2000
DOI: 10.1006/jsre.2000.5845
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The Role of Nitric Oxide, K+ATP Channels, and cGMP in the Preconditioning Response of the Rabbit

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Cited by 28 publications
(19 citation statements)
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“…Ischemic preconditioning can be chemically mimicked by the K ATP channel opener diazoxide, both in the heart (Horimoto et al, 2000) and in the brain (Munoz et al, 2003). While the site of action for diazoxide on K ATP channels remains controversial, it is generally accepted that diazoxide is a K ATP channel opener (Seino, 1999).…”
Section: Discussionmentioning
confidence: 99%
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“…Ischemic preconditioning can be chemically mimicked by the K ATP channel opener diazoxide, both in the heart (Horimoto et al, 2000) and in the brain (Munoz et al, 2003). While the site of action for diazoxide on K ATP channels remains controversial, it is generally accepted that diazoxide is a K ATP channel opener (Seino, 1999).…”
Section: Discussionmentioning
confidence: 99%
“…However, the underlying mechanism of preconditioning and/or ischemic tolerance is largely unknown. It is well established that K ATP channels play a crucial role in cytoprotection as part of ischemic preconditioning of the heart (Horimoto et al, 2000;Murry et al, 1986;Terzic, 1999), though the involvement of K ATP channels in ischemic preconditioning in the brain has not been investigated. In this study, we first reported Left: PKC level in brain from P7 animals was upregulated 6 h after hypoxic preconditioning (HPC) in comparison to control (Ctrl).…”
Section: Discussionmentioning
confidence: 99%
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“…36 Enhanced biosynthesis of NO by cNOS is essential to trigger the ischemic preconditioning phenomenon. [37][38][39][40] However, it was also reported that improved NO production by iNOS is required to mediate the antistunning and anti-infarct actions of ischemic preconditioning. 41,42 The up-regulation of this enzyme is a central mechanism whereby the myocardium protects itself from ischemia.…”
Section: Discussionmentioning
confidence: 96%
“…35) Ockalli, et al 36) suggested that the diazoxideinduced anti-ischemic effect via opening of mitoK(ATP) channels was NOdependent. This suggestion supports our result showing that ATP-channel blockage is effective in antiarrhythmia induced by thimerosal.…”
Section: Discussionmentioning
confidence: 99%