Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Cardiovascular drug reviews 14 (1996), S. 0 
    ISSN: 1527-3466
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 76 (1982), S. 114-117 
    ISSN: 1432-2072
    Keywords: Brain ; β-Adrenoceptors ; Serotonin synthesis ; Metoprolol ; ICI 118,551 ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Rats were treated subchronically (14 days) or acutely (single dose) with the β1-selective adrenoceptor antagonist metoprolol or the β2-selective adrenoceptor antagonist ICI 118,551. Metoprolol (350 mg/kg/day for 14 days, orally) significantly reduced the 5-hydroxytryptophan (5-HTP) accumulation when measured 30 min after inhibition of L-amino acid decarboxylase by NSD 1015 (100 mg/kg IP) in the limbic forebrain, the corpus striatum, the cerebral cortex, the brain stem, and in the cerebellum. ICI 118,551 (0.5 mg/kg, twice daily for 14 days, SC) also significantly reduced the 5-HTP accumulation in the same brain regions except in the corpus striatum and the brain stem. Simultaneously assayed tryptophan levels were largely unaffected. Thus sustained β-adrenoceptor blockade causes a decrease in the in vivo rate of tryptophan hydroxylation in various rat brain regions. The subchronic treatments with metoprolol or ICI 118,551 also significantly reduced the endogenous levels of 5-hydroxytryptamine (5-HT) in the various rat brain regions studied. Acute treatment with either metoprolol (2 mg/kg SC) or ICI 118,551 (0.5 mg/kg SC) did not affect the 5-HTP accumulation or the endogenous 5-HT levels in the brain regions studied. This inhibitory effect on brain 5-HT systems produced by sustained β-adrenoceptor blockade may be of significance both for the long-term cardiovascular action and for occasional neuropsychiatric side effects during β-blocking therapy.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 278 (1973), S. 1-12 
    ISSN: 1432-1912
    Keywords: Dopamine ; Tyrosine Hydroxylase ; Rat Salivary Glands ; Noradrenaline Synthesis ; Dopamine β-Hydroxylase ; Monoamine Oxidase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Endogenous levels of dopamine (DA) were measured in rat salivary glands and hearts using a new sensitive method. In these organs normally about 15 ng/g DA was found. After inhibition of the tyrosine hydroxylase or after treatment with 6-hydroxydopamine, the DA content of the organs decreased. Electrical stimulation of the cervical sympathetic rapidly increased the DA and decreased the NA content of the submaxillary gland. The increase of salivary gland DA was more marked if the dopamine β-hydroxylase (DBH) was inhibited by FLA-63. Inhibition of the monoamine oxidase (MAO) by pargyline alone did not increase the DA level of unstimulated salivary glands, nor did it enhance the increase of salivary gland DA following nerve stimulation. When pargyline was combined with FLA-63, the DA increase was not greater than after FLA-63 alone. The ganglionic blocking agent chlorisondamine completely prevented the stimulation-induced disappearance of NA and almost completely the rise in DA. It was concluded that at least the major part of the DA of heart and salivary glands is located within the adrenergic neurons and that most of the DA is converted to NA by DBH. Newly formed DA appears to become rapidly protected from MAO, probably by granular binding.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 283 (1974), S. 1-20 
    ISSN: 1432-1912
    Keywords: Extraneuronal Uptake ; Noradrenaline ; Normetanephrine ; Protriptyline ; Salivary Glands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of normetanephrine (NM) on effector cell response to noradrenaline (NA) in vivo and on extraneuronal amine uptake in vitro has been investigated in rat submaxillayr glands. Tissue slices were incubated with 3H-NA and the metabolic pattern of the radioactivity in the slices as well as of the efflux from the slices was analyzed. The level of extraneuronally retained radioactive material was found to be markedly reduced at a NM concentration of 20 μg/ml after inhibition of neuronal uptake by protriptyline (PTP). In the presence of an intact neuronal membrane pump mechanism 200 μg/ml of NM also reduced the level of radioactive material, indicating that NM has an inhibitory effect on extraneuronal and in higher concentration also on neuronal uptake and retention of NA and its metabolites. NM was found to markedly potentiate the secretory response to NA in vivo, when doses of NA larger than 1 μg were used. At lower NA doses there was no difference between NM pretreated and control rats. When neuronal uptake was prevented by pretreatment with PTP, NM was found to potentiate the secretory response to NA over the entire dose range. Inhibition by PTP of neuronal uptake only did not affect the dose-response curve for NA and data are presented which indicate that the absence of such a potentiation is due to a decreased salivary gland blood flow induced by NA after PTP pretreatment. The increased responses recorded after NM could not be ascribed to an additive effect of this amine, since NM was found to be a very weak α-receptor agonist in the rat submaxillary gland; doses of more than 1000 μg i.v. were needed to detect a secretory response. The data indicate that the extraneuronal uptake of the transmitter has a functional significance in the rat submaxillary gland by reducing high transmitter concentrations in the vicinity of the receptors.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 341 (1990), S. 215-220 
    ISSN: 1432-1912
