癌变·畸变·突变 ›› 2020, Vol. 32 ›› Issue (2): 139-144.doi: 10.3969/j.issn.1004-616x.2020.02.010

• 论著 • 上一篇    下一篇

低水平铅暴露损伤小鼠糖耐量及视网膜血管渗透性促进糖尿病视网膜病变发生

王晓会, 肖琛, 赵和平, 吴赛, 夏冬, 柳怀湘, 刘洁仪, 赵志强, 何云   

  1. 中山大学公共卫生学院, 广州市环境污染与健康风险评价重点实验室, 广东 广州 510080
  • 收稿日期:2020-01-23 修回日期:2020-03-10 出版日期:2020-03-30 发布日期:2020-04-10
  • 通讯作者: 何云,E-mail:heyun7@mail.sysu.edu.cn E-mail:heyun7@mail.sysu.edu.cn
  • 作者简介:王晓会,E-mail:wangxh56@mail2.sysu.edu.cn。
  • 基金资助:
    国家自然科学基金(81872661,81472998)

Exposure to low-level lead associated with glucose tolerance, retinal vascular permeability and diabetic retinopathy in mice

WANG Xiaohui, XIAO Chen, ZHAO Heping, WU Sai, XIA Dong, LIU Huaixiang, LIU Jieyi, ZHAO Zhiqiang, HE Yun   

  1. Guangzhou Key Laboratory of Environmental Pollution and Risk Assessment, School of Public Health, Sun Yat-sen University, Guangzhou 510080, Guangdong, China
  • Received:2020-01-23 Revised:2020-03-10 Online:2020-03-30 Published:2020-04-10

摘要: 目的: 研究低水平铅暴露对于小鼠糖耐量与视网膜血管渗透性的影响,探讨铅对糖尿病视网膜血管病变的作用。方法: 用去离子水分别配制含0(对照组)、10、100、500 mg/L醋酸铅的饮用水,48只母代小鼠摄入含醋酸铅的饮用水染毒。子代小鼠继续按母鼠相同的剂量喂饲含醋酸铅的饮用水染毒,8周龄时每个染毒剂量均分为两组,每组12只,均雌雄各半。8周组在此时收集样品,利用石墨炉火焰原子吸收法检测血铅,小鼠腹腔葡萄糖耐量试验检测糖耐量水平,眼底静脉荧光造影与小动物视网膜眼底成像技术检测眼底血管渗透性,实时荧光定量聚合酶链式反应检测视网膜血管紧密连接相关分子转录水平改变;20周组继续用醋酸铅饮用水喂养至20周龄检测上述指标。结果: 子代小鼠血铅浓度随着醋酸铅浓度的增加而升高(r8周组=0.887,r20周组=0.972,P均 < 0.05)。在100 mg/L剂量以下,染毒8周组小鼠的血铅浓度高于染毒20周组(P < 0.05);在500 mg/L剂量下,染毒8周组小鼠的血铅浓度低于染毒20周组(P < 0.01)。与对照组小鼠相比,各浓度醋酸铅染毒后的子代小鼠腹腔注射葡萄糖后2 h内血糖高于对照组小鼠,血糖随时间变化的曲线下面积积分高于对照组小鼠(P < 0.05或P < 0.01)。在染毒8周组,小鼠血糖及AUC在10 mg/L醋酸铅染毒时与对照组差异最明显,而在染毒20周组小鼠在100 mg/L醋酸铅染毒时与对照组差异最明显。在染毒8周组,小鼠未出现血管渗漏表现;与对照组小鼠相比,醋酸铅染毒小鼠在分子水平出现紧密连接相关分子ZO-1,Occludin,Claudin-1、3、5等的mRNA转录水平先升高后抑制表现(P < 0.05或P < 0.01);在染毒20周组,100和500 mg/L醋酸铅暴露条件下,小鼠视网膜血管出现渗漏;与对照组小鼠相比,醋酸铅染毒小鼠在分子水平出现紧密连接相关分子ZO-1,Occludin,Claudin-1、3、5等的mRNA转录受到抑制(P < 0.01)。结论: 铅暴露可以导致小鼠糖耐量试验中血糖升高,早期敏感剂量更低;持续性的铅暴露直接导致了视网膜血管渗漏,铅暴露可能是糖尿病视网膜血管病变等疾病的潜在危险因子。

关键词: 醋酸铅, 糖耐量, 血视网膜屏障, 渗漏, 糖尿病视网膜病变

Abstract: OBJECTIVE: To investigate the effects of low-level lead exposure on glucose tolerance and retinal vascular permeability in mice and explore the effects of lead on diabetic retinopathy. METHODS: A lead exposure mouse model was initiated beginning with the mother generation:four groups exposed to 0,10,100,500 mg/L lead acetate. Offspring were exposed continuously until the sacrifice time. Half of mice were sacrificed at 8 weeks age,named the 8-weeks group with 12 mice (male:female:1:1) in each exposure concentration level. The graphite furnace flame atomic absorption spectrometry was used to detect lead in blood,and the intraperitoneal glucose tolerance test was used to measure glucose tolerance. The fundus vein fluorescence angiography and retinal fundus imaging technology were used to detect the vascular permeability of retinal vessels. Real-time fluorescence quantitative polymerase chain reaction (qPCR) was used to detect transcription of tight junction-related molecules. The other half of mice were sacrificed at 20 weeks age,named the 20-week group. RESULTS: The blood lead concentrations of offspring increased with the increment of lead acetate exposure level(r8 week=0.887,P < 0.05;r20 week=0.972,P < 0.05). The blood lead levels were higher in the 8-week than the 20-week groups when the lead acetate exposure levels were 0,10,100 mg/L. However,the 20-week group had higher blood lead than the 8-week group when the exposure was at the 500 mg/L lead acetate exposure level (P < 0.01). Compared with the control group,the blood glucose of the exposed offspring was higher within 2 hours after intraperitoneal injection of glucose,and the area under the curve of blood glucose was higher than the control mice (P < 0.05 or P < 0.01). In the 8-week group,the blood glucose and AUC of mice exposed to 10 mg/L lead acetate showed the most significantly changes compare to the controls while those at the 20-week group was at 100 mg/L. In the 8-week group,there was no vascular leakage,but only at the molecular level,the transcriptional levels of Zona occludens protein-1(ZO-1),Occludin,Claudin-1,3,5 were increased initially and then inhibited compared with control group (P < 0.05 or P < 0.01). In the 20-week group,leakages occurred in the retinal vessels of offspring exposed to lead acetate in the 100 and 500 mg/L groups,while tight junction related molecules ZO-1,Occludin,Claudin-1,3,5 transcriptions were inhibited (P < 0.01). CONCLUSION: Lead exposure increased blood glucose in the glucose tolerance test and the dose was very low before adulthood. Persistent lead exposure directly caused leakage in the retinal blood vessels which may be a potential risk factor for diseases such as diabetic retinopathy.

Key words: lead acetate, glucose tolerance, blood retinal barrier, leakage, diabetic retinopathy

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