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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 44 (1993), S. 219-223 
    ISSN: 1432-1041
    Keywords: Trospium chloride ; Gastrointestinal motor function ; gall bladder contraction ; gastric emptying ; gastrooesophageal reflux ; orocaecal transit time ; Oesophageal pH
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The aim of this double-blind, placebo-controlled, cross-over study was to investigate the effect of trospium chloride on gall bladder contraction, gastric emptying of a liquid meal, gastrooesophageal reflux, and orocaecal transit time in healthy subjects. Gall bladder contraction was examined by ultrasonography before and after stimulation with two raw eggs. Gastric emptying was evaluated by an intubation technique and by sonography. To determine gastrooesophageal reflux and orocaecal transit time, 24-hour pH metry and a hydrogen breath test were used. The gall bladder ejection fractions were significantly lower after oral treatment with both 4×10 mg and 4×20 mg trospium compared to placebo, but no difference was seen between the two doses of drug. Gastric emptying of a liquid meal was significantly delayed after intake of 4×15 mg trospium, whilst the time course of the intragastric volume determined by ultrasound did not differ from that after placebo, suggesting an antisecretory effect of trospium on gastric secretion. The fractional time of oesophageal pH〈4 as a percentage of the entire 24-hour investigation period was significantly increased by treatment with trospium 3×15 mg per day. The orocaecal transit time of 10 g lactulose was significantly prolonged. Provided that the observed effects on gall bladder contraction, gastric emptying, and orocaecal transit time are reproduced in disease states, trospium should be regarded as a potentially useful antispasmodic agent.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 3 (1971), S. 97-101 
    ISSN: 1432-1041
    Keywords: Catapresan® ; gastric secretion ; duodenal bicarbonate secretion ; blood sugar ; insulin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Description / Table of Contents: Summary The effect of 2-(2,6-dichlorophenylamino)-2-imidazolin hydrochloride (Catapresan®) on gastric secretion, duodenal bicarbonate secretion and plasma insulin levels has been examined in clinical studies. The acidity and bicarbonate concentration were not affected, but the basal gastric secretion, and the betazol (2 mg/kg) —, pentagastrin 6 µg/kg — and insulin (0.2 U/kg) induced gastric secretion and the secretin (1 U/kg) induced duodenal bicarbonate secretion were decreased after the intravenous administration of 4 µg/kg of this substance. There was no change in blood sugar and basal insulin levels in normal persons.
    Notes: Zusammenfassung In klinischen Untersuchungen wurde der Einfluß von 2-(2,6-Dichlorphenylamino)-2-imidazolin-hydrochlorid (Catapresan®) auf die Magensaftsekretion sowie die exokrine und endokrine Pankreassekretion geprüft. Nach intravenöser Gabe von 4 µg/kg Catapresan® wird die nichtstimulierte sowie die Insulin-, Betazol-und Pentagstrin-stimulierte Säuresekretion des Magens gehemmt. Die secretininduzierte Pankreassekretion wird gleichfalls durch Catapresan® vermindert. Eine Beeinträchtigung der basalen Insulinsekretion konnte bei Personen ohne Kohlenhydratstoffwechselstörung und einer Patientin mit Hyperinsulinismus nicht nachgewiesen werden.
    Type of Medium: Electronic Resource
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