富迷迭香酸乙醇提取物对慢性脑灌注不足大鼠认知和海马长期增强的改善作用

Q4 Neuroscience
Z. Hassan, KKesevan Rajah Kumaran, Nelson Jeng Yeou Chear, Siti Najmi Syuhadaa Bakar, Thaarvena Retinasamy, Saatheeyavaane Bhuvanendran, Amin Malik Abdul Majeed, M. Shaikh, Iekhsan Othman
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引用次数: 0

摘要

慢性脑灌流不足(CCH)是血管性痴呆的主要原因之一,由脑血流量减少引起。正虹吸(Orthosiphon stamineus, OS)是一种具有显著的神经保护、抗氧化和抗炎活性的草药,因为它含有大量的迷迭香酸。本研究探讨了黄芪乙醇提取物对CCH大鼠认知功能的促智作用。CCH是由永久性双侧颈总动脉闭塞(PBOCCA)引起的。采用被动回避任务(PAT)和Morris水迷宫(MWM)测试评估认知功能,采用体内长期增强(LTP)测试评估神经可塑性。采用高效液相色谱- pda定量分析了黄芪乙醇提取物迷迭香酸的含量。在CCH大鼠中,低剂量的OS提取物显著增加了PAT的步进潜伏期,减少了MWM中的逃逸潜伏期,并挽救了高剂量的LTP损伤。这些结果有力地支持了富迷迭香酸黄芪提取物(5.088% w/w)治疗CCH所致病理性血管性痴呆的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rosmarinic acid-rich ethanolic extract of Orthosiphon stamineus ameliorates cognitive and hippocampal long-term potentiation in chronic cerebral hypoperfusion rat model
Chronic cerebral hypoperfusion (CCH) is one of the main causes of vascular dementia caused by the reduced blood flow to the brain. Orthosiphon stamineus (OS) is a medicinal herb exhibiting pronounced neuroprotective, anti-oxidant and anti-inflammatory activities due to its high rosmarinic acid content. This study investigated the nootropic effect of OS ethanolic extract on cognitive functions in CCH rats. CCH was developed by permanent bilateral occlusion of the common carotid artery (PBOCCA). Passive avoidance task (PAT) and Morris water maze (MWM) test were conducted to evaluate cognitive functions followed by in vivo long-term potentiation (LTP) for assessing neuroplasticity. The rosmarinic acid content of OS ethanolic extract was quantified using a validated HPLC-PDA. Treatment with OS ethanolic extract significantly increased step-through latency in the PAT, decreased escape latency at a low dose of OS extract in the MWM and rescued the LTP impairment at the highest dose in CCH rats. These results strongly support the effectiveness of rosmarinic acid-rich OS extract (5.088 % w/w) in treating pathological vascular dementia caused by CCH.
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来源期刊
Neuroscience Research Notes
Neuroscience Research Notes Neuroscience-Neurology
CiteScore
1.00
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21
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