Archive for the ‘Publications’ Category

Recent Graduate Student success

Friday, May 9th, 2008

Recent graduate student, Jonathan Toot, graduated in December 2007 with his PhD and is presently working at WIL Lab in Ashland as a director of Neuropharmacological Research. Here is the abstract of a recently published article from him in collaboration with several UA Biology faculty.
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Testosterone influences renal electrolyte excretion in SHR/y and WKY males

Jonathan Toot1,2 email, Cathy Jenkins1,2 email, Gail Dunphy1 email, Shannon Boehme1 email, Mike Hart1 email, Amy Milsted1 email, Monte Turner1 emailand Daniel Ely1 email

1Biology Department, The University of Akron, Akron, OH 44325-3908, USA

2School of Biomedical Sciences, Kent State University, Kent, OH 44242, USA

author email corresponding author email

BMC Physiology 2008, 8:5doi:10.1186/1472-6793-8-5

Abstract

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.