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  • Phenylephrine  (3)
  • Blood cells  (2)
  • 3-dimethylindole  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Tetrahedron Letters 35 (1994), S. 6063-6066 
    ISSN: 0040-4039
    Keywords: 2 ; 2 ; 2 ; 3-dimethylbenzofurans ; 3-dimethylindenes ; 3-dimethylindole ; Dimethyldioxirane ; deoxygenation ; dioxetanes ; epoxides ; phosphine ; phospholanes ; quinone methides ; singlet oxygen
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 282 (1974), S. 307-310 
    ISSN: 1432-1912
    Keywords: Isolated Perfused Rabbit Heart ; Phenylephrine ; dp/dt max ; Heart Rate ; Adrenolytic Drugs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In the isolated perfused rabbit heart the effect of phenylephrine on the left ventricular dp/dt max and on heart rate was investigated. 1. The positive inotropic effect of phenylephrine 3×10−7 to 3×10−6 M was abolished by the α-adrenolytic drug phentolamine (3×10−6 M), whereas the β-adrenolytic drug pindolol (10−8 M) was ineffective. On the other hand, the positive inotropic effect evoked by higher concentrations (10−5 to 10−4 M) of phenylephrine was blocked by pindolol while phentolamine was without any effect. 2. The positive chronotropic effect of phenylephrine was antagonized by pindolol. Phentolamine was ineffective. 3. The results presented here show that the ventricular myocardium of the rabbit contains both β- and α-adrenoceptors responsible for the mediation of the positive inotropic effect of phenylephrine.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 284 (1974), S. 245-261 
    ISSN: 1432-1912
    Keywords: Phenylephrine ; Isolated Organs ; Competitive Dualism in Action ; Local Anaesthesia ; Antiarrhythmic Activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The β-sympathomimetic effect of phenylephrine was investigated on the electrically driven atrium, as well as on the tracheal chain of the guinea pig. 1. Phenylephrine (PE) was found to be less effective than isoprenaline (IPN) with regard to its positive inotropic effect on the guinea-pig atrium and to its relaxing action on the tracheal chain. The intrinsic activity for PE amounted to 0.75 on the tracheal chain and to 0.45 on the atrium, when compared with IPN. 2. From these low intrinsic activities, PE was assumed to be a partial β-agonist, exerting a competitive dualism in action to IPN. This dualism could be confirmed by dose-response curves for PE in the presence of IPN and vice versa: PE behaved as a β-agonist as well as a β-antagonist. 3. The intrinsic activity of PE steadily decreased with prolongation of the incubation period. After 1 h PE had almost lost its intrinsic activity. Under these conditions the dose-response curves for IPN on the tracheal chain, as well as on atrium, were shifted to the right in a parallel manner, i.e. PE behaved as a competitive β-antagonist. 4. High concentrations of PE (10−3 M) protected the electrically driven guineapig atrium against arrhythmias induced by k-strophanthoside. The onset of both the first extrasystoles and of heart standstill, which occurred after infusion of k-strophanthoside, were delayed after preincubation with PE. 5. Phentolamine was without any influence on these antiarrhythmic properties of PE. Therefore, it could be excluded that the antiarrhythmic effect of phenylephrine is due to a stimulation of myocardial α-adrenoceptors. 6. The local anaesthetic activity of phenylephrine, as tested on the rabbit cornea, was 4 times higher than that of propranolol. 7. The effective concentrations for the β-adrenolytic, antiarrhythmic, and local anaesthetic activities of PE were clearly different. We concluded, therefore, that the different actions produced by phenylephrine were not associated with each other.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1912
    Keywords: Atrium ; Guinea Pig ; Rabbit ; Cardiostimulation ; Phenylephrine ; β-Adrenoceptors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Experiments were performed on isolated electrically driven and spontaneously beating atria from guinea pigs and rabbits in order to characterize the cardiostimulatory effect of phenylephrine as either β- or α-sympathomimetic. 1. In electrically driven left atria (1 and 2 Hz) of guinea pigs the positive inotropic effect of phenylephrine was competitively antagonized by the β-adrenolytic drug pindolol but not by the α-adrenolytic agent phentolamine. The same was true for electrically driven (2 Hz) atria of rabbits. The intrinsic activity for phenylephrine amounted to only 0.3 in the guinea-pig atrium and 0.46 in the rabbit atrium. Also in preparations from reserpine-pretreated guinea pigs the positive inotropic effect of phenylephrine was blocked by pindolol and remained uninfluenced by phentolamine. Pretreatment with reserpine did not change the intrinsic activity of phenylephrine. Three other α-sympathomimetic drugs, oxymetazoline methoxamine and naphazoline did not cause any positive inotropic effect. 