Effect of Testosterone on Potassium Channel Opening in Human Corporal Smooth Muscle Cells
Version of Record online: 18 JAN 2008
© 2008 International Society for Sexual Medicine
The Journal of Sexual Medicine
Volume 5, Issue 4, pages 822–832, April 2008
How to Cite
Han, D. H., Chae, M. R., Jung, J. H., So, I., Park, J. K. and Lee, S. W. (2008), Effect of Testosterone on Potassium Channel Opening in Human Corporal Smooth Muscle Cells. Journal of Sexual Medicine, 5: 822–832. doi: 10.1111/j.1743-6109.2007.00732.x
- Issue online: 18 JAN 2008
- Version of Record online: 18 JAN 2008
- Erectile Dysfunction;
- Potassium Channels
Introduction. In humans, the role of testosterone in sexual functions, including sexual desire, nocturnal penile erections, and ejaculatory volume, has been relatively well established. However, the effects of testosterone on intrapenile structure in humans remains controversial.
Aim. We assessed the direct effects of testosterone on potassium channels in human corporal smooth muscle cells, in an effort to understand the mechanisms inherent to the testosterone-induced relaxation of corporal smooth muscle cells at the cellular and molecular levels.
Methods. We conducted electrophysiologic studies using cultured human corporal smooth muscle cells. We evaluated the effects of testosterone on potassium channels—BKCa and KATP channels—by determining the whole-cell currents and single-channel activities. For the electrophysiologic recordings, whole-cell and cell-attached configuration patch-clamp techniques were utilized.
Main Outcome Measures. Changes in whole-cell currents and channel activities of BKCa and KATP channels by testosterone.
Results. Testosterone (200 nM) significantly increased the single-channel activity of calcium-activated potassium (BKCa) channels and whole-cell K+ currents by 443.4 ± 83.4% (at +60 mV; N = 11, P < 0.05), and this effect was abolished by tetraethylammonium (TEA) (1 mM), a BKCa channel blocker. The whole-cell inward K+ currents of the KATP channels were also increased by 226.5 ± 49.3% (at –100 mV; N = 7, P < 0.05). In the presence of a combination of vardenafil (10 nM) and testosterone (200 nM), the BKCa channel was activated to a significantly higher degree than was induced by testosterone alone.
Conclusions. The results of patch-clamp studies provided direct molecular evidence that testosterone stimulates the activity of BKCa channels and KATP channels. An understanding of the signaling mechanisms that couple testosterone receptor activation to potassium channel stimulation will provide us with an insight into the cellular processes underlying the vasorelaxant effects of testosterone. Han DH, Chae MR, Jung JH, So I, Park JK, and Lee SW. Effect of testosterone on potassium channel opening in human corporal smooth muscle cells. J Sex Med 2008;5:822–832.