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Hypertension and sex differences in the age-related renal changes when cyclooxygenase-2 activity is reduced during
Fara Sáez1, Virginia Reverte, Francisco Salazar
1Department of Physiology, Aging Institute, University of Murcia, Murcia, Spain.
Abstract:
Several studies have proposed that cyclooxygenase-2 (COX2) is involved in the regulation of nephrogenesis and that an impaired nephrogenesis may induce the development of hypertension. This study was designed to test the hypothesis that the decrease of COX2 activity leads to a reduction in nephron number, an increase in arterial pressure, and age-dependent renal alterations that are greater in male than in female rats. Arterial pressure was measured from the first to the 16th month of life in rats treated with vehicle or a COX2 inhibitor during the nephrogenic period. Stereological and histological evaluations and renal function studies were performed at different ages. Arterial pressure increased (14%; P<0.05) and nephron number decreased (17%; P<0.05) to similar levels in male and female COX2-treated rats. However, glomerular filtration rate (31%) and renal plasma flow (25%) decreased (P<0.05) in male but not in female COX2-treated rats. A greater (P<0.05) age-dependent elevation in glomerular hypertrophy was also found in male COX2-treated rats compared with their female littermates. Glomerulosclerosis and tubulointerstitial damage in renal cortex and medulla were also significantly enhanced in male but not in female aged COX2-treated rats. Our results demonstrate that the decrease in COX2 activity during renal development leads to a reduction in nephron number and to an elevation in arterial pressure that are similar in males and females. However, the consequent age-dependent deterioration of the renal structure and renal function is only significantly enhanced in male rats.
Insights
Decreased cyclooxygenase-2 (COX2) activity reduces nephron number and raises blood pressure similarly in male and female rats. However, males show greater age-dependent kidney damage and function decline.
Area of Science:
- Nephrology
- Developmental Biology
- Cardiovascular Physiology
Background:
- Cyclooxygenase-2 (COX2) is implicated in nephrogenesis.
- Impaired nephrogenesis may contribute to hypertension development.
Purpose of the Study:
- To investigate if reduced COX2 activity impacts nephron number, arterial pressure, and age-dependent renal alterations differently in male versus female rats.
- To test the hypothesis linking decreased COX2 activity to hypertension and reduced nephron count.
Main Methods:
- Rats were treated with a COX2 inhibitor or vehicle during nephrogenesis.
- Arterial pressure was monitored from 1 to 16 months.
- Stereological, histological, and renal function evaluations were performed.
Main Results:
- COX2 inhibition reduced nephron number and increased arterial pressure similarly in both sexes.
- Glomerular filtration rate and renal plasma flow declined significantly in males but not females.
- Males exhibited greater age-dependent glomerular hypertrophy, glomerulosclerosis, and tubulointerstitial damage.
Conclusions:
- Reduced COX2 activity during development lowers nephron number and elevates arterial pressure equally in male and female rats.
- Age-dependent renal structural and functional deterioration is significantly exacerbated in male rats following COX2 inhibition.
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