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  • Inorganic Chemistry  (9)
  • Fura-2  (4)
  • Cervical spine  (2)
  • 1
    ISSN: 1432-2013
    Keywords: Key words Ca2+ influx ; Fura-2 ; cAMP ; Forskolin ; Carbachol ; HT29 ; Second messenger ; Patch-clamp technique
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In HT29 colonic epithelial cells agonists such as carbachol (CCH) or ATP increase cytosolic Ca2+ activity ([Ca2+]i) in a biphasic manner. The first phase is caused by inositol 1,4,5-trisphophate-(Ins P 3-) mediated Ca2+ release from their respective stores and the second plateau phase is mainly due to stimulated transmembraneous Ca2+ influx. The present study was undertaken to examine the effect of increased adenosine 3′,5′-cyclic monophasphate (cAMP) (forskolin 10 μmol/l = FOR) on the Ca2+ transient in the presence of CCH (100 μmol/l). In unpaired experiments it was found that FOR induced a depolarization and reduced cytosolic Ca2+ ([Ca2+]i, measured as the fura-2 fluorescence ratio 340/380 nm) significantly. Dideoxyforskolin had no such effect. The effect of FOR was abolished when the cells were depolarized by a high-K+ solution. In further paired experiments utilizing video imaging in conjunction with whole-cell patch-clamp, [Ca2+]i was monitored separately for the patch-clamped cell and three to seven neighbouring cells. In the presence of CCH, FOR reduced [Ca2+]i uniformly from a fluorescence ratio (345/380) of 2.9 ± 0.12 to 1.8 ± 0.07 in the patch-clamped cell and its neighbours (n = 48) and depolarized the membrane voltage (V m) of the patch-clamped cells significantly and reversibly from −54 ± 7.4 to −27 ± 5.9 mV (n = 6). In additional experiments V m was depolarized by 15–54 mV by various increments in the bath K+ concentration. This led to corresponding reductions in [Ca2+]i. Irrespective of the cause of depolarization (high K+ or FOR) there was a significant correlation between the change in V m and change in [Ca2+]i. These data indicate that the cAMP-mediated attenuation of Ca2+ influx is caused by the depolarization produced by this second messenger.
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  • 2
    ISSN: 1432-2013
    Keywords: Ca2+ influx ; Nystatin perforated patchclamp technique ; Fura-2 ; HT29 ; ATP ; Thapsigargin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Indirect evidence has accumulated indicating a voltage dependence of the agonist-stimulated Ca2+ influx into epithelial cells. Manoeuvres expected to depolarise the membrane voltage during agonist stimulation resulted in: (1) a decrease of the sustained phase of the adenosine triphosphate (ATP, 10−5 mol/l)-induced intracellular Ca2+ transient, (2) a reduced fura-2 Mn2+-quenching rate, and (3) prevention of the refilling of the agonist-sensitive store. To quantify the change in intracellular Ca2+ as a function of membrane voltage, we measured simultaneously the intracellular Ca2+ activity ([Ca2+]i) with fura-2 and the electrical properties using the nystatin perforated patch-clamp technique in single HT29 cells. Ca2+ influx was either stimulated by ATP (10−5 mol/l) or thapsigargin (TG, 10−8 mol/l). After [Ca2+]i reached the sustained plateau phase we clamped the membrane voltage in steps of 10 mV in either direction. A stepwise depolarisation resulted in a stepwise reduction of [Ca2+]i. Similarly a stepwise hyperpolarisation resulted in a stepwise increase of [Ca2+]i (ATP: 27.5±10 nmol/l per 10 mV, n=6; TG: 19 ±7.9 nmol/l per 10 mV, n=12). The summarised data show a linear relationship between the Δ fluorescence ratio 340/380 nm change and the applied holding voltage. In unstimulated cells the same voltage-clamp protocol did not change [Ca2+]i (n=9). Under extracellular Ca2+-free conditions [Ca2+]i remained unaltered when changing the membrane voltage. These data provide direct evidence that the Ca2+ influx in epithelial cells is membrane voltage dependent. Our data indicate that small changes in membrane voltage lead to substantial changes in [Ca2+]i. This may be due either to a change of driving force for Ca2+ into the cell, or may reflect voltage-dependent regulation of the respective Ca2+ entry mechanism.
