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Vagal nerve stimulation in prevention and management of coronary heart disease
1Undurti N Das, UND Life Sciences, 13800 Fairhill Road, #321, Shaker Heights, OH 44120, United States. undurti@hotmail.com
Insights
Vagal nerve stimulation may prevent coronary heart disease (CHD) and arrhythmias by reducing inflammation. Measuring specific molecules and vagal tone can aid in predicting, preventing, and managing CHD.
Area of Science:
- Cardiovascular Science
- Neuroimmunology
Background:
- Coronary heart disease (CHD) and atherosclerosis are linked to chronic low-grade systemic inflammation.
- Congestive cardiac failure and arrhythmias contribute significantly to CHD mortality.
- Vagal stimulation exhibits anti-inflammatory properties, potentially mitigating these conditions.
Purpose of the Study:
- To explore the anti-inflammatory and anti-arrhythmic roles of vagal neurotransmitters and polyunsaturated fatty acids (PUFAs) in CHD.
- To investigate the potential of vagal nerve stimulation in preventing CHD and cardiac arrhythmias.
Main Methods:
- Review of the literature on the interplay between vagal stimulation, acetylcholine, PUFAs, and inflammatory pathways.
- Discussion of potential biomarkers for CHD and arrhythmia prediction and management.
Main Results:
- Acetylcholine, the primary vagal neurotransmitter, possesses potent anti-inflammatory effects.
- Polyunsaturated fatty acids (PUFAs) enhance acetylcholine release and are precursors to anti-inflammatory and anti-arrhythmic molecules.
- Reduced PUFA levels are observed in patients with CHD and atherosclerosis.
Conclusions:
- Vagal nerve stimulation is a promising strategy for the prevention of CHD and cardiac arrhythmias.
- Measuring specific molecules (catecholamines, acetylcholine, PUFAs, and their metabolites) and assessing vagal tone (heart rate variability) can aid in CHD prediction, prevention, and management.
Abstract:
Coronary heart disease (CHD) that is due to atherosclerosis is associated with low-grade systemic inflammation. Congestive cardiac failure and arrhythmias that are responsible for mortality in CHD can be suppressed by appropriate vagal stimulation that is anti-inflammatory in nature. Acetylcholine, the principal vagal neurotransmitter, is a potent anti-inflammatory molecule. Polyunsaturated fatty acids (PUFAs) augment acetylcholine release, while acetylcholine can enhance the formation of prostacyclin, lipoxins, resolvins, protectins and maresins from PUFAs, which are anti-inflammatory and anti-arrhythmic molecules. Furthermore, plasma and tissue levels of PUFAs are low in those with CHD and atherosclerosis. Hence, vagal nerve stimulation is beneficial in the prevention of CHD and cardiac arrhythmias. Thus, measurement of catecholamines, acetylcholine, various PUFAs, and their products lipoxins, resolvins, protectins and maresins in the plasma and peripheral leukocytes, and vagal tone by heart rate variation could be useful in the prediction, prevention and management of CHD and cardiac arrhythmias.
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