pd-0325901 has been researched along with Retinal-Degeneration* in 1 studies
1 other study(ies) available for pd-0325901 and Retinal-Degeneration
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The Role of ERK1/2 Activation in Sarpogrelate-Mediated Neuroprotection.
To characterize the mediators of 5-HT2A serotonin receptor-driven retinal neuroprotection.. Albino mice were treated intraperitoneally with saline or sarpogrelate, a 5-HT2A antagonist, immediately before light exposure (LE). Following LE, retinas were harvested for a high-throughput phosphorylation microarray to quantify activated phosphorylated proteins in G protein-coupled receptor (GPCR) signaling. To confirm microarray results and define temporal changes, Western blots of select GPCR signaling proteins were performed. Since both methodologies implicated MAPK/ERK activation, the functional significance of sarpogrelate-mediated ERK1/2 activation was examined by inhibition of ERK1/2 phosphorylation via pretreatment with the MEK inhibitor (MEKi) PD0325901. The degree of neuroprotection was evaluated with spectral-domain optical coherence tomography (SD-OCT) and electroretinography (ERG). To determine the effects of sarpogrelate on gene expression, a qPCR array measuring the expression of 84 genes involved in oxidative stress and cell death was performed 48 hours post LE.. Sarpogrelate led to an activation of the MAPK/ERK pathway. Temporal analysis further demonstrated a transient activation of ERK1/2, starting with an early inhibition 20 minutes into LE, a maximum activation at 3 hours post LE, and a return to baseline at 7 hours post LE. Inhibition of ERK1/2 with MEKi pretreatment led to attenuation of sarpogrelate-mediated neuroprotection. LE caused significant changes in the expression of genes involved in iron metabolism, oxidative stress, and apoptosis. These changes were prevented by sarpogrelate treatment.. Sarpogrelate-mediated retinal protection involves a transient activation of the MAPK/ERK pathway, although this pathway alone does not account for the full effect of neuroprotection. Topics: Acrylonitrile; Aniline Compounds; Animals; Benzamides; Blotting, Western; Diphenylamine; Electroretinography; Gene Expression Regulation; Injections, Intraperitoneal; Light; Male; MAP Kinase Signaling System; Mice; Mice, Inbred BALB C; Neuroprotection; Oxidative Stress; Phosphorylation; Radiation Injuries, Experimental; Real-Time Polymerase Chain Reaction; Receptor, Serotonin, 5-HT2A; Retina; Retinal Degeneration; Serotonin Antagonists; Succinates; Tomography, Optical Coherence | 2018 |