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尼莫地平对小鼠穿梭箱回避学习的影响:无损害反而略有改善。

Nimodipine on shuttle-box avoidance learning in mice: no impairment but slight improvement.

作者信息

Vetulani J, Battaglia M, Sansone M

机构信息

Institute of Pharmacology, PAN, Krakow, Poland.

出版信息

Pharmacol Biochem Behav. 1997 Apr;56(4):577-81. doi: 10.1016/s0091-3057(96)00421-2.

Abstract

The dihydropyridine calcium channel antagonist nimodipine was tested in mice of CD-1, C57BL/6, and DBA/2 strains subjected to shuttle-box avoidance training. In contrast with some findings of other authors showing impairment of shuttle-box avoidance learning by low doses of the drug in rats, nimodipine given IP before each training session at doses of 0.25, 0.5, 1, 2.5, or 5 mg/kg never impaired avoidance acquisition in mice. On the contrary, one dose of nimodipine (1 mg/kg) significantly improved avoidance acquisition in mice of the DBA/2 strain. The drug failed to impair avoidance performance in DBA/2 mice even if given acutely in the middle (third session) or at the end (fifth session) of the training period. The results contradict studies showing cognitive impairment induced by calcium channel blockers, and may provide some limited evidence in support of improved cognitive function in normal animals, although this effect is much less evident than in aged or brain-damaged subjects.

摘要

在接受穿梭箱回避训练的CD-1、C57BL/6和DBA/2品系小鼠中对二氢吡啶类钙通道拮抗剂尼莫地平进行了测试。与其他作者的一些研究结果相反,那些研究表明低剂量药物会损害大鼠的穿梭箱回避学习能力,而在每次训练前腹腔注射剂量为0.25、0.5、1、2.5或5mg/kg的尼莫地平从未损害小鼠的回避学习能力。相反,一剂尼莫地平(1mg/kg)显著改善了DBA/2品系小鼠的回避学习能力。即使在训练期中期(第三次训练)或末期(第五次训练)急性给药,该药物也不会损害DBA/2小鼠的回避表现。这些结果与显示钙通道阻滞剂会导致认知障碍的研究相矛盾,并且可能提供一些有限的证据来支持正常动物的认知功能得到改善,尽管这种效应远不如在老年或脑损伤个体中明显。

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