他克林对AF64A诱导的大鼠主动回避行为缺陷的影响。

N Lermontova, N Lukoyanov, T Serkova, E Lukoyanova, S Bachurin
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引用次数: 25

摘要

采用双向穿梭箱主动回避实验,研究了他克林(1,2,3,4-四氢-9-氨基吡啶)对乙胆碱偶氮离子(AF64A)诱导大鼠记忆缺损的影响。神经毒素AF64A以6 nmol (icc.v,双侧)剂量注射可引起海马区CA2和CA3的非特异性组织损伤。6 nmol处理2周后,毒素处理大鼠的AF64A主动回避表现明显恶化,学习测试中估计的正确率分别为68 +/- 3.5%和83 +/- 3.2%;P < 0.01)和滞留试验分别为53 +/- 5%和76 +/- 3.6%;P < 0.01)。在这些条件下,每日剂量为1 mg/kg的他克林慢性治疗12-14 d,可以逆转AF64A对学习(78 +/- 3.2%)和保留(72 +/- 4%)测试中主动回避表现的影响。据推测,他克林的行为影响在很大程度上取决于海马神经退行性变的严重程度。
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Effects of tacrine on deficits in active avoidance performance induced by AF64A in rats.

Effects of tacrine (1,2,3,4-tetrahydro-9-aminocridine) on memory deficits in rats treated with ethylcholine aziridinium ion (AF64A) were studied using active avoidance test in the two-way shuttle box. Neurotoxin AF64A injected at a dose of 6 nmol (i.c.v., bilaterally) causes nonspecific tissue damage in hippocampal fields CA2 and CA3. Two weeks after treatment with 6 nmol, AF64A active avoidance performance of toxin-treated rats was significantly deteriorated compared to vehicle-treated animals estimated in learning test (68 +/- 3.5 and 83 +/- 3.2% of correct responses, respectively; p < 0.01) and in retention test (53 +/- 5 and 76 +/- 3.6%, respectively; p < 0.01). Under these conditions, chronic treatment with tacrine at a daily dose of 1 mg/kg for 12-14 d reverses the effect of AF64A on the active avoidance performance both in learning (78 +/- 3.2%) and retention (72 +/- 4%) tests. It is supposed that behavioral effects of tacrine considerably depend on a severity of neurodegeneration in the hippocampus.

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