Succimer chelation normalizes reactivity to reward omission and errors in lead-exposed rats

被引:14
作者
Beaudin, Stephane A.
Stangle, Diane E.
Smith, Donald R.
Levitsky, David A.
Strupp, Barbara J.
机构
[1] Cornell Univ, Div Nutr Sci, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Psychol, Ithaca, NY 14853 USA
[3] Univ Calif Santa Cruz, Dept Biol, Santa Cruz, CA 95064 USA
基金
美国国家卫生研究院;
关键词
lead exposure; succimer; chelation; chelating agents; lead poisoning; arousal regulation; reward omission; behavior; emotion regulation; error monitoring;
D O I
10.1016/j.ntt.2006.11.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
This study evaluated the efficacy of a 3-week course of succimer treatment to alleviate behavioral deficits in rats exposed to lead (Pb) for the first 4 weeks of life. A 3 x 2 factorial design was used: three levels of lead exposure (No Pb, Moderate, and High Pb) and two levels of chelation (succimer or vehicle). Behavioral testing was conducted following chelation therapy, from 2 to 9 months of age; this report presents the results of two of the administered tasks: (1) a conditional olfactory discrimination task (baseline task), and (2) a conditional olfactory discrimination task with periodic reward omission on some correct trials (RO task). In the RO task, the performance disruption produced by committing an error on the previous trial was significantly greater for both unchelated lead-exposed groups than for controls. The High Pb rats were also more sensitive to reward omission than controls, providing converging evidence for impaired regulation of arousal or emotion. Importantly, succimer treatment was effective in normalizing the heightened reactivity of the lead-exposed animals to both errors and reward omission. In addition, non-lead-exposed rats that were treated with succimer tended to be more affected by a prior error than controls in their latency to respond on post-error trials. In sum, these findings provide new evidence that succimer chelation can significantly lessen the lasting neurobehavioral dysfunction produced by early lead exposure, but also suggest that there may be risks of administering the drug to individuals without elevated blood lead levels. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:188 / 202
页数:15
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