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Cholinergic agonists may produce preservation of myocardial ischaemia/reperfusion injury.

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.
AuthorsJ Xiong, F S Xue, Y C Xu, Q Y Yang, X Liao, W L Wang
JournalMedical hypotheses (Med Hypotheses) Vol. 73 Issue 3 Pg. 312-4 (Sep 2009) ISSN: 1532-2777 [Electronic] United States
PMID19401263 (Publication Type: Journal Article)
Chemical References
  • Cholinergic Agonists
  • Cytokines
  • Receptors, Cholinergic
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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