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      Xiaoyankangjun tablet alleviates dextran sulfate sodium-induced colitis in mice by regulating gut microbiota and JAK2/STAT3 pathway

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          Abstract

          Xiaoyankangjun tablet (XYKJP) is a traditional Chinese medicine formulation used to treat intestinal disorders in clinical practice. However, the specific therapeutic mechanism of action of XYKJP in colitis has not yet been elucidated. This study aimed to reveal the multifaceted mechanisms of action of XYKJP in treating colitis. The model established based on DSS-induced colitis in C57BL/6 mice was employed to estimate the effect of XYKJP on colitis, which was then followed by histological assessment, 16S rRNA sequencing, RT-qPCR, ELISA, and Western blot. XYKJP alleviated the symptoms of DSS-induced colitis mainly by reducing oxidative stress, inflammatory responses, and intestinal mucosal repair in colitis tissues. In addition, XYKJP regulated the intestinal flora by increasing the relative abundance of Akkermansia and Bifidobacterium and reducing the relative abundance of Coriobacteriaceae_UCG-002. Mechanistically, XYKJP increased the content of short-chain fatty acids (SCFAs) in the feces, particularly propanoic acid and butyric acid, activated their specific receptor GPR43/41, furthermore activated the Nrf2/HO-1 pathway, and suppressed the JAK2/STAT3 pathway. XYKJP significantly alleviated the symptoms of experimental colitis and functioned synergistically by regulating the intestinal flora, increasing the production of SCFAs, and activating their specific receptors, thereby repressing oxidative stress and inflammation.

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          Supplementary Information

          The online version contains supplementary material available at 10.1007/s13659-024-00468-6.

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          Gut microbiota-derived metabolites as key actors in inflammatory bowel disease

          A key role of the gut microbiota in the establishment and maintenance of health, as well as in the pathogenesis of disease, has been identified over the past two decades. One of the primary modes by which the gut microbiota interacts with the host is by means of metabolites, which are small molecules that are produced as intermediate or end products of microbial metabolism. These metabolites can derive from bacterial metabolism of dietary substrates, modification of host molecules, such as bile acids, or directly from bacteria. Signals from microbial metabolites influence immune maturation, immune homeostasis, host energy metabolism and maintenance of mucosal integrity. Alterations in the composition and function of the microbiota have been described in many studies on IBD. Alterations have also been described in the metabolite profiles of patients with IBD. Furthermore, specific classes of metabolites, notably bile acids, short-chain fatty acids and tryptophan metabolites, have been implicated in the pathogenesis of IBD. This Review aims to define the key classes of microbial-derived metabolites that are altered in IBD, describe the pathophysiological basis of these associations and identify future targets for precision therapeutic modulation.
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            Pathway paradigms revealed from the genetics of inflammatory bowel disease

            Inflammatory bowel disease (IBD) is a complex genetic disease that is instigated and amplified by the confluence of multiple genetic and environmental variables that perturb the immune- microbiome axis. The challenge of dissecting pathological mechanisms underlying IBD has spawned the development of transformative approaches in human genetics and functional genomics. Here, we describe IBD as a model disease in the context of leveraging human genetics to dissect cellular and molecular pathway interactions that control homeostasis of the mucosal immune system. Finally, we synthesize emerging insights from multiple experimental approaches into pathway paradigms and discuss future prospects for disease subtype classification and therapeutic intervention.
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              Pharmacokinetics and Bioavailability Enhancement of Baicalin: A Review

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                Author and article information

                Contributors
                Suhanwen-1@163.com
                xiangmeixian@mail.scuec.edu.cn
                Journal
                Nat Prod Bioprospect
                Nat Prod Bioprospect
                Natural Products and Bioprospecting
                Springer Nature Singapore (Singapore )
                2192-2195
                2192-2209
                12 August 2024
                12 August 2024
                December 2024
                : 14
                : 1
                : 44
                Affiliations
                [1 ]School of Pharmaceutical Sciences, South-Central Minzu University, Wuhan, 430074 Hubei People’s Republic of China
                [2 ]Department of Clinical Laboratory, Renmin Hospital of Wuhan University, ( https://ror.org/03ekhbz91) Wuhan, 430060 Hubei People’s Republic of China
                Article
                468
                10.1007/s13659-024-00468-6
                11319580
                39133435
                2f54f5e7-bda2-48f4-ad3c-48f5a53f67a2
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 24 May 2024
                : 31 July 2024
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100017718, Natural Science Foundation of Yichang Municipality;
                Award ID: 2024AFD252
                Categories
                Original Article
                Custom metadata
                © Kunming Institute of Botany, CAS 2024

                xiaoyankangjun tablet,colitis,nrf2/ho-1 pathways and jak2/stat3 pathways,tight junction proteins,gut microbiota,gpr43/41 receptor

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