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Biomedical subjects

U Heinemann

Publications and source records attributed to U Heinemann.

At least 163 records · Page 9Linked to original sources

Cholecystokinin activates CCKB-receptor-mediated Ca-signaling in hippocampal astrocytes.

Cholecystokinin-8S (CCK-8S) is the most abundant neuropeptide in the mammalian cortex and the limbic system; however, its physiological functions remained largely obscure. We studied effects of CCK on astrocytic Ca signaling, which has met considerable interest as a second messenger in astrocytic-neuronal signaling, by digital ratio-imaging of Fura-2/AM loaded rat and mouse hippocampal astrocytes in dissociated culture. Superfusion of CCK-8S (5-50 nM for 2 min) evoked repetitive Ca increases of several hundred nanomolar in a subpopulation of astrocytes. Mouse astrocytes appeared to be more responsive to CCK than rat cells with respect to the fraction of cells responding as well as to the amplitudes of Ca increases. The Ca responses persisted in the absence of extracellular Ca, indicating that release of Ca from intracellular stores is the primary source of these Ca increases. The CCK-8S-induced Ca increases were blocked by the CCKB receptor antagonist PD135158 (100 nM) but not by the CCKA antagonist lorglumide (100 nM). We surmise that astrocytes might be a major primary target for CCK in the CNS.

Animals↗

Frequency-dependent information flow from the entorhinal cortex to the hippocampus.

Storage and retrieval of information in the hippocampus is dependent on information transfer from the entorhinal cortex (EC). We studied how the separate pathways from layer II and III of the EC to the hippocampus are selected for information transfer during repetitive synaptic stimulation. Intracellular recordings were made from EC layer II and III projection cells in horizontal combined EC-hippocampal slices. Synaptic responses to stimulation of deep layers or the lateral EC with stimulus intensities approximately 70% of that required to elicit an action potential were analyzed during short trains of repetitive stimulation. The threshold intensities for induction of action potentials were in layer II cells 8.2 +/- 3.8 (SE) V, significantly larger than 4.4 +/- 1.5 V in type 1, and 5.2 +/- 3.3 V in type 2 layer III cells, respectively. During repetitive subthreshold stimulation with frequencies below 5 Hz the pathway from the EC layer II remained quiet and was preferentially activated with stimulation frequencies above 5 Hz. In contrast the EC layer III cells responded preferentially to low stimulus frequencies (<10 Hz) and became strongly inhibited when synaptically stimulated with frequencies above 10 Hz. Interestingly during stimulus frequencies between 5 and 10 Hz the likelihood that both layer II and III cells fire was large. Thus a frequency switch operates in the entrohinal cortex regulating output of layer II and III cells to the hippocampus. We suggest that such frequency dependent regulation of information flow presents a new principle of neuronal information processing.

Action Potentials↗

The Müller (glial) cell in normal and diseased retina: a case for single-cell electrophysiology.

In the retina of most vertebrates there exists only one type of macroglia, the Müller cell. Müller cells express voltage-gated ion channels, neurotransmitter receptors and various uptake carrier systems. These properties enable the Müller cells to control the activity of retinal neurons by regulating the extracellular concentration of neuroactive substances such as K+, GABA and glutamate. We show here how electrophysiological recordings from enzymatically dissociated mammalian Müller cells can be used to study these mechanisms. Müller cells from various species have Na(+)-dependent GABA uptake carriers, but only cells from primates have additional GABA receptors that activate Cl- channels. Application of glutamate analogues causes enhanced membrane currents recorded from Müller cells in situ but not from isolated cells. We show that mammalian Müller cells have no ionotropic glutamate receptors but respond to increased K+ release from glutamate-stimulated retinal neurons. This response is involved in extracellular K+ clearance and is mediated by voltage-gated (inwardly rectifying) K+ channels which are abundantly expressed by healthy Müller cells. In various cases of human retinal pathology, currents through these channels are strongly reduced or even extinguished. Another type of voltage-gated ion channels, observed in Müller cells from many mammalian species, are Na+ channels. In Müller cells from diseased human retinae, voltage-dependent Na+ currents were significantly increased in comparison to cells from control donors. Thus, the expression of glial ion channels seems to be controlled by neuronal signals. This interaction may be involved in the pathogenesis of retinal gliosis which inevitably accompanies any degeneration of retinal neurons. In particular, Müller cell proliferation may be triggered by mechanisms requiring the activation of Ca(2+)-dependent K+ channels. Ca(2+)-dependent K+ currents are easily elicitable in Müller cells from degenerating retinae and can be blocked by 1 mM TEA (tetraethylammonium). In purified Müller cell cultures, the application of 1 mM TEA greatly reduces the proliferative activity of the cells. These data clearly show that Müller cells are altered in cases of neuronal degeneration and may be crucially involved in pathogenetic mechanisms of the retina.

