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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 34 (1979), S. 575-590 
    ISSN: 1432-1106
    Keywords: Neostriatum slices ; Field potentials ; Action potentials ; EPSPs ; Intrinsic excitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Field potentials, extracellular unitary discharges and intracellular potentials evoked by intrastriatal stimulation were recorded from slices (thickness 200–400 μm) of rat neostriatum maintained in an artificial medium. The field potentials consisted of two negative waves appearing at latencies of 0.5–1.5 ms (N-1) and 2–4 ms (N-2). Extracellular unitary records showed two types of discharges, one with short but constant latencies at threshold level stimulation and the other with longer and variable latencies. In intracellular recordings the late discharge was seen to arise from EPSPs. Based on the intra- and extracellular unitary records, N-1 was identified as the population spike of antidromically or directly activated unitary discharges and N-2 as that of orthodromically activated discharges. This interpretation was substantiated by the fact that the N-2 potential was blocked in a perfusion medium containing a lower Ca++ or a higher Mg++ concentration than the standard solution. Neither interruption of ascending neostriatal inputs nor decortication 14 days prior to recording altered the configuration of the locally evoked potentials or the probability of synaptically driven discharge occurrence. Thus by intrastriatal stimulation, neostriatal neurons are activated antidromically or directly and/or orthodromically through intrinsic excitatory synapses. Since the intracellular recordings showed that neostriatal neurons can be well preserved, this preparation can be regarded as a useful tool for electrophysiological and neuropharmacological investigations on intrinsic excitatory processes in the neostriatum.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 41 (1981), S. 247-255 
    ISSN: 1432-1106
    Keywords: Hippocampal slice ; Ultrastructure ; Mossy fiber synapses
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 0.2 to 0.4 mm thick slices of guinea pig hippocampus were studied morphologically after varying periods of incubation at 36 ° C in Krebs-Ringer solution. Prior to fixation, the slices were tested for the presence of synaptically driven discharges of CA 3 neurons following mossy fiber (mf) stimulation because tissue preservation was satisfactory only in slices in which electrical responses were obtained. The fine structure of the mf layer in slices was compared with the ultrastructure of this region in hippocampal tissue fixed by transcardial perfusion or immersion of the tissue in the fixative. In the central part of the slices many intact neuronal structures of the mf layer could be seen even after 4 h of incubation. In the outer parts of the slices, neurons were swollen and vacuolated. These alterations were not observed in hippocampal tissue fixed by transcardial perfusion or by immersion. In all parts of the slices dark neurons and processes were found. Since dark neurons were also numerous in tissue blocks immersed in the fixative but were rare in perfused material, these changes were obviously caused by damage to unfixed tissue and fixation by immersion.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 37 (1979), S. 217-229 
    ISSN: 1432-1106
    Keywords: CA 3 ; Postactivation potentiation ; Longlasting ; EPSP/IPSP Changes ; Heterosynaptic potentiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary CA 3 neurons were excited synaptically by stimulation in the dentate hilus and the stratum radiatum of CA 1 in guinea pig hippocampal slices. Following repetitive stimulation (10–20 c/s, 10 s) of either stimulation site, the amplitudes of orthodromic population spikes or the probability of unitary discharges increased. Changes of the intracellularly recorded potentials were either (a) increased EPSP amplitudes associated with decreased IPSP amplitudes, or (b) increased IPSP amplitudes. A cell showing enhanced IPSPs after repetitive activation could respond with increased EPSP amplitudes and decreased IPSP amplitudes upon further repetitive activation. The potentiation, which was always preceded by a 5–10 min depression, lasted up to 3 h. This potentiation was heterosynaptic, since the responses to the non-stimulated input also changed and since the inputs were found to excite the pyramidal cells through separate synapses in double shock experiments. The heterosynaptic mode of the potentiation as well as the changes of the IPSPs indicate that not only the excitatory pathway but also the inhibitory pathway must be considered in explaining postactivation potentiation in this hippocampal field.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 39 (1980), S. 401-409 
    ISSN: 1432-1106
