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磷酯酰丝氨酸(PS)改善 TMT 诱导的大鼠记忆障碍。

Krill-Derived Phosphatidylserine Improves TMT-Induced Memory Impairment in the Rat.

机构信息

Acupuncture and Meridian Science Research Center, College of Oriental Medicine, Kyung Hee University, Seoul 130-701.

出版信息

Biomol Ther (Seoul). 2012 Mar;20(2):207-13. doi: 10.4062/biomolther.2012.20.2.207.

Abstract

The present study examined the effects of krill-derived phosphatidylserine (Krill-PS) on the learning and memory function and the neural activity in rats with trimethyltin (TMT)-induced memory deficits. The rats were administered vehicle (medium-chain triglyceride: MCT) or Krill-PS (50, 100 mg/kg, p.o.) daily for 21 days. The cognitive improving efficacy of Krill-PS in TMT-induced amnesic rats was investigated by assessing the Morris water maze test and by performing choline acetyltransferase (ChAT), acetylcholinesterase (AChE) and cAMP responsive element binding protein (CREB) immunohistochemistry. The rats with TMT injection showed impaired learning and memory of the tasks and treatment with Krill-PS produced a significant improvement of the escape latency to find the platform in the Morris water maze at the 2(nd) and 4(th) day compared to that of the MCT group (p<0.05). In the retention test, the Krill-PS+MCT groups showed increased time spent around the platform compared to that of the MCT group. Consistent with the behavioral data, Krill-PS 50+MCT group significantly alleviated the loss of acetylcholinergic neurons in the hippocampus and medial septum compared to that of the MCT group. Treatment with Krill-PS significantly increased the CREB positive neurons in the hippocampal CA1 area as compared to that of the MCT group. These results suggest that Krill-PS may be useful for improving the cognitive function via regulation of cholinergic marker enzyme activity and neural activity.

摘要

本研究考察了磷酯酰丝氨酸(PS)对三甲基锡(TMT)致记忆损伤大鼠学习记忆功能和神经活性的影响。大鼠每天给予载体(中链甘油三酯:MCT)或 PS(50、100mg/kg,po)21 天。采用 Morris 水迷宫试验评价 PS 对 TMT 致健忘大鼠的认知改善作用,并进行胆碱乙酰转移酶(ChAT)、乙酰胆碱酯酶(AChE)和 cAMP 反应元件结合蛋白(CREB)免疫组织化学染色。TMT 注射大鼠表现出学习和记忆任务受损,与 MCT 组相比,PS 治疗组在第 2 天和第 4 天的 Morris 水迷宫中找到平台的逃避潜伏期显著改善(p<0.05)。在保留测试中,PS+MCT 组与 MCT 组相比,在平台周围花费的时间增加。与行为数据一致,PS 50+MCT 组与 MCT 组相比,海马和内侧隔区乙酰胆碱能神经元的丢失明显减轻。与 MCT 组相比,PS 治疗显著增加了海马 CA1 区的 CREB 阳性神经元。这些结果表明,PS 可能通过调节胆碱能标记酶活性和神经活性,有助于改善认知功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cbe/3792220/0501d2030078/ooomb4-20-207-g001.jpg

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