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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 328 (1985), S. 354-357 
    ISSN: 1432-1912
    Keywords: Autoradiography ; β-Adrenoceptor subtypes ; Kidney ; Rat ; Guinea-pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The present autoradiographical study examines the distribution of the two β-adrenoceptor subtypes in sections of rat and guinea-pig kidney. The radioligand [125Iodo]-(-)-cyanopindolol was used for the labelling of β-adrenoceptors and the selective β-adrenoceptor blocking agents ICI 89-406 (β1-antagonist) and ICI 118-551 (β2-antagonist) were utilized to differentiate both subclasses unequivocally. β-Adrenoceptors in rat kidney were found to be almost exclusively β1. They were located mainly on glomeruli and to a lesser extent on the straight part of the distal tubules and on the cortical portion of the collecting ducts. Some β2-adrenoceptors were localized around the corticomedullary junction. Grain localization in the autoradiograms was absent in the inner medulla and papilla. Glomeruli and distal tubules of the guinea-pig kidney also possess only β1-adrenoceptors, but, in contrast to the rat, extremely high concentrations of β2-adrenoceptors were associated with the straight part of the proximal tubules in the cortex and possibly with the cortical portion of the collecting duct. Labelling was not detected on the proximal convoluted tubule in either species.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1912
    Keywords: α2-Adrenoceptors ; 3H-Clonidine binding sites ; 3H-Rauwolscine binding sites ; Noradrenergic neurons ; Serotoninergic neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary α2-adrenoceptors located presynaptically on nerve terminals are known to modulate the release of neurotransmitters from noradrenergic and serotoninergic neurons. The pre- and/or postsynaptic localization of binding sites for α2-adrenergic radioligands, the agonist 3H-clonidine and the antagonist 3H-rauwolscine, was investigated in the rat cerebral cortex by the use of specific neurotoxins. Intracerebroventricular ijections of 6-hydroxydopamine (6-OH-DA) and 5,7-dihydroxytryptamine (5,7-DHT) were used to destroy the noradrenergic and serotoninergic neurons, respectively, and the success of the treatment was controlled by measurement of tritium accumulation in cortex slices incubated with 3H-noradrenaline or 3H-serotonin. In cortical membranes, 3H-rauwolscine bound to a single site (K D about 5 nmol/l; B max 217–247 fmoles/mg protein), whereas 3H-clonidine bound to a high affinity site (K D 0.6–1.4 nmol/l) and a low affinity site (K D 6–10 nmol/l). The total number of high plus low affinity 3H-clonidine binding sites was about two thirds of the number of 3H-rauwolscine binding sites. 6-OH-DA treatment significantly increased the number of high affintiy 3H-clonidine binding sites without reducing the number of high plus low affinity binding sites, indicating a denervation supersensitivity. K D- as well as B max-values for 3H-rauwolscine remained unaltered after 6-OH-DA-treatment. Since an increase in postsynaptic α2-adrenoceptors due to 6-OH-DA-administration might have masked a loss of presynaptic α2-adrenergic binding sites, rats were chronically treated with high doses of clonidine in order to prevent a possible supersensitivity of postsynaptic receptors. Even under these conditions 6-OH-DA did not reduce the number of 3H-clonidine and 3H-rauwolscine binding sites. Injection of 5,7-DHT had no influence on binding parameters of 3H-clonidine and 3H-rauwolscine. It is concluded that in the cerebral cortex the number of postsynaptic α2-adrenoceptors is much greater than that of presynaptic α2-adrenoceptors. Therefore, the changes in the number of presynaptic α2-adrenoceptors due to destruction of noradrenergic or/and serotoninergic neurons cannot be detected by equilibrium binding studies with 3H-clonidine or 3H-rauwolscine.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1912
    Keywords: Presynaptic 5-HT autoreceptors ; 5-HT release ; Rat and pig brain cortex ; 5-HT binding sites ; 5-HT receptor subtypes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. In rat brain cortex slices preincubated with [3H]5-HT, the potencies of 17 5-HT receptor agonists to inhibit the electrically evoked3H overflow and the affinities of 13 antagonists (including several β-adrenoceptor blocking agents) to antagonize competitively the inhibitory effect of unlabelled 5-HT on evoked3H overflow were determined. 2. The affinities of the compounds for 5-HT1B and 5-HT2 binding sites in rat brain cortex membranes (labelled by [125I]cyanopindolol = [125I]-CYP in the presence of 30 μmol/l isoprenaline and [3H]ketanserin, respectively), for 5-HT1A binding sites in pig and rat brain cortex membranes (labelled by [3H]8-hydroxy-2-(di-n-propylamino)tetralin = [3H]8-OH-DPAT) and for 5-HT1C binding sites in pig choroid plexus membranes (labelled by [3H]mesulergine) were also determined. The affinities of the drugs for the various 5-HT recognition sites ranged over 4–5 log units (the functional experiments revealed the same range of differences between the drugs). 