脂肪酸结合蛋白 5 基因缺失会增强尼古丁条件性场所偏好:阐明假定的通路机制。

Future Pharmacology Pub Date : 2023-03-01 Epub Date: 2023-01-09 DOI:10.3390/futurepharmacol3010007
Nicole Roeder, Brittany Richardson, Abrianna Mihalkovic, Samantha Penman, Olivia White, John Hamilton, Ashim Gupta, Kenneth Blum, Mark S Gold, Panayotis K Thanos
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引用次数: 0

摘要

新的证据表明,内源性大麻素系统可以调节尼古丁的行为和生理效应。脂肪酸结合蛋白(FABPs)是内源性大麻素(如anandamide)的主要细胞内转运机制之一。为此,FABP 表达的变化可能同样会影响尼古丁的相关行为表现,特别是其成瘾性。以两种不同的剂量(0.1 或 0.5 毫克/千克)对 FABP5 +/+ 和 FABP5 -/- 小鼠进行了尼古丁条件性位置偏好(CPP)测试。在预调节过程中,尼古丁配对室被指定为小鼠最不喜欢的室。经过 8 天的调节后,给小鼠注射尼古丁或生理盐水。小鼠在测试日可以进入所有的药室,它们在预调日与测试日在药室中所花费的时间被用来检测药物偏好评分。CPP结果显示,FABP5 -/-小鼠对0.1 mg/kg尼古丁的位置偏好高于FABP5 +/+小鼠,而对0.5 mg/kg尼古丁的位置偏好在基因型之间没有差异。总之,FABP5 在调节尼古丁位置偏好中起着重要作用。需要进一步研究以确定其确切机制。研究结果表明,大麻素信号传导失调可能会影响尼古丁寻求行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms.

Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms.

Fatty Acid-Binding Protein 5 Gene Deletion Enhances Nicotine-Conditioned Place Preference: Illuminating the Putative Gateway Mechanisms.

Emerging evidence indicates that the endogenous cannabinoid system modulates the behavioral and physiological effects of nicotine. Fatty acid-binding proteins (FABPs) are among the primary intracellular trafficking mechanisms of endogenous cannabinoids, such as anandamide. To this end, changes in FABP expression may similarly impact the behavioral manifestations associated with nicotine, particularly its addictive properties. FABP5 +/+ and FABP5 -/- mice were tested for nicotine-conditioned place preference (CPP) at two different doses (0.1 or 0.5 mg/kg). The nicotine-paired chamber was assigned as their least preferred chamber during preconditioning. Following 8 days of conditioning, the mice were injected with either nicotine or saline. The mice were allowed to access to all the chambers on the test day, and their times spent in the drug chamber on the preconditioning versus the test days were used to examine the drug preference score. The CPP results showed that the FABP5 -/- mice displayed a higher place preference for 0.1 mg/kg nicotine than the FABP5 +/+ mice, while no CPP difference was observed for 0.5 mg/kg nicotine between the genotypes. In conclusion, FABP5 plays an important role in regulating nicotine place preference. Further research is warranted to identify the precise mechanisms. The results suggest that dysregulated cannabinoid signaling may impact nicotine-seeking behavior.

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