脑磷脂中的乙醇胺和乙烯基醚分子会调节大鼠的行为

IF 1.6 Q3 CLINICAL NEUROLOGY
NeuroSci Pub Date : 2024-11-04 DOI:10.3390/neurosci5040037
Mst Zenika Nasrin, Shuhei Kikuchi, Yasuhiro Uchimura, Mina Yoshioka, Shin-Ya Morita, Tomoya Kobayashi, Yusuke Kinoshita, Yoshio Furusho, Hitoshi Tamiaki, Daijiro Yanagisawa, Jun Udagawa
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引用次数: 0

摘要

质链磷脂是富含大脑的磷脂,在甘油骨架和烷基链之间的 sn-1 位有乙烯基醚键。以前的研究表明,质脂能调节啮齿动物的运动活动、焦虑样行为和认知功能;然而,对行为调节起作用的特定分子尚不清楚。在本研究中,我们研究了特定磷脂分子对行为的调节作用。为了确认注射脂质体中磷脂的渗透性,我们测量了静脉注射含有 ATTO 740 标记的二油酰磷脂酰乙醇胺的脂质体后的荧光强度。然后,我们比较了注射由鸡蛋磷脂酰胆碱(PC)和 1-硬脂酰-2-二十二碳六烯酰-sn-甘油-3-磷脂酰乙醇胺(PE 18:将 1-(1Z-十八烯基)-2-二十二碳六烯酰基-sn-甘油-3-磷脂酰乙醇胺(PE P-18:0/22:6)、PC 18:0/22:6、1-(1Z-十八烯基)-2-二十二碳六烯酰基-sn-甘油-3-磷脂酰乙醇胺(PE P-18:0/22:6)或 PC P-18:0/22:6 注入雄性大鼠的尾静脉。与对照组相比,在注射 Sn-1 位含有酯键的 PE 18:0/22:6 后,大鼠在开放区域中央所花费的时间明显减少。此外,与 PE 18:0/22:6 相比,PC 18:0/22:6 在新物体识别测试中的辨别率明显更高,这表明用胆碱取代乙醇胺可以增强识别记忆。我们的研究表明,磷脂中sn-1键和亲水分子的结构可以调节啮齿动物的探索行为和识别记忆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ethanolamine and Vinyl-Ether Moieties in Brain Phospholipids Modulate Behavior in Rats.

Plasmalogens are brain-enriched phospholipids with a vinyl-ether bond at the sn-1 position between the glycerol backbone and the alkyl chain. Previous studies have suggested that plasmalogens modulate locomotor activity, anxiety-like behavior, and cognitive functions in rodents; however, the specific moieties contributing to behavioral regulation are unknown. In this study, we examined the behavioral modulation induced by specific phospholipid moieties. To confirm the permeability of phospholipids in injected liposomes, we measured the fluorescence intensity following intravenous injection of liposomes containing ATTO 740-labeled dioleoylphosphatidylethanolamine. Then, we compared the behavioral effects following injection of liposomes composed of egg phosphatidylcholine (PC) and 1-stearoyl-2-docosahexaenoyl-sn-glycero-3-phosphoethanolamine (PE 18:0/22:6), PC 18:0/22:6, 1-(1Z-octadecenyl)-2-docosahexaenoyl-sn-glycero-3-phosphoethanolamine (PE P-18:0/22:6), or PC P-18:0/22:6, into the tail vein of male rats. The time spent in the central region of the open field was significantly reduced after injection of PE 18:0/22:6, harboring an ester bond at sn-1 compared to controls. Furthermore, the discrimination ratio in the novel object recognition test was significantly higher in PC 18:0/22:6 compared to PE 18:0/22:6, suggesting that the substitution of ethanolamine with choline can enhance recognition memory. We demonstrate that the structures of the sn-1 bond and the hydrophilic moiety in the phospholipids can modulate exploratory behaviors and recognition memory in rodents.

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