[谷胱甘肽乙酯对烟雾吸入性肺损伤的影响]。

Shu Zhang, F. Qi, Zhen-hua Zuo, Wei Liu, Jian-xin Wang
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Rats were sacrificed for lungs, and bronchoalveolar lavage fluid (BALF) was collected for analysis of GSH activity; and the activity of GSH, catalase (CAT) and glutathione reductase (GR) were detected in pulmonary tissue homogenate.The changes of pulmonary tissue pathology was observed through light microscope.\n\n\nRESULTS\nCompared to normal group, arterial partial pressure of oxygen (PaO(2)) in model group were decreased significantly in each time; the activity of GSH in BALF, and the activity of GSH, CAT, GR in lung tissue were also observed decreased significantly. 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引用次数: 0

摘要

目的探讨谷胱甘肽(GSH)前体谷胱甘肽乙酯(GSEt)对烟雾吸入性肺损伤大鼠的保护作用。方法采用随机数字表法将60只健康雄性SD大鼠分为正常组、模型组、GSEt高剂量组和GSEt低剂量组。建立烟雾吸入致大鼠肺损伤模型。伤后5分钟腹腔注射GSEt 50 mg/kg或150 mg/kg。分别于伤后2、12、24 h监测各组动脉血气分析。取大鼠肺,取支气管肺泡灌洗液(BALF)分析GSH活性;检测肺组织匀浆中谷胱甘肽、过氧化氢酶(CAT)和谷胱甘肽还原酶(GR)活性。光镜下观察肺组织病理变化。结果与正常组比较,模型组各时间点动脉氧分压(PaO(2))均显著降低;BALF中GSH活性及肺组织中GSH、CAT、GR活性均显著降低。与模型组比较,GSEt治疗(150 mg/kg)使PaO(2)提前12 h(82.9±7.0 mm Hg vs. 63.9±6.5 mm Hg, P<0.05), GSH活性在12 h和24 h均升高(12 h: 2.19±0.41 mg/g vs. 0.79±0.21 mg/g, 24 h: 1.75±0.47 mg/g vs. 0.67±0.10 mg/g, P<0.05);GSEt低剂量组(50 mg/kg)在24 h时CAT活性升高,GSEt高剂量组(150 mg/kg)在12 h和24 h时CAT活性升高(低剂量组24 h: 70.1±5.5 U/g vs. 56.3±5.0 U/g);高剂量组12 h: 90.9±8.1 U/g vs. 67.9±6.1 U/g, 24 h: 94.7±7.7 U/g vs. 56.3±5.0 U/g, P均<0.05);GSEt高剂量组小鼠GR活性在24 h升高(5.25±0.77 mmol/g vs. 4.37±0.64 mmol/g, P<0.05)。GSEt (150 mg/kg)给药12 h后肺组织组织学异常减轻,炎症细胞浸润减少,肺组织无点状出血。结论人参皂苷能增强肺组织抗氧化能力,对肺损伤有较好的保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effects of glutathione ethyl ester on smoke inhalation lung injury].
OBJECTIVE To investigate the effects of glutathione (GSH) precursor glutathione ethyl ester (GSEt) on smoke inhalation induced lung injury rats. METHODS Sixty healthy male Sprague-Dawley (SD) rats were divided into groups by random digits table method, which included normal group, model group, GSEt high dose group and GSEt low dose group. Smoke inhalation induced lung injury rats model was established. GSEt treatments were given through intraperitoneal injection for 50 mg/kg or 150 mg/kg 5 minutes after the injury. Arterial blood gas analysis was monitored at 2, 12 and 24 hours after injury in each group. Rats were sacrificed for lungs, and bronchoalveolar lavage fluid (BALF) was collected for analysis of GSH activity; and the activity of GSH, catalase (CAT) and glutathione reductase (GR) were detected in pulmonary tissue homogenate.The changes of pulmonary tissue pathology was observed through light microscope. RESULTS Compared to normal group, arterial partial pressure of oxygen (PaO(2)) in model group were decreased significantly in each time; the activity of GSH in BALF, and the activity of GSH, CAT, GR in lung tissue were also observed decreased significantly. Compared with model group, GSEt treatment (150 mg/kg) with the PaO(2) advanced at 12 hours (82.9±7.0 mm Hg vs. 63.9±6.5 mm Hg, P<0.05), the activity of GSH was increased at the 12 hours and 24 hours (12 hours: 2.19±0.41 mg/g vs. 0.79±0.21 mg/g, 24 hours: 1.75±0.47 mg/g vs. 0.67±0.10 mg/g, both P<0.05); the activity of CAT in GSEt low dose group (50 mg/kg) was increased at the 24 hours and the same increase was also observed in GSEt high dose group (150 mg/kg) at 12 hours and 24 hours (low dose group 24 hours: 70.1±5.5 U/g vs. 56.3±5.0 U/g; high dose group 12 hours: 90.9±8.1 U/g vs. 67.9±6.1 U/g, 24 hours: 94.7±7.7 U/g vs. 56.3±5.0 U/g, all P<0.05); the activity of GR in GSEt high dose group was increased at 24 hours (5.25±0.77 mmol/g vs. 4.37±0.64 mmol/g, P<0.05). The histological abnormality of lung tissue was alleviated after application of GSEt (150 mg/kg) 12 hours later, less inflammatory cells infiltration and no punctate hemorrhage in lung tissues. CONCLUSION GSEt can enhance antioxidant capacity in lung tissues, it have a good protection for pulmonary injury.
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