Toll-like Receptor Agonist CBLB502 Protects Against Cisplatin-induced Liver and Kidney Damage in Mice

被引:1
|
作者
Niu, Pengzhen [1 ]
Zhao, Wenyu [1 ]
Wang, Qiong [2 ,3 ]
Duan, Junzhao [2 ]
Zhu, Jie [2 ]
Fu, Hanjiang [2 ]
Wu, Yongge [1 ]
Zheng, Xiaofei [2 ]
Zhang, Daguang [4 ,5 ]
Ge, Changhui [2 ,3 ,6 ]
机构
[1] Jilin Univ, Sch Life Sci, Natl Engn Lab AIDS Vaccine, Changchun, Peoples R China
[2] Beijing Inst Radiat Med, Dept Expt Hematol & Biochem, Beijing Key Lab Radiobiol, Beijing, Peoples R China
[3] Anhui Med Univ, Grad Sch, Hefei, Peoples R China
[4] Jilin Univ, Dept Orthoped, Hosp 1, Changchun, Peoples R China
[5] Jilin Univ, Dept Obstet, Hosp 1, Changchun 130012, Peoples R China
[6] Beijing Inst Radiat Med, Dept Expt Hematol & Biochem, Beijing Key Lab Radiobiol, 27 Taiping Rd, Beijing 100850, Peoples R China
来源
IN VIVO | 2023年 / 37卷 / 05期
关键词
TLR5; agonist; CBLB502; chemotherapy protection; cisplatin; liver injury; kidney injury; ACTIVATION; COAGULATION; MECHANISMS; EXPRESSION; INJURY;
D O I
10.21873/invivo.13302
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
Background/Aim: CBLB502, a Toll-like receptor -5 agonist derived from Salmonella flagellin, exerts protective roles against irradiation and chemical drugs in mammalian tissues and stimulates tissue regeneration. This study aimed to investigate whether CBLB502 can protect against liver and kidney damage induced by the chemotherapeutic drug cisplatin (CDDP) and the underlying mechanism of the protective effect. Materials and Methods: Mice were pretreated with CBLB502 [0.2 mg/kg, intraperitoneal (i.p.) injection] 0.5 h prior to administration of CDDP (20 mg/kg, i.p. injection), and analyses of the liver and kidney indices, blood biochemistry, and histopathology were performed. Results: Pretreatment with CBLB502 alleviated CDDP-induced liver and kidney damage. RNA sequencing and bioinformatic analysis indicated that CDDP induced a similar damage-promoting gene regulation pattern in the liver and kidney. CBLB502 protected against liver and kidney damage only after CDDP treatment primarily via different pathways. However, some CBLB502-regulated genes were common between the liver and kidney, including those involved in blood coagulation, fibrinolysis, hemostasis, apoptotic regulation, NF-kappaB signaling, and response to lipopolysaccharide, suggesting a general protective effect by CBLB502. Conclusion: Our data provide insights into the protective mechanism of CBLB502 against CDDP-induced tissue damage in the liver and kidney and might provide a basis for future studies on functional genes and regulatory mechanisms that mediate protection against chemoradio-therapy-induced damage.
引用
收藏
页码:2044 / 2056
页数:13
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