4.7 Article

A diet high in sugar and fat influences neurotransmitter metabolism and then affects brain function by altering the gut microbiota

Journal

TRANSLATIONAL PSYCHIATRY
Volume 11, Issue 1, Pages -

Publisher

SPRINGERNATURE
DOI: 10.1038/s41398-021-01443-2

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Funding

  1. National Natural Science Foundation of China [81701086]
  2. Guangdong Basic and Applied Basic Research Foundation [2021A1515011338]
  3. Guangzhou Health Commission Traditional Chinese Medicine and Integrated Chinese and Western Medicine Science and Technology Project [20212A011027]
  4. GDAS' Project of Science and Technology Development [2019GDASYL- 0104007]

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The study found that a high-sugar and high-fat diet can cause dysbiosis of gut microbiota, affecting brain function and circRNA profiles. The GM byproduct trimethylamine-n-oxide affects circRNA degradation, and changes in bacterial strain abundance may influence neurotransmitter secretion.
Gut microbiota (GM) metabolites can modulate the physiology of the host brain through the gut-brain axis. We wished to discover connections between the GM, neurotransmitters, and brain function using direct and indirect methods. A diet with increased amounts of sugar and fat (high-sugar and high-fat (HSHF) diet) was employed to disturb the host GM. Then, we monitored the effect on pathology, neurotransmitter metabolism, transcription, and brain circularRNAs (circRNAs) profiles in mice. Administration of a HSHF diet-induced dysbacteriosis, damaged the intestinal tract, changed the neurotransmitter metabolism in the intestine and brain, and then caused changes in brain function and circRNA profiles. The GM byproduct trimethylamine-n-oxide could degrade some circRNAs. The basal level of the GM decided the conversion rate of choline to trimethylamine-n-oxide. A change in the abundance of a single bacterial strain could influence neurotransmitter secretion. These findings suggest that a new link between metabolism, brain circRNAs, and GM. Our data could enlarge the microbiome-transcriptome linkage library and provide more information on the gut-brain axis. Hence, our findings could provide more information on the interplay between the gut and brain to aid the identification of potential therapeutic markers and mechanistic solutions to complex problems encountered in studies of pathology, toxicology, diet, and nutrition development.

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