Animals↗

Preparation and crystallization of a cross-linked complex of bovine adrenodoxin and adrenodoxin reductase.

Bovine adrenodoxin was cross-linked to adrenodoxin reductase with 1-ethyl-3-(3-dimethyl-aminopropyl) carbodiimide. Mass spectrometry showed the reaction product to be a 1:1 complex of the two proteins with M(r) = 64,790 +/- 50. The cross-linked complex showed cytochrome c reductase activity and could be crystallized by hanging-drop vapor diffusion. Crystals of the adrenodoxin-adrenodoxin reductase complex are hexagonal, space group P6(1)22 or P6(5)22, with a = 93.26 A and c = 612.20 A and diffract to 2.9 A resolution at 100 K. Assuming two cross-linked complexes per asymmetric unit yields a reasonable V(M) of 2.97 A3/Da.

Adrenodoxin↗

Electrophysiological properties of rat subicular neurons in vitro.

The electrophysiological properties of 46 bursting cells and 39 regular firing cells were studied in the subiculum of rat combined hippocampal-entorhinal cortex slices. In bursting cells we found a significantly higher resting membrane potential than in regular firing cells. Upon hyperpolarization both cell types expressed a delayed inward rectification with a subsequent afterdepolarization. While in regular firing cells longer lasting depolarizing current injection caused a train of action potentials with a rather marked decline of discharge frequency, bursting cells displayed only little frequency accommodation. Regular firing cells usually displayed a fast and a slow afterhyperpolarization following a train of action potentials, while bursting neurons present only a slow afterhyperpolarization.

Animals↗

Blockade of voltage-gated outward K+ currents of ramified murine microglia by scorpion peptide toxins.

Microglial cells were cultured from murine neonatal brain. Ramification of isolated microglia could be induced by the application of astrocyte-conditioned medium (ACM). Voltage-gated outward potassium currents (IK) were measured in ramified microglial cells 12-24 h after their treatment with ACM. The effects of the specific K+ channel blockers charybdotoxin (CTX), noxiustoxin (NTX) and kaliotoxin (KTX) on IK of ramified microglia were studied. All these peptide toxins blocked IK in a concentration-dependent manner, while showing a high sensitivity for IK. A half-maximal effective concentration (IC50) of CTX was estimated to be 1.13 nM, while IC50 values of 1.24 nM and of 0.81 nM were calculated for KTX and for NTX, respectively. In contrast, dendrotoxin (DTX) did not show any effect on IK. It is suggested that ramified microglial cells express outward K+ currents exhibiting pharmacological properties similar to that of outward K+ currents in cytokine-activated ameboid microglia.

Animals↗

Repetitive spreading depression causes selective suppression of GABAergic function.

Cortical spreading depression (SD) represents a pathophysiological signal that has been associated with the induction of migraine and ischaemic brain damage. The properties of repetitive SDs and their effects on excitatory and inhibitory synaptic transmission were analysed in neocortical slices obtained from adult rats. The SD showed only small variations in amplitude, duration and integral when elicited four times at intervals of 30 min. Extracellularly recorded paired pulse inhibition was, however, significantly reduced by approximately 10% with each SD episode. Since excitatory synaptic transmission was unaffected, our data indicate that repetitive SD causes a selective reduction of intracortical inhibition.

