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向程窈, 于燕妮, 陈荣, 徐淋, 徐琼. Beclin-1、Bcl-2、Bax在慢性氟中毒大鼠肾脏中表达[J]. 中国公共卫生, 2016, 32(6): 798-802. DOI: 10.11847/zgggws2016-32-06-20
引用本文: 向程窈, 于燕妮, 陈荣, 徐淋, 徐琼. Beclin-1、Bcl-2、Bax在慢性氟中毒大鼠肾脏中表达[J]. 中国公共卫生, 2016, 32(6): 798-802. DOI: 10.11847/zgggws2016-32-06-20
XIANG Cheng-yao, YU Yan-ni, CHEN Rong.et al, . Expression and clinical significance of Beclin-1,Bcl-2,and Bax in renal cells of rats with exprimental fluorosis[J]. Chinese Journal of Public Health, 2016, 32(6): 798-802. DOI: 10.11847/zgggws2016-32-06-20
Citation: XIANG Cheng-yao, YU Yan-ni, CHEN Rong.et al, . Expression and clinical significance of Beclin-1,Bcl-2,and Bax in renal cells of rats with exprimental fluorosis[J]. Chinese Journal of Public Health, 2016, 32(6): 798-802. DOI: 10.11847/zgggws2016-32-06-20

Beclin-1、Bcl-2、Bax在慢性氟中毒大鼠肾脏中表达

Expression and clinical significance of Beclin-1,Bcl-2,and Bax in renal cells of rats with exprimental fluorosis

  • 摘要: 目的 观察自噬基因Beclin-1、凋亡基因Bcl-2、Bax在慢性氟中毒大鼠肾脏中的表达变化,探讨Beclin-1、Bcl-2、Bax在氟中毒肾脏损害过程中的作用。方法 将SD大鼠24只随机分为3组,每组8只,对照组(饮用含氟量 < 0.5 mg/L自来水),低、高氟组(自来水含氟量分别为50、100 mg/L);饲养9个月后,观察大鼠氟斑牙发生情况;氟离子电极法测定尿氟、骨氟含量;显微镜下观察大鼠肾组织病理形态学变化;采用免疫组织化学方法检测大鼠肾组织中Beclin-1、Bcl-2、Bax表达量;用原位杂交法测定大鼠肾脏Beclin-1 mRNA含量。结果 低氟组大鼠氟斑牙检出率为75%,高氟组为100%;与对照组比较,低、高氟组大鼠尿氟和骨氟含量分别为(10.09±0.88)、(18.09±0.89)mg/L和(5 500.84±1 093.47)、(7 477.94±1 315.88)μg /g明显升高,差异有统计学意义(P < 0.05);染氟大鼠肾脏肾小管上皮细胞水肿、间质血管扩张充血,且随染氟剂量增加损伤改变逐渐加重;与对照组比较,低、高氟组大鼠肾组织中Beclin-1、Bax表达分别为(168.90±8.68)、(146.32±10.02)和(153.74±10.56)、(134.29±9.85)明显降低(均P < 0.05);与对照组比较,低、高氟组大鼠肾组织中Bcl-2表达分别为(167.64±7.51)、(185.32±8.55)明显升高(P < 0.05);与对照组比较,低、高氟组大鼠肾组织中Beclin-1 mRNA表达分别为(166.94±13.21)、(146.11±17.66)明显降低(P < 0.05)。结论 慢性氟中毒可诱导肾小管上皮细胞自噬和凋亡相关分子的异常表达,自噬和凋亡可能共同参与慢性氟中毒肾脏损伤过程。

     

    Abstract: Objective To observe expressions of autophagy-related gene Beclin-1,apoptosis-related gene Bcl-2,and Bax in renal cells of rats with fluorosis and to explore the significance of the exprssions in renal injury associated with chronic fluorosis.Methods Twenty-four healthy Sprague-Dawley rats were randomly divided into a control group (8 rats with fluoride<0.5 mg/L in drinking water),a low fluoride group (8 rats with fluoride of 50 mg/L in drinking water)and a high fluoride group (8 rats with fluoride of 100 mg/L in drinking water).All the rats were sacrificed at 9-month of the treatment.The occurrence of dental fluorosis in the rats was observed.The fluoride content in urine and bone was determined using fluoride ion selective electrode method.Pathological changes in renal tissues were observed with optical microscopy.The protein expressions of Beclin-1,Bcl-2,Bax in renal tissues were determined with immunohistochemistry and the expression of Beclin-1 mRNA was analyzed with in situ hybridization.Results The detection rate of dental fluorosis was 75%(6/8)and 100%(8/8)for the rats of low and high fluoride group and the fluoride contents in urine were 10.09±0.88 mg/L and 18.09±0.89 mg/L and those in bone were 5 500.84±1 093.47 μg /g and 7 477.94±1 315.88 μg/g for the rats of low and high fluoride group,which were significantly higher compared to those of the rats of control group (all P < 0.05).The edema of tubular epithelial cells and obvious intersitial congestion of renal tubules were observed with light microscopy in the rats with fluoride exposure and these pathogenic changes aggravated with the increase of fluoride concentration.The expressions of Beclin-1 (168.90±8.68 and 146.32±10.02)and Bax (153.74±10.56 and 134.29±9.85)in renal tissues of the rats with low and high fluoride exposure were significantly lower than those of the rats of the control group (all P < 0.05),while the expression of Bcl-2 (167.64±7.51 and 185.32±8.55) in renal tissues of the rats of low and high fluoride group was significantly higher than that in the rats of the control group (both P < 0.05).Meanwhile the Beclin-1 mRNA expression (166.94±13.21 and 146.11±17.66)in renal tissues of the rats of low and high fluoride group decreased significantly compared to that of the rats of the control group (both P < 0.05).Conclusion Chronic fluorosis can induce autophagy and apoptosis of renal tubular epithelial cells in rats and the autophagy and apoptosis may be involved in the pathogenesis of kidney injury in chronic fluorosis.

     

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