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  • 3
    ISSN: 1432-2013
    Keywords: Key words BCECF ; Fura-2 ; pHi ; [Ca2+]i ; HT29 ; Carbachol ; Neurotensin ; ATP ; InsP3 ; Cell volume ; Calcein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  In this study we examined the influence of intracellular pH (pHi) on agonist-induced changes of intracellular Ca2+ activity ([Ca2+]i) in HT29 cells. pHi and [Ca2+]i were measured microspectrofluorimetrically using BCECF and fura-2, respectively. Buffers containing trimethylamine (TriMA), NH3/NH4 + and acetate were used to clamp pHi to defined values. The magnitudes of the peak and plateau of [Ca2+]i transients induced by carbachol (CCH, 10–6 mol/l) were greatly enhanced by an acidic pHi and nearly abolished by an alkaline pHi. The relationship between pHi and the [Ca2+]i peak was nearly linear from pHi 7.0 to 7.8. This effect of pHi was also observed at higher CCH concentrations (10–4 and 10–5 mol/l), at which the inhibitory effect of an alkaline pHi was more pronounced than the stimulatory effect of an acidic pHi. An acidic pHi shifted the CCH concentration/response curve to the left, whereas an alkaline pHi led to a rightward shift. The influence of pHi on [Ca2+]i transients induced by neurotensin (10–8 mol/l) or ATP (5 × 10–7 mol/l) was similar to its influence on those induced by CCH, but generally not as pronounced. Measurements of cellular inositol 1,4,5-trisphosphate (InsP 3) showed no changes in response to acidification with acetate (20 mmol/l) or alkalinization with TriMA (20 mmol/l). The InsP 3 increase induced by CCH was unaltered at an acidic pHi, but was augmented at an alkaline pHi. Confocal measurements of cell volume showed no significant changes induced by TriMA or acetate. Slow-whole-cell patch-clamp experiments showed no additional effect of CCH on the membrane voltage (V m) measured after TriMA or acetate application. We conclude that pHi is a physiological modulator of hormonal effects in HT29 cells, as the [Ca2+]i responses to agonists were significantly changed at already slightly altered pHi. The measurements of InsP 3, cell volume and V m show that pHi must act distally to the InsP 3 production, and not via changes of cell volume or V m.
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  • 4
    ISSN: 1432-0932
    Keywords: Biomécanique ; Rachis cervical ; Fracture de l'odontoïde ; Stabilité ; Ostéosynthèse de l'odontoïde par vis ; Biomechanics ; Cervical spine ; Odontoid fracture ; Stability ; Odontoid screw fixation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Fresh odontoid fractures of types II and III and in some cases nonunions of the odontoid can be repaired by direct anterior screw fixation preserving C1–C2 motion. The goal of this experimental study was to investigate the biomechanical stability of the fragment achieved by this direct odontoid osteosynthesis according to Böhler. Sixteen human C1–C2 segments with fractures of type II or type III were biomechanically tested in vitro under standardized conditions. Flexion and extension moments, anterior and posterior shear forces were applied, and the motion of the refixed odontoid fragment relative to C2 was determined. The results show that direct screw fixation of the odontoid under the experimental conditions provides sufficient stability for the dens fragment.
    Notes: Résumé Les fractures fraîches de l'odontoïde de type II et III et certains cas de pseudarthrose de l'odontoïde peuvent être réparés par une ostéosynthèse antérieure directe préservant la mobilité C1–C2. Le but de cette étude expérimentale était d'explorer la stabilité biomécanique permise par cette ostéosynthèse directe de l'odontoïde selon Böhler. 16 segments C1–C2 présentant des fractures de type II et III ont été testés in vitro dans des conditions bien définies. On a appliqué des moments de flexion et d'extension et des forces de cisaillement antérieur et postérieur et l'on a déterminé la mobilité du fragment odontoïdien refixé par rapport à C2. Les résultats ont montré que la fixation directe par vissage de l'odontoïde assure dans les conditions expérimentales une stabilité suffisante au fragment odontoïdien.
