Titlebook: Co-Existence and Co-Release of Classical Neurotransmitters; Ex uno plures Rafael Gutierrez Book 2009 Springer-Verlag US 2009 Nervous System

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,: Out of One, Many, signaling molecules has been long recognized and the terms “classical neurotransmitter” and “neuromodulator” have been used to label the co-released substances, often being the former of low molecular weight and the latter of high molecular weight. Indeed, the use of these terms confers a distincti

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GABA, Glycine, and Glutamate Co-Release at Developing Inhibitory Synapses,made it clear, however, that the classification of neurons and synapses as purely GABAergic, or even as purely inhibitory or excitatory, is no longer valid. In this chapter we review evidence showing that inhibitory synapses co-release multiple inhibitory neurotransmitters, and that some classical i

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GABA is the Main Neurotransmitter Released from Mossy Fiber Terminals in the Developing Rat Hippoca the interplay between glutamate and GABA, which in the immediate postnatal period is depolarizing and excitatory. Here, we review some recent data obtained in our laboratory concerning neuronal signaling at immature MF connections. MF responses were identified on the basis of their strong paired-pu

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Glutamate Co-Release by Monoamine Neurons,ral investigations have consistently reported that these neurons, including dopamine, serotonin and norepinephrine neurons establish both junctional (i.e. synaptic) and non-junctional (i.e. non-synaptic) axon terminals. The hypothesis that some of these terminals can mediate synaptic glutamate relea

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Dopamine and Serotonin Crosstalk Within the Dopaminergic and Serotonergic Systems,mine the temporal and spatial extent of the signals, but the transporters are not completely selective. Under circumstances that elevate extracellular 5-HT (such as treatment with antidepressants that block SERTs), DATs expressed on the dense DA terminals of the striatum uptake 5-HT. Subsequently, 5

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The Dual Glutamatergic/GABAergic Phenotype of Hippocampal Granule Cells,s simultaneously produces responses mediated by glutamate and GABA receptors in their postsynaptic cells. In the adult, the markers of the GABAergic phenotype and as a consequence, GABAergic transmission disappears. However, these elements can still be transiently expressed in an activity-dependent