Suppr超能文献

二异丙基氟磷酸酯抑制乙酰胆碱酯酶活性并扰乱斑马鱼的体节发生。

Diisopropylfluorophosphate inhibits acetylcholinesterase activity and disrupts somitogenesis in the zebrafish.

作者信息

Hanneman E H

机构信息

Institute of Neuroscience, University of Oregon, Eugene 97403.

出版信息

J Exp Zool. 1992 Aug 1;263(1):41-53. doi: 10.1002/jez.1402630106.

Abstract

Acetylcholinesterase (AChE) activity, localized histochemically, appeared in the nuclei of presumptive somitic mesodermal cells prior to the onset of somitogenesis. AChE activity appeared in a rostro-caudal sequence, in cells located the equivalent of five somite lengths caudal to the last formed somite. To investigate whether AChE activity was required for somitogenesis, several inhibitors of AChE activity were tested for their ability to block somitogenesis. Diisopropylfluorophosphate (DFP), a broad spectrum inhibitor of serine proteases and related enzymes, was the only AChE inhibitor tested that disrupted somitogenesis. Gastrulae at 50% epiboly exposed continuously to DFP at concentrations between 40 microM and 90 microM completed epiboly, but exhibited a dose-dependent decrease in the number of somites formed, and a parallel decrease in the caudal extent of somite innervation, by 24 hours post-fertilization (h). Fifteen somite (15h) embryos exposed to DFP at the ED50 of 70 microM for 3 hours, followed by recovery to 24h, developed abnormal somites. Approximately five normal somites formed after drug treatment before the first abnormal somite formed. The abnormal somites corresponded in location to that area of the presumptive somitic mesoderm that would have initiated AChE activity while the DFP was present. While exposed to 70 microM DFP, presumptive somites formed and motoneurons extended processes that had initiated AChE activity at the time of treatment with DFP, although at a slower than normal rate. However, embryos exposed to 1 mM DFP for 30 minutes at both the 5 and 15 somite stages, followed by recovery to 24h, developed the normal number of somites but were reduced in the caudal extent of somite innervation, and occasionally developed abnormal primary motoneurons. As with the abnormal somites, the abnormal motoneurons would have initiated AChE activity while the DFP was present. Presumptive somitic mesoderm unable to initiate AChE activity due to inhibition by DFP developed abnormally. While the effects of DFP are not limited to inhibiting AChE, the data support the "clock and wavefront" model proposed for somite formation, and support the hypothesis that AChE activity has a role in somitogenesis in zebrafish.

摘要

通过组织化学定位发现,乙酰胆碱酯酶(AChE)活性在体节发生开始之前就出现在推定的体节中胚层细胞的细胞核中。AChE活性以头-尾顺序出现,出现在位于最后形成的体节尾侧相当于五个体节长度处的细胞中。为了研究体节发生是否需要AChE活性,测试了几种AChE活性抑制剂阻断体节发生的能力。二异丙基氟磷酸酯(DFP)是一种丝氨酸蛋白酶和相关酶的广谱抑制剂,是所测试的唯一一种破坏体节发生的AChE抑制剂。处于50%外包期的原肠胚持续暴露于浓度在40微摩尔至90微摩尔之间的DFP中,能够完成外包,但在受精后24小时,形成的体节数量呈现剂量依赖性减少,体节神经支配的尾端范围也相应减少。15体节(15小时)的胚胎在70微摩尔的半数有效剂量(ED50)下暴露于DFP 3小时,然后恢复至24小时,会发育出异常的体节。在第一个异常体节形成之前,药物处理后大约形成了五个正常体节。异常体节的位置与在DFP存在时本应启动AChE活性的推定体节中胚层区域相对应。在暴露于70微摩尔DFP时,推定的体节形成,运动神经元延伸其在DFP处理时已启动AChE活性的突起,尽管速度比正常情况慢。然而,在5体节和15体节阶段均暴露于1毫摩尔DFP 30分钟,然后恢复至24小时的胚胎,形成的体节数量正常,但体节神经支配的尾端范围减小,偶尔还会发育出异常的初级运动神经元。与异常体节一样,异常运动神经元在DFP存在时本应启动AChE活性。由于DFP的抑制作用而无法启动AChE活性的推定体节中胚层发育异常。虽然DFP的作用不限于抑制AChE,但这些数据支持了为体节形成提出的“时钟和波前”模型,并支持AChE活性在斑马鱼体节发生中起作用的假说。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验