Proximal Tubular Vacuolization and Hypersensitivity to Drug-Induced Nephrotoxicity in Male Mice With Decreased Expression of the NADPH-Cytochrome P450 Reductase
Liang Ding1,2, Lei Li3, Senyan Liu3,4
1Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona.
Abstract:
The effect of variations in the expression of cytochrome P450 reductase (CPR or POR) is determined in mice with decreased POR expression to identify potential vulnerabilities in people with low POR expression. There is an age-dependent appearance of increasing vacuolization in the proximal tubules of the renal cortex in 4- to 9-month-old male (but not female) Cpr-low (CL) mice. These mice have low POR expression in all cells of the body and upregulation of lysosome-associated membrane protein 1 expression in the renal cortex. Vacuolization is also seen in extrahepatic CL and extrarenal CL male mice, but not in mice with tissue-specific Por deletion in liver, intestinal epithelium, or kidney. The occurrence of vacuolization is accompanied by increases in serum blood-urea-nitrogen levels. Male CL mice are hypersensitive to cisplatin- and gentamicin-induced renal toxicity at 3 months of age, before proximal tubular (PT) vacuoles are detectable. At doses that do not cause renal toxicity in wild-type mice, both drugs cause substantial increases in serum blood-urea-nitrogen levels and PT vacuolization in male but not female CL mice. The hypersensitivity to drug-induced renal toxicity is accompanied by increases in circulating drug levels. These novel findings demonstrate deficiency of renal function in mice with globally reduced POR expression and suggest that low POR expression may be a risk factor for drug-induced nephrotoxicity in humans.
Insights
Mice with low cytochrome P450 reductase (POR) expression exhibit kidney dysfunction and increased susceptibility to drug-induced kidney damage, highlighting potential risks for individuals with reduced POR levels.
Area of Science:
- Pharmacology
- Nephrology
- Biochemistry
Background:
- Cytochrome P450 reductase (CPR or POR) is crucial for various cellular processes.
- Variations in POR expression can impact drug metabolism and organ function.
- Understanding POR's role is vital for predicting drug toxicity.
Purpose of the Study:
- To investigate the physiological consequences of globally reduced POR expression.
- To identify potential kidney vulnerabilities in individuals with low POR levels.
- To assess the impact of low POR on drug-induced nephrotoxicity.
Main Methods:
- Generation and analysis of Cpr-low (CL) mice with globally decreased POR expression.
- Histopathological examination of renal tissues for vacuolization.
- Assessment of serum blood-urea-nitrogen levels.
- Evaluation of susceptibility to cisplatin- and gentamicin-induced nephrotoxicity.
Main Results:
- Male CL mice developed age-dependent proximal tubular vacuolization and increased blood-urea-nitrogen.
- CL mice exhibited hypersensitivity to cisplatin and gentamicin, leading to renal toxicity.
- This hypersensitivity occurred before vacuolization and was associated with increased circulating drug levels.
- Tissue-specific POR deletion did not replicate these kidney-specific effects.
Conclusions:
- Globally reduced POR expression leads to renal functional deficiency.
- Low POR expression is a potential risk factor for drug-induced nephrotoxicity in humans.
- Sex-specific differences in POR deficiency effects warrant further investigation.
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