Abstract |
The best treatment for myocardial infarction is to restore blood flow in the ischaemic region, though it will bring new myocardial damage known as myocardial ischaemia/reperfusion (I/R) injury. Both the ischaemia preconditioning and the ischaemia postcondioning have been shown to reduce the myocardial I/R injury, but their deficits restrict wide clinical availability. It has been demonstrated that inflammation plays a critical role in the I/R injury process. Also plasma levels of cytokines and inflammation response can be regulated by specifically augmenting cholinergic signaling via the efferent vagus nerve and alpha7 subunit-containing nicotinic acetylcholine receptor ( alpha7nAChR). Because cholinergic modalities, acting through vagus nerve- and/or alpha7nAChR-mediated mechanism, have been confirmed to suppress excessive inflammation during the I/R injury in kidney, liver, lung and intestine, therefore, we hypothesize that cholinergic agonists may also provide a protection for the myocardial I/R injury.
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Authors | J Xiong, F S Xue, Y C Xu, Q Y Yang, X Liao, W L Wang |
Journal | Medical hypotheses
(Med Hypotheses)
Vol. 73
Issue 3
Pg. 312-4
(Sep 2009)
ISSN: 1532-2777 [Electronic] United States |
PMID | 19401263
(Publication Type: Journal Article)
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Chemical References |
- Cholinergic Agonists
- Cytokines
- Receptors, Cholinergic
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Topics |
- Animals
- Cholinergic Agonists
(administration & dosage)
- Cytokines
(immunology)
- Humans
- Models, Cardiovascular
- Models, Immunological
- Myocardium
(immunology)
- Receptors, Cholinergic
(immunology)
- Reperfusion Injury
(immunology, prevention & control)
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