Betulinic acid protects against LPS-induced intestinal inflammatory damage via inhibiting Nrf2/TXNIP/NLRP3 signaling pathways in mice.

IF 5.4 1区 农林科学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Food & Function Pub Date : 2025-09-26 DOI:10.1039/d5fo00925a
Lijuan Zhu, Li Kong, You Huang, Zhaoping Ou, Chunlin Huang, Wenjiang Yang, Jiayu He, Mingqi Yang, Shuiping Liu, Jine Yi
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引用次数: 0

Abstract

Betulinic acid (BA) is a pentacyclic triterpenoid and found in various fruits and vegetables, known for its anti-inflammatory and antioxidant properties as well as intestinal protective roles. This study aimed to investigate the effects and mechanisms of BA on lipopolysaccharide (LPS)-induced intestinal inflammation in mice. Our results indicated that BA pretreatment alleviated LPS-induced body weight loss, morphological damage and intestinal cell apoptosis in the duodenum, jejunum, ileum and colon. BA pretreatment effectively regulated the disturbance of inflammatory cytokines in the duodenum, jejunum, ileum and colon induced by LPS. Meanwhile, BA pretreatment significantly inhibited the protein expression of TXNIP, NLRP3, ASC, caspase-1, GSDMD, IL-1β and IL-18 in the jejunum, suggesting that BA mitigated LPS-induced intestinal inflammation by inhibiting the TXNIP/NLRP3 signaling pathways. Furthermore, BA pretreatment decreased MDA content, while increasing the activities of the CAT and SOD in the jejunum. Subsequently, BA pretreatment down-regulated the protein expression of Nrf2 and HO-1 in the jejunum, indicating that BA alleviated LPS-induced intestinal oxidative impairment by inhibiting the Nrf2 signaling pathway. In conclusion, BA pretreatment exhibited protective effects on LPS-induced intestinal inflammatory damage by inhibiting Nrf2/TXNIP/NLRP3 signaling pathways in mice. This study established a theoretical foundation for the application of BA as a functional food factor in the alleviation of inflammatory bowel diseases.

白桦酸通过抑制Nrf2/TXNIP/NLRP3信号通路对lps诱导的小鼠肠道炎症损伤具有保护作用。
白桦酸(BA)是一种五环三萜,存在于各种水果和蔬菜中,以其抗炎和抗氧化特性以及肠道保护作用而闻名。本研究旨在探讨BA对脂多糖(LPS)诱导的小鼠肠道炎症的影响及其机制。结果表明,BA预处理可减轻lps诱导的大鼠体重减轻、十二指肠、空肠、回肠和结肠的形态损伤和肠细胞凋亡。BA预处理能有效调节LPS诱导的十二指肠、空肠、回肠和结肠炎性细胞因子的紊乱。同时,BA预处理可显著抑制空肠TXNIP、NLRP3、ASC、caspase-1、GSDMD、IL-1β和IL-18蛋白的表达,提示BA可能通过抑制TXNIP/NLRP3信号通路减轻lps诱导的肠道炎症。BA预处理降低了空肠MDA含量,提高了空肠CAT和SOD的活性。随后,BA预处理下调空肠Nrf2和HO-1蛋白表达,表明BA通过抑制Nrf2信号通路减轻lps诱导的肠道氧化损伤。综上所述,BA预处理通过抑制Nrf2/TXNIP/NLRP3信号通路对lps诱导的小鼠肠道炎症损伤具有保护作用。本研究为BA作为功能性食物因子在缓解炎症性肠病中的应用奠定了理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Food & Function
Food & Function BIOCHEMISTRY & MOLECULAR BIOLOGY-FOOD SCIENCE & TECHNOLOGY
CiteScore
10.10
自引率
6.60%
发文量
957
审稿时长
1.8 months
期刊介绍: Food & Function provides a unique venue for physicists, chemists, biochemists, nutritionists and other food scientists to publish work at the interface of the chemistry, physics and biology of food. The journal focuses on food and the functions of food in relation to health.
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