    Keywords: (±)-Sotalol ; (+)-Sotalol ; (−)-Sotalol ; Monophasic action potential duration ; β-Adrenoceptor affinity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The racemate (±) and the two enantiomers of sotalol were studied with regard to the effects on cardiac repolarization. In addition, the affinity to cardiac β-adrenoceptors was investigated for the enantiomers. The effect on left ventricular monophasic action potential duration was assessed in the isolated perfused guinea-pig heart and the β-adrenoceptor affinity of the compounds was studied, using α1- radioligand binding technique, in cellular membranes prepared from the left ventricular free wall of the cat. Moreover, the β-adrenoceptor blocking potency of (+)-sotalol was studied in isolated strips of guinea-pig papillary muscles. Both the racemate and the two enantiomers of sotalol caused α1- concentration-dependent prolongation of the ventricular monophasic action potential duration. The maximal effect and the concentration causing half maximal effect (EC50 = 13 μmol/l) were similar for the racemate and the enantiomers, indicating lack of stereoselectivity for this effect. The β-adrenoceptor affinity (equilibrium dissociation constant) of (+)-sotalol was 11 μmol/l and 4 μmol/l as estimated by the binding technique and in the isolated muscle strips, respectively. The affinity for (−)-sotalol, estimated by binding, was 0.6 μmol/l. Thus, at concentrations of (+)-sotalol required for α1- significant prolongation of cardiac repolarization, this isomer may cause significant β-blockade. In this study the enantiomeric purity was better than 98%, so that the degree of β-blockade may be even more pronounced if the enantiomeric purity of the (+)-enantiomer is less than 98%.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 270 (1971), S. 289-309 
    ISSN: 1432-1912
    Keywords: Amine Uptake Mechanisms ; Catecholamines ; Extraneuronal Binding ; Blood Flow ; Protriptyline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The retention of total radioactivity or3H-noradrenaline (3]H-NA) and in some experiments also its metabolites after administration of (±)-3H-NA was studied in rat hearts and salivary glandsin vitro andin vivo. Intact, atrophied and postganglionically sympathectomized (chronically denervated) glands were used. Protriptyline was administered to interfere with the neuronal amine uptake mechanism. In order to study the possible influence of amine catabolizing enzymes,3H-metaraminol was also used as substratein vitro. At a low3H-NA concentration about equal amounts of radioactivity were retained by intact and atrophied salivary gland slices and by heart slicesin vitro, while in the denervated gland smaller amounts were recovered. By increasing the3H-NA concentration significantly lower amounts of radioactive material were retained in the atrophied than in the intact salivary gland slices, indicating a reduced extraneuronal binding in the atrophied gland tissue.In vitro administration of protriptyline in different concentrations inhibited the retention of radioactivity in heart and atrophied salivary gland slices to about the same extent, while in intact salivary gland slices the effect of the drug was much less pronounced. The difference persisted after using maximally effectives protriptyline concentrations, and was attributed to the high level of NA catabolites, especially normetanephrine (NM), found in the intact glands after protriptyline. When this drug was administeredin vivo in low doses the effect was less pronounced in the atrophied gland slices than in the intact ones. As this difference disappeared when higher doses of protriptyline was administered, it was interpreted as a result of an unequal distribution of the drug by the blood flow. Maximally effective doses of protriptyline exerted at greater effect on the accumulation of total radioactivityin vivo in hearts than in salivary glands.3H-NA, however, was reduced to about the same low level in hearts as in intact salivary glands. A high amount of8H-NM in the intact glands explains this difference. Certain differences in the dose-response relationship for protriptyline between the different organs were observed, which might be attributed to differences in blood flow. Also when3H-metaraminol was used as substrate, protriptyline, when given bothin vitro andin vivo, reduced the amine retention to a greater extent in atrophied salivary gland slices than in intact ones. Since in this case an influence of monoamine oxidase and catechol-O-methyl transferase can be excluded the data point to the importance of a parenchymal uptake mechanism for amine retention.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 283 (1974), S. 21-35 
    ISSN: 1432-1912
    Keywords: Adrenergic Receptors ; Catecholamines ; Extraneuronal Uptake ; Phenoxybenzamine ; β-Receptor Blocking Agents ; Salivary Glands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of an α-receptor blocking agent, phenoxybenzamine, and a series of β-receptor blocking agents on extraneuronal uptake and retention of radioactivity after incubation of rat salivary gland slices with 3H-noradrenaline or 3H-isoprenaline has been investigated. In some experiments with 3H-noradrenaline as substrate, neuronal uptake was prevented by adding protriptyline to the incubation medium. Phenoxybenzamine reduced extraneuronal accumulation of radioactivity after both 3H-noradrenaline and 3H-isoprenaline in a concentration-dependent manner, whereas after propranolol the levels of extraneuronally retained radioactive material were markedly increased, the efflux from the slices not being diminished. Some other nonselective and selective β-receptor blocking agents with and without intrinsic activity were found to produce the same effect as propranolol upon the retention of radioactivity after incubation with 3H-noradrenaline and 3H-isoprenaline. When both phenoxybenzamine and propranolol were present in the incubation medium the effect of extraneuronally retained radioactivity after 3H-noradrenaline as well as after 3H-isoprenaline was the same as when only phenoxybenzamine was used. The metabolic pattern of the radioactivity in the slices revealed that the extraneuronally retained radioactive compounds consisted mainly of tritiated catabolites, especially 3-O-methylated ones. The relationship between the extraneuronal accumulation and adrenergic receptor mechanisms is discussed.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1432-2072
