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 language | English |
|---|---|
| Pages (from-to) | 1051-1058 |
| Number of pages | 8 |
| Journal | Experimental Physiology |
| Volume | 91 |
| Issue number | 6 |
| DOIs | |
| State | Published - Nov 2006 |
| Externally published | Yes |
Keywords
- Adrenergic alpha-1 Receptor Antagonists
- Adrenergic alpha-Antagonists
- Animals
- Electric Stimulation/methods
- Femoral Artery/physiology
- Male
- Muscle, Skeletal/blood supply
- Prazosin/pharmacology
- Purinergic P2 Receptor Antagonists
- Pyridoxal Phosphate/analogs & derivatives
- Rats
- Rats, Sprague-Dawley
- Receptors, Adrenergic, alpha-1/physiology
- Receptors, Purinergic P2/physiology
- Receptors, Purinergic P2X2
- Vasoconstriction/drug effects
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