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  • 1
    Electronic Resource
    Electronic Resource
    Inhibitory effect of tyramine-induced release of catecholamines on renin secretion (1978)
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 303 (1978), S. 139-144 
    Details
    ISSN: 1432-1912
    Keywords: α-Adrenoceptors ; Renin ; Isoprenaline ; Tyramine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of the indirect sympathomimetic agent tyramine on the isoprenaline-induced increase in plasma renin concentration was investigated in conscious rats. Tyramine caused a dose-dependent decrease in the isoprenaline-induced elevation of plasma renin concentration. Pretreatment of the rats with reserpine abolished this effect of tyramine, indicating that tyramine released catecholamines which acted on the inhibitory adrenoceptors. Pretreatment with phenoxybenzamine, an α-adrenoceptor antagonist, also abolished the inhibitory effect of tyramine on renin release, indicating that α-adrenoceptors mediated the observed inhibition of renin release. In rats with chronically denervated kidneys tyramine did not inhibit renin release. It is concluded that catecholamines which are released from renal sympathetic nerve endings can suppress renin release by activating α-adrenoceptors.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00508059
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  • 2
    Electronic Resource
    Electronic Resource
    α-Adrenoceptor-mediated inhibitory effect of the sympathetic nervous system on the isoprenaline-induced increase in plasma renin concentration (1977)
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 299 (1977), S. 77-82 
    Details
    ISSN: 1432-1912
    Keywords: α-Adrenoceptors ; Isoprenaline ; Renin ; Sympathetic nervous system
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The importance of the sympatho-adrenal system for the isoprenaline-induced increase in plasma renin concentration was investigated in conscious rats. Ganglionic blockade by trimethidinium (10 mg kg−1) increased the dose-dependent elevation of plasma renin concentration induced by isoprenaline (0.03–0.48 μg kg−1 min−1). Also treatment of the rats with guanethidine (6 mg kg−1) or reserpine (2.5 mg kg−1, given 16 and 7 h prior to the experiments) further increased the effect of isoprenaline (0.5 μg kg−1 min−1) on plasma renin concentration. Unilateral renal denervation combined with contralateral nephrectomy doubled the effect of the β-sympathomimetic amine on renin release. The α-adrenoceptor antagonist phenoxybenzamine (3 mg kg−1) also enhanced the effect of isoprenaline on this parameter. It is concluded that apart from a stimulation of renin release via β-adrenoceptors the sympathetic nervous system may inhibit renin release via stimulation of α-adrenoceptors.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00508641
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  • 3
    Electronic Resource
    Electronic Resource
    Suppression of isoprenaline-induced increase in plasma renin concentration by vasoconstrictors in rats with nonfunctioning Macula densa (1975)
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 290 (1975), S. 315-321 
    Details
    ISSN: 1432-1912
    Keywords: Isoprenaline ; Renin ; Vasoconstrictors ; Macula densa
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The mechanism of the increase in plasma renin concentration caused by the β-sympathomimetic agent isoprenaline has been further investigated. Rats were pretreated by occluding the left renal artery for 2 hrs, thus rendering the macula densa cells of this kidney nonfunctioning. After contralateral nephrectomy infusion of isoprenaline (1.5 μg/kg min) still caused a strong increase in plasma renin concentration. This increase was significantly suppressed by simultaneous infusion of angiotensin II (1.0 μg/kg min), the α-sympathomimetic amine phenylephrine (60 μg/kg min) or octapressin (10 mU/kg min). The results exclude any mediator-role of the macula densa receptors in the isoprenaline-induced release of renin. The possibility of a stimulation of renin release via the baroreceptors or a direct “secretomotoric” action of isoprenaline is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00510560
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  • 4
    Electronic Resource
    Electronic Resource
    The Inversion of the Amino Group in Vinylamine, a Flexible Model TreatmentA preliminary account of this work was given at the meeting of the Swiss Chemical Society in Geneva, October 9, 1976. (1978)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 61 (1978), S. 1418-1426 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Flexible model results for the —NH2 inversion in vinylamine are compared with microwave data published by Lovas et al. [3]. The information available on the spacing of inversion levels is found to be sufficient to rule out a planar equilibrium structure. Shifts of rotational constants upon excitation of the inversion are calculated for two predicted paths of motion derived from PRDDO geometry optimization results obtained by MiiIler & Brown [2]. Partial geometry optimization yields a path inconsistent with experiment but the path obtained from complete optimization produces shifts in excellent agreement with the observed shifts. A potential energy function compatible with experimental data on spacing of inversion levels is calculated from the observed inertia defects. The inversion angle at equilibrium is slightly smaller than the angle predicted from PRDDO calculations, and the barrier to inversion, ΔV = 1.08 ± 0.07 kcal/mol, is approximately half the PRDDO value.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19780610426
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  • 5
    Electronic Resource
    Electronic Resource
    Versuche zur Herstellung neuer Stickstoffverbindungen (1919)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 2 (1919), S. 608-611 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19190020161
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  • 6
    Electronic Resource
    Electronic Resource
    Über neue organische Phosphorverbindungen (1919)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 2 (1919), S. 612-618 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19190020162
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  • 7
    Electronic Resource
    Electronic Resource
    Ueber neue organische Phosphorverbindungen II. Phosphazine (1919)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 2 (1919), S. 619-635 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19190020163
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  • 8
    Electronic Resource
    Electronic Resource
    Über neue organische Phosphorverbindungen III. Phosphinmethylenderivate und Phosphinimine (1919)
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 2 (1919), S. 635-646 
    Details
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hlca.19190020164
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  • 9
    Electronic Resource
    Electronic Resource
    Synthese von Zuckerestern der Lysergsäure und 9,10-Dihydrolysergsäure (1979)
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 321 (1979), S. 171-174 
    Details
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis of Sugar Esters of Lysergic Acid and 9, 10-Dihydrolysergic Acid
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/prac.19793210126
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  • 10
    Electronic Resource
    Electronic Resource
    Darstellung von 5-Hydroxy-1,7-naphthyridin (1979)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1979 (1979), S. 443-445 
    Details
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 5-Hydroxy-1,7-naphthyridineN-(p-Toluenesulfonyl)glycine ester 1b reacts with 2-(bromomethyl)nicotinic ester 2 to form the nicotinic acid derivative 3b. Cyclization of 3b, by elimination of sulfinic acid, leads to the 1,7-naphthyridine derivative 7, from which the title compound 8 is formed.
    Notes: N-(p-Toluolsulfonyl)glycinester 1b reagiert mit 2-(Brommethyl)nicotinsäureester 2 zum Nicotinsäurederivat 3b. Dieses läßt sich unter Eliminierung von Sulfinsäure zum 1,7-Naphthyridin-derivat 7 cyclisieren, aus dem die im Titel genannte Verbindung 8 erhalten wird.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.197919790402
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