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  • 1
    ISSN: 1432-1912
    Keywords: Rat ; Presynaptic dopamine receptors ; Mesenteric ; Renal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In vitro studies have provided evidence that presynaptic dopamine receptors are present in the rat renal and superior mesenteric vascular beds. To confirm this in vivo, the effects of locally administered apomorphine and pergolide were studied in the in situ autoperfused renal and superior mesenteric vascular beds. Local infusion of apomorphine (1 μg · kg−1 · min−1 for 5 min) or pergolide (1 μg · kg−1 · min−1 for 5 min) into either the renal or the superior mesenteric artery had no effect on perfusion pressure per se. In the renal vascular bed, the pressure response to electrical stimulation (4 Hz, 1 ms, supramaximal voltage) was reduced to 49.8±4.8% by apomorphine and to 54.8±2.7% by pergolide; in the mesenteric vascular bed, apomorphine reduced the pressure response to electrical stimulation (4 Hz, 1 ms, supramaximal voltage) to 53.8±2.9, pergolide to 52.0±1.8%. Increases of perfusion pressure in the renal and in the mesenteric vascular bed induced by locally administered noradrenaline were not modified by apomorphine or pergolide. In both vascular beds, the inhibition of the stimulation-evoked pressure responses by apomorphine or pergolide was completely antagonized by local administration of the dopamine receptor antagonist haloperidol in a dose (1 μg · kg−1) which did not influence the inhibitory effect of the α2-adrenoceptor agonist UK-14,304; the α2-adrenoceptor antagonist rauwolscine, in a dose (100 μg · kg−1) which completely antagonized the inhibitory effect of UK-14,304, did not antagonize the inhibitory effects of apomorphine and pergolide. Local administration of rauwolscine per se increased the pressure response to stimulation at 4 Hz in both vascular beds. In contrast, local administration of haloperidol did not influence the stimulation-evoked pressure response. These results provide evidence for the presence of presynaptic, inhibitory dopamine receptors on sympathetic nerves in the rat renal and mesenteric vascular beds; these receptors could be involved in the blood pressure lowering effects of dopamine receptor agonists, such as apomorphine and pergolide.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 32 (1987), S. 639-639 
    ISSN: 1432-1041
    Keywords: α-acid glycoprotein ; hepatic impairment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 34 (1988), S. 207-209 
    ISSN: 1432-1041
    Keywords: nisoldipine ; renal dysfunction ; pharmacokinetics ; blood pressure control
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of nisoldipine have been studied after oral administration of one 10 mg tablet to 3 groups of patients: Group A (n=8) with a mean creatinine of 90 ml/min, Group B (n=8) with a mean creatinine clearance of 12 ml/min and Group C of 12 patients on maintenance haemodialysis. All of them were studied off-dialysis and 7 were also studied on a dialysis day. No significant differences were observed between Groups A, B and C (on an interdialysis day) in AUC (0–7h), tmax, Cmax and plasma protein binding. Unchanged nisoldipine could not be recovered from the urine in any patient. Haemodialysis did not significantly affect AUC, tmax and Cmax, and nisoldipine could not be detected in the dialysate. The results indicate that the dose of nisoldipine need not be changed in patients with renal dysfunction, and that a supplementary dose is not required after haemodialysis. Blood pressure in the uraemics fell more than in the patients with good renal function.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1041
    Keywords: propranolol ; oxprenolol ; phenytoin ; alpha1-acid glycoprotein ; peritoneal dialysis ; drug-protein binding ; beta-receptor blockers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The influence of continuous ambulatory peritoneal dialysis (CAPD) on the concentrations of α1-acid glycoprotein in serum and dialysate and on the serum binding of oxprenolol, propranolol and phenytoin has been studied. Before starting CAPD treatment, the serum binding of oxprenolol and propranolol was higher and that of phenytoin lower than in healthy volunteers, and the serum α1-AGP concentration was higher. During the first days to weeks after starting CAPD, the serum α1-AGP concentration rose with a concomitant increase in the binding of oxprenolol and propranolol. Subsequently, the α1-AGP level and the binding of oxprenolol and propranolol decreased to the values found before starting CAPD. The binding of phenytoin showed little change. The concentration of α1-AGP in dialysate was 2 to 5% of that in serum.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 35 (1988), S. 213-215 
