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  • Chemistry  (25)
  • Hypertension  (5)
  • 2000-2004
  • 1985-1989  (20)
  • 1975-1979  (10)
  • 1
    Electronic Resource
    Electronic Resource
    The effect of saralasin (1-Sar-8-Ala-Angiotensin II) on blood pressure in patients with cushing's syndrome (1976)
    Springer
    Journal of molecular medicine 54 (1976), S. 661-663 
    Details
    ISSN: 1432-1440
    Keywords: Cushing-Syndrom ; Hypertonie ; Renin-Aktivität ; Aldosteronismus ; Cushing's syndrome ; Hypertension ; Renin activity ; Aldosteronism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary To investigate the role of the renin angiotensin system in the pathogenesis of hypertension in Cushing's syndrome two patients with hypercorticism were infused with 20 mg saralasin (1-sar-8-alaangiotensin II) over a period of 30 minutes under constant blood pressure control. In addition, one patient with primary aldosteronism, an established form of mineralocorticoid hypertension, served as control. Neither in the two patients with Cushing's syndrome nor in the patient with primary aldosteronism could a blood pressure lowering effect of saralasin be observed. In the two patients with hypercorticism both renin activity and plasma aldosterone increased during saralasin infusion. The patient with primary aldosteronism only showed a weak increase in plasma aldosterone concentration. These results seem to exclude an important role of the renin angiotensin system in the pathogenesis of hypertension in Cushing's syndrome. The unresponsiveness of elevated blood pressure to saralasin in the two patients with hypercorticism and in the patient with primary aldosteronism indirectly supports the assumption that in patients with Cushing's syndrome increased mineralocorticoid activity may be the main factor in the pathogenesis of hypertension.
    Notes: Zusammenfassung Um die Bedeutung des Renin-Angiotensin Systems in der Pathogenese der Hypertonie bei Cushing-Syndrom zu untersuchen, wurden bei 2 Patienten mit Hyperkortizismus 20 mg Saralasin (1-Sar-8-Ala-Angiotensin II) über einen Zeitraum von 30 min unter ständiger Blutdruckkontrolle infundiert. Zusätzlich diente ein Patient mit primärem Aldosteronismus, einer etablierten Form von Mineralokortikoidhochdruck, als Kontrolle. Weder bei den 2 Patienten mit Cushing-Syndrom noch bei dem Patienten mit primärem Aldosteronismus ließ sich ein blutdrucksenkender Effekt des Saralasins nachweisen. Die beiden Patienten mit Hyperkortizismus zeigten unter Saralasin sowohl einen Anstieg der Renin-Aktivität als auch des Plasmaaldosterons. Bei dem Patienten mit primärem Aldosteronismus ließ sich nur ein geringgradiger Anstieg der Plasmaaldosteronkonzentration nachweisen. Diese Ergebnisse sprechen gegen eine wichtige Rolle des Renin-Angiotensin Systems in der Pathogenese der Hypertonie bei Cushing-Syndrom. Die Unbeeinflußbarkeit des Hochdrucks durch Saralasin bei den beiden Patienten mit Hyperkortizismus und dem Patienten mit primärem Aldosteronismus stützen indirekt die Annahme, daß bei Patienten mit Cushing-Syndrom eine erhöhte Mineralokortikoidaktivität der Hauptfaktor in der Pathogenese der Hypertonie ist.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01469145
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  • 2
    Electronic Resource
    Electronic Resource
    Weight reduction and salt restriction in hypertension: Effects on blood pressure and intracellular electrolytes (1986)
    Springer
    Journal of molecular medicine 64 (1986), S. 1183-1185 
    Details
    ISSN: 1432-1440
    Keywords: Salt restriction ; Weight reduction ; Hypertension ; Intracellular electrolytes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In 16 essential hypertensives on a program of energy restriction (800 kcal/day) with and without simultaneous salt restriction, the effects on blood pressure and intracellular Na+ and Ca2+ in red blood cells were studied. A decrease in blood pressure and intracellular free Na+ and Ca2+ was only observed in the cases of simultaneous energy and salt restriction. The beneficial effect of weight reduction in hypertension thus depends on a diminished salt intake and is probably mediated by changes in intracellular free Ca2+.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01728458
