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This Article Full Text Full Text (PDF) All Versions of this Article: 294/3/R895    most recent 00521.2007v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Mewe, M. Articles by Bauer, C. K. Search for Related Content PubMed PubMed Citation Articles by Mewe, M. Articles by Bauer, C. K.

NEUROHUMORAL CONTROL OF CARDIOVASCULAR FUNCTION

Erg K⁺ channels modulate contractile activity in the bovine epididymal duct

Institutes of ¹Vegetative Physiology and Pathophysiology and ²Pharmacology for Pharmacists, University Medical Center Hamburg-Eppendorf, Hamburg; ³Institute of Anatomy and Cell Biology, Justus-Liebig-University of Giessen, Giessen; and ⁴Center for Molecular Neurobiology Hamburg, Hamburg, Germany

Submitted 19 July 2007 ; accepted in final form 4 January 2008

The expression and functional role of ether-à-go-go-related gene (erg) K⁺ channels were examined in the bovine epididymal duct. Sperm transit through the epididymal duct relies on spontaneous phasic contractions (SC) of the peritubular smooth muscle wall. Isometric tension studies revealed SC-enhancing effects of the erg channel blockers E-4031, dofetilide, cisapride, and haloperidol and SC-suppressing effects of the activator NS-1643. In the corpus epididymidis, EC₅₀ values of 32 nM and 8.3 µM were determined for E-4031 and NS-1643, respectively. E-4031 was also able to elicit contraction in epithelium-denuded corpus segments, which lacked SC. In the cauda region, E-4031 and NS-1643 exerted effects on agonist-induced contraction similar to those observed in the proximal duct. Experiments with nifedipine and thapsigargin suggested that the excitatory effects of E-4031 depended mainly on external calcium influx and not on intracellular calcium release. Western blot and RT-PCR assays revealed the expression of both, erg1a and erg1b, in all duct regions. Because erg1b appears to predominate in the epididymal duct, patch-clamp experiments were performed on heterologously expressed erg1b channels to investigate the sensitivity of this splice variant to NS-1643. In contrast to its effects on erg1a, NS-1643 induced a concentration-dependent current increase mainly due to a marked leftward shift in erg1b channel activation by 30 mV at 10 µM, explaining the inhibitory effect of the drug on epididymal SC. In summary, these data provide strong evidence for a physiological role of erg1 channels in regulating epididymal motility patterns.

epididymis; voltage-gated potassium channel; motility; smooth muscle; Kv11 ether-à-go-go-related gene