Matches in SemOpenAlex for { <https://semopenalex.org/work/W2134579073> ?p ?o ?g. }
- W2134579073 endingPage "410" @default.
- W2134579073 startingPage "397" @default.
- W2134579073 abstract "Burst firing of dopaminergic neurons of the substantia nigra pars compacta can be induced in vitro by the glutamate agonist N-methyl-d-aspartate. It has been suggested that the interburst hyperpolarization is due to Na+ extrusion by a ouabain-sensitive pump [Johnson et al. (1992)Science258, 665–667]. We formulate and explore a theoretical model, with a minimal number of currents, for this novel mechanism of burst generation. This minimal model is further developed into a more elaborate model based on observations of additional currents and hypotheses about their spatial distribution in dopaminergic neurons [Hounsgaard (1992)Neuroscience50, 513–518; Llinás et al. (1984)Brain Res.294, 127–132]. Using the minimal model, we confirm that interaction between the regenerative, inward N-methyl-d-aspartate-mediated current and the outward Na+-pump current is sufficient to generate the slow oscillation (∼0.5 Hz) underlying the burst. The negative-slope region of the N-methyl-d-aspartate channel's current-voltage relation is indispensable for this slow rhythm generation. The time-scale of Na+-handling determines the burst's slow frequency. Moreover, we show that, given the constraints of sodium handling, such bursting is best explained mechanistically by using at least two spatial, cable-like compartments: a soma where action potentials are produced and a dendritic compartment where the slow rhythm is generated. Our result is consistent with recent experimental evidence that burst generation originates in distal dendrites [Seutin et al. (1994)Neuroscience58, 201–206]. Responses of the model to a number of electrophysiological and pharmacological stimuli are consistent with known responses observed under similar conditions. These include the persistence of the slow rhythm when the tetrodotoxin-sensitive Na+ channel is blocked and when the soma is voltage-clamped at −60 mV. Using our more elaborate model, we account for details of the observed frequency adaptation in N-methyl-d-aspartate-induced bursting, the origin of multiple spiking and bursting mechanisms, and the interaction between two different bursting mechanisms. Besides reproducing several well established firing patterns, this model also suggests that new firing modes, not yet recorded, might also occur in dopaminergic neurons. This model provides mechanistic insights and explanations into the origin of a variety of experimentally observed membrane potential firing patterns in dopaminergic neurons, including N-methyl-d-aspartate-induced bursting and its dendritic origin. Such a model, capable of reproducing a number of realistic behaviors of dopaminergic neurons, could be useful in further studies of the basal ganglia-thalamocortical motor circuit. It may also shed light on bursting that involves N-methyl-d-aspartate channel activity in other neuron types." @default.
- W2134579073 created "2016-06-24" @default.
- W2134579073 creator A5035615115 @default.
- W2134579073 creator A5061116254 @default.
- W2134579073 creator A5089830202 @default.
- W2134579073 date "1996-03-01" @default.
- W2134579073 modified "2023-10-15" @default.
- W2134579073 title "Modeling N-methyl-d-aspartate-induced bursting in dopamine neurons" @default.
- W2134579073 cites W1014586844 @default.
- W2134579073 cites W1533559637 @default.
- W2134579073 cites W1633847368 @default.
- W2134579073 cites W1840984304 @default.
- W2134579073 cites W1940417817 @default.
- W2134579073 cites W1949404224 @default.
- W2134579073 cites W1964294610 @default.
- W2134579073 cites W1982669777 @default.
- W2134579073 cites W1985940938 @default.
- W2134579073 cites W1989176150 @default.
- W2134579073 cites W1994349958 @default.
- W2134579073 cites W1999633713 @default.
- W2134579073 cites W2005452816 @default.
- W2134579073 cites W2006110610 @default.
- W2134579073 cites W2009084101 @default.
- W2134579073 cites W2009809272 @default.
- W2134579073 cites W2010359145 @default.
- W2134579073 cites W2015440166 @default.
- W2134579073 cites W2022917563 @default.
