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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Graphene oxide prevents lateral amygdala dysfunctional synaptic plasticity and reverts long lasting anxiety behavior in rats

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Author(s):
Biagioni, Audrey Franceschi [1] ; Cellot, Giada [1] ; Pati, Elisa [1] ; Lozano, Neus [2, 3] ; Ballesteros, Belen [2, 3] ; Casani, Raffaele [1] ; Coimbra, Norberto Cysne [4] ; Kostarelos, Kostas [2, 3, 5, 6] ; Ballerini, Laura [1]
Total Authors: 9
Affiliation:
[1] Int Sch Adv Studies SISSA, Neuron Physiol & Technol Lab, Neurosci, Via Bonomea 265, I-34136 Trieste - Italy
[2] CSIC, Catalan Inst Nanosci & Nanotechnol ICN2, Campus UAB, Barcelona 08193 - Spain
[3] BIST, Campus UAB, Barcelona 08193 - Spain
[4] Univ Sao Paulo FMRP USP, Dept Pharmacol, Lab Neuroanat & Neuropsychobiol, Ribeirao Preto Med Sch, Av Bandeirantes 3900, BR-14049900 Ribeirao Preto, SP - Brazil
[5] Univ Manchester, Natl Graphene Inst, Nanomed Lab, AV Hill Bldg, Oxford Rd, Manchester M13 9PL, Lancs - England
[6] Univ Manchester, Fac Biol Med & Hlth, AV Hill Bldg, Oxford Rd, Manchester M13 9PL, Lancs - England
Total Affiliations: 6
Document type: Journal article
Source: Biomaterials; v. 271, APR 2021.
Web of Science Citations: 1
Abstract

Engineered small graphene oxide (s-GO) sheets were previously shown to reversibly down-regulate glutamatergic synapses in the hippocampus of juvenile rats, disclosing an unexpected translational potential of these nanomaterials to target selective synapses in vivo. Synapses are anatomical specializations acting in the Central Nervous System (CNS) as functional interfaces among neurons. Dynamic changes in synaptic function, named synaptic plasticity, are crucial to learning and memory. More recently, pathological mechanisms involving dysfunctional synaptic plasticity were implicated in several brain diseases, from dementia to anxiety disorders. Hyper-excitability of glutamatergic neurons in the lateral nucleus of the amygdala complex (LA) is substantially involved in the storage of aversive memory induced by stressful events enabling post-traumatic stress disorder (PTSD). Here we translated in PTSD animal model the ability of s-GO, when stereotaxically administered to hamper LA glutamatergic transmission and to prevent the behavioral response featured in long-term aversive memory. We propose that s-GO, by interference with glutamatergic plasticity, impair LA-dependent memory retrieval related to PTSD. (AU)

FAPESP's process: 16/18218-0 - Nano-materials as a potential tool to anxiety disorder treatment: A pre-clinical study of carbon-based nano materials modulating neurogenesis and synapses in the hippocampus
Grantee:Audrey Franceschi Biagioni
Support type: Scholarships abroad - Research Internship - Post-doctor