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Mechanisms Underlying the Interaction Between Chronic Neurological Disorders and Microbial Metabolites via Tea Polyphenols Therapeutics

Journal

FRONTIERS IN MICROBIOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.823902

Keywords

tea polyphenols; intestinal metabolites; host health; chronic brain diseases; interaction

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Funding

  1. Zhejiang Provincial Key Research and Development Program [2020C02037]
  2. People-benefit Project of Ningbo [202002N3078]

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The hydroxyl groups and characteristic structural groups in tea polyphenols provide them with antioxidant activity, leading to anti-inflammatory effects and protection of intestinal flora and brain neurons. Microbial metabolites associated with the host have been identified as major regulators of the central nervous system. Studies on metabolites such as serotonin and short-chain fatty acids have identified multiple signaling pathways relevant to host health. However, the complexity and limitations of translating complex human diseases into animal models remain challenges. This article discusses several intestinal metabolites with research value, highlighting the interaction between tea polyphenols and chronic brain diseases mediated by the microbiota.
The number of hydroxyl groups and existence of characteristic structural groups in tea polyphenols (TP) make them have antioxidant activity, which gives TP anti-inflammatory effects, toward protecting the intestinal flora and brain neurons. Host-associated microbial metabolites are emerging as dominant modifiers of the central nervous system. As yet, the investigations on host-microbiota crosstalking remain challenging, studies focusing on metabolites such as serotonin, short-chain fatty acids, and others have pinpointed multiple actionable signaling pathways relevant to host health. However, there are still complexities and apparent limitations inherent in transforming complex human diseases to corresponding animal models. Here, we choose to discuss several intestinal metabolites with research value, as crucial areas for assessing TP-mediated chronic brain diseases interactions with microbial.

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