Heidari Somaye, Mehri Soghra, Hosseinzadeh Hossein
Pharmaceutical Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Pharmacodynamics and Toxicology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Iran J Basic Med Sci. 2017 Nov;20(11):1250-1259. doi: 10.22038/IJBMS.2017.9541.
The neurodegeneration and loss of memory function are common consequences of aging. Medicinal plants have potent protective effects against chronic neurodegenerative diseases. The aim of this study was to investigate the beneficial effects and molecular mechanisms of crocin on brain function in D-galactose (D-gal)-induced aging model in rats.
Male Wistar rats weighing 220 ± 20 g were randomly divided into six groups: control, D-gal (400 mg/kg, SC), D-gal (400 mg/kg) plus crocin (7.5, 15, 30 mg/kg, IP) and crocin alone at dose of 30 mg/kg for 8 weeks. The neuroprotective effects of crocin were evaluated by Morris water maze, determination of malondialdehyde (MDA) levels and Western blot analysis.
Crocin significantly inhibited the neurotoxic effects of D-gal through improvement of spatial learning and memory functions as well as the reduction of MDA levels. It was also found that administration of crocin up-regulated pAkt/Akt and pErk/Erk ratio which were decreased by chronic D-gal treatment. In addition, the elevated level of carboxymethyl lysine (CML), as an advance glycation product (AGE), NF-κB p65, TNFα and IL1β significantly decreased in crocin treated rats compared to D-gal group.
These findings suggest that crocin is able to enhance memory function in D-gal aging model through anti-glycative and anti-oxidative properties which finally can suppress brain inflammatory mediators (IL-1, TNF and NF-κB) formations and increase PI3K/Akt and Erk/MAPK pathways activity. Therefore, crocin can be considered as healthcare product to prevent age-related brain diseases such as Alzheimer.
神经退行性变和记忆功能丧失是衰老的常见后果。药用植物对慢性神经退行性疾病具有强大的保护作用。本研究旨在探讨西红花苷对D - 半乳糖(D-gal)诱导的大鼠衰老模型脑功能的有益作用及其分子机制。
体重220±20 g的雄性Wistar大鼠随机分为六组:对照组、D-gal组(400 mg/kg,皮下注射)、D-gal(400 mg/kg)加西红花苷组(7.5、15、30 mg/kg,腹腔注射)和单独使用30 mg/kg西红花苷组,给药8周。通过莫里斯水迷宫、丙二醛(MDA)水平测定和蛋白质免疫印迹分析评估西红花苷的神经保护作用。
西红花苷通过改善空间学习和记忆功能以及降低MDA水平,显著抑制了D-gal的神经毒性作用。还发现,给予西红花苷上调了pAkt/Akt和pErk/Erk比值,而慢性D-gal处理使其降低。此外,与D-gal组相比,西红花苷处理的大鼠中作为晚期糖基化终产物(AGE)的羧甲基赖氨酸(CML)、NF-κB p65、TNFα和IL1β的升高水平显著降低。
这些发现表明,西红花苷能够通过抗糖基化和抗氧化特性增强D-gal衰老模型中的记忆功能,最终可抑制脑内炎症介质(IL-1、TNF和NF-κB)的形成,并增加PI3K/Akt和Erk/MAPK信号通路的活性。因此,西红花苷可被视为预防阿尔茨海默病等与年龄相关的脑部疾病的保健品。