Animals↗

Comparison of effects induced by toxic applications of kainate and glutamate by glucose deprivation on area CA1 of rat hippocampal slices.

Baseline and stimulus-induced changes in [Ca2+]o and [K+]o as well as field potentials (fp's) were studied during application of the excitatory amino acids kainate or glutamate, or during glucose deprivation in area CA1 and CA3 of rat hippocampal slices. Bath application of kainate in concentrations of 1, 2, 5, 8 and 10 mM induced a sudden rapid fall of [Ca2+]o in area CA1, associated with a negative shift of the slow fp. Kainate induced disappearance of stratum radiatum (SR) as well as alveus stimulation-evoked postsynaptic fp's, with partial recovery after application of up to 2 mM kainate, but no recovery after 5 mM kainate. Only afferent volleys and repetitive SR stimulation-induced decreases of [Ca2+]o recovered after 5 mM kainate. Similar observations were made with glutamate. Only when glutamate was applied with 20 mM, irreversible disappearance of postsynaptic fp's was noted. Glucose deprivation for 60-90 min led to an initial slow decline of [Ca2+]o in area CA1 and CA3, associated with increases in [K+]o, but no significant changes in the fp baseline. Before reaching the lowest level in [Ca2+]o, stimulation of afferent and efferent fibres in area CA1 and CA3 evoked epileptiform discharges. After reaching the lowest level in [Ca2+]o, all postsynaptic potential components were irreversibly abolished, sparing afferent volleys and SR stimulation-induced decreases in [Ca2+]o. The application of the glutamate receptor antagonists 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, 30 microM) and L-2-amino-5-phosphonovalerate (2AVP, 30 microM) during glucose deprivation did not prevent irreversible loss of alveus and SR stimulation-induced postsynaptic signals. These findings suggest that glutamate release during glucose deprivation is not the main factor of acute cell damage.

2-Amino-5-phosphonovalerate↗

Effects of serotonin on different patterns of low Mg(2+)-induced epileptiform activity in the subiculum of rats studied in vitro.

The subiculum is an epilepsy-prone area within the hippocampal complex that receives a dense serotonergic innervation from the raphe nuclei. We investigated the effect of 5-HT on epileptiform activity in this region with intra- and extracellular recordings. Our data suggest that 5-HT has predominately inhibitory effects on epileptiform activity in the subiculum but in some cases could also function as a disinhibitory agent. As the subiculum is an important output station of the hippocampal complex the serotonergic innervation might influence the spread of epileptic seizures.

Animals↗

Spread of low Mg2+ induced epileptiform activity from the rat entorhinal cortex to the hippocampus after kindling studied in vitro.

Extracellular recordings were performed in in vitro combined hippocampal-entorhinal cortex (HC-EC) slices obtained from control and amygdala kindled rats to investigate the spread of epileptiform activity from the entorhinal cortex (EC) to the hippocampus (HC). Epileptiform activity was induced by lowering extracellular Mg2+ concentration. In control slices epileptiform activity was in most slices characterized by intericatal discharges and short recurrent discharges in areas CA1 and CA3 and by early seizure like events and late recurrent discharges in the EC and the subiculum. In spite of well preserved anatomical pathways in the combined HC-EC slice in which most of the fibre connectivity between the EC and the dentate gyrus (DG) is intact, seizure like events and late recurrent discharges generated in the EC had only moderate effects on the epileptiform activity in areas CA3 and CA1. In contrast in HC-EC slices obtained from kindled rats epileptiform activity generated in the EC spread to the DG and the areas CA3 and CA1. Kindling facilitates the propagation of seizure like events and late recurrent discharges through the HC-EC slice and appears to alter the filtering function of the DG.

Amygdala↗

Muscarinic activation reduces changes in [Ca2+]o evoked by stimulation of Schaffer collaterals during blocked synaptic transmission in rat hippocampal slices.

