Li S S, Zhang B, Zhang S M, Zhang Z H, Wei Y N
School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Sciences, Jinan 250062, China;Shandong Academy of Occupational Health and Occupational Medicine, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250062, China.
Shandong Academy of Occupational Health and Occupational Medicine, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250062, China.
Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. 2019 Oct 20;37(10):728-731. doi: 10.3760/cma.j.issn.1001-9391.2019.10.003.
To observe the lung injury of male rats induced by sub-chronic exposure to crotonaldehyde, and to explore the possible mechanism of injury. Forty SPF male Wistar rats were randomly divided into control group and 3 groups in each group, and each group received 0.0, 2.5, 4.5, 8.5 mg/kg body weight crotonaldehyde solution for continuous intragastric administration. 120 d, once a day. After the end of the exposure, the body weight of the rats was measured, and the lung tissues were quickly separated after cervical dislocation. The organ coefficients were calculated and histopathological examination was performed to determine malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione. Peroxidase (GSH-Px) content; ELISA was used to measure interleukin (IL) -6, IL-1β, and tumor necrosis factor (TNF) -α in lung tissues. Compared with the control group, the weight gain of the rats in the 4.5 and 8.5 mg/kg exposure groups was small, and the lung weight and organ coefficient of the exposed group decreased, the difference was statistically significant (<0.05). In the exposed group, the lung tissue structure was disordered, the alveolar wall was thickened, and inflammatory cell infiltration was observed. Compared with the control group, the MDA activity in the serum of the rats in the 4.5 mg/kg and 8.5 mg/kg groups increased, and the SOD and GSH-Px activities decreased, the difference was statistically significant (<0.05). TNF-α levels in the lung tissues of rats exposed to 4.5 mg/kg and 8.5 mg/kg, and levels of (IL) -6 and IL-1β in the lungs of rats in the 2.5, 4.5, and 8.5 mg/kg groups. Significantly increased, the difference was statistically significant (<0.05) . Crotonaldehyde may induce inflammatory and oxidative stress damage in rats by up-regulating the expression of inflammatory factors in lung tissue and changing the oxidative balance.
观察亚慢性接触巴豆醛对雄性大鼠肺损伤的影响,并探讨其可能的损伤机制。将40只SPF级雄性Wistar大鼠随机分为对照组和3个染毒组,每组分别给予0.0、2.5、4.5、8.5mg/kg体重的巴豆醛溶液连续灌胃120d,每天1次。染毒结束后,测量大鼠体重,颈椎脱臼后迅速分离肺组织,计算脏器系数并进行组织病理学检查,测定丙二醛(MDA)、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)含量;采用酶联免疫吸附测定(ELISA)法检测肺组织中白细胞介素(IL)-6、IL-1β和肿瘤坏死因子(TNF)-α水平。与对照组相比,4.5mg/kg和8.5mg/kg染毒组大鼠体重增加量少,染毒组肺重量和脏器系数降低,差异有统计学意义(P<0.05)。染毒组肺组织结构紊乱,肺泡壁增厚,可见炎性细胞浸润。与对照组相比,4.5mg/kg和8.5mg/kg组大鼠血清MDA活性升高,SOD和GSH-Px活性降低,差异有统计学意义(P<0.05)。4.5mg/kg和8.5mg/kg染毒组大鼠肺组织TNF-α水平,以及2.5、4.5、8.5mg/kg组大鼠肺组织中(IL)-6和IL-1β水平均显著升高,差异有统计学意义(P<0.05)。巴豆醛可能通过上调肺组织炎性因子表达,改变氧化平衡,诱导大鼠发生炎症和氧化应激损伤。