Exploring the mechanism of enterotoxicity mediated by the microbiome-butyrate-PPAR axis in podophyllotoxin through the toxicological evidence chain (TEC) concept

被引:2
|
作者
Duan, Jiajia [1 ,2 ]
Du, Peipei [1 ,2 ]
Jiang, Tao [1 ,2 ]
Ma, Xiao [1 ,2 ]
Sun, Jiaxing [1 ,2 ]
Liang, Jin [1 ,2 ]
Wang, Jingjing [1 ,2 ]
Liu, Chuanxin [3 ]
机构
[1] Henan Univ Sci & Technol, Affiliated Hosp 1, Dept Clin Lab, Luoyang 471003, Peoples R China
[2] Henan Univ Sci & Technol, Coll Clin Med, Luoyang 471003, Peoples R China
[3] Henan Univ Sci & Technol, Luoyang Key Lab Clin Multi & Translat Med, Endocrinol & Metab Ctr, Affiliated Hosp 1,Henan Key Lab Rare Dis, Luoyang 471003, Peoples R China
基金
中国国家自然科学基金;
关键词
podophyllotoxin; enterotoxicity; gut microbiota; metabolome; transcriptome; co-occurrence network; ULCERATIVE-COLITIS; TOPICAL BUTYRATE; DIAMINE OXIDASE; GAMMA;
D O I
10.1016/j.ecoenv.2024.116548
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Podophyllotoxin (PPT) is a lignan derived from the roots and stems of the Podophyllum plant. However, its enterotoxicity restricts its clinical application. The underlying mechanisms by which PPT exerts its action remain largely elusive. This study aimed to evaluate the molecular mechanisms underlying PPT-induced enterotoxicity utilizing the concept of toxicological evidence chain. Changes in body weight, behavior, and histopathological and biochemical markers in rats were observed. Additionally, microbiome, metabolome, and transcriptome analyses were integrated to identify potential microorganisms, metabolic markers, and major pathways using a co-occurrence network. Our findings suggested that PPT induced pathological changes in rats, including weight loss, diarrhea, and inflammation accompanied by increased levels of IFN-gamma, IL-5, IL-6, GRO/KC, and IL-12p70. The decrease in butyrate levels in the PPT group may be related to the enrichment of Firmicutes. The reduction of butyrate levels may impair the expression of PPAR gamma, subsequently promoting Escherichia-Shigella proliferation. Additionally, the suppression of PPARs pathway may result in the increased production of inflammatory factors, contributing to enterotoxicity. This study offers a novel understanding of the molecular mechanisms underlying PPT-induced enterotoxicity, making a significant contribution to developing strategies to mitigate PPT toxicity and prevent associated diseases.
引用
收藏
页数:12
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