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We are analyzing https://link.springer.com/article/10.1007/bf00165391.

Title:
Effect of long term caffeine treatment on A1 and A2 adenosine receptor binding and on mRNA levels in rat brain | Naunyn-Schmiedeberg's Archives of Pharmacology
Description:
The effect of long-term oral treatment with caffeine on A1 and A2 receptors in the rat brain was studied. Caffeine was added to the drinking water and the animals were sacrificed after a 12 day treatment period. The plasma caffeine concentration was close to 100 μM. A1 receptors were studied using quantitative autoradiography with [3H]cyclohexyladenosine (CHA). Caffeine treatment increased the number of A1 receptors in the CA3 subfield of the hippocampus from 337 to 393 fmol/mg with no change in KD (0.692 vs. 0.675 nM). A1 mRNA was measured using Northern blots and quantitative in situ hybridization. There was no increase in A1 mRNA. A2a receptors, located in dopamine rich regions of the rat brain, were studied with quantitative autoradiography using [3H]CGS 21680 as the ligand, and the A2a mRNA was determined using quantitative in situ hybridization. Caffeine treatment produced no significant change in either receptor number or mRNA, even though the apparent Bmax tended to increase from 322±8 to 352±8 fmol/mg. The results show that treatment with caffeine in a dose that causes tolerance to several effects of caffeine and increases some effects of adenosine analogues increases the number of A1 receptors without any change in A1 mRNA, suggesting that the adaptive changes are at a post-translational level. There were no significant changes in A2 receptors indicating that the two types are regulated differently and/or that the amount of endogenous agonist is sufficient to regulate A1, but not A2 receptors.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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  • Education
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What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {📈}

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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How Does Link.springer.com Make Money? {💸}

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Keywords {🔍}

google, scholar, adenosine, rat, receptor, receptors, caffeine, brain, treatment, pharmacol, article, mrna, fredholm, effects, dopamine, sci, quantitative, tolerance, theophylline, autoradiographic, res, chronic, privacy, cookies, content, effect, van, longterm, number, hippocampus, increases, access, localization, information, change, publish, search, naunynschmiedebergs, pharmacology, binding, johansson, lindefors, persson, striatum, neuroscience, mol, data, log, journal, research,

Topics {✒️}

g-protein coupled a2-receptors protein-coupled protein month download article/chapter striatal medium-sized neurons long-term oral treatment long-term theophylline treatment long-term caffeine consumption d2 dopamine receptors d1 dopamine receptor adenosine analogues increases privacy choices/manage cookies adenosine a2 receptor vivo pet study long-term treatment van der ploeg adenosine a2 receptors a2-adenosine receptors adenosine a1 receptor a1 adenosine receptor article naunyn-schmiedeberg' full article pdf central nervous system a2 receptors indicating long-term potentiation dopamine rich regions chronic neuroleptic treatment adenosine a1-receptors adenosine a1 receptors nils lindefors & bertil post-translational level chronic theophylline treatment increased receptor number beta receptor number monsma jr fj a2a receptors receptor binding european economic area apparent bmax tended related subjects oligothymidylic acid-cellulose schedule controlled responding vitro hippocampal slice human basal ganglia chain terminating inhibitors caffeine treatment increased caffeine treatment produced ddt1 mf-2 cells cross-tolerance studies drug-specific tolerance rat striatal membranes

Questions {❓}

  • Fredholm BB (1980) Are methylxanthine effects due to antagonism of endogenous adenosine?
  • Fredholm BB, Dunwiddie TV (1988) How does adenosine inhibit transmitter release?

