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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s00401-013-1145-2.

Title:
Interstitial fluid drainage is impaired in ischemic stroke and Alzheimer’s disease mouse models | Acta Neuropathologica
Description:
The interstitial fluid (ISF) drainage pathway has been hypothesized to underlie the clearance of solutes and metabolites from the brain. Previous work has implicated the perivascular spaces along arteries as the likely route for ISF clearance; however, it has never been demonstrated directly. The accumulation of amyloid β (Aβ) peptides in brain parenchyma is one of the pathological hallmarks of Alzheimer disease (AD), and it is likely related to an imbalance between production and clearance of the peptide. Aβ drainage along perivascular spaces has been postulated to be one of the mechanisms that mediate the peptide clearance from the brain. We therefore devised a novel method to visualize solute clearance in real time in the living mouse brain using laser guided bolus dye injections and multiphoton imaging. This methodology allows high spatial and temporal resolution and revealed the kinetics of ISF clearance. We found that the ISF drains along perivascular spaces of arteries and capillaries but not veins, and its clearance exhibits a bi-exponential profile. ISF drainage requires a functional vasculature, as solute clearance decreased when perfusion was impaired. In addition, reduced solute clearance was observed in transgenic mice with significant vascular amyloid deposition; we suggest the existence of a feed-forward mechanism, by which amyloid deposition promotes further amyloid deposition. This important finding provides a mechanistic link between cerebrovascular disease and Alzheimer disease and suggests that facilitation of Aβ clearance along the perivascular pathway should be considered as a new target for therapeutic approaches to Alzheimer disease and cerebral amyloid angiopathy.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Shopping

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

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.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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

The income method remains a mystery to us.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

google, scholar, article, cas, pubmed, amyloid, brain, disease, cerebral, alzheimers, clearance, angiopathy, interstitial, fluid, mouse, drainage, greenberg, perivascular, alzheimer, frosch, bacskai, neuropathol, neurol, acta, stroke, access, research, spaces, flow, usa, privacy, cookies, content, impaired, isf, imaging, deposition, model, neurobiol, amyloidbeta, neurosci, cognitive, medical, data, publish, search, steven, betensky, solutes, related,

Topics {✒️}

month download article/chapter sensory-evoked hemodynamic responses appswe/ps1de9 mouse model ldl receptor-related protein-1 plasma amyloid-beta efflux article arbel-ornath age-dependent cerebrovascular dysfunction blood-brain barrier cerebral interstitial fluid cerebral amyloid angiopathy full article pdf interstitial fluid drainage brain interstitial fluid disease mouse models robbins em amyloid β privacy choices/manage cookies transgenic mouse model blood flow observed including amyloid beta amyloid beta-protein related subjects amyloid deposition promotes katharina eikermann-haerter zhang-nunes sx kalaria rn amyloid-beta deposits amyloid beta accumulates penetrating vessel leads check access instant access cerebral capillary morphology cerebro-spinal fluid brain amyloid burden vinters hv living mouse brain high-flow microinfusion amyloid beta-peptide amyloid-beta metabolism amyloid-beta peptide photochemically initiated thrombosis smith ee harvard medical school european economic area interstitial fluid bi-exponential profile feed-forward mechanism deep cervical lymph microdialysis reveals plaque rank-sum tests

Questions {❓}

  • Launer LJ, Petrovitch H, Ross GW, Markesbery W, White LR (2008) AD brain pathology: vascular origins?

