Vorhees Charles V, Herring Nicole R, Schaefer Tori L, Grace Curtis E, Skelton Matthew R, Johnson Holly L, Williams Michael T
Division of Neurology, Department of Pediatrics, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, 3333 Burnet Avenue, Cincinnati, OH 45229, United States.
Int J Dev Neurosci. 2008 Oct;26(6):599-610. doi: 10.1016/j.ijdevneu.2008.04.002. Epub 2008 Apr 18.
Postnatal day (P)11-20 (+)-methamphetamine (MA) treatment impairs spatial learning and reference memory in the Morris water maze, but has marginal effects on learning in a labyrinthine maze. A subsequent experiment showed that MA treatment on P11-15, but not P16-20, is sufficient to induce Morris maze deficits. Here we tested the effects of P11-15 MA treatment under two different rearing conditions on Morris maze performance and path integration learning in the Cincinnati water maze in which distal cues were unavailable by using infrared illumination. Littermates were treated with 0, 10, 15, 20, or 25mg/kg MA x 4/day (2 h intervals). Half the litters were reared under standard housing conditions and half under partial enrichment by adding stainless steel enclosures. All MA groups showed impaired Cincinnati water maze performance with no significant effects of rearing condition. In the Morris maze, the MA-25 group showed impaired spatial acquisition, reversal, and small platform learning. Enrichment significantly improved Morris maze acquisition in all groups but did not interact with treatment. The male MA-25 group was also impaired on probe trial performance after acquisition and on small platform trials. A narrow window of MA treatment (P11-15) induces impaired path integration learning irrespective of dose within the range tested but impairments in spatial learning are dependent on dose. The results demonstrate that a narrower exposure window (5 days) changes the long-term effects of MA treatment compared to longer exposures (10 days).
出生后第(P)11 - 20天给予(+)-甲基苯丙胺(MA)治疗会损害莫里斯水迷宫中的空间学习和参考记忆,但对迷宫式迷宫中的学习影响较小。随后的一项实验表明,在P11 - 15天给予MA治疗足以导致莫里斯迷宫缺陷,而在P16 - 20天给予则不然。在此,我们测试了在两种不同饲养条件下,P11 - 15天给予MA治疗对莫里斯迷宫表现和路径整合学习的影响,该实验使用辛辛那提水迷宫,通过红外照明使远端线索不可用。同窝幼崽分别接受0、10、15、20或25mg/kg MA×4/天(间隔2小时)的治疗。一半的同窝幼崽在标准饲养条件下饲养,另一半通过添加不锈钢围栏进行部分富集饲养。所有MA组在辛辛那提水迷宫中的表现均受损,饲养条件无显著影响。在莫里斯迷宫中,MA - 25组在空间获取、反转和小平台学习方面表现受损。富集显著改善了所有组在莫里斯迷宫中的获取能力,但与治疗无相互作用。雄性MA - 25组在获取后的探针试验表现和小平台试验中也受损。MA治疗的一个狭窄窗口(P11 - 15)会导致路径整合学习受损,在所测试的剂量范围内与剂量无关,但空间学习受损取决于剂量。结果表明,与较长暴露时间(10天)相比,更窄的暴露窗口(5天)会改变MA治疗的长期效果。