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生物碱对啮齿类动物记忆的影响差异。

Differential effects of alkaloids on memory in rodents.

机构信息

Prime Behavior Testing Laboratories, Inc. (PBTLI), Evans, GA, 30809, USA.

Department of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, 30912, USA.

出版信息

Sci Rep. 2021 May 10;11(1):9843. doi: 10.1038/s41598-021-89245-w.

Abstract

Nicotinic acetylcholine receptors (nAChRs) play a critical role in the neuropharmacology of learning and memory. As such, naturally occurring alkaloids that regulate nAChR activity have gained interest for understanding and potentially improving memory function. In this study, we tested the acute effects of three known nicotinic alkaloids, nicotine, cotinine, and anatabine, in suppressing scopolamine-induced memory deficit in rodents by using two classic memory paradigms, Y-maze and novel object recognition (NOR) in mice and rats, respectively. We found that all compounds were able to suppress scopolamine-induced spatial memory deficit in the Y-maze spontaneous alternation paradigm. However, only nicotine was able to suppress the short-term object memory deficit in NOR, despite the higher doses of cotinine and anatabine used to account for their potential differences in nAChR activity. These results indicate that cotinine and anatabine can uniquely regulate short-term spatial memory, while nicotine seems to have more robust and general role in memory regulation in rodents. Thus, nAChR-activating alkaloids may possess distinct procognitive properties in rodents, depending on the memory types examined.

摘要

烟碱型乙酰胆碱受体(nAChRs)在学习和记忆的神经药理学中发挥着关键作用。因此,调节 nAChR 活性的天然存在的生物碱引起了人们的兴趣,以期了解并可能改善记忆功能。在这项研究中,我们使用两种经典的记忆范式,即 Y 迷宫和新物体识别(NOR),分别在小鼠和大鼠中测试了三种已知的烟碱类生物碱(尼古丁、可替宁和去甲烟碱)急性抑制东莨菪碱诱导的记忆缺陷的作用。我们发现,所有化合物都能够抑制 Y 迷宫自发交替范式中的东莨菪碱诱导的空间记忆缺陷。然而,尽管使用了更高剂量的可替宁和去甲烟碱来考虑它们在 nAChR 活性上的潜在差异,但只有尼古丁能够抑制 NOR 中的短期物体记忆缺陷。这些结果表明,可替宁和去甲烟碱可以独特地调节短期空间记忆,而尼古丁在调节啮齿动物记忆方面似乎具有更强和更普遍的作用。因此,取决于所检查的记忆类型,烟碱型乙酰胆碱受体激活生物碱在啮齿动物中可能具有不同的认知增强特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32d6/8110766/30565b842dd3/41598_2021_89245_Fig1_HTML.jpg

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