We have investigated by immunohistochemistry the cellular and subcellular distribution of the D1 dopamine receptor (D1R) in the rat striatonigral complex and its relation with the dopaminergic innervation. In the striatum, single pre-embedding immunoperoxidase and immunogold labeling demonstrate that D1R is mainly located on dendritic shafts and spines of spiny dendrites. D1R is also found in association with the plasma membrane of half of the perikarya of medium spiny neurons. Double labeling experiments allowing the simultaneous detection of D1R and of tyrosine hydroxylase (TH) demonstrate that D1R distribution does not match dopamine innervation: a majority of the receptors is located at sites distant from dopamine profiles and there is no significant D1R enrichment at sites of membrane appositions between dopamine and D1R profiles. In the substantia nigra, D1R is located at pre-synaptic sites on small diameter axons which are not in contact with TH-positive elements, and on terminal boutons forming symmetrical synapses on TH-positive or negative dendrites. These data demonstrate abundance and wide distribution of D1R at various extrasynaptic sites in the striatum and the substantia nigra, bringing strong evidence of anatomical basis for dopamine non-synaptic volume transmission in the rat striatonigral complex.
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http://dx.doi.org/10.1016/0006-8993(96)00424-6 | DOI Listing |
J Neurosci Res
January 2025
Departamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de Mexico, Mexico.
Lateralization of motor behavior, a common phenomenon in humans and several species, is modulated by the basal ganglia, a site pointed out for the interhemispheric differences related to lateralization. Our study aims to shed light on the potential role of the striatonigral D1 receptor in functional asymmetry in normal conditions through neurochemical and behavioral means. We found that D1 receptor activation and D1/D3 receptor coactivation in striatonigral neurons leads to more cAMP production by adenylyl cyclase in the striatum and GABA release in their terminals in the right hemisphere compared to the left.
View Article and Find Full Text PDFWe present an enhancer AAV toolbox for accessing and perturbing striatal cell types and circuits. Best-in-class vectors were curated for accessing major striatal neuron populations including medium spiny neurons (MSNs), direct and indirect pathway MSNs, as well as Sst-Chodl, Pvalb-Pthlh, and cholinergic interneurons. Specificity was evaluated by multiple modes of molecular validation, three different routes of virus delivery, and with diverse transgene cargos.
View Article and Find Full Text PDFBrain Res Bull
January 2023
Ribeirão Preto Medical School of the University of São Paulo (FMRP-USP), Department of Pharmacology, Laboratory of Neuroanatomy and Neuropsychobiology, Ribeirão Preto, São Paulo, Brazil; Behavioural Neuroscience Institute (INeC), Ribeirão Preto, São Paulo, Brazil; NAP-USP-Neurobiology of Emotions Research Centre (NuPNE), Ribeirão Preto Medical School of the University of São Paulo, Ribeirão Preto, São Paulo, Brazil. Electronic address:
Rationale: Several lines of evidence have demonstrated that the cannabinoid type 1 receptor (CB) is found in the caudate nucleus and putamen (CPu) in addition to the substantia nigra pars reticulata (SNpr). Here, we investigated the role of endocannabinoid neuromodulation of striato-nigral disinhibitory projections on the activity of nigro-collicular GABAergic pathways that control the expression of unconditioned fear-related behavioural responses elicited by microinjections of the GABA receptor selective antagonist bicuculline (BIC) in the deep layers of the superior colliculus (dlSC).
Methods: Fluorescent neural tract tracers were deposited in either CPu or in SNpr.
J Neurosci
January 2023
Department of Pharmacology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain
In rodents, cortical information is transferred to the (SNr) through motor and medial prefrontal (mPF) basal ganglia (BG) circuits implicated in motor and cognitive/motivational behaviors, respectively. The serotonergic 5-HT receptors are located in both of these neuronal networks, displaying topographical differences with a high expression in the associative/limbic territories, and a very low expression in the subthalamic nucleus. This study investigated whether the stimulation of 5-HT receptors could have a specific signature on the dynamic regulation of BG circuits, preferentially modulating the mPF information processing through trans-striatal pathways.
View Article and Find Full Text PDFSynapse
September 2022
Departamento de Fisiología, Biofísica y Neurociencias. Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Mexico City, Mexico.
Striatal medium-sized spiny neurons express mRNA and protein of GPR55 receptors that stimulate neurotransmitter release; thus, GPR55 could be sent to nigral striatal projections, where it might modulate GABA release and motor behavior. Here, we study the presence of GPR55 receptors at striato-nigral terminals, their modulation of GABA release, their signaling pathway, and their effect on motor activity. By double immunohistochemistry, we found the colocation of GPR55 protein and substance P in the dorsal striatum.
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