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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
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  12. Libraries
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We are analyzing https://link.springer.com/article/10.1007/s12017-020-08625-z.

Title:
Bile Acids: A Communication Channel in the Gut-Brain Axis | NeuroMolecular Medicine
Description:
Bile acids are signalling hormones involved in the regulation of several metabolic pathways. The ability of bile acids to bind and signal through their receptors is modulated by the gut microbiome, since the microbiome contributes to the regulation and synthesis of bile acids as well to their physiochemical properties. From the gut, bacteria have been shown to send signals to the central nervous system via their metabolites, thus affecting the behaviour and brain function of the host organism. In the last years it has become increasingly evident that bile acids affect brain function, during normal physiological and pathological conditions. Although bile acids may be synthesized locally in the brain, the majority of brain bile acids are taken up from the systemic circulation. Since the composition of the brain bile acid pool may be regulated by the action of intestinal bacteria, it is possible that bile acids function as a communication bridge between the gut microbiome and the brain. However, little is known about the molecular mechanisms and the physiological roles of bile acids in the central nervous system. The possibility that bile acids may be a direct link between the intestinal microbiome and the brain is also an understudied subject. Here we review the influence of gut bacteria on the bile acid pool composition and properties, as well as striking evidence showing the role of bile acids as neuroactive molecules.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Health & Fitness

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.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Link.springer.com might be cashing in, but we can't detect the method they're using.

Keywords {🔍}

pubmed, article, google, scholar, cas, bile, central, acid, acids, journal, disease, brain, receptor, gut, metabolism, research, nature, molecular, mice, sciences, microbiota, rodrigues, function, receptors, role, national, cell, neuroscience, signaling, tauroursodeoxycholic, wang, regulation, intestinal, alzheimers, proceedings, academy, parkinsons, axis, microbiome, physiology, clinical, model, neurobiology, liver, singapore, medicine, review, behavior, development, experimental,

Topics {✒️}

month download article/chapter n-methyl-d-aspartate receptors short-chain fatty acids lipopolysaccharide-induced microglial activation protein-coupled receptor responsive aci-induced neurological impairment 3beta-hydroxy-5-cholenoic acid tauro-beta-muricholic acid lc/esi-ms/ms h218/agr16/edg-5/lp nuclear receptor fxr/bar brain-gut-microbe axis regulates energy homeostasis bile acid-activated vitamin bile-acid-activated receptors central nervous system article monteiro-cardoso intestinal bile acid/farnesoid full article pdf sphingosine-1-phosphate receptor 2 sphingosine-1-phosphate receptor-2 sphingosine 1-phosphate receptor central neurochemical change brain-gut-microbe communication gut-brain axis bile acid signaling rate-limiting enzyme privacy choices/manage cookies amyloid-β deposition stimulating glucocorticoid receptor unconjugated bile acids glucose disorders bile-acid conjugations amyloid-β pathology enhanced insulin signaling nrf2 signaling pathway amyloid cascade hypothesis repressing synaptic plasticity early synaptic pathophysiology bile acid metabolism bile salt biotransformations farnesoid-x-receptor sphingolipid receptor s1pr2 nuclear receptor pxr individual bile acids free bile acids bile acids permeabilize endogenous bile acids tauroursodeoxycholic acid treatment membrane-type receptor

Questions {❓}

  • Bile in the brain?
  • Epigenetic targeting of histone deacetylase: Therapeutic potential in Parkinson’s Disease?

Schema {🗺️}

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         headline:Bile Acids: A Communication Channel in the Gut-Brain Axis
         description:Bile acids are signalling hormones involved in the regulation of several metabolic pathways. The ability of bile acids to bind and signal through their receptors is modulated by the gut microbiome, since the microbiome contributes to the regulation and synthesis of bile acids as well to their physiochemical properties. From the gut, bacteria have been shown to send signals to the central nervous system via their metabolites, thus affecting the behaviour and brain function of the host organism. In the last years it has become increasingly evident that bile acids affect brain function, during normal physiological and pathological conditions. Although bile acids may be synthesized locally in the brain, the majority of brain bile acids are taken up from the systemic circulation. Since the composition of the brain bile acid pool may be regulated by the action of intestinal bacteria, it is possible that bile acids function as a communication bridge between the gut microbiome and the brain. However, little is known about the molecular mechanisms and the physiological roles of bile acids in the central nervous system. The possibility that bile acids may be a direct link between the intestinal microbiome and the brain is also an understudied subject. Here we review the influence of gut bacteria on the bile acid pool composition and properties, as well as striking evidence showing the role of bile acids as neuroactive molecules.
         datePublished:2020-10-21T00:00:00Z
         dateModified:2020-10-21T00:00:00Z
         pageStart:99
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            Neurodegenerative disorders
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      headline:Bile Acids: A Communication Channel in the Gut-Brain Axis
      description:Bile acids are signalling hormones involved in the regulation of several metabolic pathways. The ability of bile acids to bind and signal through their receptors is modulated by the gut microbiome, since the microbiome contributes to the regulation and synthesis of bile acids as well to their physiochemical properties. From the gut, bacteria have been shown to send signals to the central nervous system via their metabolites, thus affecting the behaviour and brain function of the host organism. In the last years it has become increasingly evident that bile acids affect brain function, during normal physiological and pathological conditions. Although bile acids may be synthesized locally in the brain, the majority of brain bile acids are taken up from the systemic circulation. Since the composition of the brain bile acid pool may be regulated by the action of intestinal bacteria, it is possible that bile acids function as a communication bridge between the gut microbiome and the brain. However, little is known about the molecular mechanisms and the physiological roles of bile acids in the central nervous system. The possibility that bile acids may be a direct link between the intestinal microbiome and the brain is also an understudied subject. Here we review the influence of gut bacteria on the bile acid pool composition and properties, as well as striking evidence showing the role of bile acids as neuroactive molecules.
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         Gut microbiome
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         Internal Medicine
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External Links {🔗}(481)

Analytics and Tracking {📊}

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Libraries {📚}

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CDN Services {📦}

  • Crossref

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