Monoaminergic and Histaminergic Strategies and Treatments in Brain Diseases
Open Access
- 24 November 2016
- journal article
- review article
- Published by Frontiers Media SA in Frontiers in Neuroscience
- Vol. 10, 541
Abstract
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 treatments 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.Keywords
Funding Information
- European Cooperation in Science and Technology
- Centre National de la Recherche Scientifique
This publication has 345 references indexed in Scilit:
- Non-dopaminergic Treatments for Motor Control in Parkinson’s DiseaseDrugs, 2013
- Memantine and Cholinesterase Inhibitors: Complementary Mechanisms in the Treatment of Alzheimer’s DiseaseNeurotoxicity Research, 2013
- The noradrenaline precursor L-DOPS reduces pathology in a mouse model of Alzheimer's diseaseNeurobiology of Aging, 2012
- Vesicular monoamine transporters: Structure‐function, pharmacology, and medicinal chemistryMedicinal Research Reviews, 2011
- The overlap between neurodegenerative and vascular factors in the pathogenesis of dementiaActa Neuropathologica, 2010
- Dopamine D3 receptor stimulation underlies the development of L-DOPA-induced dyskinesia in animal models of Parkinson's diseaseNeurobiology of Disease, 2009
- Early disruptions of the blood–brain barrier may contribute to exacerbated neuronal damage and prolonged functional recovery following stroke in aged ratsNeurobiology of Aging, 2008
- Biological Actions of Drugs Affecting Serotonin and EatingObesity Research, 1995
- Loss of high-affinity α2-adrenoceptors in Alzheimer's disease: An autoradiographic study in frontal cortex and hippocampusNeuroscience Letters, 1992
- Plasma amine oxidase activities in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidaseJournal of Neural Transmission, 1991