光参对大鼠辐射性腮腺损伤的保护作用

Yidan Yao, Tingting Zhang, Kai Hu
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ROS levels in blood serum of each group were detected on the 10th, 40th and 70th days after irradiation. After parotid gland tissue was taken, the pathological changes and ultrastructural changes were observed by hematoxylin-eosin (HE) staining and transmission electron microscopy, respectively. The expression level of TNF-α in parotid gland tissue was detected by immunohistochemistry, and apoptosis of parotid cells was detected by TUNEL assay. \n \n \nResults \nThe content of ROS and the expression of TNF-α protein in the single irradiation group were simultaneously increased compared with the control group (t=-24.723, -35.013, -19.515, P<0.05; t=-13.563, 43.519, -15.249, P<0.05), while they were reduced by Sarcandra glabra in a dosage dependent manner, especially in the high dosage group of Sarcandra glabra (t=5.295, 8.138, 6.545, P<0.05; t=10.093, -7.868, 10.539, P<0.05). 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引用次数: 0

摘要

目的研究x射线照射后大鼠腮腺组织炎症反应和细胞凋亡的变化,探讨光刺草对辐射性腮腺损伤的保护作用及其可能机制。方法将120只雄性大鼠随机分为5组(每组24只):对照组、单次照射组、高剂量组(26.8 g·kg-1·d-1)、中剂量组(13.4 g·kg-1·d-1)、低剂量组(6.7 g·kg-1·d-1)联合照射。照射组大鼠腮腺接受15 Gy x线照射。各组大鼠分别于辐照后10、40、70 d用2%戊巴比妥钠(0.16 ml/100 g)麻醉,取腹主动脉血。分别于辐照后第10、40、70天检测各组血清ROS水平。取腮腺组织后,分别用苏木精-伊红(HE)染色和透射电镜观察病理变化和超微结构变化。免疫组化法检测腮腺组织中TNF-α的表达水平,TUNEL法检测腮腺细胞凋亡情况。结果与对照组相比,单次照射组ROS含量和TNF-α蛋白表达同时升高(t=-24.723, -35.013, -19.515, P<0.05;t=-13.563, 43.519, -15.249, P<0.05),且呈剂量依赖性降低,尤其是大剂量组(t=5.295, 8.138, 6.545, P<0.05;t=10.093, -7.868, 10.539, P<0.05)。对照组腮腺组织结构完整,无充血、渗出、水肿等。单次照射组,照射后10 d腮腺组织充血、水肿、炎症细胞浸润,照射后40 d出现纤维化。照射前给药后,大鼠腮腺组织的病理改变明显恢复,组织损伤程度与给药剂量呈负相关。TUNEL检测结果显示,单次照射组大鼠腮腺细胞凋亡率高于对照组(t=-4.639, -3.979, P<0.05)。结论光参可清除辐射诱导的活性氧,降低腮腺炎症反应,对腮腺具有保护作用,可能是一种潜在的辐射损伤保护剂。关键词:细胞凋亡;Sarcandra glabra;放射性腮腺损伤;活性氧;肿瘤坏死因子-α
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Protective effect of Sarcandra glabra on radiation-induced parotid injury in rats
Objective To study the changes of inflammatory response and apoptosis in parotid gland tissues of rats after X-ray irradiation, and to explore the protective effect and possible mechanism of Sarcandra glabra on radiation-induced parotid injury in rats. Methods A total of 120 male rats were randomly divided into 5 groups(24 for each): control group, single irradiation group, radiation combined with a high(26.8 g·kg-1·d-1), moderate(13.4 g·kg-1·d-1) and low(6.7 g·kg-1·d-1) dosage of Sarcandra glabra group. The parotid gland of rats in the irradiation group received 15 Gy X-ray. Rats in each group were anesthetized with 2% pentobarbital sodium (0.16 ml/100 g) at 10, 40 and 70 d after irradiation and blood was collected from abdominal aorta. ROS levels in blood serum of each group were detected on the 10th, 40th and 70th days after irradiation. After parotid gland tissue was taken, the pathological changes and ultrastructural changes were observed by hematoxylin-eosin (HE) staining and transmission electron microscopy, respectively. The expression level of TNF-α in parotid gland tissue was detected by immunohistochemistry, and apoptosis of parotid cells was detected by TUNEL assay. Results The content of ROS and the expression of TNF-α protein in the single irradiation group were simultaneously increased compared with the control group (t=-24.723, -35.013, -19.515, P<0.05; t=-13.563, 43.519, -15.249, P<0.05), while they were reduced by Sarcandra glabra in a dosage dependent manner, especially in the high dosage group of Sarcandra glabra (t=5.295, 8.138, 6.545, P<0.05; t=10.093, -7.868, 10.539, P<0.05). In the control group, the parotid gland tissue structure was intact, without congestion, exudation, edema, etc. For the single irradiation group, the parotid gland tissue became hyperemia, edema and inflammatory cell infiltration at 10 d after irradiation followed by fibrosis at 40 d after irradiation. These pathological alterations in the parotid gland tissue were significantly recovered when the rats were treated with Sarcandra glabra before irradiation, and the tissue damage was negatively correlated with drug dosage. TUNEL assay showed that the apoptosis rate of parotid gland cells in the single irradiation groups was higher than that in the control group (t=-4.639, -3.979, P<0.05). Conclusions Sarcandra glabra protects parotid gland from radiation damage by scavenging radiation-induced ROS and declining inflammatory response, and thus it may be applied as a potential protective agent for radiation injury. Key words: Apoptosis; Sarcandra glabra; Radiation induced parotid injury; ROS; TNF-α
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中华放射医学与防护杂志
中华放射医学与防护杂志 Medicine-Radiology, Nuclear Medicine and Imaging
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