- W2134579073 cites W2024246914 @default.
- W2134579073 cites W2027327558 @default.
- W2134579073 cites W2040129962 @default.
- W2134579073 cites W2052436943 @default.
- W2134579073 cites W2060317741 @default.
- W2134579073 cites W2067467155 @default.
- W2134579073 cites W2068342573 @default.
- W2134579073 cites W2069713657 @default.
- W2134579073 cites W2071812065 @default.
- W2134579073 cites W2075495671 @default.
- W2134579073 cites W2077248926 @default.
- W2134579073 cites W2081707480 @default.
- W2134579073 cites W2089151058 @default.
- W2134579073 cites W2091609447 @default.
- W2134579073 cites W2122192356 @default.
- W2134579073 cites W2258993652 @default.
- W2134579073 cites W2395686643 @default.
- W2134579073 cites W2432252618 @default.
- W2134579073 cites W4234546939 @default.
- W2134579073 cites W4251762684 @default.
- W2134579073 doi "https://doi.org/10.1016/0306-4522(95)00483-1" @default.
- W2134579073 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9053795" @default.
- W2134579073 hasPublicationYear "1996" @default.
- W2134579073 type Work @default.
- W2134579073 sameAs 2134579073 @default.
- W2134579073 citedByCount "98" @default.
- W2134579073 countsByYear W21345790732012 @default.
- W2134579073 countsByYear W21345790732013 @default.
- W2134579073 countsByYear W21345790732014 @default.
- W2134579073 countsByYear W21345790732015 @default.
- W2134579073 countsByYear W21345790732016 @default.
- W2134579073 countsByYear W21345790732017 @default.
- W2134579073 countsByYear W21345790732018 @default.
- W2134579073 countsByYear W21345790732019 @default.
- W2134579073 countsByYear W21345790732020 @default.
- W2134579073 countsByYear W21345790732021 @default.
- W2134579073 countsByYear W21345790732022 @default.
- W2134579073 countsByYear W21345790732023 @default.
- W2134579073 crossrefType "journal-article" @default.
- W2134579073 hasAuthorship W2134579073A5035615115 @default.
- W2134579073 hasAuthorship W2134579073A5061116254 @default.
- W2134579073 hasAuthorship W2134579073A5089830202 @default.
- W2134579073 hasConcept C12554922 @default.
- W2134579073 hasConcept C131453863 @default.
- W2134579073 hasConcept C137183658 @default.
- W2134579073 hasConcept C169760540 @default.
- W2134579073 hasConcept C170493617 @default.
- W2134579073 hasConcept C181911157 @default.
- W2134579073 hasConcept C185263204 @default.
- W2134579073 hasConcept C185592680 @default.
- W2134579073 hasConcept C195221683 @default.
- W2134579073 hasConcept C2776773494 @default.
- W2134579073 hasConcept C2779617337 @default.
- W2134579073 hasConcept C2780938664 @default.
- W2134579073 hasConcept C513476851 @default.
- W2134579073 hasConcept C55493867 @default.
- W2134579073 hasConcept C61174792 @default.
- W2134579073 hasConcept C66974803 @default.
- W2134579073 hasConcept C71240020 @default.
- W2134579073 hasConcept C86803240 @default.
- W2134579073 hasConceptScore W2134579073C12554922 @default.
- W2134579073 hasConceptScore W2134579073C131453863 @default.
- W2134579073 hasConceptScore W2134579073C137183658 @default.
- W2134579073 hasConceptScore W2134579073C169760540 @default.
- W2134579073 hasConceptScore W2134579073C170493617 @default.
- W2134579073 hasConceptScore W2134579073C181911157 @default.
- W2134579073 hasConceptScore W2134579073C185263204 @default.
- W2134579073 hasConceptScore W2134579073C185592680 @default.
- W2134579073 hasConceptScore W2134579073C195221683 @default.
- W2134579073 hasConceptScore W2134579073C2776773494 @default.
- W2134579073 hasConceptScore W2134579073C2779617337 @default.