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与幼年(P21 - 30或P31 - 40)或成年大鼠(P51 - 60)相比,青春期前后的大鼠(P41 - 50)对D - 甲基苯丙胺诱导的长期空间和序列学习缺陷表现出更高的易感性。

Periadolescent rats (P41-50) exhibit increased susceptibility to D-methamphetamine-induced long-term spatial and sequential learning deficits compared to juvenile (P21-30 or P31-40) or adult rats (P51-60).

作者信息

Vorhees Charles V, Reed Tracy M, Morford LaRonda L, Fukumura Masao, Wood Sandra L, Brown Carrie A, Skelton Matthew R, McCrea Anne E, Rock Stephanie L, Williams Michael T

机构信息

Division of Developmental Biology, Cincinnati Children's Research Foundation, 3333 Burnet Avenue, Cincinnati, OH 45229-3039, USA.

出版信息

Neurotoxicol Teratol. 2005 Jan-Feb;27(1):117-34. doi: 10.1016/j.ntt.2004.09.005.

Abstract

We have previously shown that P11-20 treatment with d-methamphetamine (MA) induces impaired spatial navigation in the Morris water maze (MWM), whereas P1-10 treatment does not. Little is known about the long-term behavioral consequences of MA during juvenile, adolescent, and early adult brain development. In dose-response experiments, we tested successive 10-day intervals of exposure to MA in rats (P21-30, P31-40, P41-50, and P51-60; four doses per day). MA dosing prior to P21 produces little or no toxicity; however, we observed an increased toxicity with advancing age. Across-age comparisons revealed no MWM acquisition or Cincinnati water maze (CWM) effects after MA treatment on P21-30 (2.5-10 mg/kg/dose), P31-40 (1.25-7.5 mg/kg/dose), or P51-60 (1.25-5.0 mg/kg/dose); however, significantly impaired MWM acquisition was observed after P41-50 MA treatment at the highest dose (6.25 mg/kg/dose). Learning in the CWM was also impaired in this group. No effects were seen at 1.25, 2.5, or 5 mg/kg/dose following P41-50 MA treatment. MWM reversal learning trials after P41-50 treatment showed a trend towards longer latency in all MA dose groups, but no effect on double-reversal trials. Reversal and double-reversal also showed no effects at the other exposure ages. No differences in straight channel swimming or cued learning in the MWM were seen after MA treatment at any exposure age. P41-50 is the periadolescent stage of brain development in rodents. The effects observed at this age may suggest a previously unrecognized period of susceptibility for MA-induced cognitive deficits.

摘要

我们之前已经表明,在出生后第11至20天用右旋苯丙胺(MA)进行处理会导致在莫里斯水迷宫(MWM)中空间导航受损,而在出生后第1至10天进行处理则不会。关于MA在幼年、青少年和成年早期大脑发育过程中的长期行为后果,人们了解甚少。在剂量反应实验中,我们测试了大鼠(出生后第21至30天、第31至40天、第41至50天和第51至60天;每天四个剂量)连续10天暴露于MA的情况。在出生后第21天之前给予MA几乎不会产生毒性或根本不产生毒性;然而,我们观察到随着年龄增长毒性增加。跨年龄比较显示,在出生后第21至30天(2.5至10毫克/千克/剂量)、第31至40天(1.25至7.5毫克/千克/剂量)或第51至60天(1.25至5.

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