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We are analyzing https://link.springer.com/article/10.1007/s00125-006-0334-0.

Title:
Antibiotic treatment partially protects against type 1 diabetes in the Bio-Breeding diabetes-prone rat. Is the gut flora involved in the development of type 1 diabetes? | Diabetologia
Description:
Aims/hypothesis Accumulating data suggest that the gut immune system plays a role in the development of type 1 diabetes. The intestinal flora is essential for the development of the (gut) immune system and the establishment of tolerance. It has been reported that oral administration of food and bacterial antigens early in life suppresses later development of diabetes in the Bio-Breeding diabetes-prone (BB-DP) rat. This study was designed to investigate the possible relationship between the development of diabetes and the composition of intestinal flora. Materials and methods The intestinal flora of BB-DP rats, a rat model for type 1 diabetes, was characterised long before the clinical onset of diabetes by fluorescent in situ hybridisation. In a separate experiment, BB-DP rats were treated with antibiotics and the effect on diabetes incidence and level of insulitis was analysed. Results We observed a difference in bacterial composition between rats that eventually did and those that did not develop diabetes. This difference was detectable long before clinical onset of the disease. Rats that did not develop diabetes at a later age displayed a lower amount of Bacteroides sp. Modulation of the intestinal flora through antibiotic treatment decreased the incidence and delayed the onset of diabetes. A combination of antibiotic treatment and a protective hydrolysed casein diet completely prevented diabetes in the BB-DP rat. Conclusions/interpretation Our data suggest that the intestinal flora is involved in the development of type 1 diabetes. Factors influencing composition of the intestinal flora could be a target for therapeutic intervention.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Health & Fitness
  • Science
  • Education

Content Management System {๐Ÿ“}

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 {๐Ÿ“ˆ}

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

๐ŸŒ  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? {๐Ÿ’ธ}

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

Not every website is profit-driven; some are created to spread information or serve as an online presence. Websites can be made for many reasons. This could be one of them. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {๐Ÿ”}

diabetes, rats, bbdp, treatment, flora, diet, antibiotic, intestinal, type, development, article, onset, composition, con, rat, analysis, data, effect, google, scholar, incidence, insulitis, develop, bacteria, pubmed, cas, fluorescent, shown, faecal, experiment, antigenic, load, samples, probes, developed, gut, system, bacterial, antibiotics, hydrolysed, casein, diabetic, groningen, groups, received, group, receiving, privacy, cookies, diabetologia,

Topics {โœ’๏ธ}

diabetes-preventive gluten-free diet bio-breeding diabetes-prone rat 16sย rrna-based fluorescent probes dashed linebb-dp rats bio-breeding diabetes-prone amino acids [solka-floc worchester bb-dp strain anti-staphylococcal drug fusidin universal 16sย rrna probe bb-dp rats effectiveness unmanipulated bb-dp rats specific-pathogen-free conditions bb-dp rat model pre-diabetic timepoint con+antibiotic treatment compared privacy choices/manage cookies bb-dp rats bb-dp rats [5 bb-dp rats [7] bb-dp rat bacterial group-specific probes abbreviations bb-dp future preventive measures rats received antibiotics conventional plant-based receiving hc diet hydrolysed casein diet control rats receiving figureย 1 shows binding received antibiotic treatment antibiotic treatment received increased hygienic conditions data strongly support animals developed diabetes rats developed diabetes scott fw developed diabetes show conditions privacy policy antibiotic treatment decreased combining antibiotic treatment group receiving con ain-93g diet plant-based diets short communication published filter-top cages lymphocyte-stimulatory activities cytokine gene expression terminal ileum biopsies search search develop diabetes suggests

Questions {โ“}

  • Is the gut flora involved in the development of type 1 diabetes?

