Allopurinol preconditioning attenuates renal ischemia/reperfusion injury by inhibiting HMGB1 expression in a rat model

被引:1
|
作者
Zhou, Jiang-qiao [1 ,4 ]
Qiu, Tao [1 ]
Zhang, Lu [2 ]
Chen, Zhong-bao [1 ,4 ]
Wang, Zhi-shun [2 ]
Ma, Xiao-xiong [1 ,4 ]
Li, Dongyu [3 ]
机构
[1] Wuhan Univ, Renmin Hosp, Dept Organ Transplantat, ZiYang Rd 99, Wuhan 430060, Hubei, Peoples R China
[2] Wuhan Univ, Renmin Hosp, Dept Urol, Wuhan 430060, Hubei, Peoples R China
[3] PuAi Hosp, Intens Care Unit, Anlu, Hubei, Peoples R China
[4] Wuhan Univ, Renmin Hosp, Key Lab, Hubei Prov Digest Syst Dis, Wuhan 430060, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Inflammation; Ischemia; Reperfusion; Allopurinol; Apoptosis; Rats; OXIDATIVE STRESS; ISCHEMIC-INJURY; TRANSLOCATION; APOPTOSIS; HEART; ACID;
D O I
10.1590/S0102-865020160030000005
中图分类号
R61 [外科手术学];
学科分类号
摘要
PURPOSE: To investigate the potential effects of pretreatment with allopurinol on renal ischemia/reperfusion injury (IRI) in a rat model. METHODS: Twenty four rats were subjected to right kidney uninephrectomy were randomly distributed into the following three groups (n=8): Group A (sham-operated group); Group B (ischemic group) with 30 min of renal ischemia after surgery; and Group C (allopurinol + ischemia group) pretreated with allopurinol at 50 mg/kg for 14 days. At 72 h after renal reperfusion, the kidney was harvested to assess inflammation and apoptosis. RESULTS: Pretreatment with allopurinol significantly improved renal functional and histological grade scores following I/R injury (p< 0.05). Compared with Group B, the expression levels of caspase-3 and Bax were markedly reduced in Group C, meanwhile, whereas expression of bcl-2 was clearly increased (p< 0.05). A newly described marker of inflammation, High Mobility Group Box 1(HMGB1), showed reduced expression in Group C (p< 0.05). CONCLUSION: Pretreatment with allopurinol had a protective effect on kidney ischemia/reperfusion injury, which might be related to the inhibition of HMGB1 expression.
引用
收藏
页码:176 / 182
页数:7
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