4.6 Review

General Anesthesia: A Gateway to Modulate Synapse Formation and Neural Plasticity?

期刊

ANESTHESIA AND ANALGESIA
卷 115, 期 5, 页码 1174-1182

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1213/ANE.0b013e31826a1178

关键词

-

资金

  1. Swiss National Science Foundation [31003A-130625]
  2. Swiss National Science Foundation (SNF) [31003A_130625] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

Appropriate balance between excitatory and inhibitory neural activity patterns is of utmost importance in the maintenance of neuronal homeostasis. General anesthetic induced pharmacological interference with this equilibrium results not only in a temporary loss of consciousness but can also initiate long-term changes in brain function. Although these alterations were initially considered deleterious, recent observations suggest that at least under some specific conditions, they may eventually improve neural function. The goal of this review is to provide insights into the mechanisms underlying these dual effects. Basic science issues on the important role of critical periods during neural circuitry assembly will be discussed to better understand how even brief exposures to general anesthetics could initiate context-dependent lasting changes in neuronal structure and function. Recent series of observations suggesting a developmental stage dependent impact of these drugs on synaptogenesis will then be summarized together with currently known molecular mechanisms underlying these effects. Particular emphasis will be placed on how anesthetic drugs modulate neural plasticity in the adult brain and how this may improve neural function under some pathological states. The ensemble of these new observations strongly suggests that general anesthetics should not merely be considered toxic drugs but rather acknowledged as robust, context-dependent modulators of neural plasticity. (Anesth Analg 2012;115:1174-82)

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

4.6
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