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Title: Inhibition of glutamate uptake and proton pumping in synaptic vesicles by S-nitrosylation. Author: Wolosker H, Reis M, Assreuy J, de Meis L. Journal: J Neurochem; 1996 May; 66(5):1943-8. PubMed ID: 8780021. Abstract: Nitric oxide (NO; including NO-., NO+, and NO-) was found to inhibit glutamate uptake by isolated synaptic vesicles of rat brain. This was observed when two unrelated NO donors, S-nitrosogluthathione and S-nitroso-N-acetylpenicillamine, were used. The primary target of NO is the H(+)-ATPase found in the synaptic vesicles, which leads to dissipation of the electrochemical proton gradient and inhibition of glutamate uptake. Oxyhemoglobin (12 microM) and, to a much lesser extent, methemoglobin protected the vacuolar H(+)-ATPase from inhibition. Inhibition of H+ pumping by NO was reversed by addition of 0.5 mM dithiothreitol. The results indicate that the vacuolar H(+)-ATPase from synaptic vesicles is inhibited by NO by a mechanism that involves S-nitrosylation of critical sulfhydryl groups in the enzyme. The interaction of NO with synaptic vesicles might be of importance for the understanding of the multiple effects of NO in neuro-transmission.[Abstract] [Full Text] [Related] [New Search]