4.1 Article

Domoic acid: Neurobehavioral consequences of exposure to a prevalent marine biotoxin

期刊

NEUROTOXICOLOGY AND TERATOLOGY
卷 32, 期 2, 页码 132-141

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ntt.2009.09.005

关键词

Domoic acid; Marine biotoxin; Behavior; Brain; Development

资金

  1. Pacific Northwest Center for Human Health and Ocean Studies [P50ES012762-NIH, OCE0434087- NSF]
  2. Center for Human Development and Disabilities [P51HD02274-NIH]
  3. Washington National Primate Research Center [P51RR000166-NIH]
  4. NIEHS [5R01E512459]
  5. Directorate For Geosciences
  6. Division Of Ocean Sciences [0910624] Funding Source: National Science Foundation

向作者/读者索取更多资源

Domoic acid (DA), the cause of Amnesic Shellfish Poisoning, is a naturally occurring marine biotoxin that is usually produced by the microscopic algae Pseudo-nitzschia. As is the case for other types of toxic algae, Pseudo-nitzschia outbreaks are becoming more frequent. Acute high-dose symptomology in humans includes vomiting, cramping, coma and death as well as neurological effects such as hallucinations, confusion and memory loss. Experimental studies and medical reports have collectively shown that DA exposure primarily affects the hippocampal regions of the brain and is associated with seizures and the disruption of cognitive processes. The neurobehavioral signature of DA is unique in that it includes transient and permanent changes in memory function that resemble human antegrade amnesia. Experimental studies with adult nonhuman primates have established that DA is a dose-dependent emetic that produces clinical and neuropathological changes consistent with excitotoxicity. Behavioral evaluations of treated rodents have shown that hyperactivity and stereotypical scratching are the first functional markers of toxicity. Mid-dose treatment is associated with memory impairment and behavioral hyperreactivity, suggesting changes in arousal and/or emotionality. At higher doses, DA treatment results in frank neurotoxicity that is characterized by seizures, status epilepticus and death in treated animals. The route of DA exposure is important and influences the severity of effects; intraperitoneal and intravenous treatments produce classic signs of poisoning at significantly lower doses than oral exposure. While developmental studies are few, DA readily crosses the placenta and enters the fetal brain. Domoic acid is not associated with congenital dysmorphia but is linked to persistent changes in motor behavior and cognition in exposed offspring. Comparative research suggests that functional losses associated with DA can be persistent and injuries to the CNS can be progressive. Long-term studies will be necessary to accurately track the expression of DA-related injury, in health and behavior, over the lifespan. (C) 2009 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.1
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据