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Abstract #24518 Published in IGR 11-3
Differential Modulation of MAPKs in Relation to Increased Intraocular Pressure in the Aqueous Humor of Rat Eye Injected with Hyaluronic Acid
Shmulevich A; Beit-Yannai ECurrent Eye Research 2009; 34: 466-475
PURPOSE: To explore the presence of several mitogem-activated protein kinases in the aqueous humor and to follow changes in levels and activity along chronic elevated intraocular pressure. MATERIAL AND METHODS: Intra-anterior chamber once-a-week injections of hyaluronic acid were used as a rat model of induced elevated intraocular pressure. Saline-injected rats served as control and the counter untreated eye was used as sham group. Aqueous humor was taken at different timepoints and analyzed by Western blot analysis for Erk, JNK, AP1, and NOS in the phosphorylated active form and total protein expression. RESULTS: Phosphorylated Erk was detected in the aqueous humor of the entire tested groups. In rats exposed to elevated intraocular pressure for longer than two weeks, a significant increase in the Erk activation was found. Total Erk expression following the hyaluronic acid injections significantly increased. Higher incidence of phosphorylated 46kD JNK was found in the aqueous humor of the hyaluronic acid injection (63%) versus the saline and sham groups (43%). Rats with elevated intraocular pressure after two weeks expressed significantly higher pJNK than the short-term injected hyaluronic acid, saline, and sham groups. The amount of the two JNK isomers declined in the hyaluronic acid injected rats, reaching significance when the elevated intraocular pressure is longer than two weeks versus sham. Among the tested samples, 74% expressed the different NOS isoforms independent of the treatment. Along with the “non responders,” the majority were from the sham group. There is a significant decrease in the total amount of the three isoforms in the hyaluronic acid injected rats after two weeks versus the sham and saline groups. CONCLUSIONS: We suggest that these signaling molecules might be a new target for intervention, opening new possibilities for intraocular pressure management.
Dr. A. Schmulevich, Clinical Pharmacology Department, The Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel
Classification:
3.5 Molecular biology incl. SiRNA (Part of: 3 Laboratory methods)
2.6.3 Compostion (Part of: 2 Anatomical structures in glaucoma > 2.6 Aqueous humor dynamics)
5.1 Rodent (Part of: 5 Experimental glaucoma; animal models)
