Synapses compute and transmit information to connect neural circuits and are at the basis of brain operations. Alterations in their function contribute to a vast range of neuropsychiatric and neurodegenerative disorders and synapse-based therapeutic intervention, such as selective inhibition of synaptic transmission, may significantly help against serious pathologies. Graphene is a two-dimensional nanomaterial largely exploited in multiple domains of science and technology, including biomedical applications. In hippocampal neurons in culture, small graphene oxide nanosheets (s-GO) selectively depress glutamatergic activity without altering cell viability. Glutamate is the main excitatory neurotransmitter in the central nervous system and growing evidence suggests its involvement in neuropsychiatric disorders. Here we demonstrate that s-GO directly targets the release of presynaptic vesicle. We propose that s-GO flakes reduce the availability of transmitter, via promoting its fast release and subsequent depletion, leading to a decline ofglutamatergic neurotransmission. We injected s-GO in the hippocampus in vivo, and 48 h after surgery ex vivo patch-clamp recordings from brain slices show a significant reduction in glutamatergic synaptic activity in respect to saline injections.

Graphene oxide flakes tune excitatory neurotransmission in vivo by targeting hippocampal synapses / Rauti, Rossana; Medelin, Manuela; Newman, Leon; Vranic, Sandra; Reina, Giacomo; Bianco, Alberto; Prato, Maurizio; Kostarelos, Kostas; Ballerini, Laura. - In: NANO LETTERS. - ISSN 1530-6984. - 19:5(2019), pp. 2858-2870. [10.1021/acs.nanolett.8b04903]

Graphene oxide flakes tune excitatory neurotransmission in vivo by targeting hippocampal synapses

Rauti, Rossana
Investigation
;
Medelin, Manuela
Membro del Collaboration group
;
Ballerini, Laura
Conceptualization
2019

Abstract

Synapses compute and transmit information to connect neural circuits and are at the basis of brain operations. Alterations in their function contribute to a vast range of neuropsychiatric and neurodegenerative disorders and synapse-based therapeutic intervention, such as selective inhibition of synaptic transmission, may significantly help against serious pathologies. Graphene is a two-dimensional nanomaterial largely exploited in multiple domains of science and technology, including biomedical applications. In hippocampal neurons in culture, small graphene oxide nanosheets (s-GO) selectively depress glutamatergic activity without altering cell viability. Glutamate is the main excitatory neurotransmitter in the central nervous system and growing evidence suggests its involvement in neuropsychiatric disorders. Here we demonstrate that s-GO directly targets the release of presynaptic vesicle. We propose that s-GO flakes reduce the availability of transmitter, via promoting its fast release and subsequent depletion, leading to a decline ofglutamatergic neurotransmission. We injected s-GO in the hippocampus in vivo, and 48 h after surgery ex vivo patch-clamp recordings from brain slices show a significant reduction in glutamatergic synaptic activity in respect to saline injections.
19
5
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https://doi.org/10.1021/acs.nanolett.8b04903
https://pubs.acs.org/doi/10.1021/acs.nanolett.8b04903#
Rauti, Rossana; Medelin, Manuela; Newman, Leon; Vranic, Sandra; Reina, Giacomo; Bianco, Alberto; Prato, Maurizio; Kostarelos, Kostas; Ballerini, Laura
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11767/89920
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