Synergistic action of hypoosmolarity and glutamine in inducing acute swelling of retinal glial (Müller) cells

✍ Scribed by Anett Karl; Antje Wurm; Thomas Pannicke; Katja Krügel; Marta Obara-Michlewska; Peter Wiedemann; Andreas Reichenbach; Jan Albrecht; Andreas Bringmann

• Publisher: John Wiley and Sons
• Year: 2010
• Tongue: English
• Weight: 729 KB
• Volume: 59
• Category: Article
• ISSN: 0894-1491
• DOI: 10.1002/glia.21095

✦ Synopsis

Abstract

High blood ammonia, elevated glutamine, and hyponatremia are pathogenic factors contributing to astrocytic swelling and brain edema in liver failure. We investigated the effects of hypoosmolarity, ammonia, and glutamine on the induction of glial cell swelling in freshly isolated slices of the rat retina. Glutamine, but not ammonia or hypoosmolarity per se, evoked a rapid (within one minute) swelling of retinal glial (Müller) cell bodies under hypoosmotic conditions. Under isoosmotic conditions, glutamine evoked a delayed swelling after 10 min of exposure. The effect of glutamine was concentration‐dependent, with half‐maximal and maximal effects at ∼ 0.1 and 0.5 mM. Glutamine in hypoosmotic solution induced a dissipation of the mitochondrial membrane potential. The effects on the mitochondrial membrane potential and the glial soma size were reduced by (i) agents which inhibit the transfer of glutamine into mitochondria and its hydrolysis there, (ii) inhibition of the mitochondrial permeability transition, (iii) inhibitors of oxidative‐nitrosative stress, and (iv) inhibitors of phospholipase A~2~ and cyclooxygenase. Glutamine‐induced glial swelling was also prevented by ATP and adenosine, acting at adenosine A~1~ receptors. The data suggest that hypoosmolarity accelerates the swelling‐inducing effect of glutamine on retinal glial cells, and that swelling induction by glutamine is mediated by inducing oxidative‐nitrosative stress, inflammatory lipid mediators, and mitochondrial dysfunction. © 2010 Wiley‐Liss, Inc.