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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 17 (1973), S. 190-205 
    ISSN: 1432-1106
    Keywords: K+ specific microelectrodes ; Extracellular space ; Diffusion in brain tissue ; Cortical DC potentials
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Steady state and transient values of intracortical potassium were measured with K+ sensitive microelectrodes. Resting intracortical K+ activity is low and resembles that of cerebrospinal fluid. Elevation of intracortical K+ was brought about by electrophoretic injection of K+ by a constant current source from a KCl containing micropipette at fixed distances from the recording electrode. The intracortical K+ responses to electrophoretic K+ injection were compared with those in a medium of 150 mM/l NaCl plus 3 mM/l KCl. The dependence of intracortical K+ steady state levels on electrophoretic currents is nearly linear, but the K+ response in the cortex was about six times higher than in saline. Half times (T1/2) of the rising and falling phases of K+ during current steps were found to be prolonged by the same degree in the cortex. The distribution of [K+]0 appears to be dominated by free diffusion with an apparent diffusion coefficient of 1/6 that in the medium. Primarily diffusional redistribution may also apply to K+ which is released by direct cortical stimulation. K+ released by brief stimulation distributes faster than K+ during and after prolonged continuous stimulation with average T1/2 of 1.2 and 3.0 sec respectively in accordance with diffusion from instantaneous and continuous point sources. For small [K+]0 changes, deviations from diffusional kinetics were found to be about one-fifth of absolute [K+]0 values and became predominant at times longer than 10 T1/2. They can be ascribed to K+ uptake mechanisms. DC recorded cortical surface potentials reveal close relations to the slopes of intracortical potassium activity.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Extracellular space ; Na+ and Cl− concentration ; Effects of metabolism on osmolarity ; Epilepsy ; Cerebral cortex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Extracellular Na+- and Cl−-concentrations ([Na+]o, [Cl−]o) were recorded with ion-selective microelectrodes during repetitive stimulation and stimulus-induced self-sustained neuronal afterdischarges (SAD) in the sensorimotor cortex of cats. In all cortical layers [Na+]o initially decreased by 4–7 mM. In depths of more than 600 μm below the cortical surface such decreases usually turned into increases of 2–6 mM during the course of the SADs, whereas in superficial layers [Na+]o never rose above its resting level. [Cl−]o always showed an increase in the course of the SADs often preceded by an initial small decrease. The average increase at a depth of 1,000 μm was about 7 mM. [Cl−]o reached peak values at about the end of the ictal period, whereas [Na+]o reached its maximum shortly after the end of the SAD, at times when [K+]o was still elevated above the baseline concentration. These data indicate that the extracellular osmolarity can increase during SAD by up to 30 mM. Such an increase in osmolarity can be explained by an increase in the number of intracellular particles, caused by cleavage of larger molecules during enhanced metabolism. This could lead to cell-swelling due to passive water influx from the extracellular space (ES). However, the resulting reduction of the size of the ES is calculated to be less than 10% for an increase in intracellular osmolarity by 30 mOsm. This value is too small as compared to previously measured ES-reductions under similar conditions (i.e., 30% reduction at 1,000 μm; Dietzel et al. 1980). Reductions of the size of the ES that accompany the observed changes in the ionic environment, are quantitatively explained on the basis of the extended glial buffering mechanism described in the preceding paper.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 11 (1970), S. 431-447 
    ISSN: 1432-1106
    Keywords: Ammonium ; Postsynaptic inhibition ; Motoneuronal potentials ; Microelectrode iontophoresis ; Spinal cord
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Potential changes were investigated which follow the intra- and extracellular electrophoretic injection of NH4 + and also the intravenous application of neutral ammonium salts. The common effect found in all kinds of application is a depolarizing shift of the IPSP-equilibrium potential (EIPSP) towards the resting potential. Inhibitory transmission is preserved but produces considerably reduced hyperpolarizing potential changes at normal resting potentials. In addition, ammonium ions produce short term shifts of resting and overshoot potentials with intracellular application. The latter changes can be explained under the assumption that NH4 + partly substitutes for Na+ as for the action potential generation. The observed reversible reduction of EIPSP has high sensitivity towards extracellular and systemic NH4 + application as compared to intracellular injection. The time course of the depolarizing shift of EIPSP, especially its restitution, was shortest in extracellular application. It is suggested that ammonium release from the internal site produces the long term effects observed on the IPSP after intracellular injection. The externally effective dosages correspond to intracerebral NH4 +-concentrations which are reported for preconvulsive states of various kinds of metabolically induced epilepsies.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1106
    Keywords: Axonal flow ; Excitation ; Single-cell-injection ; Autoradiography ; Cat Motoneurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Tritiated glycine has been injected intracellularly into cat motoneurons by means of cross barrel iontophoresis through microelectrodes. The amino acid is incorporated into proteins in the cell body and the synthesized radioactive proteins have been localized by autoradiography. The single-cell-injection technique has several advantages over the usual intraperitoneal, intravenous or intrathecal injection, e.g. distribution of the radiochemical is strictly confined to the injected neuron; the amount of injected substance can be estimated; it is easy to investigate simultaneously electrophysiological and morphological characteristics of a defined neuron. Since the injected cell body releases radioactive proteins into the axon, the transport of these substances can be studied under various conditions. In this study the influence of antidromic stimulation has been studied. Stimulated motoneurons demonstrate higher radioactivity in their cell bodies than unstimulated ones, reflecting an increased protein synthesis. The differences are even more pronounced in the axons of stimulated cells when compared with unstimulated ones. A significant, higher amount of radioactive material — up to 100% increase as demonstrated by silver grain counting — can be seen in the axons of stimulated neurons. Although considerable differences seem to exist for the quantity of the exported proteins no significant differences have been detected for the velocity of transportation. In axons of stimulated and unstimulated neurons proteins advance toward the periphery at the same rate.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 27 (1977), S. 237-243 
