Optogenetic versus electrical stimulation of dopamine terminals in the nucleus accumbens reveals local modulation of presynaptic release
Year: 2015
Type: article
Abstract: The nucleus accumbens is highly heterogeneous, integrating regionally distinct afferent projections and accumbal interneurons, resulting in diverse local microenvironments. Dopamine (DA) neuron terminals similarly express a heterogeneous collection of terminal receptors that modulate DA signaling. Cyclic voltammetry is often used to probe DA terminal dynamics in brain slice preparations; however, this method traditionally requires electrical stimulation to induce DA release. Electrical stimulation excites all of the neuronal processes in the stimulation field, potentially introducing simultaneous, multi‐synaptic modulation of DA terminal release. We used optogenetics to selectively stimulate DA terminals and used voltammetry to compare DA responses from electrical and optical stimulation of the same area of tissue around a recording electrode. We found that with multiple pulse stimulation trains, optically stimulated DA release increasingly exceeded that of electrical stimulation. Furthermore, electrical stimulation produced inhibition of DA release across longer duration stimulations. The GABAB antagonist, CGP 55845, increased electrically stimulated DA release significantly more than light stimulated release. The nicotinic acetylcholine receptor antagonist, dihydro‐β‐erythroidine hydrobromide, inhibited single pulse electrically stimulated DA release while having no effect on optically stimulated DA release. Our results demonstrate that electrical stimulation introduces local multi‐synaptic modulation of DA release that is absent with optogenetically targeted stimulation. image The nucleus accumbens is highly heterogeneous, integrating regionally distinct afferent projections and accumbal interneurons, resulting in diverse microenvironments. Local electrical stimulation excites all of the neuronal processes in the stimulation field, potentially modulating the dopamine signal ‐ measured using cyclic voltammetry. Optogenetically targeting light stimulation to dopamine terminals (blue) reduces the cholinergic and GABAergic modulatory effects on stimulated dopamine release.
Source: Journal of Neurochemistry
DOI: 10.1111/jnc.13177
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: green
Awards: G1611948964, Translational Studies on Early-life Stress and Vulnerability to Alcohol Addiction, Center for the Neurobiology of Addiction Treatment, nAChR sensitivity and individual differences in drug abuse vulnerability, G7565021924, Animal Models of Cocaine Addiction, G9000034230, G9000134263, G9000156666, Multidisciplinary Training in the Biology of Alcohol Addiction, Alcohol/Stress Effects on Kappa Opioid Receptors in the Amygdala and Accumbens
OpenAlex ID: W1506576978
