TY - JOUR
T1 - Monoaminergic and histaminergic strategies and treatments in brain diseases
AU - Di Giovanni, Giuseppe
AU - Strac, Dubravka Svob
AU - Sole, Montse
AU - Unzeta, Mercedes
AU - Tipton, Keith F.
AU - Mück-Šeler, Dorotea
AU - Bolea, Irene
AU - Corte, Laura Della
AU - Perkovic, Matea Nikolac
AU - Pivac, Nela
AU - Smolders, Ilse J.
AU - Stasiak, Anna
AU - Fogel, Wieslawa A.
AU - De Deurwaerdère, Philippe
PY - 2016/1/1
Y1 - 2016/1/1
N2 - © 2016 Di Giovanni, Svob Strac, Sole, Unzeta, Tipton, Mück-Šeler, Bolea, Della Corte, Nikolac Perkovic, Pivac, Smolders, Stasiak, Fogel and De Deurwaerdère. The monoaminergic systems are the target of several drugs for the treatment of mood, motor and cognitive disorders as well as neurological conditions. In most cases, advances have occurred through serendipity, except for Parkinson's disease where the pathophysiology led almost immediately to the introduction of dopamine restoring agents. Extensive neuropharmacological studies first showed that the primary target of antipsychotics, antidepressants, and anxiolytic drugs were specific components of the monoaminergic systems. Later, some dramatic side effects associated with older medicines were shown to disappear with new chemical compounds targeting the origin of the therapeutic benefit more specifically. The increased knowledge regarding the function and interaction of the monoaminergic systems in the brain resulting from in vivo neurochemical and neurophysiological studies indicated new monoaminergic targets that could achieve the efficacy of the older medicines with fewer side-effects. Yet, this accumulated knowledge regarding monoamines did not produce valuable strategies for diseases where no monoaminergic drug has been shown to be effective. Here, we emphasize the new therapeutic and monoaminergic-based strategies for the treatment of psychiatric diseases. We will consider three main groups of diseases, based on the evidence of monoamines involvement (schizophrenia, depression, obesity), the identification of monoamines in the diseases processes (Parkinson's disease, addiction) and the prospect of the involvement of monoaminergic mechanisms (epilepsy, Alzheimer's disease, stroke). In most cases, the clinically available monoaminergic drugs induce widespread modifications of amine tone or excitability through neurobiological networks and exemplify the overlap between therapeutic approaches to psychiatric and neurological conditions. More recent developments that have resulted in improved drug specificity and responses will be discussed in this review.
AB - © 2016 Di Giovanni, Svob Strac, Sole, Unzeta, Tipton, Mück-Šeler, Bolea, Della Corte, Nikolac Perkovic, Pivac, Smolders, Stasiak, Fogel and De Deurwaerdère. The monoaminergic systems are the target of several drugs for the treatment of mood, motor and cognitive disorders as well as neurological conditions. In most cases, advances have occurred through serendipity, except for Parkinson's disease where the pathophysiology led almost immediately to the introduction of dopamine restoring agents. Extensive neuropharmacological studies first showed that the primary target of antipsychotics, antidepressants, and anxiolytic drugs were specific components of the monoaminergic systems. Later, some dramatic side effects associated with older medicines were shown to disappear with new chemical compounds targeting the origin of the therapeutic benefit more specifically. The increased knowledge regarding the function and interaction of the monoaminergic systems in the brain resulting from in vivo neurochemical and neurophysiological studies indicated new monoaminergic targets that could achieve the efficacy of the older medicines with fewer side-effects. Yet, this accumulated knowledge regarding monoamines did not produce valuable strategies for diseases where no monoaminergic drug has been shown to be effective. Here, we emphasize the new therapeutic and monoaminergic-based strategies for the treatment of psychiatric diseases. We will consider three main groups of diseases, based on the evidence of monoamines involvement (schizophrenia, depression, obesity), the identification of monoamines in the diseases processes (Parkinson's disease, addiction) and the prospect of the involvement of monoaminergic mechanisms (epilepsy, Alzheimer's disease, stroke). In most cases, the clinically available monoaminergic drugs induce widespread modifications of amine tone or excitability through neurobiological networks and exemplify the overlap between therapeutic approaches to psychiatric and neurological conditions. More recent developments that have resulted in improved drug specificity and responses will be discussed in this review.
KW - Antidepressant
KW - Antiparkinsonian treatments
KW - Antipsychotic
KW - Drug addiction
KW - Monoamine oxidase inhibitor
KW - Multi-target pharmacology
KW - Neurodegenerative diseases
KW - Stroke
U2 - 10.3389/fnins.2016.00541
DO - 10.3389/fnins.2016.00541
M3 - Review article
SN - 1662-4548
VL - 10
JO - Frontiers in Neuroscience
JF - Frontiers in Neuroscience
IS - NOV
M1 - 541
ER -