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Prevention of antibiotic-associated metabolic syndrome in mice by intestinal alkaline phosphatase.

Publication ,  Journal Article
Economopoulos, KP; Ward, NL; Phillips, CD; Teshager, A; Patel, P; Mohamed, MM; Hakimian, S; Cox, SB; Ahmed, R; Moaven, O; Kaliannan, K ...
Published in: Diabetes, obesity & metabolism
May 2016

To examine whether co-administration of intestinal alkaline phosphatase (IAP) with antibiotics early in life may have a preventive role against metabolic syndrome (MetS) in mice.A total of 50 mice were allocated to four treatment groups after weaning. Mice were treated with azithromycin (AZT) ± IAP, or with no AZT ± IAP, for three intermittent 7-day cycles. After the last treatment course, the mice were administered a regular chow diet for 5 weeks and subsequently a high-fat diet for 5 weeks. Body weight, food intake, water intake, serum lipids, glucose levels and liver lipids were compared. 16S rRNA gene pyrosequencing was used to determine the differences in microbiome composition.Exposure to AZT early in life rendered mice susceptible to MetS in adulthood. Co-administration of IAP with AZT completely prevented this susceptibility by decreasing total body weight, serum lipids, glucose levels and liver lipids to the levels of control mice. These effects of IAP probably occur as a result of changes in the composition of specific bacterial taxa at the genus and species levels (e.g. members of Anaeroplasma and Parabacteroides).Co-administration of IAP with AZT early in life prevents mice from susceptibility to the later development of MetS. This effect is associated with alterations in the composition of the gut microbiota. IAP may represent a novel treatment against MetS in humans.

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Published In

Diabetes, obesity & metabolism

DOI

EISSN

1463-1326

ISSN

1462-8902

Publication Date

May 2016

Volume

18

Issue

5

Start / End Page

519 / 527

Related Subject Headings

  • Weight Gain
  • Weaning
  • Obesity
  • Molecular Typing
  • Mice, Inbred C57BL
  • Metabolic Syndrome
  • Male
  • Intestinal Mucosa
  • Gastrointestinal Microbiome
  • Feces
 

Citation

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Chicago
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Economopoulos, K. P., Ward, N. L., Phillips, C. D., Teshager, A., Patel, P., Mohamed, M. M., … Hodin, R. A. (2016). Prevention of antibiotic-associated metabolic syndrome in mice by intestinal alkaline phosphatase. Diabetes, Obesity & Metabolism, 18(5), 519–527. https://doi.org/10.1111/dom.12645
Economopoulos, K. P., N. L. Ward, C. D. Phillips, A. Teshager, P. Patel, M. M. Mohamed, S. Hakimian, et al. “Prevention of antibiotic-associated metabolic syndrome in mice by intestinal alkaline phosphatase.Diabetes, Obesity & Metabolism 18, no. 5 (May 2016): 519–27. https://doi.org/10.1111/dom.12645.
Economopoulos KP, Ward NL, Phillips CD, Teshager A, Patel P, Mohamed MM, et al. Prevention of antibiotic-associated metabolic syndrome in mice by intestinal alkaline phosphatase. Diabetes, obesity & metabolism. 2016 May;18(5):519–27.
Economopoulos, K. P., et al. “Prevention of antibiotic-associated metabolic syndrome in mice by intestinal alkaline phosphatase.Diabetes, Obesity & Metabolism, vol. 18, no. 5, May 2016, pp. 519–27. Epmc, doi:10.1111/dom.12645.
Economopoulos KP, Ward NL, Phillips CD, Teshager A, Patel P, Mohamed MM, Hakimian S, Cox SB, Ahmed R, Moaven O, Kaliannan K, Alam SN, Haller JF, Goldstein AM, Bhan AK, Malo MS, Hodin RA. Prevention of antibiotic-associated metabolic syndrome in mice by intestinal alkaline phosphatase. Diabetes, obesity & metabolism. 2016 May;18(5):519–527.
Journal cover image

Published In

Diabetes, obesity & metabolism

DOI

EISSN

1463-1326

ISSN

1462-8902

Publication Date

May 2016

Volume

18

Issue

5

Start / End Page

519 / 527

Related Subject Headings

  • Weight Gain
  • Weaning
  • Obesity
  • Molecular Typing
  • Mice, Inbred C57BL
  • Metabolic Syndrome
  • Male
  • Intestinal Mucosa
  • Gastrointestinal Microbiome
  • Feces