Liu Gang, Song Dongmei, Jiang Yu, Zhu Liqing, Ge Yun
Department of Emergency, University-Town Hospital of Chongqing Medical University, Chongqing 401331, China. Corresponding author: Jiang Yu, Email:
Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2015 Apr;27(4):280-4. doi: 10.3760/cma.j.issn.2095-4352.2015.04.011.
To investigate the expression of heme oxygenase-1 (HO-1) in lung tissue of mice with acute paraquat poisoning, and discuss its pathological mechanism.
Fifty-eight healthy male mice were randomly divided into control group (n = 8) and poisoned group (n = 50). The mice in poisoned group were lavaged with 20% paraquat (50 mg/kg), and those in control group with equal amount of normal saline. The mice were sacrificed on the day of experiment in control group, and those in poisoned group at 6 hours and 1, 3, 7, 14 days after poisoning. The lung tissue was harvested to observe the changes in pathology of lung with hematoxylin and eosin (HE) staining. The positive expression of HO-1 was determined with immunohistochemistry, and the protein expression of HO-1 was determined with Western Blot. The contents of superoxide dismutase (SOD) and malonaldehyde (MDA) were determined.
The mice showed shortness of breath and signs of exhaustion 1 hour after poisoning, getting worse on 3-5 days, but returned to normal 14 days after poisoning. Under the light microscope, it showed that the control group had no significant pathological changes in lung tissue. One day after the ingestion, pulmonary alveolar structure disorder, obvious hemorrhage, edema and infiltration of inflammatory cells were found. At 3 days, the pathological changes in the lung tissue were more pronounced. They were less pronounced on 7 days, and inflammatory changes disappeared on 14th day, but alveolar structure disorder remained. Immunohistochemical test showed that HO-1 was seldom expressed in the lung tissue, and a little amount was expressed in the mucosal epithelial cells of the airway in control group. It was shown that inflammatory cell and endothelial were mainly distributed in the mucosal epithelial cells of airway 1 day after poisoning followed by a gradually decrease tendence, and came to normal level of control group 7 days after poisoning. It was shown by Western Blot that HO-1 (gray value) in lung tissue increased 6 hours after poisoning (2.438 ± 0.467 vs. 0.475 ± 0.167, P < 0.01), peaked at 1 day (9.200 ± 0.940 vs. 0.475 ± 0.167, P < 0.01), continued to increase till 7 days after poisoning, and it lowered to normal level thereafter (0.825 ± 0.260 vs. 0.475 ± 0.167, P > 0.05). The SOD activity (μU/L) in lung tissue was lowered 6 hours after poisoning, and it was significantly lower than that of control group (649.681 ± 13.951 vs. 1 167.051 ± 15.744, P < 0.01), and it continued to decrease up to 14 days after poisoning ( 859.733 ± 121.079 vs. 1 167.051 ± 14.744, P < 0.01). MDA content (μmol/L) in the lung tissue homogenate was elevated 6 hours after poisoning with significant difference compared with that of the control group (4.542 ± 0.266 vs. 3.705 ± 0.176, P < 0.01). It peaked on day 1 (5.956 ± 0.281 vs. 3.705 ± 0.176, P < 0.01), then it declined and reached normal level 3 days after poisoning (4.134 ± 0.168 vs. 3.705 ± 0.176, P > 0.05).
HO-1 expression was increased significantly in lung tissue of mice with acute paraquat poisoning, which may be considered as an important protection mechanism against paraquat poisoning.
探讨血红素加氧酶-1(HO-1)在急性百草枯中毒小鼠肺组织中的表达情况,并探讨其病理机制。
将58只健康雄性小鼠随机分为对照组(n = 8)和中毒组(n = 50)。中毒组小鼠用20%百草枯(50 mg/kg)灌胃,对照组小鼠用等量生理盐水灌胃。对照组小鼠在实验当天处死,中毒组小鼠在中毒后6小时、1、3、7、14天处死。取肺组织,用苏木精-伊红(HE)染色观察肺组织病理学变化。采用免疫组织化学法检测HO-1的阳性表达,采用蛋白质免疫印迹法检测HO-1的蛋白表达。检测超氧化物歧化酶(SOD)和丙二醛(MDA)的含量。
中毒后1小时小鼠出现呼吸急促、疲惫症状,3 - 5天症状加重,但中毒后14天恢复正常。光镜下可见,对照组肺组织无明显病理变化。摄入后1天,肺泡结构紊乱,有明显出血、水肿及炎性细胞浸润。3天时,肺组织病理变化更明显。7天时变化减轻,14天时炎症改变消失,但肺泡结构紊乱仍存在。免疫组织化学检测显示,HO-1在对照组肺组织中很少表达,仅在气道黏膜上皮细胞中有少量表达。中毒后1天可见炎性细胞和内皮细胞主要分布于气道黏膜上皮细胞,随后呈逐渐下降趋势,中毒后7天恢复至对照组正常水平。蛋白质免疫印迹法显示,中毒后6小时肺组织中HO-1(灰度值)升高(2.438 ± 0.467 vs. 0.475 ± 0.167,P < 0.01),1天时达到峰值(9.200 ± 0.940 vs. 0.475 ± 0.167,P < 0.01),中毒后7天持续升高,此后降至正常水平(0.825 ± 0.260 vs. 0.475 ± 0.167,P > 0.05)。中毒后6小时肺组织中SOD活性(μU/L)降低,显著低于对照组(649.681 ± 13.951 vs. 1 167.051 ± 15.744,P < 0.01),中毒后14天仍持续降低(859.733 ± 121.079 vs. 1 167.051 ± 14.744,P < 0.01)。中毒后6小时肺组织匀浆中MDA含量(μmol/L)升高,与对照组相比有显著差异(4.542 ± 0.266 vs. 3.705 ± 0.176,P < 0.01)。1天时达到峰值(5.956 ± 0.281 vs. 3.705 ± 0.176,P < 0.01),随后下降至中毒后3天恢复正常水平(4.134 ± 0.168 vs. 3.705 ± 0.176,P > 0.05)。
急性百草枯中毒小鼠肺组织中HO-1表达显著增加,这可能是对抗百草枯中毒的重要保护机制。