Schema {🗺️}

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         headline:Effect of long term caffeine treatment on A1 and A2 adenosine receptor binding and on mRNA levels in rat brain
         description:The effect of long-term oral treatment with caffeine on A1 and A2 receptors in the rat brain was studied. Caffeine was added to the drinking water and the animals were sacrificed after a 12 day treatment period. The plasma caffeine concentration was close to 100 μM. A1 receptors were studied using quantitative autoradiography with [3H]cyclohexyladenosine (CHA). Caffeine treatment increased the number of A1 receptors in the CA3 subfield of the hippocampus from 337 to 393 fmol/mg with no change in KD (0.692 vs. 0.675 nM). A1 mRNA was measured using Northern blots and quantitative in situ hybridization. There was no increase in A1 mRNA. A2a receptors, located in dopamine rich regions of the rat brain, were studied with quantitative autoradiography using [3H]CGS 21680 as the ligand, and the A2a mRNA was determined using quantitative in situ hybridization. Caffeine treatment produced no significant change in either receptor number or mRNA, even though the apparent Bmax tended to increase from 322±8 to 352±8 fmol/mg. The results show that treatment with caffeine in a dose that causes tolerance to several effects of caffeine and increases some effects of adenosine analogues increases the number of A1 receptors without any change in A1 mRNA, suggesting that the adaptive changes are at a post-translational level. There were no significant changes in A2 receptors indicating that the two types are regulated differently and/or that the amount of endogenous agonist is sufficient to regulate A1, but not A2 receptors.
         datePublished:
         dateModified:
         pageStart:407
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         sameAs:https://doi.org/10.1007/BF00165391
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            Striatum
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      headline:Effect of long term caffeine treatment on A1 and A2 adenosine receptor binding and on mRNA levels in rat brain
      description:The effect of long-term oral treatment with caffeine on A1 and A2 receptors in the rat brain was studied. Caffeine was added to the drinking water and the animals were sacrificed after a 12 day treatment period. The plasma caffeine concentration was close to 100 μM. A1 receptors were studied using quantitative autoradiography with [3H]cyclohexyladenosine (CHA). Caffeine treatment increased the number of A1 receptors in the CA3 subfield of the hippocampus from 337 to 393 fmol/mg with no change in KD (0.692 vs. 0.675 nM). A1 mRNA was measured using Northern blots and quantitative in situ hybridization. There was no increase in A1 mRNA. A2a receptors, located in dopamine rich regions of the rat brain, were studied with quantitative autoradiography using [3H]CGS 21680 as the ligand, and the A2a mRNA was determined using quantitative in situ hybridization. Caffeine treatment produced no significant change in either receptor number or mRNA, even though the apparent Bmax tended to increase from 322±8 to 352±8 fmol/mg. The results show that treatment with caffeine in a dose that causes tolerance to several effects of caffeine and increases some effects of adenosine analogues increases the number of A1 receptors without any change in A1 mRNA, suggesting that the adaptive changes are at a post-translational level. There were no significant changes in A2 receptors indicating that the two types are regulated differently and/or that the amount of endogenous agonist is sufficient to regulate A1, but not A2 receptors.
      datePublished:
      dateModified:
      pageStart:407
      pageEnd:414
      sameAs:https://doi.org/10.1007/BF00165391
      keywords:
         Quantitative receptor autoradiography
         In situ hybridization
         Northern blot
         Tolerance
         Hippocampus
         Striatum
         Pharmacology/Toxicology
         Neurosciences
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         name:Springer-Verlag
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            type:ImageObject
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            name:Björn Johansson
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                  name:Karolinska Institutet
                  address:
                     name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Susanne Ahlberg
            affiliation:
                  name:Karolinska Institutet
                  address:
                     name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
                     type:PostalAddress
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            type:Person
            name:Ingeborg van der Ploeg
            affiliation:
                  name:Karolinska Institutet
                  address:
                     name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Stefan Brené
            affiliation:
                  name:Karolinska Institutet
                  address:
                     name:The Department of Molecular Neurobiology, Karolinska Institutet, Stockholm, Sweden
                     type:PostalAddress
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            name:Nils Lindefors
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                  name:Karolinska Institutet
                  address:
                     name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
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                  name:Karolinska Institutet
                  address:
                     name:The Department of Molecular Neurobiology, Karolinska Institutet, Stockholm, Sweden
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            name:Håkan Persson
            affiliation:
                  name:Karolinska Institutet
                  address:
                     name:The Department of Molecular Neurobiology, Karolinska Institutet, Stockholm, Sweden
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            name:Bertil B. Fredholm
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      name:Susanne Ahlberg
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            address:
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               type:PostalAddress
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            name:Karolinska Institutet
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               name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
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            type:Organization
      name:Stefan Brené
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            name:Karolinska Institutet
            address:
               name:The Department of Molecular Neurobiology, Karolinska Institutet, Stockholm, Sweden
               type:PostalAddress
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      name:Nils Lindefors
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            address:
               name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
               type:PostalAddress
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               type:PostalAddress
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      name:Håkan Persson
      affiliation:
            name:Karolinska Institutet
            address:
               name:The Department of Molecular Neurobiology, Karolinska Institutet, Stockholm, Sweden
               type:PostalAddress
            type:Organization
      name:Bertil B. Fredholm
      affiliation:
            name:Karolinska Institutet
            address:
               name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
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      name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
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      name:The Department of Molecular Neurobiology, Karolinska Institutet, Stockholm, Sweden
      name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
      name:The Department of Molecular Neurobiology, Karolinska Institutet, Stockholm, Sweden
      name:The Department of Molecular Neurobiology, Karolinska Institutet, Stockholm, Sweden
      name:The Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden
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