Frequency and pattern dependence of adrenergic and purinergic vasoconstriction in rat skeletal muscle arteries

Heidi A. Kluess, John B. Buckwalter, Jason J. Hamann, Darren S. Delorey, Philip S. Clifford

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Sympathetic nerves fire in bursts followed by brief periods of quiescence. Periods of quiescence may be a valuable part of coding for different neurotransmitters. We compared adrenergic- and non-adrenergic-mediated vasoconstriction with repeating burst patterns versus constant frequency stimulation. Seventeen rats were killed, and the femoral arteries dissected out and mounted in organ tissue baths at 37°C and pH 7.4. Field stimulation was applied to artery rings from five rats at constant frequencies of 2-6 Hz for 144 impulses. In 12 rats, artery rings were stimulated with two burst pattern protocols consisting of repeating pairs, triplets, quadruplets or sextuplets performed using either 8 or 30 Hz as the instantaneous frequency for a total of 144 impulses. All protocols were repeated with the P2 purinergic antagonist pyridoxal-phosphate-6-azophenyl-2′4′-disulphonic acid (PPADs; 0.42 m) or the α1-antagonist prazosin (1.59 μm). Tension was decreased by the addition of the P2 antagonist PPADs (P < 0.05). Prazosin abolished tension at all constant frequencies (P < 0.05). P2 and α1-antagonism decreased tension with 8 and 30 Hz burst pattern field stimulation. However, the magnitude of decrease in tension with prazosin was less with burst patterns compared to the same average constant frequencies (P < 0.05). It appears that P2X receptors and α1-receptors in the femoral artery are sensitive to frequency and patterns of electrical stimulation.

Original languageEnglish
Pages (from-to)1051-1058
Number of pages8
JournalExperimental Physiology
Volume91
Issue number6
DOIs
StatePublished - Nov 2006
Externally publishedYes

Fingerprint

Dive into the research topics of 'Frequency and pattern dependence of adrenergic and purinergic vasoconstriction in rat skeletal muscle arteries'. Together they form a unique fingerprint.

Cite this