology, University of Toronto, Ontario, Canada.
Insights
Kidney P-glycoprotein (P-gp) expression increases with age in young children, leading to higher digoxin clearance rates. This finding helps explain why children need larger digoxin doses per body weight.
Area of Science:
- Pharmacology
- Developmental Biology
- Nephrology
Background:
- Digoxin elimination primarily occurs via renal glomerular filtration and P-glycoprotein (P-gp) mediated tubular secretion.
- Young children require higher digoxin doses per kilogram of body weight than adults, a phenomenon not fully understood.
Purpose of the Study:
- To investigate the age-dependent expression of renal P-gp in developing mice.
- To correlate P-gp expression levels with changes in digoxin clearance rates across different age groups.
Main Methods:
- Semi-quantitative RT-PCR was used to analyze mdr1a and mdr1b (P-gp) ontogeny in mouse kidneys at various ages (birth to 45 days).
- Pharmacokinetic studies of digoxin were conducted in mice of the same age groups to determine clearance rates.
Main Results:
- P-gp (mdr1a and mdr1b) expression was minimal at birth and Day 7, significantly increasing by Day 21.
- Digoxin clearance rates peaked at Day 21, showing a significant positive correlation with P-gp expression levels.
Conclusions:
- Increased renal P-gp expression after weaning in mice contributes to enhanced digoxin clearance.
- This age-dependent increase in P-gp may explain the higher digoxin dosage requirements in young children.
Abstract:
Digoxin is eliminated mainly by the kidney through glomerular filtration and P-glycoprotein (P-gp) mediated tubular secretion. Toddlers and young children require higher doses of digoxin per kilogram of bodyweight than adults, although the reasons for this have not been elucidated. We hypothesized there is an age-dependant increase in P-gp expression in young children. The objectives of this study were to elucidate age-dependant expression of renal P-gp and its correlation with changes in the clearance rate of digoxin. FVB mice were killed at different ages to prepare total RNA for P-gp expression studies. Semi-quantitative RT-PCR was conducted to analyze mdr1a and mdr1b ontogeny in the kidney at: birth, 7, 14, 21, 28 and 45-d old adults. The pharmacokinetics of digoxin (7 microg/kg) was studied in mice of the same age groups. Newborn and Day 7 levels of both mdr1a and mdr1b were marginal. Day 21 mdr1b levels were significantly higher than both Day 14 and Day 28 levels. Digoxin clearance rates were the highest at Day 21, with significant correlation between P-gp expression and clearance values. Increases in digoxin clearance rates after weaning may be attributed, at least in part, to similar increases in P-gp expression.
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