Altered neurotransmitter release, vesicle recycling and presynaptic structure in the pilocarpine model of temporal lobe epilepsy
Author(s) -
Chirag Upreti,
Rafael Otero,
Carlos Partida,
Frank Skinner,
Ravi Thakker,
Luis F. Pacheco Otalora,
Zhenyu Zhou,
Giorgi Maglakelidze,
Jana Velı́šková,
Libor Velı́šek,
Dwight K. Romanovicz,
Theresa A. Jones,
Patric K. Stanton,
Emilio R. Garrido-Sanabria
Publication year - 2012
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awr341
Subject(s) - status epilepticus , pilocarpine , synaptic vesicle , hippocampal formation , neuroscience , mossy fiber (hippocampus) , neurotransmitter , epilepsy , postsynaptic potential , active zone , hippocampus , chemistry , biology , biophysics , vesicle , biochemistry , central nervous system , dentate gyrus , receptor , membrane
In searching for persistent seizure-induced alterations in brain function that might be causally related to epilepsy, presynaptic transmitter release has relatively been neglected. To measure directly the long-term effects of pilocarpine-induced status epilepticus on vesicular release and recycling in hippocampal mossy fibre presynaptic boutons, we used (i) two-photon imaging of FM1-43 vesicular release in rat hippocampal slices; and (ii) transgenic mice expressing the genetically encoded pH-sensitive fluorescent reporter synaptopHluorin preferentially at glutamatergic synapses. In this study we found that, 1-2 months after pilocarpine-induced status epilepticus, there were significant increases in mossy fibre bouton size, faster rates of action potential-driven vesicular release and endocytosis. We also analysed the ultrastructure of rat mossy fibre boutons using transmission electron microscopy. Pilocarpine-induced status epilepticus led to a significant increase in the number of release sites, active zone length, postsynaptic density area and number of vesicles in the readily releasable and recycling pools, all correlated with increased release probability. Our data show that presynaptic release machinery is persistently altered in structure and function by status epilepticus, which could contribute to the development of the chronic epileptic state and may represent a potential new target for antiepileptic therapies.
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