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本文引用的文献

1
A genome-wide Drosophila screen for heat nociception identifies α2δ3 as an evolutionarily conserved pain gene.全基因组果蝇热伤害感受筛选鉴定 α2δ3 为一个进化保守的疼痛基因。
Cell. 2010 Nov 12;143(4):628-38. doi: 10.1016/j.cell.2010.09.047.
2
Light-avoidance-mediating photoreceptors tile the Drosophila larval body wall.避光介导的感光器覆盖在果蝇幼虫的体壁上。
Nature. 2010 Dec 16;468(7326):921-6. doi: 10.1038/nature09576. Epub 2010 Nov 10.
3
Optogenetically Induced Olfactory Stimulation in Drosophila Larvae Reveals the Neuronal Basis of Odor-Aversion behavior.果蝇幼虫中光遗传学诱导的嗅觉刺激揭示了气味厌恶行为的神经基础。
Front Behav Neurosci. 2010 Jun 2;4:27. doi: 10.3389/fnbeh.2010.00027. eCollection 2010.
4
Analysis of Drosophila TRPA1 reveals an ancient origin for human chemical nociception.分析果蝇的 TRPA1 揭示了人类化学伤害感受的古老起源。
Nature. 2010 Mar 25;464(7288):597-600. doi: 10.1038/nature08848. Epub 2010 Mar 17.
5
Nociceptors: a phylogenetic view.伤害感受器:系统发生观点。
J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2009 Dec;195(12):1089-106. doi: 10.1007/s00359-009-0482-z. Epub 2009 Oct 11.
6
Cytokine signaling mediates UV-induced nociceptive sensitization in Drosophila larvae.细胞因子信号传导介导果蝇幼虫中紫外线诱导的伤害性致敏。
Curr Biol. 2009 May 26;19(10):799-806. doi: 10.1016/j.cub.2009.03.062. Epub 2009 Apr 16.
7
Behavioral dissection of Drosophila larval phototaxis.果蝇幼虫趋光性的行为剖析
Biochem Biophys Res Commun. 2009 May 1;382(2):395-9. doi: 10.1016/j.bbrc.2009.03.033. Epub 2009 Mar 12.
8
Drosophila painless is a Ca2+-requiring channel activated by noxious heat.果蝇的“无痛”蛋白是一种由有害热激活的、需要钙离子的通道。
J Neurosci. 2008 Oct 1;28(40):9929-38. doi: 10.1523/JNEUROSCI.2757-08.2008.
9
Transient receptor potential channels in sensory neurons are targets of the antimycotic agent clotrimazole.感觉神经元中的瞬时受体电位通道是抗真菌剂克霉唑的作用靶点。
J Neurosci. 2008 Jan 16;28(3):576-86. doi: 10.1523/JNEUROSCI.4772-07.2008.
10
Nociceptive neurons protect Drosophila larvae from parasitoid wasps.伤害感受神经元保护果蝇幼虫免受寄生蜂侵害。
Curr Biol. 2007 Dec 18;17(24):2105-2116. doi: 10.1016/j.cub.2007.11.029. Epub 2007 Nov 29.

成长之痛:果蝇幼虫伤害防御反应的发育

Growing pains: development of the larval nocifensive response in Drosophila.

作者信息

Sulkowski Mikolaj J, Kurosawa Mathieu S, Cox Daniel N

机构信息

School of Systems Biology, George Mason University, Manassas, Virginia 20120, USA.

出版信息

Biol Bull. 2011 Dec;221(3):300-6. doi: 10.1086/BBLv221n3p300.

DOI:10.1086/BBLv221n3p300
PMID:22186918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4209481/
Abstract

The ability to perceive and avoid harmful substances or stimuli is key to an organism's survival. The neuronal cognate of the perception of pain is known as nociception, and the reflexive motion to avoid pain is termed the nocifensive response. As the nocifensive response is an ancient and evolutionarily conserved behavioral response to nociceptive stimuli, it is amenable to study in relatively simple and genetically tractable model systems such as Drosophila. Recent studies have taken advantage of the useful properties of Drosophila larvae to begin elucidating the neuronal connectivity and molecular machinery underlying the nocifensive response. However, these studies have primarily utilized the third-instar larval stage, and many mutations that potentially influence nociception survive only until earlier larval stages. Here we characterize the nocifensive responses of Drosophila throughout larval development and find dramatic changes in the nature of the behavior. Notably, we find that prior to the third instar, larvae are unable to perform the characteristic "corkscrew-like roll" behavior. Also, we identify an avoidance behavior consistent with a nocifensive response that is present immediately after larval hatching, representing a paradigm that may be useful in examining mutations with an early lethal phenotype.

摘要

感知并避开有害物质或刺激的能力是生物体生存的关键。对疼痛的感知在神经元层面被称为伤害感受,而避免疼痛的反射性动作则被称为伤害防御反应。由于伤害防御反应是对伤害性刺激的一种古老且在进化上保守的行为反应,因此适合在相对简单且具有遗传易处理性的模型系统(例如果蝇)中进行研究。最近的研究利用了果蝇幼虫的有用特性,开始阐明伤害防御反应背后的神经元连接和分子机制。然而,这些研究主要利用的是三龄幼虫阶段,许多可能影响伤害感受的突变仅存活到更早的幼虫阶段。在这里,我们描述了果蝇在整个幼虫发育过程中的伤害防御反应,并发现了行为性质的显著变化。值得注意的是,我们发现三龄之前的幼虫无法做出典型的“螺旋状翻滚”行为。此外,我们识别出一种与伤害防御反应一致的回避行为,这种行为在幼虫孵化后立即出现,代表了一种可能有助于研究具有早期致死表型突变的范例。