    ISSN: 1432-1106
    Keywords: Ca++ selective microelectrodes ; Ca++ activity ; K+ activity ; Seizure ; Cerebral cortex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Extracellular calcium and potassium activities (aCa and aK) as well as neuronal activity were simultaneously recorded with ion-sensitive electrodes in the somatosensory cortex of cats. Baseline aCa was 1.2–1.5 mM/1, baseline a k 2.7–3.2 mM/1. Transient decreases in aCa and simultaneous increases in aK were evoked by repetitive stimulation of the contralateral forepaw, the nucleus ventroposterolateralis thalami and the cortical surface. Considerable decreases in aCa (by up to 0.7 mM/1) were found during seizure activity. A fall in aCa preceded the onset of paroxysmal discharges and the rise in aK after injection of pentylene tetrazol. The decrease in aCa led also the rise in aK during cyclical spike driving in a penicillin focus. It is concluded that alterations of Ca++ dependent mechanisms participate in the generation of epileptic activity.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1106
    Keywords: Extracellular space ; K+ regulation ; Spatial K+ buffering ; Epilepsy ; Cerebral cortex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The time course of local changes of the extracellular space (ES) was investigated by measuring concentration changes of repeatedly injected tetramethylammonium (TMA+) and choline (Ch+) ions for which cell membranes are largely impermeable. After stimulus-induced extracellular [K+] elevations the δ[TMA+] and δ[Ch+] signals recorded with nominally K+-selective liquid ion-exchanger microelectrodes increased by up to 100%, thus indicating a reduction of the ES down to one half of its initial size. The shrinkage was maximal at sites where the K+ release into the ES was also largest. At very superficial and deep layers, however, considerable increases in extracellular K+ concentration were not accompanied by significant reductions in the ES. These findings can be explained as a consequence of K+ movement through spatially extended cell structures. Calculations based on a model combining the spatial buffer mechanism of Kuffler and Nicholls (1966) to osmolarity changes caused by selective K+ transport through primarily K+ permeable membranes support this concept. Following stimulation additional iontophoretically induced [K+]o rises were reduced in amplitude by up to 35%, even at sites where maximal decreases of the ES were observed. This emphasizes the importance of active uptake for K+ clearance out of the ES.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    European biophysics journal 13 (1986), S. 259-271 
    ISSN: 1432-1017
    Keywords: Sodium channels ; patch-clamp ; sensory neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Physics
    Notes: Abstract Isolated Na currents were studied in cultured chick sensory neurons using the patch clamp technique. On membrane depolarization, whole cell currents showed the typical transient and voltage-dependent time course as in nerve fibres. Na currents appeared at about-40 mV and reached maximum amplitude at around-10 mV. At low voltages (-30 to 0 mV), their turning-on was sigmoidal and inactivation developed exponentially. The ratio of inactivation time constants was found to be smaller than in squid axons and comparable to that of mammalian nodes of Ranvier. Peak conductance and steady-state inactivation were strongly voltage-dependent, with maximum slopes at-17 and-40 mV, respectively. The reversal potential was close to the Nernst equilibrium potential, indicating a high degree of ion-selectivity for the channel. Addition of 3μM TTX, or replacement of Na by Choline in the external bath, abolished these currents. Internal pronase (1 mg/ml) and N-bromoacetamide (0.4 mM) made inactivation incomplete, with little effect on its rate of decay. Single Na channel currents were studied in outside-out membrane patches, at potentials between-50 and-20 mV. Their activation required large negative holding potentials (-90 mV). They were fully blocked by addition of TTX (3 μM) to the external bath. At-40 mV their mean open time was about 2ms and the amplitude distribution could be fitted by a single Gaussian curve, indicating the presence of a homogeneous population of channels with a conductance of 11±2 pS. Probability of opening increased and latency to first opening decreased with increasing depolarization. Inactivation of the channel became faster with stronger depolarizations, as measured from the inactivation time course of sample averages. Internal pronase (0.1 mg/ml) produced effects on inactivation comparable to those on whole cell currents. Openings of the channel had a tendency to occur in bursts and showed little inactivation during pulses of 250 ms duration. The open lifetime of the channel at low potentials (-50,-40 mV) was only three times larger than in control patches, suggesting that Na channels in chick sensory neurons can close several times before entering an inactivating absorbing state.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 560 (1989), 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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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 560 (1989), 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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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 250 (1974), S. 574-576 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Experiments were performed on two bursting pacemaker neurones in the right parietal ganglion5. One of these produces no fast outward current6?9 and is therefore useful as a control for possible artefacts due to activation or inactivation of an additional outward current. Electrodes of 2?20 ??, ...
    Type of Medium: Electronic Resource
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