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1 Maternal & Fetal Health Research Centre, Division of Human Development, The University of Manchester, Manchester, United Kingdom
* To whom correspondence should be addressed. E-mail: mark.wareing{at}manchester.ac.uk.
In the placental vasculature, where oxygenation may be an important regulator of vascular reactivity, there is a paucity of data on the expression of potassium (K) channels, important mediators of vascular smooth muscle tone. We therefore addressed the expression and function of several K channel subtypes in human placentas. The expression of KV2.1, KV9.3, BKCa, KIR6.1 and TASK1 in chorionic plate arteries, veins and placental homogenate was assessed by RT-PCR and Western Blotting. Functional activity of K channels was assessed pharmacologically in small chorionic plate arteries and veins by wire myography using 4-aminopyridine, iberiotoxin, pinacidil and anandamide. Experiments were performed at 20%, 7% and 2% oxygen to assess the effect of oxygenation on the efficacy of K channel modulators. KV2.1, KV9.3, BKCa, KIR6.1 and TASK1 channels were all demonstrated to be expressed at the message level. KV2.1, BKCa, KIR6.1 and TASK1 were all demonstrated at the protein level. Pharmacological manipulation of voltage-gated and ATP-sensitive channels produced the most marked modifications in vascular tone, in both arteries and veins. We conclude that K channels play an important role in controlling placental vascular function.
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