Navigation überspringen
Universitätsbibliothek Heidelberg
Status: Bibliographieeintrag

Verfügbarkeit
Standort: ---
Exemplare: ---
heiBIB
 Online-Ressource
Verfasst von:Swandulla, Dieter [VerfasserIn]   i
 Misgeld, Ulrich [VerfasserIn]   i
Titel:Development and properties of synaptic mechanisms in a network of rat hypothalamic neurons grown in culture
Verf.angabe:D. Swandulla and U. Misgeld
E-Jahr:1990
Jahr:01 Sep 1990
Umfang:14 S.
Teil:volume:64
 year:1990
 number:3
 pages:715-726
 extent:14
Fussnoten:Gesehen am 08.04.2021
Titel Quelle:Enthalten in: Journal of neurophysiology
Ort Quelle:Bethesda, Md. : Soc., 1938
Jahr Quelle:1990
Band/Heft Quelle:64(1990), 3, Seite 715-726
ISSN Quelle:1522-1598
Abstract:1. Dissociated neurons from embryonic rat hypothalamus (E14-15) were cultured on a glial background monolayer for up to three months. Dendrites of cells 7-14 days in culture (DIC) intracellularly stained with the fluorescent dye Lucifer yellow were thin and smooth, and multiple growth cones could be observed. The length of the dendrites of older cells did not differ much, but dendrites were thicker and branched more profoundly, forming a complicated network. Growth cones were rare, but few spine-like protrusions could be observed. 2. Randomly occurring depolarizing potentials were recorded in 60% of the cells 7-14 DIC and in 90% of the cells 21 DIC. Activity became phasic when the gamma-aminobutyric acid (GABA) antagonists picrotoxin or bicuculline were applied. After 21 DIC the majority of the cells showed burst discharges, whereas only approximately 10% of the cells 7 DIC exhibited bursting. 3. With low [Cl] in the recording pipette, spontaneous activity consisted of hyperpolarizing and depolarizing potentials at -40-mV membrane potential. Some spontaneous activity persisted with Na channels blocked by tetrodotoxin (TTX, 0.3-1 microM), and when reducing the external [Ca]o from 5 to 0.3 mM. Picrotoxin blocked part of the activity, and the remaining activity was blocked by kynurenic acid. 4. Bursts of action potentials were superimposed on rhythmically occurring clusters of excitatory synaptic potentials (EPSPs), which had a steep rising phase and decayed within hundreds of milliseconds. Bursts of similar appearance could be triggered by brief (10 ms) depolarizing current injections, and a few cells had properties indicative for endogenous pacemakers. 5. From 7 DIC on, all cells responded to GABA and to the GABA agonist muscimol. Under voltage clamp, zero current potential depended on the Cl gradient across the membrane and corresponded to the zero current potential of picrotoxin-sensitive postsynaptic currents. 6. After 21 DIC all cells responded to glutamate and its agonist quisqualate. Under voltage clamp, nanomolar concentrations of quisqualate (100-500 nM) induced long-lasting inward currents, which did not decay substantially during prolonged drug application. Quisqualate concentrations greater than 1 microM induced a diphasic inward-current response consisting of an initial fast current transient followed by a maintained current component. With internal Cs replacing K and Na and external TTX (0.3 microM), both current components reversed sign at approximately 8 mV, as predicted by the Nernst equation for currents through channels that were permeable for monovalent cations. 7. Focal applications of GABA and muscimol elicited larger currents when applied near the soma than when applied to the dendrites.(ABSTRACT TRUNCATED AT 400 WORDS)
DOI:doi:10.1152/jn.1990.64.3.715
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1152/jn.1990.64.3.715
 Volltext: https://journals.physiology.org/doi/abs/10.1152/jn.1990.64.3.715
 DOI: https://doi.org/10.1152/jn.1990.64.3.715
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:1753329833
Verknüpfungen:→ Zeitschrift

Permanenter Link auf diesen Titel (bookmarkfähig):  https://katalog.ub.uni-heidelberg.de/titel/68721234   QR-Code
zum Seitenanfang