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  • 5
    ISSN: 1432-0932
    Keywords: Biomécanique ; Rachis cervical ; Fracture de l'odontoïde ; Instabilité atlanto-axoïdienne ; Arthrodèse atlanto-axoïdienne postérieure ; Biomechanics ; Cervical spine ; Odontoid fracture ; Atlantoaxial instability ; Posterior atlantoaxial fusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Unstable C1-C2 segments are generally treated surgically. Depending on the indication a direct screw fixation of the odontoid or a C1-C2 arthrodesis is a possible technique. In this experimental in vitro study the three different atlantoaxial fusion techniques by Gallie, Brooks, and Magerl were compared biomechanically. Sixteen human C1-C2 segments with odontoid fractures of type II and III were investigated under standardized conditions. Flexion and extension moments, anterior, and posterior shear forces, left and right torsional moments were applied, and the motion of C1 relative to C2 was determined. The results of this investigation show clearly that the segments treated with the technique by Magerl with transarticular screws achieved the highest stiffness, compared to the wiring methods of Brooks and Gallie. These differences were most evident for posterior shear forces and for torsional moments. For these load conditions the ratio of stiffness Magerl: Brooks: Gallie was about 10:2:1. Significant differences for the plastic deformation of the differently fixed C1-C2 segments were found within the first few load/unload cycles, which give information about the relationship between primary and long-term stability.
    Notes: Résumé L'instabilité C1-C2 est le plus souvent traitée chirurgicalement. Selon l'indication, peuvent être proposées soit une ostéosynthèse par vissage direct de l'odontoïde, soit une arthrodèse C1-C2. Dans cette étude expérimentale in vitro, on a comparé au plan biomécanique, les trois différentes techniques d'arthrodèse atlanto-axoïdiennes, selon Gallie, Brooks et Magerl. 16 segments C1-C2 présentant des fractures de type II et III ont été testés in vitro dans des conditions bien définies. On a appliqué des moments de flexion et d'extension, des forces de cisaillement antérieur et postérieur et des moments de torsion vers la droite et vers la gauche, et l'on a analysé la mobilité de C1-C2. Les résultats de cette investigation ont clairement démontré que les segments traités par la technique de Magerl avec des vis transarticulaires, présentaient la plus grande rigidité, en comparaison des méthodes de cerclage de Brooks et de Gallie. Ces différences étaient plus évidentes dans le cas du cisaillement postérieur et de la torsion. Dans ces conditions de contrainte, le rapport de rigidité Magerl/Brooks/Gallie était de 10/2/1. Des différences significatives de déformation plastique ont été retrouvées entre les différentes fixations C1-C2 au cours des premiers cycles de mise en charge et décharge, qui renseignent sur la relation entre la stabilité primaire et à long terme.
