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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 275 (1972), S. 251-261 
    ISSN: 1432-1912
    Keywords: Tritium-Labelled Hexamethonium Derivatives ; Whole Body Autoradiography ; Distribution ; Accumulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary On each nitrogen atom of 3H-hexamethonium one methyl group was replaced either by a n-propyl, N-n-propylphthalimide or n-nonyl group. By means of whole-body autoradiography the influence of the different substituents on the distribution pattern was studied in mice after i.v. or s.c. injection. Increasing the chain length of the substituents caused an enhanced accumulation of the respective compounds into secreting tissues, heart muscle, and liver, and an augmentation of biliary excretion. The affinity of the bis-quaternary ammonium compounds for cartilaginous tissues was also altered. The physiological “barriers” between blood and brain or blood and the aqueous humor of the eye, were highly effective against the compounds studied, whereas the placenta could be penetreted by these derivatives.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 283 (1974), S. 331-334 
    ISSN: 1432-1912
    Keywords: Chlorphentermine ; Phospholipids ; Lung Tissue ; Isolated Macrophages
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Chronic treatment of rats with chlorphentermine (44 mg/kg, per day, i.p. for 8 weeks) alters the lipid metabolism both of lung tissue and of alveolar macrophages (AM). Calculated for one lung three times more lipid could be extracted from lung tissue and ten times more from AM, compared with controls. The molar ratio lipids: chlorphentermine is 10∶1 in the lung tissue and 7∶1 in AM. It reflects the remarkable binding of this drug to lipids, which is supposed to be the reason for the reduced breakdown mainly of phospholipids.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 323 (1983), S. 145-148 
    ISSN: 1432-1912
    Keywords: Dopamine vascular receptors ; Gastrointestinal tract ; Cat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of intravenous infusion of dopamine (10 and 25 μg·kg−1·min−1 consecutively) on visceral blood flow distribution was examined in anesthetized cats using the microsphere technique and electromagnetic flowmetry. Arterial blood pressure did not change in response to dopamine infusion, but blood flow through the superior mesenteric artery, and blood flow in the mucosa-submucosa of the gastric antrum and various gut segments increased significantly. During infusion of the high dose the increase was most marked in the mucosa-submucosa of the antrum (+355%) and distal colon (+371%). By contrast, blood flow decreased in the muscularis-serosa of the gut segments investigated, in the spleen, pancreas, and the hepatic arterial bed. The increase in blood flow through the superior mesenteric artery was blocked by the dopamine antagonist bulbocapnine (10 mg/kg i.v.). The results suggest that the receptors mediating the dopamine-induced vasodilation in the gastrointestinal tract are located in the resistance vessels of the mucosa-submucosa.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 279 (1973), S. 207-210 
    ISSN: 1432-1912
    Keywords: Chlorphentermine ; Phospholipids ; NMR ; Binding Studies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Chlorphentermine which is known to interfere with lipid metabolism in vivo shows strong interaction with phosphatidylcholine in NMR-binding studies. This complexation is supposed to alter the phospholipid metabolism thus giving rise to intracellular accumulation of lipids. No significant interaction was observed for phentermine.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 288 (1975), S. 261-268 
    ISSN: 1432-1912
    Keywords: Chlorphentermine ; Lipids ; Lung ; Liver ; Adrenals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In three species chronic treatment with the anorectic drug chlorphentermine causes a profound alteration of the phospholipid/lipid metabolism in the organism, resulting in an increase of the fractions of phospholipids and lipids, e.g. in lungs, livers and adrenals. The results are interpreted as drug-induced generalized phospholipidosis, which is caused by amphiphilic drugs, like chlorphentermine and others. Its extent depends on several factors, like content, pattern and turnover rate of phospholipids in different organs, and on the species.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 312 (1980), S. 77-83 
    ISSN: 1432-1912
    Keywords: Dopamine ; Diuresis ; Renal blood flow ; Sympathetic activity ; Cat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of intravenous (i.v.) and intraarterial (i.a.) injection and infusion of dopamine (DA) on renal hemodynamics, regional sympathetic activity and kidney function were investigated in anaesthetized cats. In response to the i.v. bolus injection of DA (25 μg/kg), mean arterial blood pressure (MABP) was increased by 19.7%, renal blood flow (RBF) by 16.6%, and regional sympathetic discharges were inhibited. The principal effect of i.a. bolus injection of DA into the renal artery was vasoconstriction. Vasodilation was observed neither after lower doses of DA nor after pretreatment with phenoxybenzamine. During continuous i.v. infusion of 10 μg DA kg−1 min−1 MABP, RBF, renal sympathetic discharges and glomerular filtration rate (GFR) did not change, whereas urine volume was increased by 120.5%, sodium excretion by 99.7%, chloride excretion by 143.2%, and potassium excretion by 31.9%. Urine osmolality was decreased and osmolal clearance increased. Raising the DA dose to 25 μg kg−1 min−1 resulted in a fall of GFR, but the diuretic response was not significantly different from that of the low dose. Bulbocapnine (6 mg/kg i.v.) antagonized the DA-induced diuresis. In conclusion, the diuretic effect of DA in the cat is not dependent on a change in RBF, GFR or renal sympathetic activity. This suggests that a tubular site of action is primarily responsible for DA diuresis.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 270 (1971), S. 419-427 
    ISSN: 1432-1912
    Keywords: Tritium Labelled Hexamethonium ; Whole Body Autoradiography ; Distribution ; Accumulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Distribution and accumulation of intravenously and subcutaneously injected tritium-labelled hexamethonium has been studied in mice using autoradiography of whole body sections. The bis-quaternary ammonium compound is rapidly distributed over the organism and excreted mainly by the kidneys, less with the bile. Due to its affinity to “negative binding sites” it combines with acid mucopolysaccharides and is accumulated therefore considerably in connective and cartilaginous tissues. 30 min after either injection route the general distribution pattern of hexamethonium in the organism is characterized as follows (decreasing order): Kidneys, urinary tract, cartilage and connective tissue ≫ lungs 〉 blood, liver 〉 heart and skeletal muscle, gastric and intestinal wall 〉 spleen 〉 adipose tissue, brain and spinal cord.
    Type of Medium: Electronic Resource
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