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作 者:周永田[1] 徐旭东[1] 刘正亮[1] 谢林[1] 秦占霞[1] 马娟[1] 史春霞[1] 沙海洋[1]
机构地区:[1]山东省职业卫生与职业病防治研究院康复理疗科,济南250002
出 处:《中国公共卫生》2007年第4期474-476,共3页Chinese Journal of Public Health
基 金:山东省医科院2004年科研项目(2004-0023)
摘 要:目的观察HgCl2对大鼠脊髓星形胶质细胞的影响。方法SD大鼠30只,雌雄各半,体重160~200 g。随机分为3组,每组10只。大剂量组按17 mg/kg(1/4 LD50)经口灌胃HgCl2溶液,1次/d。小剂量组按8.5 mg/kg(1/8 LD50)经口灌胃HgCl2溶液,1次/d。对照组经口灌胃生理盐水2 ml,1次/d,3组均连续灌胃(20±2)d。染汞组建成亚急性汞中毒模型后,各组均处死5只雄鼠,留5只雌鼠作药物干预试验。染汞组用二巯丙磺钠注射液(DMPS)按28 mg/kg腹腔注射驱汞2个疗程,小剂量组仅用DMPS,大剂量组在用DMPS的期间内,按29.22/(kg.d)经口灌胃己酮可可碱(POF)溶液14 d。实验结束后处死全部动物,灌注固定取出脊髓L5-6节并制成病理切片。用免疫组化链酶亲和素-生物素-过氧化物酶聚合物(SABC)法测定脊髓胶质纤维酸性蛋白(GFAP)。结果大、小剂量组GFAP平均灰度均显著低于对照组,阳性细胞率均显著高于对照组。DMPS+POF显著降低GFAP阳性细胞率,提高平均灰度值,单纯应用DMPS无此作用。结论亚急性HgCl2中毒大鼠脊髓GFAP表达上调,POF能够有效抑制星形胶质细胞激活。Objective To observe the effect of HgCl2 on the astroeyte in spinal cord. Methods Thirty SD rats(15♀, 15 ♂, weighting 160 -- 200g) were randomized into 3 groups of 10(5 ♀, 5 ♂ ) each. Group A and group B received HgCl2 juice at a dose of 17mg/kg( 1/4 LD50), 8.5 mg/kg( 1/8 LD50) respectively by gavage daily. Group C received 0.9 % saline 2 ml by garage daily. To found the sub- acute mercury poisoning rat model within(20 ± 2) days. Then male rats in each group were dissected and the chelator(DMPS) was injected into the abdomen of female rats of group A and B at a dose of 28 mg/kg for 2 periods . Group A received DMPS+ POF(pentoxifylline) and group B received DMPS only. The POF was used at a dose of 29.22 mg/kg by garage daily for 14 days . The rats were all dissected and the spinal cord (L5 - 6) were gotten after the trial finished. Then the pathological section of spinal cord was made from and GFAP was detected . Results The average gray scale in group A and group B are all less and the positive cell rate are all larger signlfieantly compaired with control group. The POF depress the activation of astrocyte significantly. Conclusion Sub - acute poisoning of HgCl2 enhance GFAP level significantly in spinal cord, and POF depresses the activation of astrocyte.
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