Key result
TENS increases pacing tolerance and improves lactate metabolism without reversal by naloxone.
Why the study?
The mechanisms underlying the effects of transcutaneous electrical nerve stimulation (TENS) on pacing-induced angina pectoris and catecholamine metabolism were unclear, including the role of opioid pathways.
Does naloxone reverse the beneficial effects of TENS on pacing-induced angina pectoris in patients with severe coronary artery disease?
RCT (n=11)
Double-blind
Random order
Does naloxone reverse the beneficial effects of TENS on pacing-induced angina pectoris in patients with severe coronary artery disease?
The beneficial effects of TENS on pacing-induced angina are not mediated by beta-endorphins, as they are not reversed by high-dose naloxone.
Answers are grounded in this paper and cite their sources.
TENS benefits in pacing-induced angina persist after high-dose naloxone; challenges beta-endorphin mediation and supports investigation of non-opioid mechanisms.
Two invasive studies (invasive study I and invasive study II) showed positive effects of transcutaneous electrical nerve stimulation (TENS) in pacing-induced angina pectoris in terms of increased tolerance to pacing, improved lactate metabolism and less anginal pain. Invasive study I demonstrated a decrease in left ventricular afterload by TENS treatment as reflected by a fall in systolic blood pressure, and this fact was thought to be explained by reduced sympathetic activity since arterial levels of epinephrine and norepinephrine dropped during TENS in TENS responders. In invasive study II, the influence of naloxone on the effects of TENS in pacing-induced angina pectoris was studied in 11 patients with severe coronary artery disease. The patients were catheterized and treated with TENS on 2 occasions; one with a single intravenous (i.v.) dose of saline as placebo and one with a single i.v. dose of 50 mg naloxone, double-blind, in random order. Treatment with TENS increased tolerance to pacing (P less than 0.01 with placebo and P less than 0.01 with naloxone, respectively) and improved lactate metabolism (P less than 0.05 with placebo and P less than 0.01 with naloxone, respectively). The positive effects of TENS were thus reproducible and not reversed by single i.v. doses of naloxone. The results of this study indicate that the effects of TENS on the heart are not mediated by beta-endorphin but do not exclude activation of more short-acting opioids like delta or kappa receptor agonists (met-enkephalin and/or dynorphin) since naloxone has a low affinity for these receptors. It is also possible that non-opioid mechanisms are of importance.(ABSTRACT TRUNCATED AT 250 WORDS)
No takes yet. Share an insight, caveat, or question.
Mannheimer et al. (1990) conducted an RCT in Pacing-induced angina pectoris in severe coronary artery disease (n=11). Transcutaneous electrical nerve stimulation (TENS) with naloxone vs. Transcutaneous electrical nerve stimulation (TENS) with saline placebo was evaluated on Tolerance to pacing (p=<0.01). Transcutaneous electrical nerve stimulation (TENS) increased tolerance to pacing and improved lactate metabolism, and these effects were not reversed by a single i.v. dose of naloxone.
Synapse has enriched 10 related papers. Consider them for comparative context: