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1.
Gesundheitswesen ; 80(S 02): S88-S96, 2018 Mar.
Article in German | MEDLINE | ID: mdl-27006988

ABSTRACT

BACKGROUND: Men have a higher risk of mortality than women and react much more sensitively to status-related stressors. The relationship between hierarchical rank and health, mediated on the HPA axis, delivers possible explanations for the more pronounced male sensitivity. In this context, the construct of status unease has attracted a lot of attention in recent years. It links social comparison with a reduced general wellbeing and considers it to be a major risk factor for various diseases. METHODS: An analysis of secondary data from the Socio-Economic Panel (SOEP) was used to analyze the extent to which subjective dissatisfaction with one's own standard of living is associated with an increased gender-related mortality risk. The statistical modeling of the question was carried out by performing gender-disaggregated Cox proportional hazard models. The unbalanced sub-sample consisted of 6 454 men (685 deaths) and 6 908 women (618 deaths). RESULTS: Dissatisfaction with one's standard of living has a significant influence on the mortality risk of men but not women: Men with low satisfaction have nearly a twice as high risk of mortality than the reference group (HR=1,95, 95% CI 1,48-2,58), men with moderate satisfaction a 25% higher mortality risk (HR=1,26, 95% CI 1,08-1,49). Furthermore, subjective status shows stronger dose-response relationships than objective status parameters. CONCLUSION: Dissatisfaction with one's standard of living turns out to be a clear predictor for male mortality. Stress reactions due to disparaging social comparison processes triggered by the HPA-axis could be a central cause. The results indicate that the standardized inclusion of subjective status indicators should be considered in social-epidemiological analysis. The distinctive gender difference also points out that gender-sensitive epidemiological data analysis is reasonable.


Subject(s)
Financing, Personal , Hypothalamo-Hypophyseal System , Mortality , Personal Satisfaction , Stress, Psychological , Female , Germany , Humans , Male , Pituitary-Adrenal System , Sex Factors , Socioeconomic Factors
2.
Gesundheitswesen ; 75(6): 340-50, 2013 Jun.
Article in German | MEDLINE | ID: mdl-22932831

ABSTRACT

BACKGROUND: Externalising behavior problems involve a huge developmental risk potential as they can substantially interface with the parallel process of establishing and forming identity in peer groups during adolescence while simultaneously coping with expectations regarding academic achievement and behaviour. Therefore adolescents with externalising behavior constitute a potential target audience for health promotion. AIM OF THE STUDY: The purpose of this paper is to clarify in what kind of social contexts externalising behavior problems are associated with decreased subjective health in adolescence. METHOD: An analysis of secondary data from the KiGGS study (Robert Koch-Institute, 2009) was undertaken. Calculations of logistic regression models for boys and girls were performed on the basis of preceding stratifications using the indicator subjective health and including relevant social demographic factors. OUTCOME: Externalising adolescents face a higher risk of decreased subjective health than inconspicuous adolescents of the same age group, while there is a gender-specific difference (boys OR 2.76; girls OR 1.48). The gender-specific differences in subjective health appraisal found in inconspicuous adolescents cannot be verified in adolescents with externalising behaviour. Related to social demographic predictors a classic social gradient for girls is verified whereas externalising behaviour in boys is predominantly associated from high social class and decreased subjective health. In multivariate procedures a higher odds ratio for decreased subjective health becomes apparent for adolescents who ascend or descend in relation to their education level as well as for adolescents from higher social classes who had to repeat a school year. CONCLUSION: Adolescents with externalising behavior frequently rate their health situation as being bad. The fact that it is primarily boys with behavior problems and boys who are intergenerational mobile educationwise who exhibit decreased psychosocial well-being, indicates that an increased context related exclusion risk (ostracism) is an essential health risk factor. Micro-groups of adolescents facing risk of being ostracised appear to be an essential target group for prevention and health promotion which so far is not being taken into consideration on the basis of school type related recommendations.


Subject(s)
Attitude to Health , Diagnostic Self Evaluation , Health Status , Mental Disorders/epidemiology , Mental Disorders/psychology , Personal Satisfaction , Self-Assessment , Adolescent , Age Distribution , Child , Female , Germany/epidemiology , Humans , Male , Mental Disorders/diagnosis , Personal Autonomy , Prevalence , Sex Distribution , Social Behavior , Socioeconomic Factors
3.
J Neurochem ; 93(4): 812-24, 2005 May.
Article in English | MEDLINE | ID: mdl-15857385

ABSTRACT

NMDA receptors are involved in a variety of brainstem functions. The excitatory postsynaptic NMDA currents of pre-Botzinger complex interneurons and hypoglossal motoneurons, which are located in the medulla oblongata, show remarkably fast deactivation kinetics of approximately 30 ms compared with NMDA receptors in other types of neurons. Because structural heterogeneity might be the basis for physiological properties, we examined the expression of six NMDA receptor subunits (NMDAR1, NR2A-2D, and NR3A) plus eight NMDR1 splice variants in pre-Botzinger complex, hypoglossal and, for comparison, neurons from the nucleus of the solitary tract in young rats using single cell multiplex RT-PCR. Expression of NR2A, NR2B, and NR2D was observed in all three cell types while NR3A was much more abundant in pre-Botzinger complex interneurons, which belong to the rhythm generator of respiratory activity. In hypoglossal neurons, the NMDAR1 splice variants NMDAR1-4a and NMDAR1-4b were found. In neurons of the nucleus of the solitary tract, instead of NMDAR1-4b, the NMDAR1-2a splice variant was detected. This differential expression of modulatory splice variants might be the molecular basis for the characteristic functional properties of NMDA receptors, as neurons expressing a special NMDAR1 splice variant at the mRNA level show fast kinetics compared with neurons lacking this splice variant.


Subject(s)
Brain Stem/cytology , Neurons/physiology , Receptors, N-Methyl-D-Aspartate/classification , Receptors, N-Methyl-D-Aspartate/metabolism , Respiration , Valine/analogs & derivatives , 6-Cyano-7-nitroquinoxaline-2,3-dione/pharmacology , Animals , Animals, Newborn , Blotting, Northern/methods , Brain Stem/metabolism , Electric Stimulation/methods , Excitatory Amino Acid Agonists/pharmacology , Excitatory Amino Acid Antagonists/pharmacology , Excitatory Postsynaptic Potentials/drug effects , Excitatory Postsynaptic Potentials/radiation effects , In Vitro Techniques , Membrane Potentials/drug effects , Membrane Potentials/physiology , Membrane Potentials/radiation effects , N-Methylaspartate/pharmacology , Neurons/drug effects , Patch-Clamp Techniques/methods , Protein Subunits/classification , Protein Subunits/genetics , Protein Subunits/metabolism , RNA, Messenger/biosynthesis , Rats , Receptors, N-Methyl-D-Aspartate/genetics , Restraint, Physical/methods , Reverse Transcriptase Polymerase Chain Reaction/methods , Valine/pharmacology
4.
J Theor Biol ; 208(3): 329-43, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11207094

ABSTRACT

Patch clamp recordings of excitatory postsynaptic currents (EPSCs) in central neurons reveal large fluctuations in amplitudes and decay times of AMPA-receptor-mediated EPSCs. By using Monte Carlo simulations of synaptic transmission in brainstem interneurons, we tested several hypothesis that could account for the observed variability. The coefficient of variation (CV) of 0.5 for miniature amplitudes cannot be explained by fluctuations in vesicle content or receptor distribution, but is traced to variations in receptor number, which is estimated as 77+/-39 receptors per bouton. As the variability of rise times reflects fluctuations in size of the post-synaptic density and heterogeneity of the receptor distribution, the relatively small CV=0.37 of experimentally determined values points to a homogeneous arrangement of receptors. Within our model the large variability of decay times (CV=0.49) can only be explained by fluctuations in the transmitter time course (mean residence times of 0.4+/-0.13 ms), presumably resulting from heterogeneities in synaptic morphology. Hence, our simulations indicate that different noise sources control the variability of amplitudes, rise and decay times. In particular, the distribution of decay times yields information about the synaptic transmission process, which cannot be obtained from other observables.


Subject(s)
Computer Simulation , Excitatory Postsynaptic Potentials/physiology , Models, Neurological , Presynaptic Terminals/physiology , Animals , Monte Carlo Method , Patch-Clamp Techniques , Rats , Receptors, AMPA/physiology
5.
Pflugers Arch ; 440(2): 322-32, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10898534

ABSTRACT

Intracellular calcium signals are critical for modulation of neuronal function, and also for pathophysiological states during human neurodegenerative disease, such as Morbus Alzheimer and amyotrophic lateral sclerosis (ALS). We investigated intracellular calcium signals in motoneurones of the nucleus hypoglossus from the mouse, which were maintained in a functionally intact state of rhythmic, respiratory-related activity. Simultaneous patch-clamp recordings and calcium imaging demonstrated that rhythmic inspiratory-related clusters of action potential (AP) discharges are paralleled by calcium oscillations both in somatic and dendritic compartments. Calcium oscillations resulted primarily from the AP-induced opening of voltage-dependent calcium channels in the soma and dendrites. Dendritic calcium transients differed from somatic responses in their kinetics, amplitude, voltage dependence and regulation of basal calcium levels. Based on a combination of infrared differential interference contrast optics, microfluorimetric calcium imaging and electrophysiological patch-clamp recordings, our results demonstrate that the brainstem slice preparation is an attractive model system to study the integration and superposition of calcium signals in a functionally intact neuronal net.


Subject(s)
Brain Stem/physiology , Calcium/metabolism , Nerve Net/physiology , Periodicity , Action Potentials/physiology , Animals , Calcium Signaling , Dendrites/metabolism , In Vitro Techniques , Mice , Models, Neurological , Motor Neurons/metabolism , Motor Neurons/physiology , Oscillometry , Patch-Clamp Techniques , Sodium/physiology , Time Factors , Tissue Distribution
6.
J Physiol ; 525 Pt 2: 433-45, 2000 Jun 01.
Article in English | MEDLINE | ID: mdl-10835045

ABSTRACT

Motoneurones are particularly vulnerable both in human forms of amyotrophic lateral sclerosis (ALS) and corresponding animal models of the disease. While most motoneurone populations are selectively impaired, oculomotor neurones are essentially resistant to ALS-related damage. Motoneurone vulnerability has been closely linked to disruptions of calcium signalling. To investigate underlying events, we performed a quantitative analysis of calcium homeostasis in oculomotor neurones from mice by simultaneous patch-clamp recordings in sliced tissue and microfluorometric-calcium measurements. Somatic calcium dynamics were investigated by using a computer-controlled microfluorometric system. In oculomotor neurones, basal calcium concentrations were around 80 nM and depolarisation-induced calcium responses were observed for membrane voltages positive to -40 u1u1u approximately mV1 approximately . Endogenous calcium homeostasis was quantified by using the 'added buffer' approach. The recovery phase of depolarisation-induced calcium transients was well approximated by a mono-exponential function with a decay time constant that showed a linear dependence on dye concentration. The extrapolated time constant in the absence of indicator dye was 1.7 +/- 0.2 s (n = 11 cells, 21C). Endogenous calcium binding ratios (kappa(s)) were found to be 264 +/- 25 (n = 11 cells), indicating that 99.6 % of cytosolic calcium ions were taken up by endogenous buffers. Recovery of calcium transients was characterised by an 'effective' extrusion rate gamma = 156 +/- 20 s-1 (n = 11 cells, 21 C). Endogenous calcium binding ratios in oculomotor neurones were 5- to 6-fold larger compared with those of more vulnerable motoneurones in the nucleus hypoglossus and spinal cord. In a first order approximation, they reduced the volume of local calcium elevations around open calcium channels, lowered peak amplitudes of global calcium transients for a given influx and prolonged calcium recovery times for a given set of uptake and extrusion mechanisms. With respect to motoneurone degeneration, our measurements suggest that the exceptional stability of oculomotor neurones partially results from a specialised calcium homeostasis based on high buffering capacities. Furthermore, they indicate that cellular adaptations that account for rapid calcium signalling in hypoglossal and spinal motoneurones enhance their vulnerability during ALS-related motoneurone disease.


Subject(s)
Amyotrophic Lateral Sclerosis/metabolism , Calcium Signaling , Motor Neuron Disease/metabolism , Oculomotor Nerve/metabolism , Animals , Buffers , Disease Models, Animal , Fluorescent Dyes , Fura-2 , Homeostasis , Humans , In Vitro Techniques , Kinetics , Membrane Potentials , Mice , Models, Neurological , Nerve Degeneration/metabolism , Neurons/metabolism , Oculomotor Nerve/cytology , Patch-Clamp Techniques
7.
J Neurochem ; 74(4): 1335-45, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10737588

ABSTRACT

Brainstem nuclei serve a diverse array of functions in many of which ionotropic glutamate receptors are known to be involved. However, little detailed information is available on the expression of different glutamate receptor subunits in specific nuclei. We used RT-PCR in mice to analyze the glutamate receptor subunit composition of the pre-Bötzinger complex, the hypoglossal nucleus, the nucleus of the solitary tract, and the inferior olive. Analyzing 15 receptor subunits and five variants, we found all four alpha-amino-3-hydroxy-5-methyl-4-propionic acid (AMPA) and six NMDA receptor (NR) subunits as well as three of five kainate (KA) receptors (GluR5, GluR6, and KA1) to be expressed in all nuclei. However, some distinct differences were observed: The inferior olive preferentially expresses flop variants of AMPA receptors, GluR7 is more abundant in the pre-Bötzinger complex than in the other nuclei, and NR2C is most prominent in the nucleus of the solitary tract. In single hypoglossal motoneurons and interneurons of the pre-Bötzinger complex investigation of GluR2 editing revealed strong expression of the GluR2-R editing variant, suggesting low Ca2+ permeability of AMPA receptors. Thus, Ca2+-permeable AMPA receptors are unlikely to be the cause for the reported selective vulnerability of hypoglossal motoneurons during excitotoxic events.


Subject(s)
Alternative Splicing/physiology , Brain Stem/cytology , Neurons/physiology , Receptors, Glutamate/genetics , Animals , Antisense Elements (Genetics) , Gene Expression/physiology , Genetic Heterogeneity , Mice , Neurons/chemistry , Receptors, AMPA/genetics , Receptors, Kainic Acid/genetics , Receptors, N-Methyl-D-Aspartate/genetics , Reverse Transcriptase Polymerase Chain Reaction
8.
J Neurophysiol ; 82(6): 2936-46, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10601430

ABSTRACT

A quantitative analysis of activity-related calcium dynamics was performed in motoneurons of the nucleus hypoglossus in the brain stem slice preparation from mouse by simultaneous patch-clamp and microfluorometric calcium measurements. Motoneurons were analyzed under in vitro conditions that kept them in a functionally intact state represented by rhythmic, inspiratory-related bursts of excitatory postsynaptic currents and associated action potential discharges. Bursts of electrical activity were paralleled by somatic calcium transients resulting from calcium influx through voltage-activated calcium channels, where each action potential accounted for a calcium-mediated charge influx around 2 pC into the somatic compartment. Under in vivo conditions, rhythmic-respiratory activity in young mice occurred at frequencies up to 5 Hz, demonstrating the necessity for rapid calcium elevation and recovery in respiratory-related neurons. The quantitative analysis of hypoglossal calcium homeostasis identified an average extrusion rate, but an exceptionally low endogenous calcium binding capacity as cellular parameters accounting for rapid calcium signaling. Our results suggest that dynamics of somatic calcium transients 1) define an upper limit for the maximum frequency of respiratory-related burst discharges and 2) represent a potentially dangerous determinant of intracellular calcium profiles during pathophysiological and/or excitotoxic conditions.


Subject(s)
Calcium/physiology , Hypoglossal Nerve/physiology , Motor Neurons/physiology , Algorithms , Animals , Brain Stem/cytology , Brain Stem/physiology , Electrophysiology , Fluorescent Dyes , Fluorometry , Fura-2 , Homeostasis/physiology , Hypoglossal Nerve/cytology , In Vitro Techniques , Membrane Potentials/physiology , Mice , Patch-Clamp Techniques , Respiratory Mechanics/physiology , Spinal Cord/cytology , Spinal Cord/physiology
9.
J Physiol ; 520 Pt 2: 485-502, 1999 Oct 15.
Article in English | MEDLINE | ID: mdl-10523417

ABSTRACT

1. A quantitative analysis of endogenous calcium homeostasis was performed on 65 motoneurones in slices of the lumbar spinal cord from 2- to 8-day-old mice by simultaneous patch-clamp and microfluorometric calcium measurements. 2. Somatic calcium concentrations were monitored with a temporal resolution in the millisecond time domain. Measurements were performed by using a monochromator for excitation and a photomultiplier detection system. 3. Somatic calcium signalling was investigated during defined voltage-clamp protocols. Calcium responses were observed for membrane depolarizations positive to -50 mV. A linear relation between depolarization time and free calcium concentrations ([Ca2+]i) indicated that voltage-dependent calcium influx dominated the response. 4. Endogenous calcium homeostasis was quantified by using the 'added buffer' approach. In the presence of fura-2 and mag-fura-5, calcium transients decayed according to a monoexponential function. Decay-time constants showed a linear dependence on dye concentration and the extrapolated constant in the absence of indicator dye was 371 +/- 120 ms (n = 13 cells, 21 C). 5. For moderate elevations (< 1 microM), recovery kinetics of depolarization-induced calcium transients were characterized by a calcium-independent, 'effective' extrusion rate gamma = 140 +/- 47 s-1 (n = 13 cells, 21 C). 6. The endogenous calcium binding ratio for fixed buffers in spinal motoneurones was kappaB' = 50 +/- 17 (n = 13 cells), indicating that less than 2 % of cytosolic calcium ions contributed to [Ca2+]i. 7. Endogenous binding ratios in spinal motoneurones were small compared to those found in hippocampal or cerebellar Purkinje neurones. From a functional perspective, they provided motoneurones with rapid dynamics of cytosolic [Ca2+]i for a given set of influx, extrusion and uptake mechanisms. 8. With respect to pathophysiological conditions, our measurements are in agreement with a model where the selective vulnerability of spinal motoneurones during excitotoxic conditions and motoneurone disease partially results from low endogenous calcium buffering.


Subject(s)
Calcium/metabolism , Motor Neurons/metabolism , Spinal Cord/metabolism , Animals , Calcium Channels/metabolism , Fluorometry , Fura-2/analogs & derivatives , Homeostasis , Mice , Motor Neuron Disease/metabolism , Patch-Clamp Techniques , Protein Binding , Purkinje Cells/metabolism
10.
J Physiol ; 515 ( Pt 1): 119-31, 1999 Feb 15.
Article in English | MEDLINE | ID: mdl-9925883

ABSTRACT

1. The rhythmically active respiratory network in the brainstem slice of the mouse was investigated under in vitro conditions using patch clamp and microfluorometric techniques. Rhythmic respiratory activity persisted over the whole course of an experiment. 2. Electrophysiologically recorded rhythmic activity in respiratory neurones was accompanied by oscillations in intracellular calcium, which displayed a maximal concentration of 300 nM and decayed to basal levels with a mean time constant of 1.6 +/- 0.9 s. 3. Elevations of calcium concentrations were highly correlated with the amplitude of rhythmic membrane depolarization of neurones, indicating that they were initiated by a calcium influx across the plasma membrane through voltage-gated calcium channels. 4. Voltage clamp protocols activating either high voltage-activated (HVA) or both HVA and low voltage-activated (LVA) calcium channels showed that intracellular calcium responses were mainly evoked by calcium currents through HVA channels. 5. Somatic calcium signals depended linearly on transmembrane calcium fluxes, suggesting that calcium-induced calcium release did not substantially contribute to the response. 6. For calcium elevations below 1 microM, decay time constants were essentially independent of the amplitude of calcium rises, indicating that calcium extrusion was adequately approximated by a linear extrusion mechanism. 7. Cytosolic calcium oscillations observed in neurones of the ventral respiratory group provide further evidence for rhythmic activation of calcium-dependent conductances or second messenger systems participating in the generation and modulation of rhythmic activity in the central nervous system.


Subject(s)
Brain Stem/physiology , Calcium Signaling/physiology , Neurons/physiology , Respiratory Muscles/innervation , Animals , Brain Stem/cytology , Cell Membrane/drug effects , Cytophotometry , Electrophysiology , In Vitro Techniques , Ion Channel Gating/physiology , Medulla Oblongata/cytology , Medulla Oblongata/physiology , Membrane Potentials/physiology , Mice , Patch-Clamp Techniques
11.
Eur J Neurosci ; 10(1): 64-70, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9753114

ABSTRACT

Subtype-specific pharmacological compounds represent important tools to identify the molecular components of synaptically activated glutamate receptors in central neurones. Here, we utilized a collection of subtype-specific antagonists and modulators to investigate the functional profile of glutamate receptors in identified synapses in thin slices of the cerebellum, hippocampus and brain stem. During whole-cell patch-clamp recordings alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate/kainate (AMPA/KA) receptor-mediated synaptic currents (EPSCs) in cerebellar Purkinje cells were (i) prolonged by 100 microM cyclothiazide, (ii) not significantly changed after preincubation in 10 microM concanavalin A, (iii) not affected by 1 microM Evans Blue or polyamine toxin analogue N-(4-hydroxyphenylpropanolyl)-spermine (NHPPS), but (iv) significantly reduced by high (> or = 100 microM) concentrations of Evans Blue. These pharmacological properties were distinct from those observed in hippocampal granule cells and brain stem interneurones and markedly different from those of recombinant glutamate receptor channels GluR1-GluR6 previously investigated in heterologous expression systems.


Subject(s)
Receptors, AMPA/physiology , Receptors, Kainic Acid/physiology , Synapses/chemistry , Synapses/physiology , 6-Cyano-7-nitroquinoxaline-2,3-dione/pharmacology , Animals , Antihypertensive Agents/pharmacology , Benzothiadiazines/pharmacology , Brain Stem/chemistry , Brain Stem/cytology , Cerebellum/chemistry , Cerebellum/cytology , Coloring Agents/pharmacology , Concanavalin A/pharmacology , Evans Blue/pharmacology , Excitatory Amino Acid Antagonists/pharmacology , Excitatory Postsynaptic Potentials/drug effects , Excitatory Postsynaptic Potentials/physiology , Hippocampus/chemistry , Hippocampus/cytology , Interneurons/chemistry , Interneurons/drug effects , Patch-Clamp Techniques , Polyamines/pharmacology , Rats , Rats, Wistar , Receptors, AMPA/antagonists & inhibitors , Receptors, Kainic Acid/antagonists & inhibitors , Spermine/analogs & derivatives , Tetrodotoxin/pharmacology
12.
J Physiol ; 511 ( Pt 1): 105-17, 1998 Aug 15.
Article in English | MEDLINE | ID: mdl-9679167

ABSTRACT

1. Simultaneous patch clamp and rapid microfluorometric calcium measurements were performed on sixty-five motoneurones in slices of the nucleus hypoglossus in the brainstem of 2- to 6-day-old mice. 2. Hypoglossal motoneurones were particularly vulnerable to mechanical or metabolic stress during isolation of in vitro slice preparations. Therefore, experimental conditions were optimized for functional integrity, as judged by spontaneous rhythmic activity of hypoglossal nerves (XII). 3. Calcium concentrations in the cell soma were monitored with a temporal resolution in the millisecond time domain during depolarizing voltage steps. Ratiometric fluorescence measurements were made using a rapid monochromator (switching tau < 10 ms), a photomultiplier tube and the calcium sensitive dyes fura-2 and mag-fura-5. 4. Dynamics of somatic calcium transients were investigated as a function of the concentration of calcium indicator dye in the cell. Decays of calcium transients were approximated to a single exponential component and decay time constants showed a linear dependence on dye concentration. The extrapolated decay time in the absence of indicator dye was 0.7 +/- 0.2 s, suggesting rapid somatic calcium dynamics under physiological conditions. 5. By a process of back-extrapolation, the 'added buffer' method, a calcium binding ratio of 41 +/- 12 (9 cells) was obtained indicating that 98% of the calcium ions entering a hypoglossal motoneurone were bound by endogenous buffers. 6. Endogenous calcium binding ratios in hypoglossal motoneurones were small compared with those of other neurones with comparable size or geometry. Accordingly, our measurements suggest that the selective vulnerability of hypoglossal motoneurones to calcium-related excitotoxicity might partially result from low concentrations of calcium buffers in these cells.


Subject(s)
Brain Stem/physiology , Calcium/metabolism , Hypoglossal Nerve/physiology , Motor Neurons/physiology , Spinal Cord/physiology , Animals , Fura-2 , In Vitro Techniques , Kinetics , Membrane Potentials , Mice , Patch-Clamp Techniques , Spectrometry, Fluorescence , Time Factors , Vagus Nerve/physiology
13.
J Theor Biol ; 188(2): 227-40, 1997 Sep 21.
Article in English | MEDLINE | ID: mdl-9379674

ABSTRACT

We present a minimal kinetic model for excitatory synaptic transmission to cerebellar Purkinje cells. The main components are a kinetic model for a single glutamate receptor, which is calibrated with the help of patch clamp data, and a mean field approximation for the dynamics of a population of channels, which generate an EPSC. The resulting minimal model of the parallel fiber-Purkinje cell synapse is used to estimate the dynamics of glutamate in the synaptic cleft and to clarify the role of receptor desensitization in synaptic transmission. We also apply the model to different aspects of synaptic modulation, like long-term depression and potentiation by pharmacological application of ampakines. In the framework of the minimal model these effects can be understood as the result of modified receptor kinetics.


Subject(s)
Models, Neurological , Purkinje Cells/physiology , Synaptic Transmission , Animals , Depression, Chemical , Excitatory Postsynaptic Potentials/drug effects , Glutamic Acid/physiology , Kinetics , Purkinje Cells/drug effects , Pyrrolidinones/pharmacology , Receptors, Glutamate/drug effects , Receptors, Glutamate/physiology , Synaptic Transmission/drug effects
14.
J Neurophysiol ; 78(1): 82-91, 1997 Jul.
Article in English | MEDLINE | ID: mdl-9242263

ABSTRACT

Excitatory synaptic transmission was investigated in interneurons of the parvocellular nucleus tractus solitarius (pNTS) by performing patch-clamp experiments in thin slice preparations from rat brain stem. Stimulation of single afferent fibers evoked excitatory postsynaptic currents (EPSCs) mediated by glutamate receptors of the DL-alpha-amino-3-hydroxy-5-methylisoxazole-propionic acid (AMPA) and N-methyl-D-aspartate types. AMPA-receptor-mediated EPSCs displayed decay time constants of 3.5 +/- 1.2 (SD) ms (13 cells), which were slow compared with EPSC decay time constants in neurons of the cerebellum or hippocampus. Slow EPSC decay was not explained by dendritic filtering, because the passive membrane properties of pNTS interneurons provided favorable voltage-clamp conditions. Also, the slowness of EPSC decay did not result from slow deactivation of AMPA receptors (0.7 +/- 0.2 ms, 5 cells), which was investigated during rapid application of agonist to outside-out patches. Comparison of AMPA receptor kinetics with EPSC decay time constants suggested that the slow time course of EPSCs resulted from the prolonged presence of glutamate in the synaptic cleft.


Subject(s)
Interneurons/physiology , Receptors, AMPA/physiology , Solitary Nucleus/physiology , Synaptic Transmission/physiology , Animals , Excitatory Amino Acid Agonists/pharmacology , In Vitro Techniques , Kinetics , Patch-Clamp Techniques , Rats , Rats, Wistar
15.
Neuropharmacology ; 36(11-12): 1489-501, 1997.
Article in English | MEDLINE | ID: mdl-9517419

ABSTRACT

To determine the molecular components of neuronal glutamate receptors, it is important to identify pharmacological tools that allow differentiation between different glutamate receptor types. Here, we utilized the naphthalene derivative Evans Blue (EB) and a collection of other subtype-specific compounds (polyamine toxins, concanavalin A, cyclothiazide) to compare the pharmacological profile of neuronal and recombinant glutamate receptors GluR1-GluR6 expressed in Xenopus oocytes. Submicromolar concentrations of EB selectively reduced the activity of homomeric glutamate receptors GluR1, GluR2(Q) and GluR4. Applied at concentrations above 100 microM, EB potentiated kainate responses of receptors GluR1, GluR3 and GluR4, while receptors GluR2(Q) and GluR6(Q) were completely blocked. Similar experiments were performed on identified neurones in brain slices and after injection of rat brain RNA in Xenopus oocytes. Neuronal kainate responses were (i) potentiated by 100 microM cyclothiazide, (ii) slightly blocked after preincubation in 10 microM concanavalin A, and (iii) not significantly affected by either low (< 1 microM) or high (> 100 microM) concentrations of EB. Their pharmacological properties were markedly different from those of recombinant glutamate receptor channels GluR1-GluR6 investigated in heterologous expression systems.


Subject(s)
Ion Channels/metabolism , Neurons/metabolism , Oocytes/metabolism , Receptors, Glutamate/biosynthesis , Animals , Brain Chemistry/drug effects , Brain Chemistry/genetics , Chimera , Electrophysiology , Evans Blue/pharmacology , Ion Channels/genetics , Oligonucleotides, Antisense/metabolism , RNA/biosynthesis , Rats , Receptors, AMPA/metabolism , Receptors, Glutamate/genetics , Receptors, Kainic Acid/genetics , Receptors, Kainic Acid/metabolism , Recombinant Proteins/metabolism , Xenopus laevis
16.
Eur J Neurosci ; 7(12): 2508-12, 1995 Dec 01.
Article in English | MEDLINE | ID: mdl-8845956

ABSTRACT

The prion protein (PrP) plays a pivotal role in transmissible spongiform encephalopathies such as Creutzfeldt-Jakob disease in humans and scrapie and bovine spongiform encephalopathy in animals. Previous experiments have suggested that the normal cellular prion protein (PrPc) is involved in synaptic function in the hippocampus. Here, we utilized the controlled recording conditions of the patch-clamp technique to investigate the synaptic function of prion protein in cerebellar Purkinje cells. By performing whole-cell and outside-out patch-clamp experiments in thin slices, we investigated synaptic transmission in prion protein knockout mice (PrP-null) and control animals. In PrP-null mice, the kinetics of GABA- and glutamate receptor-mediated currents showed no significant deviation from those in control animals. In contrast to previous results in hippocampal neurons, our findings support the view that synaptic transmission is unimpaired in prion protein-deficient mice.


Subject(s)
Cerebellum/metabolism , Prions/metabolism , Synaptic Transmission/physiology , Animals , Creutzfeldt-Jakob Syndrome/metabolism , Kinetics , Membrane Potentials/physiology , Mice , Mice, Inbred Strains , Patch-Clamp Techniques , Purkinje Cells/metabolism , gamma-Aminobutyric Acid/pharmacology
17.
Neuron ; 12(6): 1331-43, 1994 Jun.
Article in English | MEDLINE | ID: mdl-7912092

ABSTRACT

In the molecular layer of the cerebellar cortex, Purkinje cells and interneurons receive a common excitatory input from parallel fibers. The AMPA/kainate receptor-mediated parallel fiber excitatory postsynaptic current (EPSC) recorded in Purkinje cells decays much more slowly than that recorded in interneurons. We show that this slowness of decay does not result from dendritic filtering and that it is unlikely to reflect the deactivation kinetics of the postsynaptic receptors. Agents blocking glutamate uptake prolong the EPSC in Purkinje cells. We conclude that the slow EPSC decay results from the continued presence of transmitter glutamate. This may be due to retarded transmitter diffusion around spines or to cross-talk between neighboring active synapses.


Subject(s)
Glutamates/metabolism , Glutamates/pharmacology , Purkinje Cells/physiology , Receptors, Glutamate/physiology , Synapses/physiology , Synaptic Transmission/physiology , Animals , Aspartic Acid/pharmacology , Cerebellar Cortex/drug effects , Cerebellar Cortex/physiology , Dendrites/physiology , Electric Stimulation , Evoked Potentials/drug effects , Evoked Potentials/physiology , Glutamic Acid , In Vitro Techniques , Interneurons/drug effects , Interneurons/physiology , Male , Mathematics , Models, Neurological , Nerve Fibers/physiology , Purkinje Cells/drug effects , Rats , Rats, Wistar , Receptors, AMPA/physiology , Receptors, Glutamate/drug effects , Receptors, Kainic Acid/physiology , Synaptic Transmission/drug effects
18.
Biophys J ; 65(5): 1837-43, 1993 Nov.
Article in English | MEDLINE | ID: mdl-7507716

ABSTRACT

The molecular processes associated with voltage-dependent opening and closing (gating) of ion channels were investigated using a new preparation from plant cells, i.e., voltage and calcium-activated ion channels in radish root vacuoles. These channels display a main single channel conductance of approximately 90 pS and are characterized by long activation times lasting several hundreds of milliseconds. Here, we demonstrate that these channels have a second kinetically distinct activation mode which is characterized by even longer activation times. Different membrane potential protocols allowed to switch between the fast and the slow mode in a controlled and reversible manner. At transmembrane potentials of -100 mV, the ratio between the fast and slow activation time constant was around 1:5. Correspondingly, activation times lasting several seconds were observed in the slow mode. The molecular process controlling fast and slow activation may represent an effective modulator of voltage-dependent gating of ion channels in other plant and animal systems.


Subject(s)
Ion Channels/metabolism , Plants/metabolism , Biophysical Phenomena , Biophysics , Calcium/metabolism , Electrophysiology , Ion Channel Gating/physiology , Membrane Potentials , Models, Biological , Vacuoles/metabolism , Vegetables/metabolism
19.
Proc Natl Acad Sci U S A ; 90(14): 6528-32, 1993 Jul 15.
Article in English | MEDLINE | ID: mdl-8393569

ABSTRACT

Joro spider toxin (JSTX) is one of the most potent antagonists of glutamatergic AMPA/KA (alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate/kainate) receptor channels in invertebrates and vertebrates. A differential blocking effect on certain types of glutamatergic synapses--e.g., parallel and climbing fiber synaptic inputs to rat cerebellar Purkinje neurons--has been shown by using a synthetic analog of the spider toxin. By investigating the molecular basis of the JSTX action on the recombinant AMPA/KA receptors GluR1-GluR4 and GluR6 expressed in Xenopus oocytes, we found that submicromolar concentrations of JSTX exert a subunit-specific block. Thus, receptor subunits forming a receptor channel with a linear current-voltage (I-V) relationship (GluR1/2, GluR2/3, and GluR6) were not affected, while receptor subunits with rectifying I-V relationships (GluR1, GluR3, GluR4, and GluR1/3) were reversibly blocked by JSTX. By using receptor-subunit mutants obtained by site-directed mutagenesis, we have identified a single amino acid position (glutamine in the proposed second transmembrane domain) that is critical for the JSTX block. Since this site has previously been shown to control the I-V relationship of the AMPA/KA receptor channel and to participate in the regulation of the channel's permeability for calcium ions, our findings suggest that JSTX binds close to the central pore region of the channel.


Subject(s)
Neurotoxins/genetics , Receptors, Glutamate/drug effects , Spider Venoms/genetics , Amino Acid Sequence , Animals , Arginine/genetics , Calcium/metabolism , Conductometry , Glutamine/genetics , Molecular Sequence Data , Neurotoxins/pharmacology , Oocytes , Protein Biosynthesis , Receptors, AMPA , Receptors, Glutamate/biosynthesis , Receptors, Kainic Acid , Recombinant Proteins/biosynthesis , Recombinant Proteins/drug effects , Sequence Homology, Amino Acid , Spider Venoms/pharmacology , Structure-Activity Relationship , Xenopus
20.
Proc Natl Acad Sci U S A ; 90(2): 605-9, 1993 Jan 15.
Article in English | MEDLINE | ID: mdl-7678460

ABSTRACT

Excitatory synaptic transmission in the mammalian central nervous system is mediated predominantly by glutamate receptor (GluR) channels of the alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate/kainate (AMPA/KA) receptor type. A major improvement in our understanding of glutamatergic synaptic transmission has been achieved after the identification of quinoxalinediones (e.g., 6-cyano-7-nitroquinoxaline-2,3-dione) as specific antagonists of AMPA/KA receptors. In addition to their effects on neurons, quinoxalinediones were also shown to block glutamate-induced responses mediated by recombinant AMPA/KA receptor channels expressed in heterologous systems, irrespective of their particular subunit composition. Here we report the identification of an AMPA/KA receptor antagonist that selectively blocks a subset of AMPA/KA receptors. We found that Evans blue, a biphenyl derivative of naphthalene disulfonic acid, blocks at low concentrations (IC50 = 355 nM for the subunit combination GluR1,2) KA-mediated responses of the subunits GluR1, GluR1,2, GluR1,3, and GluR2,3 expressed in Xenopus oocytes but not responses of GluR3 or GluR6. The blocking action of Evans blue was partially reversible and did not compete with KA for the agonist binding site. These findings suggest not only that Evans blue is a potent tool for elucidating the functional role of specific AMPA/KA receptor subtypes for excitatory synaptic transmission but also that it may also represent a powerful starting point for clinically useful drugs that are able to reduce the excitatory drive in specific neuronal populations of the central nervous system.


Subject(s)
Evans Blue/pharmacology , Excitatory Amino Acid Antagonists , Ion Channels/drug effects , Animals , Kainic Acid/metabolism , Oocytes/physiology , Protein Conformation/drug effects , Quisqualic Acid , Receptors, AMPA , Receptors, Glutamate/classification , Receptors, Glutamate/genetics , Receptors, Glutamate/metabolism , Receptors, Kainic Acid , Recombinant Proteins/drug effects , Structure-Activity Relationship , Xenopus
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