Chlorogenic acid attenuates cyclophosphamide-induced rat interstitial cystitis

被引:20
|
作者
Luo, Jing [1 ]
Yang, Chengfei [1 ]
Luo, Xing [1 ]
Yang, Yang [1 ]
Li, Jia [1 ]
Song, Bo [1 ]
Zhao, Jiang [1 ]
Li, Longkun [1 ]
机构
[1] Army Mil Med Univ, Affiliated Hosp 2, Dept Urol, Chongqing, Peoples R China
基金
中国国家自然科学基金;
关键词
NF-KAPPA-B; BLADDER PAIN SYNDROME; INFLAMMATION; PATHWAYS; PREVALENCE; EXPRESSION; STRESS; WOMEN; MODEL; MICE;
D O I
10.1016/j.lfs.2020.117590
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aims: This study aimed to investigate the therapeutic effect and molecular mechanism of chlorogenic acid (CGA) on cyclophosphamide (CYP)-induced rat interstitial cystitis (IC). Materials and methods: An animal model of IC was established by intraperitoneal injection of CYP in female Sprague-Dawley rats. Eighty rats were randomly assigned to four groups: negative control (NC), NC treated with CGA (NC + CGA), IC, and IC treated with CGA (IC + CGA). Bladder urination function was assessed by analyzing urodynamic parameters. The expression of apoptosis-related proteins and inflammatory biomarkers in bladder specimens was detected using western blot and immunohistochemistry analysis. Key findings: Compared with the IC group, bladder urinary function was significantly improved in the IC + CGA group. CGA treatment reduced inflammatory damage in the bladder tissue of IC rats. Caspase3 and Bax expression was higher while Bcl-2 expression was lower in the IC group compared to the IC + CGA group. In addition, there were significant differences between the groups in the expression levels of inflammatory biomarkers in the bladder tissue. Furthermore, CGA could inhibit CYP-induced MAPK/NF-κB phosphorylation in the rat bladder tissue. Significance: In a CYP-induced rat model of IC, CGA could reduce inflammation and apoptosis, thus partially restoring bladder function, and the MAPK/NF-κB pathway was probably involved in it. © 2020 Elsevier Inc.
引用
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页数:8
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