2. In spontaneously beating atria of either guinea pigs or rabbits the positive chronotropic effect of phenylephrine was competitively inhibited by pindolol. Phentolamine proved to be without any effect. The intrinsic activity for the positive chronotropic effect with 0.52 in guinea-pig atria and 0.47 in rabbit atria was less than that of isoprenaline (1.0). 3. The results presented here show that at least on atria only β-adrenoceptors are of functional importance.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 67 (1989), S. 799-803 
    ISSN: 1432-1440
    Keywords: Cystic Fibrosis ; Blood cells ; Beta-adrenoceptors ; Cyclic AMP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Several in vivo and in vitro studies have suggested that children suffering from cystic fibrosis (CF) might have a general defect of beta-adrenoceptors on the cell surface which might account for an unbalanced secretory process. In order to investigate if this view holds true, we determined the beta-adrenoceptor density and affinity on lymphocytes by means of radioligand studies using 125-iodo-cyano-pindolol (125-ICYP) in 20 children with CF. Cyclic AMP (cAMP) response was also investigated after specific beta-adrenoceptor stimulation with isoprenaline (IPN) and after direct stimulation of the adenylate cyclase with forskolin in lymphocytes. Children with CF and controls have identical numbers and affinities of beta-adrenoceptors on lymphocytes. The cyclic AMP response was identical in CF- and in age-matched control children regardless whether adenylate cyclase was stimulated directly or via beta-adrenoceptors. In conclusion, the data support the view that no general adrenoceptor or adenylate cyclase defect exists in CF. As several studies have found abnormal reactions to adrenergic stimuli in CF patients, we presume that there is a defect beyond the level of adrenergic receptors and cAMP which remains to be identified.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1076
    Keywords: Bronchial asthama ; Adrenergic theory ; α- and β-adrenoceptors ; Blood cells ; Age-dependent maturation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Among the possible mechanisms which may cause wheezing or asthmatic episodes a genetically determined β-adrenoceptor blockade and a hyperresponsiveness of α-andrenoceptors has been postulated. Evidence to support this hypothesis stems from an increased bronchial sensitivity to β-blockers, a reduced formation of cyclic AMP in response to β-adrenergic stimulation and enhanced α-adrenergic responses in asthmatic subjects. The recent development of techniques for measuring the specific, high-affinity binding of radiolabeled α-and β-adrenergic antagonists made it possible to study α- and β-adrenoceptors in vitro. Based upon the assumption that a change in the number and/or affinity of adrenergic receptors might be a general phenomenon, we have performed α- and β-receptor binding studies on lymphocytes and platelets from wheezing infants and asthmatic children as well as of infants, children, and adults not suffering from these diseases. Using 125[I]-cyanopindolol (ICYP) and 3[H]-yohimbine (HYOH) as highly specific ligands for α- and β-adrenoceptors, the following results were obtained: (1) Lymphocytes and platelets from control subjects and asthamatics bound similar amounts of ICYP and HYOH and thus showed no differences either in the number or the affinity of α- and β-adrenoceptors. Lymphocytes and platelets of wheezing and nonwheezing infants also bound the same amounts of the radioligands. (2) In asthmatic children receiving 4×2 puffs salbutamol β-adrenoceptor were down-regulated and this may mimic β-adrenoceptor blockade. (3) When subjects were divided into four categories according to age (0–5, 5–10, 10–20 years, adults) the number of β-adrenoceptor binding sites showed an age-dependent increase. The number and affinity of α-adreneceptor binding sites on platelets was neither influenced by age nor disease. It is concluded that the α- and β-adrenoceptors of wheezing infants and asthmatic children at least on blood cells are normal. However the β-adrenoceptors show an age-dependent maturation process, which may account for an unresponsiveness to β-adrenoceptor agonists in wheezing infants.
    Type of Medium: Electronic Resource
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