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Published on: November 17, 2018
Effects of Polymannuronic Acid on the Intestinal Microbiota in Mice after Long-Term Intragastric Administration
Abstract:
Polymannuronic acid (PM) is an alginate oligosaccharide derived from brown algae with a characterized structure and excellent biological activities. Herein, mice were given different doses of PM through 30-day-long-term intragastric administration, and the contents of the jejunum, ileum, and colon were analyzed by 16S rRNA gene sequencing technology for microbial diversity, and relevant experiments were verified according to the analysis results so as to comprehensively evaluate the effects of PM on the intestinal flora. The PM (400 mg/kg and 100 mg/kg) could regulate the microflora balance at the phylum level and increase the microflora richness in the jejunum, ileum, and colon of the mice. The PM could induce more strains that are negatively correlated with Escherichia, thereby reducing the relative abundance of Escherichia. Analysis of bacterial function showed that high and low doses of PM could promote lipid metabolism in the bacterial communities. Moreover, the PM could reduce serum total cholesterol and cholesterol ester levels in a concentration-dependent manner. High-dose PM could lead to colonic intestinal inflammation by increasing the relative abundance of multiple bacterial groups in the jejunum, ileum, and colon. Moreover, high-dose PM could increase lipopolysaccharide-binding protein and interleukin-1β levels. Therefore, the dose of PM plays an important role in its efficacy, and its biological activity is dosedifferent.
Insights
Polymannuronic acid (PM) from brown algae impacts gut microbiota. While beneficial at lower doses, high doses of PM can cause colonic inflammation in mice.
Area of Science:
- Marine biotechnology
- Microbiome research
- Algal oligosaccharides
Background:
- Polymannuronic acid (PM), an alginate oligosaccharide from brown algae, possesses known biological activities.
- Intestinal flora plays a crucial role in host health and metabolism.
Purpose of the Study:
- To comprehensively evaluate the effects of different doses of PM on the intestinal flora in mice.
- To investigate the dose-dependent biological activities of PM on gut microbiota and host physiology.
Main Methods:
- Mice received varying doses of PM via intragastric administration for 30 days.
- 16S rRNA gene sequencing analyzed microbial diversity in the jejunum, ileum, and colon.
- Bacterial function, serum cholesterol, and inflammatory markers were assessed.
Main Results:
- PM (100 and 400 mg/kg) modulated microflora balance and increased richness in all intestinal segments.
- PM reduced the relative abundance of *Escherichia* and promoted bacterial lipid metabolism.
- High-dose PM increased colonic intestinal inflammation, lipopolysaccharide-binding protein, and interleukin-1β levels.
- PM demonstrated a dose-dependent effect on serum total cholesterol and cholesterol ester levels.
Conclusions:
- PM exhibits dose-dependent effects on the gut microbiota and host, influencing microbial balance, lipid metabolism, and inflammation.
- Lower doses of PM may beneficially regulate intestinal flora, while high doses can induce adverse inflammatory responses.
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