Katariina Seppälä , Inés Reigada , Olli Matilainen , Tomi Rantamäki , Leena Hanski
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引用次数: 0
摘要
线虫的透明性使其能够在显微镜下对细胞过程进行活体成像,但由于其运动活动频繁,因此需要将其固定。在此,我们利用视频记录和基于红外线的自动活动追踪技术介绍了氯胺酮对成年眼镜蛇的类似麻醉作用。氯胺酮可在类似于传统固定剂叠氮化钠(NaN3)产生麻痹的浓度(20-50 mM)下导致可逆的运动阻滞。在 20 mM 氯胺酮的固定水平下,可以进行荧光和明视野成像。暴露于氯胺酮后,蠕虫的运动活性完全恢复,而且没有观察到急性毒性。然而,暴露于20毫摩尔氯胺酮后立即出现了明显的化学感觉缺陷。氯胺酮的短期处理并未显示出 SKN-1(skinhead-1)激活的迹象,而 SKN-1 是与 NaN3 相关的应激反应的标志物。总之,我们的研究结果表明氯胺酮具有作为一种无毒线虫固定剂的潜力,并合理地将秀丽隐杆线虫作为了解其药理学的模式生物。
Transparency of Caenorhabditis elegans enables microscopic in vivo imaging of cellular processes, but immobilization is required due to high locomotor activity. Here, anesthetic-like effects of dissociate anesthetic ketamine in adult C. elegans are presented using video recordings and infrared-based automated activity tracking. Ketamine caused a reversible blockade of locomotion at a similar concentration (20–50 mM) at which conventionally used immobilizing agent sodium azide (NaN3) produces paralysis. The levels of immobilization at 20 mM ketamine enabled fluorescent and brightfield imaging. The worms’ locomotory activity recovered fully after ketamine exposure and no acute toxicity was observed. However, a marked chemosensation deficiency was noted immediately after 20 mM ketamine exposure. Short-term ketamine treatment did not show signs of SKN-1 (skinhead-1) activation, a marker of the stress response associated with NaN3. In sum, our results show ketamine’s potential as a non-toxic nematode immobilizing agent and rationalize C. elegans as a model organism to understand its pharmacology.
期刊介绍:
Neuroscience publishes papers describing the results of original research on any aspect of the scientific study of the nervous system. Any paper, however short, will be considered for publication provided that it reports significant, new and carefully confirmed findings with full experimental details.