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  • 3
    Electronic Resource
    Electronic Resource
    Cellular calcium metabolism in primary hypertension (1987)
    Springer
    Journal of molecular medicine 65 (1987), S. 155-160 
    Details
    ISSN: 1432-1440
    Keywords: Hypertension ; Ca2+
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Several disturbances of cellular Ca2+ metabolism have been described in essential hypertension and in the spontaneously hypertensive rat. Possibly the elevation of intracellular free Ca2+ concentration in arterial smooth muscle cells is one important step in the pathogenesis of primary hypertension. In most studies a decreased energy-dependent Ca2+ transport has been proposed as a mechanism. However, disturbances in cellular Ca2+ metabolism, which can be exclusively ascribed to essential hypertension, have not yet been found. The cause of altered cellular Ca2+ transport in primary hypertension may either be a genetically determined defect of membrane transport or a still-unidentified humoral factor.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01728224
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  • 4
    Electronic Resource
    Electronic Resource
    Treatment of resistant hypertension by phlebotomy (1985)
    Springer
    Journal of molecular medicine 63 (1985), S. 762-764 
    Details
    ISSN: 1432-1440
    Keywords: Phlebotomy ; Hypertension
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In 15 essential hypertensives resistant against a standard triple combination of antihypertensive drugs phlebotomy was performed. Mean arterial pressure was lowered from 140.1±12.2 mm Hg to 123.8±14.9 mm Hg after 14 days. No serious side effects were observed. The duration of the hypoptensive effect of phlebotomy was about 4 weeks. Phlebotomy can be used in addition to drug treatment in resistant essential hypertension.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01733828
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  • 5
    Electronic Resource
    Electronic Resource
    Renin, aldosterone and arterial pressure responses to acute β-adrenergic receptor blockade in hypertensive patients (1976)
    Springer
    Journal of molecular medicine 54 (1976), S. 775-782 
    Details
    ISSN: 1432-1440
    Keywords: Akute β-Rezeptorenblockade ; Hypertension ; Renin ; Aldosteron ; Tag-Nacht-Rhythmus ; Acute β-receptor blockade ; Hypertension ; Renin ; Aldosterone ; Day-night rhythm
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary The effect of acute (intravenous) β-adrenergic blockade with propranolol or pindolol on arterial pressure (BP), plasma renin activity (PRA), and plasma concentration of aldosterone (PA) was evaluated in 20 essential hypertensive men. BP, PRA and PA were determined during continuous recumbency overnight (8 p.m. to 6 a.m.) every 30 min. Two groups of patients were observed. Patients of group I exhibited a characteristic day-night rhythm of PRA with low values before midnight and large increases early in the morning. Conversely, no rhythm and very low PRA values were observed in patients of group II. BP was higher in group II than in group I. In group I following intravenous propranolol or pindolol, BP fell within minutes and levels as well as rhythms of PRA were converted to those of group II without treatment. In group II day-night profiles of PRA and BP remained unchanged. Rhythm and concentration of PA in the two groups were not influenced by either drug. In 4 patients of group I infusion of angiotensin II inhibitor did not lower BP. The observations suggest that in the two groups dissimilarities in rhythms of PRA as well as in BP responses to β-blockade may reflect differences in neuro-adrenergic tone.