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  • 6
    ISSN: 1432-2013
    Keywords: Key words CO2/HCO3 ; NH3/NH4+ ; pHi ; [Ca2+]i ; Fura-2 ; BCECF ; Ca2+ store ; Ca2+ influx ; Inositol 1 ; 4 ; 5-trisphosphate ; Epithelia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The influence of intracellular pH (pHi) on intracellular Ca2+ activity ([Ca2+]i) in HT29 cells was examined microspectrofluorometrically. pHi was changed by replacing phosphate buffer by the diffusible buffers CO2/HCO3 –or NH3/NH4 + (pH 7.4). CO2/HCO3 –buffers at 2,5 or 10% acidified pHi by 0.1, 0.32 and 0.38 pH units, respectively, and increased [Ca2+]i by 8–15 nmol/l. This effect was independent of the extracellular Ca2+ activity and the filling state of thapsigargin-sensitive Ca2+ stores. Removing the CO2/HCO3 –buffer alkalinized pHi by 0.14 (2%), 0.27 (5%), and 0.38 (10%) units and enhanced [Ca2+]i to a peak value of 20, 65, and 143 nmol/l, respectively. Experiments carried out with Ca2+-free solution and with thapsigargin showed that the [Ca2+]i transient was due to release from intracellular pools and stimulated Ca2+ entry. NH3/NH4 + (20 mmol/l) induced a transient intracellular alkalinization by 0.6 pHunits and increased [Ca2+]i to a peak (Δ [Ca2+]i = 164 nmol/l). The peak [Ca2+]i increase was not influenced by removal of external Ca2+, but the decline to basal [Ca2+]i was faster. Neither the phospholipase C inhibitor U73122 nor the inositol 1,4,5-trisphosphate (InsP 3) antagonist theophylline had any influence on the NH3/NH4 +-stimulated [Ca2+]i increase, whereas carbachol-induced [Ca2+]i transients were reduced by more than 80% and 30%, respectively. InsP 3 measurements showed no change of InsP 3 during exposure to NH3/NH4 +, whereas carbachol enhanced the InsP 3 concentration, and this effect was abolished by U73122. The pHi influence on ”capacitative” Ca2+ influx was also examined. An acid pHi attenuated, and an alkaline pHi enhanced, carbachol- and thapsigargin-induced [Ca2+]i influx. We conclude that: (1) an alkaline pHi releases Ca2+ from InsP 3-dependent intracellular stores; (2) the store release is InsP 3 independent and occurs via an as yet unknown mechanism; (3) the store release stimulates capacitative Ca2+ influx; (4) the capacitative Ca2+ influx activated by InsP 3 agonists is decreased by acidic and enhanced by alkaline pHi. The effects of pHi on [Ca2+]i should be of relevance under many physiological conditions.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 153-156 
    ISSN: 0044-2313
    Keywords: Tripotassium oxide chloride ; preparation ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Crystal Structures of α- and β-K3OClThe orange coloured compound K3OCl has been prepared. It exists in a low temperature modification (α-K3OCl) and a high temperature modification (β-K3OCl). The transition temperature is 364 ± 5 K. The crystal structures were determined by x-ray diffraction. α-K3OCl crystallizes at room temperature in the orthorhombic space group Pbnm (Z = 4) with the cell parameters a = b = 723.9(2) pm and c = 1 027.7(2) pm in the anti-GdFeO3-structure type. The high temperature modification β-K3OCl crystallizes (Z = 1) in the cubic space group Pm3m in the β-Ag3SI-structure type with a = 516.2(2) pm (T = 393 K).
    Notes: Die orangefarbene Verbindung K3OCl wurde dargestellt. Sie tritt in einer Tieftemperaturmodifikation (α-K3OCl) und in einer Hochtemperaturmodifikation (β-K3OCl) auf. Die Umwandlungstemperatur beträgt 364 ± 5 K. Die Kristallstrukturen wurden durch Röntgenstrukturanalyse aufgeklärt. α-K3OCl kristallisiert bei Raumtemperatur in der orthorhombischen Raumgruppe Pbnm (Z = 4) mit den Gitterkonstanten a = b = 723,9(2) pm und c = 1 027,7(2) pm im anti-GdFeO3-Strukturtyp. Die Hochtemperaturmodifikation, β-K3OCl, kristallisiert mit Z = 1 in der kubischen Raumgruppe Pm3m im β-Ag3SI-Strukturtyp mit a = 516,2(2) pm (T = 393 K).
    Additional Material: 3 Ill.
