期刊
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS
卷 1840, 期 6, 页码 1923-1932出版社
ELSEVIER
DOI: 10.1016/j.bbagen.2014.01.030
关键词
Nitric oxide; [H-3]GABA release; Synaptic vesicle acidification; Mitochondrial membrane potential; S-nitrosylation; Exocytosis
资金
- National Academy of Sciences of Ukraine
Background: Nitric oxide (NO) is an important presynaptic modulator of synaptic transmission. Here, we aimed to correlate the release of the major inhibitory neurotransmitter GABA with intracellular events occurring in rat brain axon terminals during their exposure to NO in the range of nanomolar-low micromolar concentrations. Methods: Using [H-3]GABA and fluorescent dyes (Fluo 4-AM, acridine orange and rhodamine 6G), the following parameters were evaluated: vesicular and cytosolic GABA pools, intracellular calcium concentration, synaptic vesicle acidification, and mitochondrial membrane potential. Diethylamine NONOate (DEA/NO) and S-nitroso-N-acetylpenicillamine (SNAP) were used as NO donors. Results: DEA/NO and SNAP (in the presence of dithiothreitol (DTT)) stimulated external Ca2+-independent [H-3] GABA release, which was not attributed to a rise in intracellular calcium concentration. [H-3]GABA release coincided with increasing GABA level in cytosol and decreasing the vesicular GABA content available for exocytotic release. There was a strong temporal correlation between NO-induced increase in cytosolic [GABA] and dissipation of both synaptic vesicle proton gradient and mitochondria' membrane potential. Dissipation was reversible, and recovery of both parameters correlated in time with re-accumulation of [H-3]GABA into synaptic vesicles. The molar ratio of DTT to SNAP determined the rate and duration of the recovery processes. Conclusions: We suggest that NO can stimulate GABA release via GABA transporter reversal resulting from increased GABA levels in cytosol. The latter is reversible and appears to be due to S-nitrosylation of key proteins, which affect the energy status of the pre-synapse. General significance: Our findings provide new insight into molecular mechanism(s) underlying the presynaptic action of nitric oxide on inhibitory neurotransmission. (C) 2014 Elsevier B.V. All rights reserved.
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