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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Der Anaesthesist 44 (1995), S. 880-883 
    ISSN: 1432-055X
    Keywords: Schlüsselwörter Elektrische Zwerchfellstimulation ; Atemhilfe ; Respiratorische Insuffizienz ; Key words Electrical diaphragm stimulation ; Assisted respiration ; Respiratory distress
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Abstract Neoplastic or traumatic lesions of the brain stem or the upper spinal cord frequently cause respiratory insufficiency necessitating permanent mechanical ventilation. If the integrity of the diaphragm and its nerves is not affected, adequate ventilation can be achieved by electric stimulation of the phrenic nerves [1, 3, 5, 6]. Diaphragm pacing systems mean the patients can be independent of ventilator treatment. This is a psychological advantage for the patient, giving him or her the option of living in less specialized medical care units and perhaps even at home [4, 9]. Case report. We report the case of a 47-year-old man with a brain stem tumour, which was resected in large pieces. During the postoperative period an increasingly severe respiratory insufficiency developed, which finally made continuous mechanical ventilation necessary. After the viability of the phrenic nerves and contractility of the diaphragm had been shown by direct stimulation of the nerves to be still intact, it was decided that a diaphragm pacer system should be implanted. A “Diaphragm Pacer System S232 G” (Avery Laboratories, Glen Cove, N.Y., USA: external transmitter, antenna, implanted electrode and receiver) was implanted. Using a supraclavicular approach, phrenic nerve electrodes were placed around each nerve and connected with subcutaneous implants of radio signal receivers. Six days after implantation phrenic nerves were stimulated for a first short period. External antenna loops were taped to the skin over the implanted receiver sites (Fig. 3). The impulses produced by the transmitter were delivered via these antenna loops and led to contraction of the diaphragm, providing almost normal respiration. The duration of stimulation was increased stepwise from 1 h a day to full-time stimulation. Three weeks after implantation of the diaphragm pacer system the patient could be totally weaned from mechanical ventilation. After a further 2 weeks it was possible to discharge him from the intensive care unit, and he was then transferred to a rehabilitation centre.
    Notes: Zusammenfassung Wir berichten über den Fall eines 47jährigen Patienten mit einer durch einen Stammhirntumor bedingten respiratorischen Insuffizienz, die eine vollständige maschinelle Beatmung erforderlich machte. Nachdem die volle Funktionsfähigkeit von Zwerchfellmuskulatur und der Nn. phrenici nachgewiesen worden war, wurde dem Patienten ein Phrenicus-Stimulationssystem implantiert. Der Patient konnte danach innerhalb von drei Wochen vollständig vom Respirator entwöhnt werden. Fünf Wochen nach Implantation des Systems wurde er aus der Betreuung einer neurochirurgischen Intensivstation in eine Rehabilitationsklinik verlegt.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 418 (1991), S. 238-247 
    ISSN: 1432-2013
    Keywords: Isolated cardiocytes ; Whole cell recording ; Reoxygenation ; Increased net current ; Transient inward current ; Ca current
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Single myocytes were isolated from ventricles of adult guinea-pig hearts. The patch-clamp technique in the whole-cell configuration was used to study ionic currents. Experiments were performed in an experimental chamber that allowed the cells to be exposed to a sufficiently low O2 pressure to cause metabolic inhibition after 4–35 min (mean 14.1 min, n=20), which was indicated by the appearance of a large time-independent K current. Reoxygenation about 1 min after the first extra outward current was observed caused this current to vanish completely within 2–6 s if the calcium inside the pipette was buffered to negligible values with 20 mmol/l EGTA. With only 10 μM EGTA in the pipette, reoxygenation was followed by an arrhythmogenic period of 10–150 s duration, which was dominated by three types of event: (a) transient inward currents (I ti) developed during the first 5–10 s (26 cells); (b) the net current was increased by a factor of 1.9±0.4 (mean±SD, n=17) yielding a reversal potential for the increased component of −77±4 mV (mean±SD, n=4); and (c) the Ca current decreased by 20%–100% within the first 5–10 s. At the end of the arrhythmogenic period, I ti vanished, the net current recovered completely, and the Ca current recovered partially. At −45 mV, increasing preceding depolarization enlarged the amplitude of both the I ti and the net current, Iti being about four times more increased than the net current. The suppression of the Ca current was independent of the phase of the preceding I ti. We conclude that in isolated cardiocytes, after the induction of an anoxia-induced K current, reoxygenation causes a period of up to 150 s of cytosolic Ca overload, during which I ti is triggered, the net current is enhanced, and the Ca current is suppressed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 418 (1991), S. 248-260 
