Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/22618
Title: Monoaminergic mechanisms in epilepsy may offer innovative therapeutic opportunity for monoaminergic multi-target drugs
Authors: Svob Strac, Dubravka
Pivac, Nela
Smolders, Ilse J.
Fogel, Wieslawa A.
De Deurwaerdere, Philippe
Di Giovanni, Giuseppe
Keywords: Epilepsy
Anticonvulsants
Astrocytes
Microglia
Issue Date: 2016
Publisher: Frontiers Research Foundation
Citation: Svob Strac, D., Nela, P., Smolders, I. J., Fogel, W. A., De Deurwaerdere, P., & Di Giovanni, G. (2016). Monoaminergic mechanisms in epilepsy may offer innovative therapeutic opportunity for monoaminergic multi-target drugs. Frontiers in Neuroscience, 10, 492.
Abstract: A large body of experimental and clinical evidence has strongly suggested that monoamines play an important role in regulating epileptogenesis, seizure susceptibility, convulsions, and comorbid psychiatric disorders commonly seen in people with epilepsy (PWE). However, neither the relative significance of individual monoamines nor their interaction has yet been fully clarified due to the complexity of these neurotransmitter systems. In addition, epilepsy is diverse, with many different seizure types and epilepsy syndromes, and the role played by monoamines may vary from one condition to another. In this review, we will focus on the role of serotonin, dopamine, noradrenaline, histamine, and melatonin in epilepsy. Recent experimental, clinical, and genetic evidence will be reviewed in consideration of the mutual relationship of monoamines with the other putative neurotransmitters. The complexity of epileptic pathogenesis may explain why the currently available drugs, developed according to the classic drug discovery paradigm of “one-molecule-one-target,” have turned out to be effective only in a percentage of PWE. Although, no antiepileptic drugs currently target specifically monoaminergic systems, multi-target directed ligands acting on different monoaminergic proteins, present on both neurons and glia cells, may represent a new approach in the management of seizures, and their generation as well as comorbid neuropsychiatric disorders.
URI: https://www.um.edu.mt/library/oar//handle/123456789/22618
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