Astrocytes protect neurons from ammonia toxicity

• Published in: Neurochemical research 2005-10, Vol.30 (10), p.1311-1318
• Main Authors: Rao, K V Rama, Panickar, K S, Jayakumar, A R, Norenberg, M D
• Format: Article
• Language: English
• Subjects: Ammonia - toxicity; Animals; Apoptosis - drug effects; Astrocytes - cytology; Astrocytes - drug effects; Astrocytes - metabolism; Caspase 3; Caspases - metabolism; Cells, Cultured; Coculture Techniques; Free Radicals - metabolism; Humans; L-Lactate Dehydrogenase - metabolism; Membrane Potentials - physiology; Mitochondria - metabolism; Neurons - cytology; Neurons - drug effects; Neurons - metabolism; Rats
• ISSN: 0364-3190; 1573-6903
• DOI: 10.1007/s11064-005-8803-2

Ammonia is a neurotoxin that is implicated in the CNS dysfunction associated with hepatic encephalopathy, urea cycle disorders, Reye's syndrome and other neurological conditions. While in vivo studies suggest that astrocytes are the principal target of ammonia toxicity, recent in vitro investigations suggest that neurons may also be directly affected by ammonia. To further examine the issue of neural cell sensitivity to ammonia, pure rat cortical neuronal cultures, as well as co-cultures of neurons and astrocytes, were exposed to 5 mM NH4Cl for 48 h. Cultures were examined for morphological changes by light microscopy, measures of cell death, free radical production and changes in the mitochondrial inner membrane potential. Ammonia caused extensive degenerative changes in pure cultured neurons, while such neuronal changes were minor in the co-cultures. Similarly, processes of pure cultured neurons displayed a significant loss of the mitochondrial inner membrane potential, as compared to neurons in co-cultures. Cell death (LDH release) in ammonia-treated neuronal cultures was twice as great as untreated controls, while in co-cultures ammonia did not significantly increase cell death. Free radical production at 3 min was increased (69%, P