Schema {๐Ÿ—บ๏ธ}

WebPage:
      mainEntity:
         headline:Antibiotic treatment partially protects against type 1 diabetes in the Bio-Breeding diabetes-prone rat. Is the gut flora involved in the development of type 1 diabetes?
         description:Accumulating data suggest that the gut immune system plays a role in the development of type 1 diabetes. The intestinal flora is essential for the development of the (gut) immune system and the establishment of tolerance. It has been reported that oral administration of food and bacterial antigens early in life suppresses later development of diabetes in the Bio-Breeding diabetes-prone (BB-DP) rat. This study was designed to investigate the possible relationship between the development of diabetes and the composition of intestinal flora. The intestinal flora of BB-DP rats, a rat model for type 1 diabetes, was characterised long before the clinical onset of diabetes by fluorescent in situ hybridisation. In a separate experiment, BB-DP rats were treated with antibiotics and the effect on diabetes incidence and level of insulitis was analysed. We observed a difference in bacterial composition between rats that eventually did and those that did not develop diabetes. This difference was detectable long before clinical onset of the disease. Rats that did not develop diabetes at a later age displayed a lower amount of Bacteroides sp. Modulation of the intestinal flora through antibiotic treatment decreased the incidence and delayed the onset of diabetes. A combination of antibiotic treatment and a protective hydrolysed casein diet completely prevented diabetes in the BB-DP rat. Our data suggest that the intestinal flora is involved in the development of type 1 diabetes. Factors influencing composition of the intestinal flora could be a target for therapeutic intervention.
         datePublished:2006-07-01T00:00:00Z
         dateModified:2006-07-01T00:00:00Z
         pageStart:2105
         pageEnd:2108
         sameAs:https://doi.org/10.1007/s00125-006-0334-0
         keywords:
            Antibiotics
            BB-DP rats
            Insulitis
            Intestinal flora
            Type 1 diabetes
            Internal Medicine
            Metabolic Diseases
            Human Physiology
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         isPartOf:
            name:Diabetologia
            issn:
               1432-0428
               0012-186X
            volumeNumber:49
            type:
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               PublicationVolume
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                        name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
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                     name:University Medical Center Groningen, University of Groningen
                     address:
                        name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
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         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Antibiotic treatment partially protects against type 1 diabetes in the Bio-Breeding diabetes-prone rat. Is the gut flora involved in the development of type 1 diabetes?
      description:Accumulating data suggest that the gut immune system plays a role in the development of type 1 diabetes. The intestinal flora is essential for the development of the (gut) immune system and the establishment of tolerance. It has been reported that oral administration of food and bacterial antigens early in life suppresses later development of diabetes in the Bio-Breeding diabetes-prone (BB-DP) rat. This study was designed to investigate the possible relationship between the development of diabetes and the composition of intestinal flora. The intestinal flora of BB-DP rats, a rat model for type 1 diabetes, was characterised long before the clinical onset of diabetes by fluorescent in situ hybridisation. In a separate experiment, BB-DP rats were treated with antibiotics and the effect on diabetes incidence and level of insulitis was analysed. We observed a difference in bacterial composition between rats that eventually did and those that did not develop diabetes. This difference was detectable long before clinical onset of the disease. Rats that did not develop diabetes at a later age displayed a lower amount of Bacteroides sp. Modulation of the intestinal flora through antibiotic treatment decreased the incidence and delayed the onset of diabetes. A combination of antibiotic treatment and a protective hydrolysed casein diet completely prevented diabetes in the BB-DP rat. Our data suggest that the intestinal flora is involved in the development of type 1 diabetes. Factors influencing composition of the intestinal flora could be a target for therapeutic intervention.
      datePublished:2006-07-01T00:00:00Z
      dateModified:2006-07-01T00:00:00Z
      pageStart:2105
      pageEnd:2108
      sameAs:https://doi.org/10.1007/s00125-006-0334-0
      keywords:
         Antibiotics
         BB-DP rats
         Insulitis
         Intestinal flora
         Type 1 diabetes
         Internal Medicine
         Metabolic Diseases
         Human Physiology
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1007%2Fs00125-006-0334-0/MediaObjects/125_2006_334_Fig1_HTML.gif
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1007%2Fs00125-006-0334-0/MediaObjects/125_2006_334_Fig2_HTML.gif
      isPartOf:
         name:Diabetologia
         issn:
            1432-0428
            0012-186X
         volumeNumber:49
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         name:Springer-Verlag
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            type:ImageObject
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            name:S. Brugman
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                  name:University Medical Center Groningen, University of Groningen
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                  address:
                     name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
                     type:PostalAddress
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            name:J. T. J. Visser
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                  name:University Medical Center Groningen, University of Groningen
                  address:
                     name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
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            name:A. C. M. Wildeboer-Veloo
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                  name:University Medical Center Groningen
                  address:
                     name:Department of Medical Microbiology, University Medical Center Groningen, Groningen, The Netherlands
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            name:H. J. M. Harmsen
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                  name:University Medical Center Groningen
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                     name:Department of Medical Microbiology, University Medical Center Groningen, Groningen, The Netherlands
                     type:PostalAddress
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            name:J. Rozing
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                  name:University Medical Center Groningen, University of Groningen
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                     name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
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            name:University Medical Center Groningen, University of Groningen
            address:
               name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
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            name:University Medical Center Groningen, University of Groningen
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               name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
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      name:J. T. J. Visser
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            name:University Medical Center Groningen, University of Groningen
            address:
               name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
               type:PostalAddress
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      name:A. C. M. Wildeboer-Veloo
      affiliation:
            name:University Medical Center Groningen
            address:
               name:Department of Medical Microbiology, University Medical Center Groningen, Groningen, The Netherlands
               type:PostalAddress
            type:Organization
      name:H. J. M. Harmsen
      affiliation:
            name:University Medical Center Groningen
            address:
               name:Department of Medical Microbiology, University Medical Center Groningen, Groningen, The Netherlands
               type:PostalAddress
            type:Organization
      name:J. Rozing
      affiliation:
            name:University Medical Center Groningen, University of Groningen
            address:
               name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
               type:PostalAddress
            type:Organization
      name:N. A. Bos
      affiliation:
            name:University Medical Center Groningen, University of Groningen
            address:
               name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
      name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
      name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
      name:Department of Medical Microbiology, University Medical Center Groningen, Groningen, The Netherlands
      name:Department of Medical Microbiology, University Medical Center Groningen, Groningen, The Netherlands
      name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
      name:Department of Cell Biology, Immunology Section, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands

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