Functional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine.

The dorsal striatum comprises a continuum of distinct functional domains, limbic, associative, and sensorimotor. In the primate it exclusively subdivides further into two nuclei, the putamen and caudate. Dopamine (DA) transmission is differentially affected between these nuclei in neurodegenerative...

Full description

Bibliographic Details
Main Authors: Cragg, S, Hille, C, Greenfield, S
Format: Journal article
Language:English
Published: 2002
_version_ 1826298769866489856
author Cragg, S
Hille, C
Greenfield, S
author_facet Cragg, S
Hille, C
Greenfield, S
author_sort Cragg, S
collection OXFORD
description The dorsal striatum comprises a continuum of distinct functional domains, limbic, associative, and sensorimotor. In the primate it exclusively subdivides further into two nuclei, the putamen and caudate. Dopamine (DA) transmission is differentially affected between these nuclei in neurodegenerative diseases such as Parkinson's and by psychostimulants such as cocaine. Because rodent systems can offer only limited insight into DA systems of the human brain, a fuller appreciation of DA transmission and its role in dysfunction requires direct study in primates. DA behavior was explored in the major functional domains of the caudate nucleus and compared with the putamen, using fast-scan cyclic voltammetry in striatal sections from the marmoset (Callithrix jacchus). There was domain-specific variation in extracellular DA transients [i.e., concentration ([DA](o)) released by a single stimulus and the rate maximum of DA uptake, V(max)]. Across nuclei, functional rather than anatomical regions were differentiated by these dynamics. The largest, fastest DA transients were at motor-associated loci. Evoked [DA](o) at physiological frequencies was differently frequency-sensitive between functional domains but not between anatomical nuclei. In contrast, presynaptic depression was not an index of regional differentiation, recovering with similar kinetics at all loci. Within a given functional domain of dorsal striatum, the dynamics of DA release and uptake are similar for the putamen and the caudate nucleus. Conversely, distinct functional domains are defined by these DA dynamics, in a manner more marked in primates than in rodents. These data from the primate brain highlight differences in DA availability that may be central to DA function and dysfunction in the human.
first_indexed 2024-03-07T04:51:52Z
format Journal article
id oxford-uuid:d53df99b-c80f-4904-ba49-309752262002
institution University of Oxford
language English
last_indexed 2024-03-07T04:51:52Z
publishDate 2002
record_format dspace
spelling oxford-uuid:d53df99b-c80f-4904-ba49-3097522620022022-03-27T08:24:34ZFunctional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d53df99b-c80f-4904-ba49-309752262002EnglishSymplectic Elements at Oxford2002Cragg, SHille, CGreenfield, SThe dorsal striatum comprises a continuum of distinct functional domains, limbic, associative, and sensorimotor. In the primate it exclusively subdivides further into two nuclei, the putamen and caudate. Dopamine (DA) transmission is differentially affected between these nuclei in neurodegenerative diseases such as Parkinson's and by psychostimulants such as cocaine. Because rodent systems can offer only limited insight into DA systems of the human brain, a fuller appreciation of DA transmission and its role in dysfunction requires direct study in primates. DA behavior was explored in the major functional domains of the caudate nucleus and compared with the putamen, using fast-scan cyclic voltammetry in striatal sections from the marmoset (Callithrix jacchus). There was domain-specific variation in extracellular DA transients [i.e., concentration ([DA](o)) released by a single stimulus and the rate maximum of DA uptake, V(max)]. Across nuclei, functional rather than anatomical regions were differentiated by these dynamics. The largest, fastest DA transients were at motor-associated loci. Evoked [DA](o) at physiological frequencies was differently frequency-sensitive between functional domains but not between anatomical nuclei. In contrast, presynaptic depression was not an index of regional differentiation, recovering with similar kinetics at all loci. Within a given functional domain of dorsal striatum, the dynamics of DA release and uptake are similar for the putamen and the caudate nucleus. Conversely, distinct functional domains are defined by these DA dynamics, in a manner more marked in primates than in rodents. These data from the primate brain highlight differences in DA availability that may be central to DA function and dysfunction in the human.
spellingShingle Cragg, S
Hille, C
Greenfield, S
Functional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine.
title Functional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine.
title_full Functional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine.
title_fullStr Functional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine.
title_full_unstemmed Functional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine.
title_short Functional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine.
title_sort functional domains in dorsal striatum of the nonhuman primate are defined by the dynamic behavior of dopamine
work_keys_str_mv AT craggs functionaldomainsindorsalstriatumofthenonhumanprimatearedefinedbythedynamicbehaviorofdopamine
AT hillec functionaldomainsindorsalstriatumofthenonhumanprimatearedefinedbythedynamicbehaviorofdopamine
AT greenfields functionaldomainsindorsalstriatumofthenonhumanprimatearedefinedbythedynamicbehaviorofdopamine