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Journal ArticleDOI

Understanding the Molecular Mechanisms of the Interplay Between Herbal Medicines and Gut Microbiota.

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TLDR
More advanced experimental designs are recommended for future study, such as overall chemical characterization of gut microbiota‐metabolized HMs, direct microbial analysis of HM‐targeted gut microbiota, and precise gut microbiota research model development, to further elucidate the interactions between HMs and gut microbiota.
Abstract
Herbal medicines (HMs) are much appreciated for their significant contribution to human survival and reproduction by remedial and prophylactic management of diseases. Defining the scientific basis of HMs will substantiate their value and promote their modernization. Ever-increasing evidence suggests that gut microbiota plays a crucial role in HM therapy by complicated interplay with HM components. This interplay includes such activities as: gut microbiota biotransforming HM chemicals into metabolites that harbor different bioavailability and bioactivity/toxicity from their precursors; HM chemicals improving the composition of gut microbiota, consequently ameliorating its dysfunction as well as associated pathological conditions; and gut microbiota mediating the interactions (synergistic and antagonistic) between the multiple chemicals in HMs. More advanced experimental designs are recommended for future study, such as overall chemical characterization of gut microbiota-metabolized HMs, direct microbial analysis of HM-targeted gut microbiota, and precise gut microbiota research model development. The outcomes of such research can further elucidate the interactions between HMs and gut microbiota, thereby opening a new window for defining the scientific basis of HMs and for guiding HM-based drug discovery.

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Journal ArticleDOI

Pharmacological basis and new insights of quercetin action in respect to its anti-cancer effects

TL;DR: The evidence for the pharmacological potential and inhibition of quercetin on cancers, supporting the viewpoint that quercETin should be adequately considered as a therapeutic agent against various cancers is summarized.
Journal ArticleDOI

Gut Microbiota, Short-Chain Fatty Acids, and Herbal Medicines.

TL;DR: Current knowledge aboutSCFAs origination, the role of SCFAs in health and disease, the influence of herbal medicine on SCF as production and the corresponding mechanisms are summarized.
Journal ArticleDOI

Gut microbiota, a new frontier to understand traditional Chinese medicines.

TL;DR: This review summarized the interactions between TCM and gut microbiota, and the pharmacological effects and features of metabolites produced during interactions betweenTCM and Gut microbiota, focusing on gut microbiota and metabolites.
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Panax ginseng and Panax quinquefolius: From pharmacology to toxicology.

TL;DR: The aim of this review is to provide a simple and extensive overview of the pharmacokinetics and pharmacodynamics of P. ginseng and P. quinquefolius, focusing on the clinical evidence which has shown particular effectiveness in specific diseases, such as dementia, diabetes mellitus, respiratory infections, and cancer.
Journal ArticleDOI

Gut Microbiota and Nonalcoholic Fatty Liver Disease: Insights on Mechanisms and Therapy.

TL;DR: This review reviews the main roles of gut microbiota in mediating the development of NAFLD, and the advances in gut microbiota-targeted therapies forNAFLD in both the experimental and clinical studies, as well as the conclusions on the prospect of gut microbiome-targeting therapies in the future.
References
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Journal ArticleDOI

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TL;DR: It is shown that the relative proportion of Bacteroidetes is decreased in obese people by comparison with lean people, and that this proportion increases with weight loss on two types of low-calorie diet.
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Pathogenic Escherichia coli

TL;DR: Few microorganisms are as versatile as Escherichia coli; it can also be a highly versatile, and frequently deadly, pathogen.
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Natural Products as Sources of New Drugs from 1981 to 2014

TL;DR: This contribution is a completely updated and expanded version of the four prior analogous reviews that were published in this journal in 1997, 2003, 2007, and 2012, and the time frame has been extended to cover the 34 years from January 1, 1981, to December 31, 2014, for all diseases worldwide, and from 1950 (earliest so far identified) to December 2014 for all approved antitumor drugs worldwide.
Journal ArticleDOI

Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010

TL;DR: This review is an updated and expanded version of the three prior reviews and adds a new designation, "natural product botanical" or "NB", to cover those botanical "defined mixtures" that have now been recognized as drug entities by the FDA and similar organizations.
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