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Synapsin‐regulated synaptic transmission from readily releasable synaptic vesicles in excitatory hippocampal synapses in mice
Author(s) -
Hvalby Øivind,
Jensen Vidar,
Kao HungTeh,
Walaas S. Ivar
Publication year - 2006
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2005.100685
Subject(s) - synapsin , synapsin i , excitatory postsynaptic potential , synaptic augmentation , neuroscience , synaptic vesicle , synapse , neurotransmission , biology , hippocampal formation , excitatory synapse , inhibitory postsynaptic potential , vesicle , biochemistry , receptor , membrane
The effects of synapsin proteins on synaptic transmission from vesicles in the readily releasable vesicle pool have been examined by comparing excitatory synaptic transmission in hippocampal slices from mice devoid of synapsins I and II and from wild‐type control animals. Application of stimulus trains at variable frequencies to the CA3‐to‐CA1 pyramidal cell synapse suggested that, in both genotypes, synaptic responses obtained within 2 s stimulation originated from readily releasable vesicles. Detailed analysis of the responses during this period indicated that stimulus trains at 2–20 Hz enhanced all early synaptic responses in the CA3‐to‐CA1 pyramidal cell synapse, but depressed all early responses in the medial perforant path‐to‐granule cell synapse. The synapsin‐dependent part of these responses, i.e. the difference between the results obtained in the transgene and the wild‐type preparations, showed that in the former synapse, the presence of synapsins I and II minimized the early responses at 2 Hz, but enhanced the early responses at 20 Hz, while in the latter synapse, the presence of synapsins I and II enhanced all responses at both stimulation frequencies. The results indicate that synapsins I and II are necessary for full expression of both enhancing and decreasing modulatory effects on synaptic transmission originating from the readily releasable vesicles in these excitatory synapses.