Griffin Síle M, Lehtinen Markus J, Meunier Johann, Ceolin Laura, Roman Francois J, Patterson Elaine
IFF Health & Biosciences, Danisco Sweeteners Oy, Kantvik, Finland.
Amylgen SAS, Montferrier-sur-Lez, France.
Nutr Neurosci. 2023 Mar;26(3):254-264. doi: 10.1080/1028415X.2022.2042915. Epub 2022 Mar 3.
Insufficient sleep is a serious public health epidemic in modern society, impairing memory and other cognitive functions. In this study, partial sleep deprivation (SD) was used to induce cognitive impairment in mice to determine the effects of probiotics on subsequent cognitive deficits.
Lp-115 (Lp-115), Lpc-37 (Lpc-37), subsp. 420 (B420) and their combination were administered to mice subjected to partial SD and compared with non-SD and SD vehicle groups. Mice were administered a daily oral gavage containing either 1 × 10 colony forming units (CFU) of single-strain, 1.5 × 10 CFU of multi-strain (5 × 10 CFU/strain), or vehicle for thirty days prior to and for nine days during a behavioural test paradigm. The novel object recognition (NOR) test, spontaneous alternation Y-maze (Y-maze), and the step-through passive avoidance (STPA) task were applied to evaluate learning and memory performance following partial SD.
Partial SD had a significant impact on cognitive function in vehicle mice. Intervention with Lpc-37 significantly improved recognition memory deficits in the NOR test, spatial working memory deficits in the Y-maze, and contextual long-term memory impairments in the STPA task, in mice subjected to partial SD compared to the SD vehicle group. The multi-strain significantly improved recognition memory deficits in the NOR test and spatial working memory deficits in the Y-maze in mice subjected to partial SD compared to the SD vehicle group.
These findings demonstrate that Lpc-37 and the multi-strain may play a role in alleviating memory impairments and improve cognitive function in partially sleep-deprived mice.
睡眠不足是现代社会中一种严重的公共卫生问题,会损害记忆力和其他认知功能。在本研究中,采用部分睡眠剥夺(SD)诱导小鼠认知障碍,以确定益生菌对后续认知缺陷的影响。
将Lp-115(Lp-115)、Lpc-37(Lpc-37)、亚种420(B420)及其组合给予部分睡眠剥夺的小鼠,并与非睡眠剥夺和睡眠剥夺对照剂组进行比较。在行为测试范式前30天及测试期间9天,每天给小鼠口服含1×10菌落形成单位(CFU)单菌株、1.5×10 CFU多菌株(5×10 CFU/菌株)或对照剂。应用新物体识别(NOR)测试、自发交替Y迷宫(Y迷宫)和穿梭式被动回避(STPA)任务来评估部分睡眠剥夺后的学习和记忆表现。
部分睡眠剥夺对对照剂组小鼠的认知功能有显著影响。与睡眠剥夺对照剂组相比,用Lpc-37干预可显著改善部分睡眠剥夺小鼠在NOR测试中的识别记忆缺陷、Y迷宫中的空间工作记忆缺陷以及STPA任务中的情境长期记忆损伤。与睡眠剥夺对照剂组相比,多菌株可显著改善部分睡眠剥夺小鼠在NOR测试中的识别记忆缺陷和Y迷宫中的空间工作记忆缺陷。
这些发现表明,Lpc-37和多菌株可能在减轻部分睡眠剥夺小鼠的记忆损伤和改善认知功能方面发挥作用。