Schema {🗺️}

WebPage:
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         headline:Interstitial fluid drainage is impaired in ischemic stroke and Alzheimer’s disease mouse models
         description:The interstitial fluid (ISF) drainage pathway has been hypothesized to underlie the clearance of solutes and metabolites from the brain. Previous work has implicated the perivascular spaces along arteries as the likely route for ISF clearance; however, it has never been demonstrated directly. The accumulation of amyloid β (Aβ) peptides in brain parenchyma is one of the pathological hallmarks of Alzheimer disease (AD), and it is likely related to an imbalance between production and clearance of the peptide. Aβ drainage along perivascular spaces has been postulated to be one of the mechanisms that mediate the peptide clearance from the brain. We therefore devised a novel method to visualize solute clearance in real time in the living mouse brain using laser guided bolus dye injections and multiphoton imaging. This methodology allows high spatial and temporal resolution and revealed the kinetics of ISF clearance. We found that the ISF drains along perivascular spaces of arteries and capillaries but not veins, and its clearance exhibits a bi-exponential profile. ISF drainage requires a functional vasculature, as solute clearance decreased when perfusion was impaired. In addition, reduced solute clearance was observed in transgenic mice with significant vascular amyloid deposition; we suggest the existence of a feed-forward mechanism, by which amyloid deposition promotes further amyloid deposition. This important finding provides a mechanistic link between cerebrovascular disease and Alzheimer disease and suggests that facilitation of Aβ clearance along the perivascular pathway should be considered as a new target for therapeutic approaches to Alzheimer disease and cerebral amyloid angiopathy.
         datePublished:2013-07-02T00:00:00Z
         dateModified:2013-07-02T00:00:00Z
         pageStart:353
         pageEnd:364
         sameAs:https://doi.org/10.1007/s00401-013-1145-2
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            Amyloid β
            Cerebral amyloid angiopathy
            Interstitial fluids
            Ischemic stroke
            Perivascular space
            Pathology
            Neurosciences
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      headline:Interstitial fluid drainage is impaired in ischemic stroke and Alzheimer’s disease mouse models
      description:The interstitial fluid (ISF) drainage pathway has been hypothesized to underlie the clearance of solutes and metabolites from the brain. Previous work has implicated the perivascular spaces along arteries as the likely route for ISF clearance; however, it has never been demonstrated directly. The accumulation of amyloid β (Aβ) peptides in brain parenchyma is one of the pathological hallmarks of Alzheimer disease (AD), and it is likely related to an imbalance between production and clearance of the peptide. Aβ drainage along perivascular spaces has been postulated to be one of the mechanisms that mediate the peptide clearance from the brain. We therefore devised a novel method to visualize solute clearance in real time in the living mouse brain using laser guided bolus dye injections and multiphoton imaging. This methodology allows high spatial and temporal resolution and revealed the kinetics of ISF clearance. We found that the ISF drains along perivascular spaces of arteries and capillaries but not veins, and its clearance exhibits a bi-exponential profile. ISF drainage requires a functional vasculature, as solute clearance decreased when perfusion was impaired. In addition, reduced solute clearance was observed in transgenic mice with significant vascular amyloid deposition; we suggest the existence of a feed-forward mechanism, by which amyloid deposition promotes further amyloid deposition. This important finding provides a mechanistic link between cerebrovascular disease and Alzheimer disease and suggests that facilitation of Aβ clearance along the perivascular pathway should be considered as a new target for therapeutic approaches to Alzheimer disease and cerebral amyloid angiopathy.
      datePublished:2013-07-02T00:00:00Z
      dateModified:2013-07-02T00:00:00Z
      pageStart:353
      pageEnd:364
      sameAs:https://doi.org/10.1007/s00401-013-1145-2
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         Alzheimer’s disease
         Amyloid β
         Cerebral amyloid angiopathy
         Interstitial fluids
         Ischemic stroke
         Perivascular space
         Pathology
         Neurosciences
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                  address:
                     name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
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            name:Katharina Eikermann-Haerter
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                  name:Massachusetts General Hospital and Harvard Medical School
                  address:
                     name:Stroke and Neurovascular Regulation Laboratory, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
                     type:PostalAddress
                  type:Organization
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            name:Steven Hou
            affiliation:
                  name:Massachusetts General Hospital and Harvard Medical School
                  address:
                     name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Julia L. Gregory
            affiliation:
                  name:Massachusetts General Hospital and Harvard Medical School
                  address:
                     name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Lingzhi Zhao
            affiliation:
                  name:Massachusetts General Hospital and Harvard Medical School
                  address:
                     name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
                     type:PostalAddress
                  type:Organization
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                  name:Harvard School of Public Health
                  address:
                     name:Department of Biostatistics, Harvard School of Public Health, Boston, USA
                     type:PostalAddress
                  type:Organization
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            name:Matthew P. Frosch
            affiliation:
                  name:Massachusetts General Hospital and Harvard Medical School
                  address:
                     name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
                     type:PostalAddress
                  type:Organization
                  name:Massachusetts General Hospital and Harvard Medical School
                  address:
                     name:C.S. Kubik Laboratory for Neuropathology, Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
                     type:PostalAddress
                  type:Organization
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            name:Steven M. Greenberg
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                  name:Massachusetts General Hospital and Harvard Medical School
                  address:
                     name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
                     type:PostalAddress
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            name:Brian J. Bacskai
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                  name:Massachusetts General Hospital and Harvard Medical School
                  address:
                     name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
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      volumeNumber:126
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         name:Department of Biostatistics, Harvard School of Public Health, Boston, USA
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      name:Massachusetts General Hospital and Harvard Medical School
      address:
         name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
         type:PostalAddress
      name:Massachusetts General Hospital and Harvard Medical School
      address:
         name:C.S. Kubik Laboratory for Neuropathology, Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
         type:PostalAddress
      name:Massachusetts General Hospital and Harvard Medical School
      address:
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      name:Eloise Hudry
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            name:Massachusetts General Hospital and Harvard Medical School
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            address:
               name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
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            name:Massachusetts General Hospital and Harvard Medical School
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               name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
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            name:Massachusetts General Hospital and Harvard Medical School
            address:
               name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
               type:PostalAddress
            type:Organization
            name:Massachusetts General Hospital and Harvard Medical School
            address:
               name:C.S. Kubik Laboratory for Neuropathology, Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
               type:PostalAddress
            type:Organization
      name:Steven M. Greenberg
      affiliation:
            name:Massachusetts General Hospital and Harvard Medical School
            address:
               name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
               type:PostalAddress
            type:Organization
      name:Brian J. Bacskai
      affiliation:
            name:Massachusetts General Hospital and Harvard Medical School
            address:
               name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
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      name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:Stroke and Neurovascular Regulation Laboratory, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:Department of Biostatistics, Harvard School of Public Health, Boston, USA
      name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:C.S. Kubik Laboratory for Neuropathology, Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
      name:Alzheimer Research Unit, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA
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External Links {🔗}(193)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Particles.js
  • Prism.js

CDN Services {📦}

  • Crossref

3.99s.