Protein kinase B (Akt) and mitogen-activated protein kinase p38α in retinal ischemic post-conditioning

John C. Dreixler, Ajay Sampat, Afzhal R. Shaikh, Michael Alexander, Marcus M. Marcet, Steven Roth

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

In previous studies, it was shown that post-conditioning, a transient period of brief ischemia following prolonged severe ischemia in the retina, could provide significant improvement in post-ischemic recovery, attenuation of cell loss, and decreased apoptosis. However, the mechanisms of post-conditioning in the retina have not been elucidated. We hypothesized that two kinases, mitogen-activated protein kinase p38α and protein kinase B (Akt), were involved in the mechanism of post-conditioning. Ischemia was induced in rat retina in vivo. Recovery after ischemia followed by 8 min of post-conditioning early in the reperfusion period after prolonged ischemia was assessed functionally (electroretinography) and histologically at 7 days after ischemia. We examined the role of p38α and Akt subtypes 1-3 in post-conditioning by intravitreal injection of interfering RNA 6 h prior to ischemia and post-conditioning and compared the results to injection of non-silencing interfering RNA sequence. The blockade of p38α significantly decreased the recovery after ischemia and post-conditioning, and enhanced cell loss and disorganization of the retina. Blockade of Akt1, and to a lesser degree, Akt2, significantly decreased the recovery after ischemia and enhanced cell loss and disorganization. These differences in the effects of blockade of Akt subtypes were not explainable by distribution of Akt subtypes in the retina, which were similar. In conclusion, both p38 and Akt are essential components of the neuroprotection induced by post-ischemic conditioning in the retina.

Original languageEnglish (US)
Pages (from-to)309-320
Number of pages12
JournalJournal of Molecular Neuroscience
Volume45
Issue number2
DOIs
StatePublished - Oct 1 2011
Externally publishedYes

Fingerprint

Ischemic Postconditioning
Proto-Oncogene Proteins c-akt
p38 Mitogen-Activated Protein Kinases
Ischemia
Retina
MAP Kinase Kinase Kinases
Electroretinography
Intravitreal Injections
Reperfusion
RNA
Apoptosis

Keywords

  • Akt
  • p38
  • Post-conditioning
  • Retinal ischemia

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience

Cite this

Protein kinase B (Akt) and mitogen-activated protein kinase p38α in retinal ischemic post-conditioning. / Dreixler, John C.; Sampat, Ajay; Shaikh, Afzhal R.; Alexander, Michael; Marcet, Marcus M.; Roth, Steven.

In: Journal of Molecular Neuroscience, Vol. 45, No. 2, 01.10.2011, p. 309-320.

Research output: Contribution to journalArticle

Dreixler, John C. ; Sampat, Ajay ; Shaikh, Afzhal R. ; Alexander, Michael ; Marcet, Marcus M. ; Roth, Steven. / Protein kinase B (Akt) and mitogen-activated protein kinase p38α in retinal ischemic post-conditioning. In: Journal of Molecular Neuroscience. 2011 ; Vol. 45, No. 2. pp. 309-320.
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