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[TSP-1及其受体CD47在百草枯诱导的大鼠肺纤维化发病机制中的作用]

[The roles of TSP-1 and its receptor CD47 in pathogenesis of paraquat-induced pulmonary fibrosis in rats].

作者信息

Zhang J, Liu K X, Gao W, Xie X S

机构信息

Department of Nephrology, Second Clinical Medical Institution of North Sichuan Medical College (Nanchong Central Hospital) , Nanchong 637000, China.

出版信息

Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2017 Dec 20;35(12):881-887. doi: 10.3760/cma.j.issn.1001-9391.2017.12.001.

Abstract

To establish a rat model of paraquat (PQ) -induced pulmonary fibrosis and observe the changes in thrombospondin-1 (TSP-1) and its receptor CD47 in lung tissue, and to investigate their roles in the pathogenesis of PQ-induced pulmonary fibrosis. Fifty-four clean adult male Sprague-Dawley rats were randomly divided into normal control group (=6) and 2 h, 12 h, 1 d, 3 d, 7 d, and 14 d PQ poisoning groups (=8 per group). A rat model of PQ poisoning was established by a single gavage of 20 wt.% PQ solution (50 mg/kg). Flow cytometry was used to determine the concentration of reactive oxygen species (ROS) in blood and lung tissue. Enzyme-linked immunosorbent assay was used to determine the concentrations of hydroxyl radicals, malondialdehyde, and hydroxyproline in lung tissue. HE staining and Masson staining were used to observe the pathological damage of lung tissue after PQ poisoning. The expression of TSP-1 and CD47 in lung tissue was measured by Immunohistochemistry. Compared with the normal control group, the 2 h to 7 d PQ poisoning groups showed significant increases in ROS fluorescence intensity in red blood cells and lung tissues and the concentrations of malondialdehyde and hydroxyl radicals in lung tissue (<0.05) , and the 14 d PQ poisoning group had a significant increase in the concentration of hydroxyproline in lung tissue (<0.05). HE staining showed that the 2 h to 7 d PQ poisoning groups had significantly higher semiquantitative pathological scores of pulmonary alveolitis than the normal control group (<0.05). The Masson staining showed that the 7 d and 14 d PQ poisoning groups had significantly higher semiquantitative pathological scores of pulmonary fibrosis than the normal control group (<0.05). Compared with the normal control group, all PQ poisoning groups (except the 12 h group) had significantly increased expression of TSP-1 in lung tissue (<0.05) , and all PQ poisoning groups (except the 1 d group) had significantly increased expression of CD47 in lung tissue (<0.05). Within 2 h after PQ poisoning, the expression of TSP-1 and CD47 was positively correlated with the concentrations of ROS, hydroxyl radicals, and malondialdehyde and the degree of pulmonary alveolitis (<0.01) ; at 1 d after PQ poisoning, the expression of TSP-1 and CD47 was positively correlated with the concentration of hydroxyproline in lung tissue (<0.01) . The expression of TSP-1 and CD47 is closely related to oxidative stress and subsequent pulmonary fibrosis, and they may be involved in the development and progression of pulmonary alveolitis and subsequent pulmonary fibrosis in rats with PQ poisoning.

摘要

建立百草枯(PQ)诱导的大鼠肺纤维化模型,观察肺组织中血小板反应蛋白-1(TSP-1)及其受体CD47的变化,并探讨它们在PQ诱导的肺纤维化发病机制中的作用。将54只清洁级成年雄性Sprague-Dawley大鼠随机分为正常对照组(n = 6)和PQ中毒2 h、12 h、1 d、3 d、7 d及14 d组(每组n = 8)。通过单次灌胃20 wt.% PQ溶液(50 mg/kg)建立PQ中毒大鼠模型。采用流式细胞术检测血液和肺组织中活性氧(ROS)浓度。采用酶联免疫吸附测定法检测肺组织中羟自由基、丙二醛和羟脯氨酸浓度。采用苏木精-伊红(HE)染色和Masson染色观察PQ中毒后肺组织的病理损伤。采用免疫组织化学法检测肺组织中TSP-1和CD47的表达。与正常对照组相比,PQ中毒2 h至7 d组红细胞和肺组织中ROS荧光强度以及肺组织中丙二醛和羟自由基浓度显著升高(P < 0.05),PQ中毒14 d组肺组织中羟脯氨酸浓度显著升高(P < 0.05)。HE染色显示,PQ中毒2 h至7 d组肺泡炎半定量病理评分显著高于正常对照组(P < 0.05)。Masson染色显示,PQ中毒7 d和14 d组肺纤维化半定量病理评分显著高于正常对照组(P < 0.05)。与正常对照组相比,所有PQ中毒组(12 h组除外)肺组织中TSP-1表达显著升高(P < 0.05),所有PQ中毒组(1 d组除外)肺组织中CD47表达显著升高(P < 0.05)。PQ中毒后2 h内,TSP-1和CD47的表达与ROS、羟自由基和丙二醛浓度及肺泡炎程度呈正相关(P < 0.01);PQ中毒1 d时,TSP-1和CD47的表达与肺组织中羟脯氨酸浓度呈正相关(P < 0.01)。TSP-1和CD47的表达与氧化应激及随后的肺纤维化密切相关,它们可能参与了PQ中毒大鼠肺泡炎及随后肺纤维化的发生发展过程。

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