    Keywords: Intrinsic cholinergic excitation ; Nicotinic receptors ; Fast excitation ; Muscarinic receptors ; Slow excitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary An in vitro slice technique was employed to study the receptors involved in intrinsic cholinergic excitation in the rat neostriatum. The locally evoked synaptic potentials were suppressed by antinicotinic agents, mecamylamine (10 μM), d-tubocurarine (3 μM) or hexamethonium (100 μM), but not by the antimuscarinic agent atropine (100 μM). If the slices were exposed to an acetylcholinesterase (AChE)-inhibitor (paraoxon 1–20 μM, physostigmine 0.1–0.5 μM), the synaptic potentials were potentiated. The amplitude of the orthodromic population spike increased, and it was further facilitated when the stimulus frequencies were raised from 1–3 Hz to 10–30 Hz. The frequency facilitation following exposure to an AChE-inhibitor was blocked by atropine (1–100 μM). Intracellular recording indicated that a slow depolarizing potential caused the frequency potentiation of the orthodromic discharges. Apparently rat neostriatum is similar to cholinergic systems in sympathetic ganglia and spinal Renshaw cells, in that nicotinic receptors mediate fast excitation and muscarinic receptors mediate slow excitation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 45 (1982), S. 108-114 
    ISSN: 1432-1106
    Keywords: Neostriatal slices ; Depolarizing IPSPs ; Pentobarbital ; 4-aminopyridine ; GABA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In neostriatal slices pretreated with sodium pentobarbital (100 μM) and 4-aminopyridine (50 μM), intrastriatal stimulation elicited EPSPs followed by a slowly decaying depolarization which lasted about 200 ms and was associated with a membrane conductance increase and a suppression of spike potentials. This depolarizing inhibitory synaptic action could be blocked by picrotoxin (50 μM) or bicuculline (50 μM). The reversal potential for the slowly decaying depolarization was −57 to −62 mV, i.e. it was positive with respect to the resting membrane potential (¯x = −67 mV). GABA, injected into the tissue in the vicinity of the recording electrode by pressure application, or added to the perfusate (10 μM−1 mM), depolarized the cells and reduced both the membrane resistance and the amplitude of EPSPs. The reversal potential of GABA depolarization was found in a potential range approximating that of the slowly decaying depolarization. These results are compatible with the assumption that GABA is the transmitter of an intrinsic inhibition in rat neostriatum, but indicate that GABA-mediated IPSPs of neostriatal cells in vitro are depolarizing at the resting membrane potential. The possible reasons for this are discussed.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 733 (1994), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    European journal of neuroscience 3 (1991), S. 0 
    ISSN: 1460-9568
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Single electrode current clamp and voltage clamp recordings were employed to study the effects of noradrenergic agonists and a cholinergic agonist (carbachol, Cch) on the resting membrane potential of CA3 neurons in guinea pig hippocampal slices. Stimulation of muscarinic and β-adrenergic receptors depolarized, and stimulation of α1-adrenergic receptor hyperpolarized, CA3 neurons but the membrane potential changes were small. Hyperpolarizations or outward currents induced by baclofen, adenosine or serotonin (5-HT) were strongly potentiated by α-noradrenergic agonists and suppressed by Cch at concentrations ten times lower than those having any direct effects on membrane potential. Both the enhancement of the baclofen-induced hyperpolarization by phenylephrine and its suppression by Cch were pronounced at low concentrations of baclofen, but diminished at higher concentrations. The modulatory effects persisted after blockade of sodium spikes by tetrodotoxin and after blockade of fast inhibitory and excitatory synaptic transmission by picrotoxin and 6-cyano-7-nitroquinoxaline-2,3-dione. Our data suggest that, through the postsynaptic interaction with ligands activating potassium conductance, noradrenergic and muscarinic receptor stimulation can exert a stronger inhibitory and excitatory effect on CA3 pyramidal neurons at their resting membrane potential than would be expected from the changes in membrane potential induced by these neuromodulators on their own.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 416 (1990), S. 247-253 
    ISSN: 1432-2013
