T
Tamás F. Freund
Researcher at Hungarian Academy of Sciences
Publications - 237
Citations - 33521
Tamás F. Freund is an academic researcher from Hungarian Academy of Sciences. The author has contributed to research in topics: Hippocampal formation & Parvalbumin. The author has an hindex of 96, co-authored 235 publications receiving 31361 citations. Previous affiliations of Tamás F. Freund include Pázmány Péter Catholic University & University of Szeged.
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Journal ArticleDOI
Long-Term Plasticity of Endocannabinoid Signaling Induced by Developmental Febrile Seizures
Kang Chen,Anna Ratzliff,Lutz G.W. Hilgenberg,Attila I. Gulyás,Attila I. Gulyás,Tamás F. Freund,M. D. Smith,Thien P. Dinh,Daniele Piomelli,Ken Mackie,Ivan Soltesz +10 more
TL;DR: It is shown that the activity-dependent, retrograde inhibition of GABA release by endogenous cannabinoids is persistently enhanced in the rat hippocampus following a single episode of experimental prolonged febrile seizures during early postnatal development.
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Phase Segregation of Medial Septal GABAergic Neurons during Hippocampal Theta Activity
TL;DR: In this paper, the authors used in vivo juxtacellular recording and filling in the medial septum followed by immunocytochemical identification of the recorded cells containing parvalbumin to determine their firing pattern, phase relationship with hippocampal theta, morphology, and to reveal their involvement in the generation of hippocampal hippocampus theta activity.
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Subcellular localization of type 1 cannabinoid receptors in the rat basal ganglia
TL;DR: The present data are consistent with a role of endocannabinoids in the control of GABA, but not glutamate, release in the basal ganglia via presynaptic CB1 receptors, but also call the attention to possible non-CB1-mediated effects of widely used cannabinoid ligands on action potential generation.
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Correlated morphological and neurochemical features identify different subsets of vasoactive intestinal polypeptide-immunoreactive interneurons in rat hippocampus.
TL;DR: The correlation of these features with the content of neurochemical markers strongly suggests that vasoactive intestinal polypeptide-immunoreactive interneurons are specialized for distinct inhibitory functions in the hippocampal network.
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Interneurons are the local targets of hippocampal inhibitory cells which project to the medial septum
TL;DR: Electron microscopic analysis provided evidence that the axon terminals of CA1‐HS cells form symmetrical synapses selectively on GABAergic interneurons, both locally and in the CA3 region, ideally suited to synchronize neuronal activity along the septo‐hippocampal axis.