食欲嗅觉记忆诱导的求偶行为。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Journal of neurogenetics Pub Date : 2019-03-01 Epub Date: 2019-04-08 DOI:10.1080/01677063.2019.1593978
Yuya Onodera, Rino Ichikawa, Kanta Terao, Hiromu Tanimoto, Nobuhiro Yamagata
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引用次数: 3

摘要

食物奖励和有害惩罚等强化信号可以改变多种行为。这在果蝇中是正确的,果蝇可以通过气味和糖奖励或电击惩罚来调节。尽管学习调节了各种各样的行为,但条件反应传统上是通过改变选择中的气味偏好来衡量的,而其他记忆引导的行为几乎没有被研究过。本研究采用视频记录和半自动化处理管道,对果蝇糖联想学习后的条件气味反应进行了详细分析。轨迹分析显示,多种行为成分随着对奖励气味的条件处理而改变。值得注意的是,我们发现侧翼伸展(D. melanogaster求偶行为的标志)在有奖励气味的情况下明显增加。引人注目的是,蘑菇体输出的遗传破坏并没有损害条件求爱的增加,但明显削弱了条件气味方法。我们的研究结果强调了条件反应的复杂性及其独特的调节机制,这可能是果蝇协调而复杂的记忆引导行为的基础。
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Courtship behavior induced by appetitive olfactory memory.

Reinforcement signals such as food reward and noxious punishment can change diverse behaviors. This holds true in fruit flies, Drosophila melanogaster, which can be conditioned by an odor and sugar reward or electric shock punishment. Despite a wide variety of behavior modulated by learning, conditioned responses have been traditionally measured by altered odor preference in a choice, and other memory-guided behaviors have been only scarcely investigated. Here, we analyzed detailed conditioned odor responses of flies after sugar associative learning by employing a video recording and semi-automated processing pipeline. Trajectory analyses revealed that multiple behavioral components were altered along with conditioned approach to the rewarded odor. Notably, we found that lateral wing extension, a hallmark of courtship behavior of D. melanogaster, was robustly increased specifically in the presence of the rewarded odor. Strikingly, genetic disruption of the mushroom body output did not impair conditioned courtship increase, while markedly weakening conditioned odor approach. Our results highlight the complexity of conditioned responses and their distinct regulatory mechanisms that may underlie coordinated yet complex memory-guided behaviors in flies.

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来源期刊
Journal of neurogenetics
Journal of neurogenetics 医学-神经科学
CiteScore
4.40
自引率
0.00%
发文量
13
审稿时长
>12 weeks
期刊介绍: The Journal is appropriate for papers on behavioral, biochemical, or cellular aspects of neural function, plasticity, aging or disease. In addition to analyses in the traditional genetic-model organisms, C. elegans, Drosophila, mouse and the zebrafish, the Journal encourages submission of neurogenetic investigations performed in organisms not easily amenable to experimental genetics. Such investigations might, for instance, describe behavioral differences deriving from genetic variation within a species, or report human disease studies that provide exceptional insights into biological mechanisms
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