    Notes: Zusammenfassung Der Einfluß einer akuten (intravenösen) β-Rezeptorenblockade mit Propranolol oder Pindololauf den Blutdruck (RR), die Plasma-Reninaktivität (PRA) und die Plasma-Aldosteronkonzentration (PA) wurde bei 20 Männern mit essentieller Hypertension untersucht. RR, PRA und PA wurden am liegenden Patienten nachts (20.00–6.00 Uhr) alle 30 min bestimmt. Zwei Gruppen von Patienten konnten unterschieden werden: Patienten der Gruppe I wiesen einen charakteristischen Tag-Nacht-Rhythmus in der Plasma-Reninaktivität auf, mit niedrigen Werten vor Mitternacht und hohen Werten am frühen Morgen. Im Gegensatz hierzu hatten die Patienten der Gruppe II sehr niedrige PRA-Werte; ein Rhythmus für PRA ließ sich nicht nachweisen. RR war höher in der Gruppe II als in Gruppe I. Nach Infusion von Propranolol oder Pindolol kam es in der Gruppe I zu einem schnellen RR-Abfall. Das Verhalten des Tag-Nacht-Profils für PRA war nach der β-Blockade vergleichbar mit demjenigen der Gruppe II vor der β-Blockade. In der Gruppe II blieben RR und Tag-Nacht-Profil von PRA unter β-Blockade unverändert. Rhythmus und Konzentration von PA wurden in beiden Gruppen nicht beeinflußt. Bei 4 Patienten der Gruppe I führte Angiotensin II-Blockade zu keiner RR-Senkung. Die Ergebnisse sind mit der Annahme vereinbar, daß die Unterschiede im Renin-Rhythmus und im Blutdruckverhalten nach akuter β-Rezeptorenblockade durch eine unterschiedliche neuroadrenerge Aktivität der beiden Gruppen bedingt sind.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01614294
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  • 6
    Electronic Resource
    Electronic Resource
    Der Metabolismus des Retinoids Ro 10-9359. Isolierung und Identifizierung der Hauptmetaboliten aus Plasma, Urin und Faeces des Menschen sowie aus der Galle der Ratte Synthese von drei Urinmetaboliten (1977)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 60 (1977), S. 2309-2325 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Metabolism of the Retinoid Ro 10-9359. Isolation and Identification of the Major Metabolites in Human Plasma, Urine and Feces Synthesis of Three Urinary MetabolitesAfter oral administration of therapeutic doses of the 3H-labelled aromatic retinoic acid analog (retinoid) Ro 10-9359 (ethyl all-trans-9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-2,4,6,8-nonatetraenoate) to humans 75 and 15% of the 3H-dose were excreted within the first five days in the feces and the urine, respectively. Using chromatographic procedures including high pressure liquid chromatography 18 metabolites could be isolated from human urine. Their structures were elucidated by mass spectrometry and FT-1H-NMR. spectroscopy. In these urinary metabolites the tetraene side chain of the parent compound Ro 10-9359 is shortened. The radioactivity of the identified urinary metabolites accounted for about 11% of the dose. Three urinary metabolites were synthesized. The main part of the radioactivity excreted within the first five days in the feces consisted of unchanged drug (60% of the dose). A smaller (amount 15% of the dose) could not be identified. The unchanged drug and a major metabolite, the corresponding acid, were found in human plasma.In an experiment with bile-duct cannulated rats the radioactively labelled retinoid Ro 10-9359 was injected intravenously. About 70% of the 3H-dose was excreted in the bile, within the first 48 hours. The whole radioactivity of the rat bile consisted of polar metabolites. No unchanged drug could be found. After enzymatic hydrolysis of the bile conjugates three metabolites were isolated. The main metabolite (49% of the i.v. dose) was a conjugate of the corresponding acid of the parent drug, already found as free compound in human plasma. The other bile metabolites (9 and 7% of the i.v. dose) had an intact side chain, too.An enterohepatic recycling of the bile metabolites was observed in the rat.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19770600722
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  • 7
    Electronic Resource
    Electronic Resource
    Alkylaminopyridines and some Analogues as Derivatives for the structure elucidation of long aliphatic chains by mass spectrometryDedicated to Professor Edgar Lederer, Gif-sur-Yvette, on the occasion of his 70th birthday (1978)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 61 (1978), S. 1287-1295 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several long chain primary alcohols (saturated, monoolefinic and methyl branched) have been converted via their mesylates into various long chain alkylated aromatic compounds with basic character, and their mass spectra compared. The spectra of 2-alkylaminopyridines and to some extent those of 3-alkylaminopyridines exhibit most clearly the structure of the aliphatic chain, allowing the localization of branchings and double bonds.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19780610411
