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Subunit Contributes to Delayed Rectifier K+ Currents in Myocytes From Rabbit Corpus Cavernosum





From the Departments of * Physiology and
Biophysics,
Gastroenterology and Hepatology,
and
Urology, Mayo Clinic, Rochester,
Minnesota.
| Correspondence to: Simon J. Gibbons, PhD, Department of Physiology and Biophysics, Mayo Clinic, Guggenheim 8, 200 First St SW, Rochester, MN 55905. |
-dendrotoxin (200 nM), a Kv1
channel blocker, had no effect. The nucleotide sequence of K+
channel subunits was determined by polymerase chain reaction-based cloning
techniques using RNA derived from cavernosal muscle strips and single
identified myocytes. Molecular cloning techniques identified the full-length
sequence of the rabbit ortholog of the Kv2.2
subunit. This sequence
contains 911 amino acid residues and is 92% identical to the recently revised
human Kv2.2 sequence. Identified cavernosal myocytes of the type used in
physiological recordings expressed Kv2.2 messenger RNA. We conclude that Kv2.2
subunits contribute to whole-cell currents in rabbit canvernosal
myocytes. Further, Kv currents play a role in regulating membrane
potential and hence excitability in rabbit cavernosal myocytes.
Key words: Penile erection, potassium channels, patch clamp techniques, smooth muscle, molecular cloning
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