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西红花中的活性成分西红花醛可减轻阿尔茨海默病淀粉样β诱导的大鼠模型的认知功能障碍:潜在机制。

Safranal, an active ingredient of saffron, attenuates cognitive deficits in amyloid β-induced rat model of Alzheimer's disease: underlying mechanisms.

机构信息

Department of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Neurophysiology Research Center, Shahed University, Tehran, Iran.

出版信息

Metab Brain Dis. 2019 Dec;34(6):1747-1759. doi: 10.1007/s11011-019-00481-6. Epub 2019 Aug 17.

Abstract

Alzheimer's disease (AD) is the most prevalent neurodegenerative amyloid disorder with progressive deterioration of cognitive and memory skills. Despite many efforts, no decisive therapy yet exists for AD. Safranal is the active constituent of saffron essential oil with antioxidant, anti-inflammatory, and anti-apoptotic properties. In this study, the possible beneficial effect of safranal on cognitive deficits was evaluated in a rat model of AD induced by intrahippocampal amyloid beta (Aβ). Safranal was daily given p.o. (0.025, 0.1, and 0.2 ml/kg) post-surgery for 1 week and finally learning and memory were evaluated in addition to assessment of the involvement of oxidative stress, inflammation, and apoptosis. Findings showed that safranal treatment of amyloid β-microinjected rats dose-dependently improved cognition in Y-maze, novel-object discrimination, passive avoidance, and 8-arm radial arm maze tasks. Besides, safranal attenuated hippocampal level of malondialdehyde (MDA), reactive oxygen species (ROS), protein carbonyl, interleukin 1β (IL-1β), interleukin 6 (IL-6), tumor necrosis factor α (TNFα), nuclear factor-kappa B (NF-kB), apoptotic biomarkers including caspase 3 and DNA fragmentation, glial fibrillary acidic protein (GFAP), myeloperoxidase (MPO), and acetylcholinesterase (AChE) activity and improved superoxide dismutase (SOD) activity and mitochondrial membrane potential (MMP) with no significant effect on nitrite, catalase activity, and glutathione (GSH). Furthermore, safranal prevented CA1 neuronal loss due to amyloid β. In summary, safranal treatment of intrahippocampal amyloid beta-microinjected rats could prevent learning and memory decline via neuronal protection and at a molecular level through amelioration of apoptosis, oxidative stress, inflammation, cholinesterase activity, neutrophil infiltration, and also by preservation of mitochondrial integrity.

摘要

阿尔茨海默病(AD)是最常见的神经退行性淀粉样变疾病,其认知和记忆能力逐渐恶化。尽管做了很多努力,但目前仍没有针对 AD 的决定性疗法。藏红花醛是藏红花精油的活性成分,具有抗氧化、抗炎和抗细胞凋亡作用。在这项研究中,通过海马内β淀粉样蛋白(Aβ)微注射诱导 AD 的大鼠模型评估了藏红花醛对认知缺陷的可能有益作用。藏红花醛在手术后每天口服(0.025、0.1 和 0.2 ml/kg)1 周,最后评估学习和记忆能力,以及评估氧化应激、炎症和细胞凋亡的参与情况。结果表明,藏红花醛治疗 Aβ微注射大鼠可剂量依赖性地改善 Y 迷宫、新物体识别、被动回避和 8 臂放射臂迷宫任务中的认知能力。此外,藏红花醛可降低海马丙二醛(MDA)、活性氧(ROS)、蛋白羰基、白细胞介素 1β(IL-1β)、白细胞介素 6(IL-6)、肿瘤坏死因子 α(TNFα)、核因子-κB(NF-κB)、细胞凋亡生物标志物包括半胱氨酸天冬氨酸蛋白酶 3 和 DNA 片段、胶质纤维酸性蛋白(GFAP)、髓过氧化物酶(MPO)和乙酰胆碱酯酶(AChE)的水平,提高超氧化物歧化酶(SOD)活性和线粒体膜电位(MMP),对亚硝酸盐、过氧化氢酶活性和谷胱甘肽(GSH)无显著影响。此外,藏红花醛可预防由于 Aβ引起的 CA1 神经元丢失。总之,藏红花醛治疗海马内 Aβ微注射大鼠可通过神经元保护和在分子水平上通过改善细胞凋亡、氧化应激、炎症、胆碱酯酶活性、中性粒细胞浸润以及维持线粒体完整性来预防学习和记忆能力下降。

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