The rat hippocampal slice preparation and blockers of postsynaptic glutamate receptors (6-nitro-7-sulphamoylbenzo(f)quinoxaline-2,3-dione (NBQX) 10 microM; DL-2-amino-5-phosphonovaleric acid (APV) 30 microM) were used to study the effects of muscarinic activation on stimulus-induced decreases in [Ca2+]o presumably due to presynaptic Ca-influx. Perfusion with carbachol (100-200 microM) transiently reduced these changes in [Ca2+]o. Blockade of this muscarinic effect by pirenzepine (200 microM) and prolongation of this effect after prolonged lithium (1 mM) incubation suggest involvement of the muscarinic M1 receptor subtype. These findings suggest, that activation of M1 receptors might contribute to inhibition of excitatory synaptic transmission by inhibiting presynaptic Ca-influx. In this way, the muscarinic enhancement of excitatory input may be limited to non-deleterious levels.

2-Amino-5-phosphonovalerate↗

Effects of glutamate receptor agonists on presumed presynaptic Ca(2+)-signals in juvenile rat hippocampal area CA1.

The physiological role of presynaptic glutamate receptors in controlling presynaptic Ca(2+)-influx and thereby transmitter release is unknown. To test if presynaptic Ca(2+)-uptake in the hippocampus is controlled by glutamate autoreceptors, we created a hippocampal slice preparation for investigation of presumed presynaptic Ca(2+)-signals with ion-sensitive microelectrodes after lesioning of post-synaptic neurons by glucose deprivation. After prolonged glucose deprivation in slices from juvenile animals of postnatal days 13-15 and 20-22, stratum radiatum (SR) and alveus stimulation-induced postsynaptic field potential (fp) components were irreversibly abolished in area CA1, whereas SR stimulation still evoked afferent volleys. Repetitive stimulation of the SR still induced small decreases in the extracellular Ca2+ concentration ([Ca2+]o), but repetitive alveus stimulation no longer induced decreases in [Ca2+]o, suggesting a complete damage of pyramidal cells. In lesioned slices the remaining SR stimulation-induced small decreases in [Ca2+]o presumably reflect presynaptic Ca(2+)-influx. These small decreases in [Ca2+]o were reversibly reduced by kainate, RS-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), N-methyl-D-aspartate (NMDA) and L-glutamic acid (glutamate), without effects on afferent volleys.

Animals↗

Modulation of A-currents by [K+]o in acutely isolated pyramidal neurones of juvenile rat entorhinal cortex and hippocampus.

Pyramidal neurones of the entorhinal cortex and of hippocampal areas CA1 and CA3 were acutely isolated from juvenile rats. The effect of lowering the concentration of extracellular potassium ions ([K+]o) on fast transient A-currents (IA) was studied using the whole-cell configuration of the patch-clamp technique. Upon lowering [K+]o from 5.4 to 0 mM amplitudes of IA in all pyramidal neurones were reduced only at test potentials positive to -20 mV, but were increased at potentials below -20 mV. Omission of magnesium ions from the intracellular perfusate resulted in an increase of IA in external K+-free solution at any potential tested. Moreover, when [K+]o was reduced steady-state activation and inactivation curves of IA were shifted in the hyperpolarizing direction.

Animals↗

Crystals of the chemically synthesized acceptor stem of tRNAAla from Escherichia coli diffracting to high resolution.

The acceptor stem of tRNA(Ala) from E. coli has been chemically synthesized and crystallized. This duplex contains a G.U base pair in position 3-70, which is the main identity element for alanyl-tRNA synthetase from E. coli. The crystals are stable in the X-ray beam for a long period of time and diffract to 1.7 A resolution. The monoclinic crystals reveal a C2 space group with a = 35.0, b = 47.5, c = 26.2 A, beta = 102.3 degrees and one acceptor stem per asymmetric unit.

Journal Article↗

Proton modulation of outward K+ currents in interferon-gamma-activated microglia.

