[Signaling mechanism of neuroprotective effect of ischemic preconditioning of brain].
Leonid N. Maslov
Abstract
Leonid N. Maslov
Abstract
Analysis of published data indicates that Ras-protein and kinases PI3K, Akt, MEK1/2, ERK1/2, PKC, CaMKII are involved in the signaling mechanism of ischemic preconditioning. In addition, it is established that cyclooxigenase-2, NO-synthase and mitK(ATP)-channel are involved in delayed preconditioning. Signaling mechanism of early ischemic preconditioning of brain is remained unstudied.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Analysis of published data indicates that Ras-protein and kinases PI3K, Akt, MEK1/2, ERK1/2, PKC, CaMKII are involved in the signaling mechanism of ischemic preconditioning. In addition, it is established that cyclooxigenase-2, NO-synthase and mitK(ATP)-channel are involved in delayed preconditioning. Signaling mechanism of early ischemic preconditioning of brain is remained unstudied.
Key concepts: Ischemic preconditioning, Mechanism (biology), Neuroprotection, Protein kinase B, Neuroscience, PI3K/AKT/mTOR pathway, Kinase, Protein kinase C