Ginkgo biloba extract (EGb 761) attenuates lung injury induced by intestinal ischemia/reperfusion in rats: Roles of oxidative stress and nitric oxide

被引:58
作者
Liu, Ke-Xuan [1 ]
Wu, Wei-Kang
He, Wei
Liu, Chui-Liang
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Anesthesiol, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Inst Integrated Tradit Chinese Med & Western Med, Guangzhou 510080, Guangdong, Peoples R China
[3] Guangdong Provincial Peoples Hosp, Dept Anesthesiol, Guangzhou 510080, Guangdong, Peoples R China
[4] Guangdong Provincial Hosp Tradit Chinese Med, Dept Anesthesiol, Guangzhou 510120, Guangdong, Peoples R China
关键词
ginkgo biloba extract; intestine; reperfusion injury; lung; adult respiratory distress syndrome; vascular permeability; nitric oxide; lipid peroxidation;
D O I
10.3748/wjg.v13.i2.299
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the effect of ginkgo biloba extract (EGb 761) on lung injury induced by intestinal ischemia/ reperfusion (II/R). METHODS: The rat model of II/R injury was produced by clamping the superior mesenteric artery for 60 min followed by reperfusion for 180 min. The rats were randomly allocated into sham, II/R, and EGb +II/R groups. In EGb +II/R group, EGb 761 (100 mg/kg per day) was given via a gastric tube for 7 consecutive days prior to surgery. Rats in II/R and sham groups were treated with equal volumes of the vehicle of EGb 761. Lung injury was assessed by light microscopy, wet-to-dry lung weight ratio (W/D) and pulmonary permeability index (PPI). The levels of malondialdehyde (MDA) and nitrite/nitrate (NO2-/NO3-), as well as the activities of superoxide dismutase (SOD) and myeloperoxidase (MPO) were examined. Western blot was used to determine the expression of inducible nitric oxide synthase (NOS). RESULTS: EGb 761 markedly improved mean arterial pressure and attenuated lung injury, manifested by the improvement of histological changes and significant decreases of pulmonary W/D and PPI (P < 0.05 or 0.01). Moreover, EGb 761 markedly increased SOD activity, reduced MDA levels and MPO activity and suppressed NO generation accompanied by down-regulation of NOS expression (P < 0.05 or 0.01). CONCLUSION: The results indicate that EGb 761 has a protective effect on lung injury induced by E /R, which may be related to its antioxidant property and suppressions of neutrophil accumulation and iNOS-induced NO generation. EGb 761 seems to be an effective therapeutic agent for critically ill patients with respiratory failure related to H /R. (c) 2007 The WJG Press. All rights reserved.
引用
收藏
页码:299 / 305
页数:7
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