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We are analyzing https://link.springer.com/article/10.1007/s11302-012-9299-2.

Title:
Anti-inflammatory effects of purine nucleosides, adenosine and inosine, in a mouse model of pleurisy: evidence for the role of adenosine A2 receptors | Purinergic Signalling
Description:
Adenosine and its metabolite, inosine, have been described as molecules that participate in regulation of inflammatory response. The aim of this study was to investigate the effect of adenosine and inosine in a mouse model of carrageenan-induced pleurisy as well as the participation of adenosine receptors in this response. Injection of carrageenan into the pleural cavity induced an acute inflammatory response characterized by leukocyte migration, pleural exudation, and increased release of interleukin-1β and tumor necrosis factor-α in pleural exudates. The treatment with adenosine (0.3–100 mg/kg, i.p.) and inosine (0.1–300 mg/kg, i.p.) 30 min before carrageenan injection reduced significantly all these parameters analyzed. Our results also demonstrated that A2A and A2B receptors seem to mediate the adenosine and inosine effects observed, since pretreatment with selective antagonists of adenosine A2A (ZM241385) and A2B (alloxazine) receptors, reverted the inhibitory effects of adenosine and inosine in pleural inflammation. The involvement of A2 receptors was reinforced with adenosine receptor agonist CGS21680 treatment, since its anti-inflammatory effects were reversed completely and partially with ZM241385 and alloxazine injection, respectively. Moreover, the combined treatment with subeffective dose of adenosine (0.3 mg/kg) and inosine (1.0 mg/kg) induced a synergistic anti-inflammatory effect. Thus, based on these findings, we propose that inosine contributes with adenosine to exert anti-inflammatory effects in pleural inflammation, reinforcing the notion that endogenous nucleosides play an important role in controlling inflammatory diseases. This effect is likely mediated by the activation of adenosine A2 subtype receptors and inhibition of production or release of pro-inflammatory cytokines.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
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Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

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What is the average monthly size of link.springer.com audience?

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


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We don't see any clear sign of profit-making.

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Keywords {🔍}

google, scholar, adenosine, pubmed, cas, article, pharmacol, inflammation, inosine, receptors, receptor, effects, antiinflammatory, role, inflammatory, eltzschig, pleurisy, hasko, szabo, model, pleural, rev, linden, mouse, acute, exp, med, ther, physiol, eur, privacy, cookies, content, signalling, effect, carrageenan, release, activation, mice, pharmacology, clin, cronstein, shock, publish, search, purinergic, silva, almeida, adair, santos,

Topics {✒️}

tumor necrosis factor-α month download article/chapter carrageenan-induced lung injury neca-induced anti-inflammatory effects anti-inflammatory flavonoid glycoside serine/threonine protein phosphatase exert anti-inflammatory effects endogenous anti-inflammatory agent de almeida cabrini rat carrageenin-induced pleurisy adenosine-dependent pulmonary inflammation synergistic anti-inflammatory effect full article pdf da silva acute tubular necrosis carrageenan-induced pleurisy purinergic signalling 8 purinergic receptor agonists excessive vascular adhesion a3 adenosine receptor privacy choices/manage cookies vascular nucleoside transporters author information authors adenosine a2 receptors nf-kappab activation pathways anti-inflammatory effects adenosine a2b receptors adenosine receptor induction related aglycone flavonoids a3 adenosine receptors anti-inflammatory activity receptor-specific knockouts adenosine receptor agonists related subjects experimental acute pancreatitis eltzschig hk a2b receptor activation inflammatory responses induced macrophage inflammatory protein alpha s-linked pro-inflammatory effects surface adenosine deaminase collagen-induced arthritis pro-inflammatory cytokines endogenous signaling molecules inflammatory organ damage drug newly discovered receptor-mediated mechanisms inosine effects observed inosine reduces inflammation

Questions {❓}

  • Law WR (2006) Adenosine receptors in the response to sepsis: what do receptor-specific knockouts tell us?

