Why the study?
Does testosterone manipulation influence renal sodium and potassium excretion in SHR/y and WKY male rats?
Does testosterone manipulation influence renal sodium and potassium excretion in SHR/y and WKY male rats?
Testosterone influences renal electrolyte excretion through an androgen receptor-dependent mechanism, without differential Y-chromosome involvement between WKY and SHR/y males.
Rat data on androgen effects on sodium excretion warrant no clinical practice change; leaves open human mechanistic studies.
BACKGROUND: The Y-chromosome (Yc) and testosterone (T) increase blood pressure and may also influence renal electrolyte excretion. Therefore, the goal of this study was to determine if the Yc combined with T manipulation could influence renal Na and K excretion. METHODS: To investigate the role of the Yc and T, consomic borderline hypertensive (SHR/y) and normotensive Wistar-Kyoto (WKY) rat strains were used (15 weeks) in three T treatment groups: castrate, castrate with T implant and gonadally intact males. Urine was collected (24 hrs at 15 weeks of age) for Na and K measurements by flame photometry. RT-PCR was used to demonstrate the presence of renal androgen receptor (AR) transcripts. Plasma T and aldosterone were measured by RIA. In another experiment the androgen receptor was blocked using flutamide in the diet. RESULTS: Na and K excretion were decreased by T in SHR/y and WKY. AR transcripts were identified in SHR/y and WKY kidneys. Plasma aldosterone was decreased in the presence of T. Blockade of the AR resulted in a significant increase in Na excretion but not in K excretion in both SHR/y and WKY males. CONCLUSION: T influences electrolyte excretion through an androgen receptor dependent mechanism. There was not a differential Yc involvement in electrolyte excretion between WKY and SHR/y males.
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Toot et al. (2008) studied this question.
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