Korean J Physiol Pharmacol.
1999 Oct;3(5):507-512.
Effect of prostaglandins D2, E2 and I2 on the regulation of KATP channel activity in rat cardiac myocytes
- Affiliations
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- 1Department of Pharmacology, Chonnam National University Medical School, Kwangju, 501-190 South Korea.
- 2Department of Physiology, College of Veterinary Medicine, Chonnam National University, Kwanaju 501-190, Korea.
Abstract
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Contribution of prostaglandins D2, E2 and I2 (PGD2, PGE2 and PGI2) on
the regulation of ATP-sensitive K+ channel (KATP channel) was
investigated in isolated single rat ventricular cardiac myocytes using
the patch clamp technique. PGD2, PGE2 and PGI2 did not affect KATP
channel activity in the inside-out patch, but increased channel
activity in a dose-dependent manner when the channel activities were
attenuated by the administration of 100 muM ATP to the internal
solution in the inside-out patch. Channel activations by the
prostaglandins were abolished by 50 muM glibenclamide, a KATP channel
blocker. Dose-response curves of relative channel activity against the
ATP concentrations of internal solution in the inside-out patch were
shifted to the right in the presence of those three prostaglandins. The
rank order of the channel stimulatory potencies (as IC50 for ATP)
calculated from the dose-response curves were PGI2 < PGD2 < PGE2.
Conductance of the channel was not changed by those three
prostaglandins. In conclusion, we suggest that prostaglandins D2, E2
and I2 are involved in the regulation of KATP channel activity in
certain circumstances, and that those three prostaglandins may cause
myocardial relaxation by opening KATP channels, thus protecting the
heart from ischema.