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  • 8
    ISSN: 0044-2313
    Keywords: Inter alkali metal chalcogenides ; rubidium lithium selenide ; X-ray ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Crystal Structure of RbLiSeRbLiSe is in the system Rb2Se/Li2Se the only ternary phase without mixed crystals of the binary compounds. The single crystal X-ray investigation of this yellow hygroscopic compound leads to the tetragonal space group P4/nmm (Z = 2) with the lattice constants a = 461.6(1) and c = 748.2(3) pm. Its crystal structure confirms a simple rule of expected structure types for inter alkali metal chalcogenides of the general formula ABX.
    Notes: Im System Rb2Se/Li2Se wurde RbLiSe als einzige Phase gefunden. Mischkristallbildung konnte nicht beobachtet werden. Die gelbe, sehr hygroskopische Verbindung kristallisiert nach Einkristalluntersuchungen tetragonal in der Raumgruppe P4/nmm (Z = 2) mit den Gitterkonstanten a = 461,6(1) und c = 748,2(3) pm. Als Vertreter des anti-PbFCl-Strukturtyps befolgt RbLiSe eine von uns empirisch ermittelte „Regel“ zur Struktursystematik der ternären Interalkalimetallchalkogenide des Formeltyps ABX.
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 390 (1972), S. 273-279 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On bisphenyl-bis(dipyridyl) chromium(II) and lithium tetraphenylo chromate(II)By reaction of Ph2CHCrCl2 · 2 THF with two moles of phenyl lithium Ph2CHCrPh2 is obtained in solution. With this solution we prepared the new Cr(II) compounds CrPh2 · 2 bipy and Li2Ph4 · 4 THF by addition of 2,2′-bipyridine and two moles of further phenyl lithium, respectively. During this reactions the diphenylmethyl group is cleaved under reduction of Cr(III) to Cr(II). Li2CrPh4 · 4 THF is an example of a new group of high spin organochromates(II).
    Notes: Ausgehend vom Ph2CHCrCl2 · 2 THF wird mit Lithiumphenyl Ph2CHCrPh2 in Lösung hergestellt. Setzt man diese Lösungen mit 2,2′-Dipyridyl bzw. Lithiumphenyl als weitere Donoren um, so kommt es zum reduktiven Zerfall, wobei aus den primären Additionsprodukten die Diphenylmethylgruppe abgespalten wird. Es entstehen CrPh2 · 2 Dipy bzw. Li2CrPh4 · 4 THF als Verbindungen des zweiwertigen Chroms. Die letzte Verbindung gehört in eine neue Gruppe von magnetisch normalen Oganochromaten(II).
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  • 10
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Kristallstrukturen der Titelkomplexe, deren einer zwei verschiedene Carbonylmetall-Einheiten, deren anderer zwei verschiedene Brückenliganden besitzt, wurden bestimmt. Die Stereochemie des Cr—Ni-Komplexes entspricht der Erwartung, seine Metall - Metall-Bindung ist jedoch kürzer als der Durchschnittswert aus den entsprechenden Cr2- bzw. Ni2-Verbindungen. Bei dem Fe2-Komplex ist die Gesamt-Molekülgeometrie ebenfalls normal, doch der Metall - Metall-Abstand ist deutlich kürzer als erwartet. Die Verkürzung der Metall - Metall-Bindungen steht bei beiden Komplexen in Zusammenhang mit der Minimisierung der intramolekularen sterischen Hinderung.Stereochemistry of the Metal - Metal Bond.Structures of the Compounds (CO)4Cr[μ-PMe2]2Ni(CO)2 and (CO)3Fe[μ-PMe2, μ-I]Fe(CO)3. Each with Two Different Complex HalvesThe crystal structures of the title complexes, one of which has two different carbonylmetal units and the other has two different bridging ligands, were determined. The stereochemistry of the Cr—Ni complex is as expected, its metal - metal bond however is shorter than the average value of the corresponding Cr2 and Ni2 compounds. For the Fe2 complex the overall molecular geometry is also normal, but the metal - metal distance is considerably shorter than expected. The shortening of the metal - metal bonds is in both complexes correlated with the minimization of intramolecular steric strain.
    Additional Material: 2 Ill.
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