    ISSN: 1432-1041
    Keywords: Isosorbide dinitrate ; isosorbide mononitrates ; exercise ; plasma concentrations ; first pass effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary As the fall in hepatic blood flow caused by exercise is expected to decrease the elimination of high extraction drugs, the influence of exercise on the fate of the anti-anginal drug isosorbide dinitrate has been assessed. Isosorbide dinitrate 10 mg was given orally, after an overnight fast, on 2 different days to 7 healthy volunteers and the plasma concentrations of the parent compound and its mononitrate metabolites were measured. Heavy bicycle exercise from the 45 th to the 105 th min after intake of the drug on one of the experimental days did not change the plasma isosorbide dinitrate concentrations as compared to those on the rest day. The concentrations of both mononitrates were lower on the exercise day, but the difference was already present before the exercise started.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1041
    Keywords: nimodipine ; pharmacokinetics ; haemodynamics ; cardiopulmonary resuscitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary As the pharmacokinetics of a drug may be altered in haemodynamically compromised patients, the plasma concentrations and haemodynamic effects of the calcium entry blocker nimodipine have been examined in patients resuscitated after out-of-hospital cardiac arrest. In 7 patients nimodipine was infused at increasing rates up to 30 µg·kg−1·h−1. The plasma concentrations increased with increasing dose; at the highest dose a mean steady-state plasma concentration of 22.1 ng·ml−1 was obtained, and the mean plasma clearance was 1.4 l·kg−1·h−1. There were no marked changes in mean arterial blood pressure or heart rate. In 9 other patients nimodipine was given as a bolus infusion of 10 µg·kg−1 over 3 min, followed by a continuous infusion of 30 µg·kg−1·h−1. A mean steady-state plasma concentration of 17.6 ng·ml−1 was obtained and the mean plasma clearance was 1.9 l·kg−1·h−1. Heart rate did not change significantly, but the mean arterial blood pressure fell. The data indicate that in patients resuscitated after cardiac arrest, the pharmacokinetics of nimodipine are not markedly different from patients with other conditions, e.g. subarachnoid haemorrhage. However, if a loading dose is given to obtain a steady-state concentration sooner, there will be a fall in arterial blood pressure.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 329 (1985), S. 146-151 
    ISSN: 1432-1912
    Keywords: Apomorphine ; Pergolide ; Autoperfused rat hindquarters ; Dopamine receptors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of locally administered apomorphine and pergolide were studied in the isolated autoperfused hindquarters of the rat, in an attempt to assess the possible role of presynaptic dopamine receptors at the level in the hypotensive effect of these dopamine agonists. Local infusion of apomorphine (1μg·kg−1·min−1 for 5 min) or pergolide (1μg·kg−1·min−1 for 5 min) [into the hindquarters] did not alter perfusion pressure per se, but reduced the pressor response to electrical stimulation of the lumbar sympathetic chains for the whole frequency range used during a cumulative frequency-response curve (0.25–16 Hz, 1 ms, supramaximal voltage). Apomorphine and pergolide reduced the pressor response elicited by 4 Hz electrical stimulation (applied until maximum response was reached) to 54.8±7.1% and 53.9±1.7% respectively, but they did not modify similar increases of perfusion pressure produced by locally administered noradrenaline. The inhibition by apomorphine and pergolide of the 4 Hz stimulation-evoked pressor response was completely antagonized by local administration of the dopamine antagonist haloperidol (1μg·kg−1), but was not influenced by the α2-antagonist rauwolscine (100μg·kg−1). This dose of rauwolscine antagonized the inhibitory effect of the α2-agonist UK-14,304, which was not influenced by haloperidol. Local administration of rauwolscine increased the pressor response to stimulation at 4 Hz by 37.4–46.2%. In contrast, local administration of haloperidol did not influence the 4 Hz stimulation-evoked pressor response. These results indicate that dopamine receptors are pressent on the sympathetic innervation of the vascular bed in the rat hindquarters but do not provide evidence for a physiological role of these receptors in modulating peripheral sympathetic neurotransmission. Stimulation of these receptors, leading to a decrease of noradrenaline release and thus of vasomotor tone, might—at least in part—explain the blood pressure lowering effects of intravenous apomorphine and pergolide in the rat.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of clinical monitoring and computing 6 (1989), S. 67-73 