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  • 8
    Electronic Resource
    Electronic Resource
    N-Alkyl-2-pyrrolidones as Derivatives for the Structure Elucidation of Long-chain Primary Alcohols by Mass SpectrometryDedicated to Professor Dr. Walter Boguth on the occasion of his 60th birthday (1977)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 60 (1977), S. 1203-1208 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: One unsaturated and three branched long-chain primary alcohols have been converted into N-alkyl-2-pyrrolidones for investigation by mass spectrometry. The EI. mass spectra of these derivatives have been found to exhibit unambiguously the branching points and, albeit less clearly, the position of a double bond in the chain.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19770600408
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  • 9
    Electronic Resource
    Electronic Resource
    Synthese von [2]-Catenanen aus [2]-Rotaxanen (1988)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 121 (1988), S. 961-970 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of [2]-Catenanes from [2]-RotaxanesStarting from the rotaxane 18a a mixture of catenane 21 and rotaxane 23 is obtained by attaching a polymethylene bridge between the methylene groups in α-position of the sulfonyl groups. The isocyclic catenane 28 containing a 28- and a 46-membered ring is obtained from the catenane 21 by splitting the bonds between the bridgehead atoms and the sulfonyl groups. The 1H-, 13C-NMR, and mass spectra of this compounds are discussed.
    Notes: Ausgehend von dem Rotaxan 18a wird durch Angliederung einer Polymethylenbrücke zwischen den beiden zu den Sulfonylgruppen α-ständigen Methylengruppen ein Gemisch von Catenan 21 und Rotaxan 23 synthetisiert. Aus 21 wird nach Spaltung der Bindungen zwischen den Brückenkopfatomen und den Sulfonylgruppen das isocyclische Catenan 28, bestehend aus einem 28-und einem 46-gliedrigen Ring, erhalten. Die 1H-, 13C-NMR-Spektren und Massenspektren dieser Verbindung werden diskutiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19881210522
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  • 10
    Electronic Resource
    Electronic Resource
    Gezielte Synthese von translationsisomeren [3]-Catenanen (1986)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 119 (1986), S. 1374-1399 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Directed Synthesis of Translationally Isomeric [3]-Catenanes1)In a multi-step reaction sequence the tetrahydroxymetacyclophane 12c is synthesized. Acetalisation with 1,25-dichloro-13-pentacosanone followed by nitration and reduction afforded the diamine 13c. By cyclization of this compound in 2-pentanol with sodium carbonate and sodium iodide under high dilution conditions the monomeric products 16, 17, and 18 are obtained in yields of 21.4, 7.7, and 0.9%, respectively. On the basis of mass, 13C NMR and 1H NMR spectra the structure of these compounds is discussed. Starting from the precatenane 16 the [3]-catenanes 25a, b,c and 26a, b, c are obtained in a multi-step reaction sequence. The structure of these compounds is confirmed by mass, 13C NMR, and 1H NMR spectroscopic investigations.
    Notes: In einer vielstufigen Synthese wird das Tetrahydroxymetacyclophan 12c synthetisiert. Durch Acetalisierung mit 1,25-Dichlor-13-Pentacosanon, nachfolgender Nitrierung und Reduktion wird das Diamin 13c erhalten. Dessen Cyclisierung in 2-Pentanol in Gegenwart von Natriumcarbonat und Natriumiodid unter Verdünnungsbedingungen ergibt die monomeren Cyclisierungsprodukte 16, 17 und 18 in Ausbeuten von 21.4. 7.7 und 0.9%. Die Struktur dieser Verbindungen wird anhand der Massen-, 13C- und 1H-NMR-Spektren diskutiert. In einer mehrstufigen Reaktionsfolge werden aus dem Prä-[3]-catenan 16 die [3]-Catenane 25a, b, c und 26a, b, c erhalten. Die Struktur dieser Verbindungen wird durch 13C-NMR, 1H-NMR- und massenspektroskopische Untersuchungen bewiesen.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19861190424
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