    Keywords: Beta-2-receptor agonist ; Salbutamol ; Monoamine synthesis ; Serotonin ; Noradrenaline ; Dopamine ; Antidepressant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Subchronic (5 mg/kg SC, twice daily for 14 days) but not acute administration of the beta-2-adrenoceptor agonist salbutamol to rats caused a significant increase in the accumulation of 5-hydroxytryptophan in the limbic forebrain, the corpus striatum and the cerebral cortex when measured during 30 min after inhibition of l-amino acid decarboxylase by NSD 1015 (100 mg/kg IP). Simultaneously assayed tryptophan concentrations in the same brain regions were not affected. These results indicate an increase in the in vivo rate of tryptophan hydroxylation in the brain, produced by subchronic salbutamol administration. The effect of salbutamol treatment on brain catecholamine (CA) utilization was estimated by studying the disappearance of CA in the brain after inhibition of tyrosine hydroxylase by alpha-methyltyrosine methyl ester (H 44/68) 250 mg/kg IP, 3.5 h before sacrifice. Subchronically but not acutely administered salbutamol caused both a significant increase in endogenous noradrenaline (NA) levels and an increased NA utilization. Dopamine levels and turnover were, however, not altered by either acute or subchronic treatment. The activation, probably centrally elicited, of brain NA and 5-hydroxytryptamine systems by the subchronic salbutamol regimen supports the concept of beta-adrenoceptor mediated regulation of brain monoamine systems, and could contribute to the clinically reported antidepressant activity of beta-2-adrenoceptor agonists.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 1432-2072
    Keywords: Beta-adrenoceptors ; Locomotor activity ; Propranolol ; Apomorphine ; Clonidine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The present study was undertaken in order to clarify the possible involvement of a central betaadrenoceptor mediated action on the stimulation of locomotor activity by the dopamine agonist apomorphine and the noradrenergic agonist clonidine. The effect of pretreatment with various doses of d-and dl-propranolol on apomorphine- and apomorphine plus clonidine-induced locomotor stimulation in reserpinized mice was measured in photocell activity chambers. Pretreatment with dl-propranolol prolonged the duration of apomorphine-induced locomotor stimulation without affecting the maximal level of activity. A similar tendency was seen after pretreatment with the d-form of propranolol, which has a much lower beta-receptor blocking activity. The potentiation by clonidine of the apomorphine-induced locomotor stimulation in reserpinized mice was dose-dependently reduced by pretreatment with dl-propranolol whereas d-propranolol was found to be ineffective. The results indicate that central beta-receptor mechanisms might be involved in the apomorphine plus clonidine-induced locomotor stimulation of reserpinized mice.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 10
    ISSN: 1573-7241
    Keywords: almokalant ; class III antiarrhythmic drugs ; monophasic action potentials ; frequency dependence ; ventricular paced QT intervals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The aim of the present study was to assess the frequency dependency of the effects of almokalant, a selective class III antiarrhythmic drug, on ventricular repolarization using recordings of monophasic action potentials and measurements of ventricular paced QT intervals. Twenty male volunteers were studied during almokalant infusion aiming at plasma concentrations (Cpl) of 20, 50, 100, and 150 nmol/l. The duration of monophasic action potential at 90% repolarization (MAPD) was measured during incremental and premature ventricular extrastimulation. The ventricular paced QT interval was measured during incremental stimulation from the apical region (RVAPEX) and the outflow tract (RVOT) of the right ventricle, and the frequency dependence was analyzed using a linear regression model. At an almokalant dose of Cpl≥50, there was a significant prolongation of the MAPD of 10–15%. The prolongation was of equal magnitude at all paced cycle lengths (CL). The MAPD of ventricular extrasystoles increased in parallel over the range of coupling intervals studied and was significantly prolonged at Cpl 100 and 150. The ratio between the MAPD of the extrasystoles and preceding beats was unaltered after almokalant infusion. The ventricular paced QT intervals increased during almokalant infusion in a similar manner as that of the MAPD. During RVAPEX stimulation, the prolongation was more pronounced at low heart rates, an effect that was not seen during RVOT stimulation. Almokalant significantly prolonged the MAPD at dose levels Cpl≥50. There was no evidence of a frequency dependence of this effect. The ventricular paced QT intervals were prolonged in a similar manner as that of the MAPD, and this effect exhibited a small reverse frequency dependence during RVAPEX stimulation.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...