    Keywords: Medulla oblongata ; Chemoreceptor ; Extracellular pH ; Hypoxia ; Hypercapnia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effects of extracellular pH changes on neurons in slices of the rat ventral medulla oblongata were investigated by extracellular recording. Changes in discharge rate were correlated with pH changes in the tissue next to the recorded cell, as measured by H+-selective microelectrodes. pH was altered by varying the bicarbonate concentration ([HCO3 −]) in the superfusion solution. In 136 out of 316 neurons, the number of spontaneous or electrically evoked discharges per unit time increased with decreasing pH and decreased with increasing pH. Changes of only 0.01–0.04 pH unit were effective in these pH-sensitive neurons. The response was transient; the discharge rate returned to the control value within a few minutes. The pH sensitivity persisted in the presence of 0.5 μM atropine, 20 μM bicuculline and after replacing Ca2+ by Mg2+ in the superfusion solution to reduce synaptic transmission. The response to the same pH decrease was stronger when increasing PCO2 than when reducing [HCO3 −]0. The pH-induced response significantly increased during hypoxia. The results show that in the ventral medulla oblongata neurons exist that transiently respond to small decreases and increases of pH. The pH sensitivity is an intrinsic property of these neurons; it is not due to a synaptic mechanism but is modulated by PCO2 and PO2.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 407 (1986), S. 482-487 
    ISSN: 1432-2013
    Keywords: Neostriatal slice ; Ca-spike ; Acetylcholine ; Carbachol ; Physostigmine ; Atropine ; Barium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Intracellular recording from neostriatal neurons in rat brain slices revealed effects of the acetylcholine (ACh) agonist carbachol (Cch, 1–10 μmol/l), of the anticholinesterase physiostigmine (10 μmol/l) and of the muscarinic antagonist atropine (10 μmol/l) on plateau potentials elicited in the presence of K-blockers were Cadependent, elicited in the presence of K-blockers were Cadependent, since they persisted in Na-free solution, were resistant to tetrodotoxin (TTX, 3 μmol/l) and blocked by Cd (0.1–0.5 mmol/l). Cch reduced the duration of the plateau potentials and made them more susceptible to fatigue. These effects were antagonized by atropine (1–10 μmol/l), but not by Ba (100–200 μmol/l) or 4-aminopyridine (4-AP, 0.5 mmol/l). Physostigmine (10 μmol/l) had the same atropine-sensitive effects as Cch on the plateau potential. Atropine (10 μmol/l), by itself, prolonged the duration of the plateau potential. High concentrations (100 μmol/l) of Cch did not further reduce the duration of the plateau potential, instead, the duration re-increased with prolonged exposure. The re-increase of the plateau-spike duration was later masked by bursting activity. The opposing effects of low and high concentrations of Cch on the plateau potential duration corresponded to effects of this drug on intrastriatally evoked EPSPs in that low concentrations of Cch reduced the EPSP amplitude, but high concentrations re-increased it after a transient decrease. It is concluded that the muscarinic effect of Ach in the neostriatum is to modulate Ca-influx and that this effect is exerted in a tonic manner.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 414 (1989), S. 139-144 
    ISSN: 1432-2013
    Keywords: GABAB-receptor ; Baclofen ; Inhibition ; GABAA-receptor ; Inhibitory neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Intracellular recordings were made from electrophysiologically identified inhibitory neurons in the dentate hilus. (−)Baclofen (0.1–0.5 μmol/l), applied by the bath, strongly hyperpolarized inhibitory neurons, reduced their input resistance and induced outward currents under voltage clamp at holding potential of −60 mV in cells recorded with KCl-filled electrodes. Increasing the (−)baclofen concentration (up to 1 μmol/l) did not increase the amplitude of the outward current, but increased its duration. (−)Baclofen depressed Cl-dependent IPSPs evoked by perforant path stimulation in inhibitory neurones, granule cells and CA3 neurons. In the case of inhibitory neurons and CA3 neurons, depression of IPSPs, membrane hyperpolarization and increase in membrane conductance concurred. All effects were blocked by BaCl2 (1 mmol/l) in the superfusate. In the case of granule cells, depression of IPSPs by (−)balcofen out-lasted an only small membrane hyperpolarization, conductance increase or outward current. High concentrations (up to 10 μmol/l) of (−)baclofen depressed evoked IPSPs of granule cells for an extended period of time, but the other effects remained small and transient. IPSPs elicited in granule cells by microdrop application of glutamate to the dentate hilus were also blocked by (−)baclofen, but spontaneous IPSPs were only reduced in amplitude. We suggest that the blockade of GABAA receptor-mediated IPSPs of hippocampal neurons by the GABAB receptor agonist (−)baclofen can be explained by a K-dependent hyperpolarization of inhibitory neurons.
    Type of Medium: Electronic Resource
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