Schema {🗺️}

WebPage:
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         headline:Anti-inflammatory effects of purine nucleosides, adenosine and inosine, in a mouse model of pleurisy: evidence for the role of adenosine A2 receptors
         description:Adenosine and its metabolite, inosine, have been described as molecules that participate in regulation of inflammatory response. The aim of this study was to investigate the effect of adenosine and inosine in a mouse model of carrageenan-induced pleurisy as well as the participation of adenosine receptors in this response. Injection of carrageenan into the pleural cavity induced an acute inflammatory response characterized by leukocyte migration, pleural exudation, and increased release of interleukin-1β and tumor necrosis factor-α in pleural exudates. The treatment with adenosine (0.3–100 mg/kg, i.p.) and inosine (0.1–300 mg/kg, i.p.) 30 min before carrageenan injection reduced significantly all these parameters analyzed. Our results also demonstrated that A2A and A2B receptors seem to mediate the adenosine and inosine effects observed, since pretreatment with selective antagonists of adenosine A2A (ZM241385) and A2B (alloxazine) receptors, reverted the inhibitory effects of adenosine and inosine in pleural inflammation. The involvement of A2 receptors was reinforced with adenosine receptor agonist CGS21680 treatment, since its anti-inflammatory effects were reversed completely and partially with ZM241385 and alloxazine injection, respectively. Moreover, the combined treatment with subeffective dose of adenosine (0.3 mg/kg) and inosine (1.0 mg/kg) induced a synergistic anti-inflammatory effect. Thus, based on these findings, we propose that inosine contributes with adenosine to exert anti-inflammatory effects in pleural inflammation, reinforcing the notion that endogenous nucleosides play an important role in controlling inflammatory diseases. This effect is likely mediated by the activation of adenosine A2 subtype receptors and inhibition of production or release of pro-inflammatory cytokines.
         datePublished:2012-03-29T00:00:00Z
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      headline:Anti-inflammatory effects of purine nucleosides, adenosine and inosine, in a mouse model of pleurisy: evidence for the role of adenosine A2 receptors
      description:Adenosine and its metabolite, inosine, have been described as molecules that participate in regulation of inflammatory response. The aim of this study was to investigate the effect of adenosine and inosine in a mouse model of carrageenan-induced pleurisy as well as the participation of adenosine receptors in this response. Injection of carrageenan into the pleural cavity induced an acute inflammatory response characterized by leukocyte migration, pleural exudation, and increased release of interleukin-1β and tumor necrosis factor-α in pleural exudates. The treatment with adenosine (0.3–100 mg/kg, i.p.) and inosine (0.1–300 mg/kg, i.p.) 30 min before carrageenan injection reduced significantly all these parameters analyzed. Our results also demonstrated that A2A and A2B receptors seem to mediate the adenosine and inosine effects observed, since pretreatment with selective antagonists of adenosine A2A (ZM241385) and A2B (alloxazine) receptors, reverted the inhibitory effects of adenosine and inosine in pleural inflammation. The involvement of A2 receptors was reinforced with adenosine receptor agonist CGS21680 treatment, since its anti-inflammatory effects were reversed completely and partially with ZM241385 and alloxazine injection, respectively. Moreover, the combined treatment with subeffective dose of adenosine (0.3 mg/kg) and inosine (1.0 mg/kg) induced a synergistic anti-inflammatory effect. Thus, based on these findings, we propose that inosine contributes with adenosine to exert anti-inflammatory effects in pleural inflammation, reinforcing the notion that endogenous nucleosides play an important role in controlling inflammatory diseases. This effect is likely mediated by the activation of adenosine A2 subtype receptors and inhibition of production or release of pro-inflammatory cytokines.
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         Inosine
         Carrageenan
         Pleurisy
         Adenosine receptors
         Biomedicine
         general
         Pharmacology/Toxicology
         Human Physiology
         Neurosciences
         Cancer Research
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                     name:Graduate Program in Pharmacology, Department of Pharmacology, Center of Biological Sciences, Federal University of Paraná, Curitiba, Brazil
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            affiliation:
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                  address:
                     name:Graduate Program in Pharmacology, Department of Pharmacology, Center of Biological Sciences, Federal University of Paraná, Curitiba, Brazil
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      name:Morgana Duarte da Silva
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            name:Federal University of Santa Catarina
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               name:Laboratory of Neurobiology of Pain and Inflammation, Department of Physiological Sciences, Federal University of Santa Catarina, Florianopolis, Brazil
               type:PostalAddress
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      name:Daniela de Almeida Cabrini
      affiliation:
            name:Federal University of Paraná
            address:
               name:Graduate Program in Pharmacology, Department of Pharmacology, Center of Biological Sciences, Federal University of Paraná, Curitiba, Brazil
               type:PostalAddress
            type:Organization
      name:Adair R. S. Santos
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            name:Federal University of Paraná
            address:
               name:Graduate Program in Pharmacology, Department of Pharmacology, Center of Biological Sciences, Federal University of Paraná, Curitiba, Brazil
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      name:Graduate Program in Pharmacology, Department of Pharmacology, Center of Biological Sciences, Federal University of Paraná, Curitiba, Brazil
      name:Graduate Program in Pharmacology, Department of Pharmacology, Center of Biological Sciences, Federal University of Paraná, Curitiba, Brazil
      name:Laboratory of Neurobiology of Pain and Inflammation, Department of Physiological Sciences, Federal University of Santa Catarina, Florianopolis, Brazil
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