    ISSN: 1573-2614
    Keywords: signal processing ; EEG and EMG monitoring ; propofol in continuous infusion ; propofol bloodconcentration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Computer Science , Medicine
    Notes: Summary Propofol has been used as IV induction (2 mg/kg) and maintenance agent (150 µg/kg/min and 100 µg/kg/min after 30 min), combined with N2O/O2 in 16 premedicated (atropine 0.5 mg, Thalamonal 2 ml IM) and mechanically ventilated patients, having ear surgery or arthroscopy. Cranial biopotentials were analysed by 2 different techniques: 1. The Anesthesia and Brain Activity Monitor (ABM Datex) providing the zero crossing frequency (ZXF) as a value for the mean frequency of the EEG signal during a considered time interval, the mean integrated voltage (MIV) as a mean value of the amplitude of the same EEG signal and the spontaneous electromyography of the frontal muscle (SEMG). 2. The EEG trend monitor (rough signal, spectral analysis (S.A.), procentual display). The EEG changes, recorded during propofol anesthesia, are comparable with both techniques. Induction is characterised by a decrease in ZXF, caused by a procentual increase in the low frequency bands (the delta band represents more than 80% of the total power). During the perfusion period an increase in the power of the alpha band (10% to 40%) and a decrease in the delta band is noticed. The ZXF regains its original value. At the end of the procedure the ZXF increases (beta band to more than 30%). A correlation was looked for between the EEG changes and the propofol blood concentrations. The higher the propofol blood concentrations, the more pronounced the low frequency bands. The appearance of beta waves or a ZXF greater than 10 Hz indicates pending arrousal.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-2959
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The short-term tests performed in vitro on different systems, from phage to human cells, or in vivo, on laboratory animals, allow only a qualitative estimate of the action of mutagenic agents, and the extrapolation of such experimental results to man may encounter many difficulties. Direct biomonitoring of populations exposed to chemicals could represent a more realistic approach for an evaluation of the hazards to man. Certain methods are still under development. Nevertheless, other ones can already by used routinely, e.g. the cytogenetic observations on peripheral blood lymphocytes and the Ames test for mutagenic substances in urine, and can provide useful suggestions how to set threshold limits for chemical substances encountered in the working environment.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1612-1112
    Keywords: Reversed-Phase Chromatography ; Fluorescence detection ; Ampicillin ; Plasma ; Broncho-alveolar lavage fluid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A high performance liquid chromatographic analysis of ampicillin in plasma and broncho-alveolar lavage fluid, using amoxicillin as internal standard, is described. The samples are deproteinated with trichloroacetic acid. For both ampicillin and amoxicillin, a fluorescent degradation product is formed in the presence of mercury(II)-chloride, after alkaline degradation and acid hydrolysis. Chromatography is done on a Spherisorb 5 ODS column using methanol-water (60∶40) with PicRB-7 (1-heptane sulphonic acid) as mobile phase and fluorescence detection (Ext 345 nm, Em 425 nm). Calibration curves for ampicillin were linear over the concentration range 1–100 μg/ml in 100 μl plasma samples and over the concentration range 20–2000 ng/ml in 0.5 ml samples of broncho-alveolar lavage fluid. Quantitative analyses with relative standard deviations of less than 10% are achieved.
    Type of Medium: Electronic Resource
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