3. There were no significant correlations between the affinities of the drugs at 5-HT1C and 5-HT2 binding sites and their potencies or affinities, determined for the 5-HT autoreceptors. In contrast, significant correlations were found between the potencies or affinities of the drugs for the autoreceptors and their affinities at 5-HT1A or 5-HT1B binding sites; the best correlations were obtained with the 5-HT1B binding site. 4. Some of the drugs investigated were not included in the correlation since their agonistic or antagonistic effects on the autoreceptors were weak and pEC30 or apparent pA2 values could not be determined (〈5.5). Among these drugs, 8-OH-DPAT, TVX Q 7821 (2-(4-(4-(2-pyrimidin-yl)-1-piperazinyl)-butyl)-1,2-benzisothiazol-3(2H)one-1,1-dioxide) and spiperone showed a very low affinity for 5-HT1B binding sites (pKD〈5.3), but a high affinity for 5-HT1A binding sites (pKD〉7.2). 5. In conclusion, the evidence indicates that the presynaptic 5-HT autoreceptor belongs to the 5-HT1B receptor subtype.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 333 (1986), S. 335-341 
    ISSN: 1432-1912
    Keywords: Postsynaptic 5-HT1 receptors ; Adenylate cyclase ; Rat hippocampus ; 5-HT1A, 5-HT1B, 5-HT1C, 5-HT2 receptor subtypes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Serotonin (5-HT) stimulated adenylate cyclase activity in homogenates of rat hippocampus. This effect was pharmacologically characterised with a series of agonists and antagonists of various structural classes. 2. These compounds where also tested in radioligand binding studies using selective ligands for the various subtypes of 5-HT1 and 5-HT2 receptors. 5-HT1A, 5-HT1B and 5-HT1C recognition sites were labelled with [3H]8-OH-DPAT ([3H]8-hydroxy-2-(di-n-propylamino)-tetralin) in pig cortex membranes, [125I]CYP([125I]iodocyanopindolol) in rat cortex and [3H]mesulergine in pig choroid plexus membranes, respectively. 3. The rank order of potency of 13 agonists stimulating adenylate cyclase activity in homogenates of rat hippocampus was in good agreement with the rank order of affinity of these agonists for the 5-HT1A binding site: N,N-dipropyl-5-carboxamidotryptamine (DP-5-CT)〉5-carboxamidotryptamine (5-CT)〉8-OH-DPAT〉5-HT〉 5-methoxytryptamine (5-OCH3T)〉d-LSD〉5-methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (RU 24969)〉α-methylserotonin (α-CH3-5-HT)〉dopamine〉2-methylserotonin (2-CH3-5-HT). The correlation between the respective potencies and affinities of these agonists was r=0.934, P〈0.001. 4. There was no correlation between stimulation of adenylate cyclase activity by these agonists and their affinity for 5-HT1B, 5-HT1C or 5-HT2 binding sites. r=0.381–0.108, P〈0.20–0.73. 5. Potent antagonists at D-1 receptors (SCH 23390), 5-HTM receptors (ICS 205-930), 5-HT2-receptors (ketanserin) and 5-HT1C-receptors (mesulergine) antagonised the 5-HT stimulated adenylate cyclase activity only at very high concentrations. In contrast, spiperone and metitepin were potent antagonists of the effect of 5-CT and 5-HT on adenylate cyclase. The use of these selective antagonists allowed to exclude the possibility that 5-HT stimulates adenylate cyclase activity in rat hippocampus through D-1, 5-HTM, 5-HT2 or 5-HT1C receptors. 6. These data support the concept that 5-HT stimulated adenylate cyclase activity in rat hippocampus is mediated by a 5-HT1A receptor.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 316 (1985), S. 126-131 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] We describe a new class of drugs that selectively block serotonin M-receptors on peripheral neurones. Because of their high affinity, some of these drugs are the most potent of any pharmacological class yet reported. They have allowed the identification of three M-receptor subtypes, one of which is ...
    Type of Medium: Electronic Resource
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  • 6
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    Unknown
    Urbana, etc. : Periodicals Archive Online (PAO)
    American Journal of Psychology. 74:4 (1961:Dec.) 569 
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 198 (1963), S. 39-74 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] IN a recent article on binocular vision1, it was stated that a necessary condition for the stereoscopic fusion of a pair of disparate patterns is that they should be presented simultaneously, or at least that there should be temporal overlap in the presentation of the two patterns. Some ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Applied microbiology and biotechnology 24 (1986), S. 71-74 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The effect of some sugars in different concentrations and some nitrogeneous organic constituents in 2% yeast extract (basal medium) on production of cyclopiazonic acid (CA) by Penicillium verrucosum var. cyclopium was studied at room temperature. Maximum CA production was observed after 14 days in a medium containing 2% yeast extract +2.5% sucrose. Ammonium lactate had a negative effect on the production of CA by the test culture. Nitrogeneous organic constituents such as peptone and tryptone did not enhance the yield of CA in the medium. After an initial drop in the pH, a general increase in pH was observed as the incubation time increased. Curdled milk was also found to be a suitable medium for the production of CA by the mold culture.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1438-2385
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1438-2385
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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