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段蕾, 阎智伟, 刘莹, 聂继盛. 慢性苯并[a]芘暴露对大鼠学习记忆及谷氨酸受体影响[J]. 中国公共卫生, 2013, 29(7): 1004-1006. DOI: 10.11847/zgggws2013-29-07-20
引用本文: 段蕾, 阎智伟, 刘莹, 聂继盛. 慢性苯并[a]芘暴露对大鼠学习记忆及谷氨酸受体影响[J]. 中国公共卫生, 2013, 29(7): 1004-1006. DOI: 10.11847/zgggws2013-29-07-20
DUAN Lei, YAN Zhi-wei, LIU Ying.et al, . Effects of chronic benzo[a]pyrene exposure on learning and memory and metabotropic glutamate receptor in rats[J]. Chinese Journal of Public Health, 2013, 29(7): 1004-1006. DOI: 10.11847/zgggws2013-29-07-20
Citation: DUAN Lei, YAN Zhi-wei, LIU Ying.et al, . Effects of chronic benzo[a]pyrene exposure on learning and memory and metabotropic glutamate receptor in rats[J]. Chinese Journal of Public Health, 2013, 29(7): 1004-1006. DOI: 10.11847/zgggws2013-29-07-20

慢性苯并a芘暴露对大鼠学习记忆及谷氨酸受体影响

Effects of chronic benzoapyrene exposure on learning and memory and metabotropic glutamate receptor in rats

  • 摘要: 目的探讨慢性苯并a芘暴露对大鼠学习记忆损伤及代谢性谷氨酸受体的影响。方法将40只SD大鼠按照体重随机分为对照组、苯并a芘低、中、高剂量组(1.0、2.5、6.25 mg/kg),每组8只,腹腔注射染毒13周;用Morris水迷宫检测大鼠学习记忆能力,免疫印迹法(Western-blot)检测大鼠脑组织海马代谢性谷氨酸受体(mGluR1、mGluR2、mGluR3)表达。结果 与对照组比较,苯并a芘中、高剂量组大鼠平均潜伏期(18.34±7.09)、(24.0±12.76)s明显延长(P<0.05),高剂量组目标象限停留时间(29.00±3.64)s与穿越平台次数(4.11±1.36)次明显减少(P<0.01),随着染毒剂量增加,大鼠海马组织mGluR1、mGluR2蛋白表达增高,高剂量组大鼠海马组织mGluR1、mGluR2蛋白表达(1.09±0.29)、(0.85±0.14)明显高于对照组(0.56±0.13)、(0.54±0.15),差异均有统计学意义(P<0.05),mGluR3蛋白表达在各组之间差异不明显。结论 慢性苯并a芘暴露可导致大鼠大脑海马组织代谢性谷氨酸受体表达增高,这可能是引发学习记忆能力受损的机制之一。

     

    Abstract: Objective To explore effects of chronic benzoapyrene (BaP) exposure on learning and memory and metabotropic glutamate receptor in rats.Methods Forty male Sprague-Dawley rats were randomly assigned to one of the five groups:blank control,solvent control,1.0,2.5,and 6.25 mg/kg·bw of BaP (8 mice in each group).The rats received intraperitoneal injection treatment for 13 weeks.Morris water maze was employed to test the learning and memory behavior.The expression of metabotropic glutamate receptor 1 (m GluR1),metabotropic glumate receptor 2 (mGluR2) in the hippocampus were detected with western-blot.Results Morris water maze test showed that the rats exposed 2.5 and 6.25 mg/kg·bw BaP had increased latencies (18.34±7.09 s and 24.0±12.76 s) (P<0.05 for all).The rats exposed to 6.25 mg/kg·bw BaP had prolonged time passing the aim target (22.14±14.96 s,P<0.01),decreased number of crossing platform (4.11±1.36) and swimming time in the target area (29.00±3.64 s,P<0.01)compared with the those of the rats in control and low-dose group.The results of western-bolt test demonstrated that the expression of mGluR1 and mGluR2 in the hippocampus of 6.25mg/kg·bw BaP(1.09±0.29 and 0.85±0.14) group were significantly higher than those of the control group (0.56±0.13 and 0.54±0.15 (P<0.05),while mGluR3 showed no statistically significant difference between the groups.Conclusion Chronic BaP exposure can lead to cognitive dysfunction and overexpression of mGluR1 and mGluR2,which may be one of the mechanisms of learning and memory impairment induced by BP.

     

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