Original Contributions |
From the Institut de Pharmacologie Moléculaire et Cellulaire, CNRS-UPR 411, Valbonne, France.
Correspondence to Pierre Pacaud, PhD, Institut de Pharmacologie Moléculaire et Cellulaire, CNRS-UPR 411, 660 Route des Lucioles, Sophia Antipolis, 06560 Valbonne, France. E-mail pacaud{at}ipmc.cnrs.fr
AbstractIn cutaneous veins where
purinergic neurotransmission is more prominent compared with in deep
vessels, physiological and pathological roles of
nerve-released ATP have been described. Neuronally released ATP has
been reported to act through activation of unidentified ionotropic P2X
receptor(s). This study analyzed P2X receptor subtypes
expressed in human saphenous vein smooth muscle and their
physiological functions. Transcripts for both
hP2X1 receptors, already identified in other smooth
muscles, and, surprisingly, hP2X7 receptors known to be
responsible for the cytotoxic effect of ATP in macrophages were
detected by Northern blot analysis in total RNA from saphenous
vein smooth muscle. ATP and other P2X receptor agonists
[
ß-methylene-ATP, 2-methylthio-ATP, and
2',3'-(4-benzoyl)benzoyl-ATP] dose-dependently contracted venous
rings, but the contraction induced by 2-methylthio-ATP was more
transient than that evoked by the other P2X agonists. The effect of
hP2X1 agonists involved the activation of a rapidly
desensitizing cation current recorded in freshly isolated myocytes.
The action of hP2X7 receptor agonists was related to a
maintained nondesensitizing cation current. In addition,
hP2X7 receptor activation formed membrane pores that were
permeable to large molecules. hP2X1 and hP2X7
receptors coexpressed in COS cells did not associate to form
heteromultimers. Our data indicate that both hP2X1
and hP2X7 receptors are expressed as 2 separated
populations of channels in human saphenous vein myocytes and are
involved in ATP-induced tension. We suggest that cell lysis consequent
to hP2X7 receptorinduced pore formation contributes to
the disorganization and decrease in the amount of contractile myocytes
in the media of varicose veins.
Key Words: cation channel purinoceptor vein smooth muscle
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