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机构地区:[1]郑州大学第一附属医院神经内科,郑州450052 [2]郑州大学第一附属医院老年病科,郑州450052
出 处:《中国实用神经疾病杂志》2010年第15期16-17,共2页Chinese Journal of Practical Nervous Diseases
基 金:广东省自然科学基金资助项目(编号000825)
摘 要:目的观察纳洛酮对铝致学习记忆减退大鼠海马锥体细胞凋亡的影响。方法采用慢性氯化铝灌胃方法,制备学习记忆减退大鼠模型后随机分为模型组和纳洛酮治疗组,另设正常对照组。纳洛酮治疗组大鼠连续7 d腹腔注射纳洛酮。采用脱氧核苷酸末端转移酶介导的脱氧尿苷酸-生物素切口末端标记法,原位检测凋亡细胞,流式细胞仪检测凋亡率。结果纳洛酮组大鼠海马锥体细胞的凋亡率为(6.4±1.6)%,模型组(9.6±1.9)%,差异有统计学意义(P<0.05);纳洛酮组大鼠凋亡细胞数为(7.5±1.9),模型组(12.8±2.2),差异有统计学意义(P<0.05)。结论纳洛酮能减少铝致学习记忆减退大鼠海马锥体细胞的凋亡。Objective To observe the effects of naloxone on apoptosis of hippocampus pyramidal neurons in rats with aluminum-induced learning and memory impairment. Methods Aluminum-induced learning and memory impairment model was established by gavages of aluminum chloride (600 mg/kg) for 3 months. Rats were divided into three groups,viz, Naloxone trea- ted rats (NAL 0.8 mg/kg, ip daily for 7 days), nontreated model rats and normal controls. The apoptosis in situ in hippocam- pus pyramidal neurons of the three groups of rats was investigated with a TdT-mediated dUTP nicked labeling (TUNEL) method. The apoptotic rate of neurons was measured by flow cytometry. Results The apoptosis ratio of hippocampus cell in the NAL group (6.4± 1.6)% was significantly decreased compared to nontreated model rats (9.6± 1.9)% (P〈0.05). The number of apoptotic pyramidal neurons in the CA1 region of hippocampus in the NAL group(7.5 ± 1.9) was significantly decreased compared to nontreated model rats (12.8±2.2) (P〈0.05). Conclusion Naloxone could decrease the apoptosis of pyramidal neurons in rats with aluminum induced learning and memory impairment.
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