    ISSN: 1432-2013
    Keywords: Isolated cardiocytes ; Transient inward current ; Current-voltage relationship ; Kinetics ; Na/Ca exchanger
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Transient inward currents (I ti), activated by a rise in intracellular Ca concentration, are believed to trigger cardiac arrhythmias in reperfused hearts. In this report, I ti in isolated cardiocytes from the guinea-pig were evoked by reoxygenation following a period of anoxia of between 4 min and 35 min. Reoxygenation was performed 1 min after the full development of an anoxia-induced time-independent K current. This current disappeared within 2–6 s and in the following 10 s I ti developed to maximum amplitude. I ti were evoked using a constant pulse pattern (holding potential V h=−45 mV; test potential V t=+10 mV; pulse duration 350 ms; frequency 1 Hz). In more than 95% of the cells, I ti at the holding potential I ti (−45 mV) declined with a time constant of τ=670±240 ms (mean±SD, n=17). In two cells, undamped oscillatory currents were observed. The amplitude of I ti (-45 mV) was proportional to the amplitude and duration of the preceding depolarizing test pulse. Test pulses of long duration (500 ms and 1000 ms, mean ± SD) to potentials positive to +10 mV produced slowly decaying tail currents (τ=391±51 ms, mean ± SD), which superimposed with I ti (−45 mV). The current/voltage relationship of I ti peaked between −30 mV and −10 mV and approximated zero at the most positive potentials, i.e. no reversal of I ti was found up to +80 mV. Using double-pulse protocols (prepulse potential +40 mV), I ti were enhanced at potentials negative to −30 mV and were also present in the range of the normal resting potential of ventricular heart cells. The instantaneous current-voltage relationship was monotone between −50 mV and +40 mV. Because of the dependence of I ti on the preceding depolarization, the instantaneous current-voltage relationship provides more reliable information on the voltage dependence of I ti. The interval between two subsequent I ti (−45 mV) values was 237±35 ms (mean ± SD, n=27) and depended on the amplitude of I ti (−45 mV) to increase by 5.2±0.5% (mean ± SD) per 100 pA decrease in I ti (−45 mV). A simple noise analysis showed that if one assumes that ionic channels are responsible for the generation of I ti (−45 mV), their unitary conductance cannot exceed 0.36 pS. We conclude that reoxygenation-induced I ti are triggered by a cyclic release of Ca from the sarcoplasmic reticulum and provide evidence that they are mediated by the electrogenic Na/Ca exchanger. The arrhythmogenic potency of reoxygenation-induced I ti is demonstrated under current-clamp conditions.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 416 (1990), S. 207-209 
    ISSN: 1432-2013
    Keywords: Isolated cardiocytes ; Anoxia ; AP shortening ; K current ; Ca current
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Whole cell currents were measured in isolated cardiocytes of guinea pig under anoxic conditions (pO2 〈0.5 torr). After 2 to 32 (mean 11.2) minutes of anoxia, time independent outward currents developed gradually which had a linear current-voltage relation between -100 and +20 mV and reversed at the resting potential of the cells (-82 to -90 mV). After 20 to 170 (mean 38) seconds, the amplitude of these outward currents saturated (3.6±0.5 nA at +10 mV, n=23). Reoxygenation within one minute after the appearance of the first extra outward currents led in most cells (〉90%) to their complete disappearance in 2 to 4 (mean 2.87, n=15) seconds. Ca currents were not affected at the time when the first extra outward currents occurred. It is concluded that (i) the anoxia-induced outward current is carried by K+ ions probably through KATP channels which open at intracellular ATP concentrations below 1 mmol/l (Noma and Shibasaki 1985) and (ii) this degree of ATP depletion does not affect normal Ca channel function.
    Type of Medium: Electronic Resource
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