Whole-cell outward potassium currents (IK) were measured in interferon (IFN)-gamma-activated cultured murine microglial cells. Acidification of the external milieu moved the threshold of activation of IK in a depolarizing direction, while alkalinization showed the opposite effect. A shift of more than 20 mV of the steady-state activation and inactivation curves of IK in hyperpolarizing direction was measured when pH was changed from 5.8 to 7.8. The time-dependent inactivation of IK was slower when superfusing cells with acid solutions than with alkaline ones. In contrast, variations in the pH of the intracellular solution did not alter kinetics of IK. However, alkalinization of the internal solution from a pH of 5.8 to 7.8 led to a two-fold increase in the current density of IK.

Animals↗

Low Mg2+ induced epileptiform activity in the subiculum before and after disconnection from rat hippocampal and entorhinal cortex slices.

The subiculum is an area within the hippocampal complex which participates strongly in ictaform activity generated in the entorhinal cortex (EC). To study the properties of epileptiform activity with intra- and extracellular recording techniques in the subiculum, combined slices containing the EC, subiculum and hippocampus were prepared with and without surgical disconnection of the subiculum from the EC and area CA1. For induction of epileptiform activity extracellular magnesium was lowered. After acute disconnection of the subiculum from the cornu ammonis and the EC, seizure like events similar to those in the more intact preparation did develop. These were characterized by slow negative field potential shifts and, in intracellular recordings by sustained depolarization shifts lasting for 10-43 s. This activity could develop into late recurrent discharges of 1-2 s. These data indicate that the subiculum may be an important zone for epileptogenesis in temporal lobe epilepsy.

Animals↗

Crystallization and preliminary X-ray characterization of the Methanothermus fervidus histones HMfA and HMfB.

HMfA and HMfB are histone proteins from the thermophilic archaeon Methanothermus fervidus. They wrap DNA into nucleosome-like structures and appear to represent the basic core histone fold. HMfA was crystallized in space groups P4(2)2(1)2 and P2(1)2(1)2(1). HMfB crystallized in space group P2(1)2(1)2, while a selenomethionine-substituted variant, SeMet-HMfB, yielded crystals in C222(1). In all crystal forms HMfA, HMfB, or SeMet-HMfB may be present as homodimers.

Bacterial Proteins↗

Effects of T-type, L-type, N-type, P-type, and Q-type calcium channel blockers on stimulus-induced pre- and postsynaptic calcium fluxes in rat hippocampal slices.

The contribution of T-, L-, N-, P-, and Q-type Ca2+ channels to pre- and postsynaptic Ca2+ entry during stimulus-induced high neuronal activity in area CA1 of rat hippocampal slices was investigated by measuring the effect of specific blockers on stimulus-induced decreases in extracellular Ca2+ concentration ([Ca2+]o). [Ca2+]o was measured with ion-selective electrodes in stratum radiatum (SR) and stratum pyramidale (SP), while Ca2+ entry into neurons was induced with stimulus trains (20 Hz for 10 s) alternately delivered to SR and the alveus, respectively. The [Ca2+]o decreases recorded in SR in response to SR stimulation represented mainly presynaptic Ca2+ entry (Capre), while [Ca2+]o decreases recorded in SP in response to alvear stimulation were predominantly based on postsynaptic Ca2+ entry (Capost). Ethosuximide and trimethadione were ineffective in concentrations up to 1 mM. At 10 mM, they reduced Capost and, much less, also Capre. Nimodipine (25 microM) reduced Capost and, to a minor extent, Capre. omega-Agatoxin IVA (0.4-1 microM) and omega-contoxin MVIIC (1 microM) also reduced both Capre and Capost, but with a stronger action on Capre. omega-Conotoxin GVIA (3-8 microM) reduced Capost without effect on Capre. We conclude that during stimulus-induced, high-frequency neuronal activity Capost is carried by P/Q-, N-, and L- type channels and probably a further channel type different from these channels. Capre includes at least P/Q- and possibly L-type channels. N-type channels did not contribute to Capre in our experiments. Since ethosuximide and trimethadione were only effective in high concentrations, their action may be unspecific. Thus, T-type channels do not seem to play a major part in Ca2+ entry in this situation.

Animals↗