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Molecular Assessment of Traditional Mongolian Medicine Tongola-5 in Lactulose Induced Diarrhea: An in vivo Study

体内 下调和上调 乳果糖 腹泻 体外 转录组 药理学 肠道菌群 生物 微生物学 基因表达 医学 生物化学 基因 内科学 生物技术
作者
Chunli Ma,Qiqige Buren,M.M. van der Eerde,Min Qing,Xiufang Bao,Linyun Zhao,Lili Cao,Xin Zhang,Qigeqi Bai,Mei‐Ling Chen,Mei Hong,Yulong Bao,Hua Lian
出处
期刊:Drug Design Development and Therapy [Dove Medical Press]
卷期号:Volume 19: 6145-6181
标识
DOI:10.2147/dddt.s527657
摘要

To elucidate the mechanisms underlying the therapeutic effects of Tonglaga-5 (TLG5) in the treatment of chronic diarrhea. The chemical compositions of TLG5 in both in vitro and systemic circulation were analyzed using UPLC-Q/TOF MSE. Network pharmacology was applied to predict the therapeutic effects of TLG5 on chronic diarrhea. Molecular docking was utilized to assess the binding affinity between key bioactive compounds and their corresponding targets. A total of 24 male Sprague-Dawley (SD) rats were randomly assigned to three groups: control, model, and TLG5 treatment. Corresponding administration included a standard diet, a high-lactose diet of varying concentrations, and TLG5 by gavage during modeling. Transcriptomic analysis was employed to assess gene expression changes in intestinal tissues. Alterations in the intestinal microbiota were evaluated using 16S rRNA sequencing. qPCR and immunohistochemistry technologies were adopted to analyze the expression of genes and proteins associated with intestinal barrier integrity. ELISA was performed to quantify levels of bile acids and short-chain fatty acids (SCFAs). UPLC-Q/TOF MSE identified 118 compounds in vitro and 52 in the systemic circulation. Network pharmacological analysis revealed that the in vitro and in vivo components of TLG5 were associated with five core targets and five key compounds, respectively. RNA sequencing analysis showed that TLG5 treatment inhibited the inflammatory pathway. 16S rRNA sequencing demonstrated that TLG5 administration led to an upregulation of beneficial microbial populations and a concomitant downregulation of pathogenic bacteria. The TLG5 treatment group presented a reduction in necrotic areas and inflammatory cell infiltration, as well as preservation of the mucosal structure, with a marked decline in inflammatory lesions. Moreover, TLG5 treatment resulted in a significant increase in the levels of SCFAs and bile acids in the cecum. TLG5 exerts therapeutic effects on chronic diarrhea through multiple mechanisms, including modulation of intestinal microbiota diversity, enhancement of intestinal barrier function, and attenuation of inflammatory responses.

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