Affiliation:
1. From the Department of Physiology, School of Medicine, University of Maryland, Baltimore, Md.
Abstract
Confocal microscopy of fluo-4 fluorescence in pressurized rat mesenteric small arteries subjected to low-frequency electrical field stimulation revealed Ca
2+
transients in perivascular nerves and novel, spatially localized Ca
2+
transients in adjacent smooth muscle cells. These muscle Ca
2+
transients occur with a very brief latency to the stimulus pulse (most <3 ms). They are wider (≈5 μm) and last longer (t
1/2
, 145 ms) than Ca
2+
sparks. They are abolished by the purinergic receptor (P2X) antagonist suramin, but they are totally unaffected by the α
1
-adrenoceptor antagonist prazosin or by capsaicin (which inhibits the function of perivascular sensory nerves). We conclude that these novel Ca
2+
transients represent Ca
2+
entering smooth muscle cells through P2X receptors activated by ATP released from sympathetic nerves, and we therefore call them “junctional Ca
2+
transients” or jCaTs. As expected from spontaneous neurotransmitter release, jCaTs also occur spontaneously, with characteristics identical to evoked jCaTs. Visualization of sympathetic neurotransmission shows that purinergic components dominate at low frequencies of sympathetic nerve fiber activation.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine,Physiology
Cited by
51 articles.
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