Department of Anatomy, Afzalipour School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.
Institute of Neuropharmacology, Kerman Neuroscience Research Center, Kerman University of Medical Sciences, Kerman, Iran.
Brain Behav. 2024 Sep;14(9):e70010. doi: 10.1002/brb3.70010.
The hippocampus is susceptible to damage, leading to negative impacts on cognition. Conditioned medium (CM) obtained from adipose tissue-derived mesenchymal stem cells (MSCs) and acetylsalicylic acid (ASA) have shown neuroprotective effects independently. This study explored the synergistic potential of ASA and CM from adipose-derived MSCs against hippocampal injury.
Adult male Wistar rats received bilateral hippocampal ethidium bromide (EB) injections to induce hippocampal damage. Rats were treated with ASA and/or CM derived from adipose tissue MSCs every 48 h for 16 days. Behavioral tests (open field test, Morris water maze, novel object recognition, and passive avoidance), oxidative stress, Western blot analysis of brain-derived neurotrophic factor (BDNF) and cerebral dopamine neurotrophic factor (CDNF) expression, and hippocampal histological investigation were conducted.
Administration of EB caused impairments in spatial, recognition, and passive avoidance memory, as well as heightened oxidative stress, reduced BDNF/CDNF expression, and pyramidal cell loss in the hippocampal CA1 region. Administration of ASA, CM, or a combination of both mitigated these hippocampal damages and cognitive deficits, elevated BDNF and CDNF levels, and alleviated the CA1 necrosis caused by EB. Moreover, co-administering ASA and CM resulted in greater improvements in spatial memory compared to administering ASA alone, suggesting possible synergistic interactions.
The ability of ASA, CM obtained from adipose tissue-derived MSCs, and their combination therapy to alleviate hippocampal injuries highlights their promising therapeutic potential as a neuroprotection strategy against brain damage. Our findings provide preliminary evidence of the potential synergistic effects of ASA and CM, which warrants further investigations.
海马体易受损,导致认知功能受到负面影响。脂肪组织来源的间充质干细胞(MSCs)的条件培养基(CM)和乙酰水杨酸(ASA)已被证明具有独立的神经保护作用。本研究探讨了 ASA 和脂肪来源 MSC 的 CM 联合应用于海马损伤的协同潜力。
成年雄性 Wistar 大鼠接受双侧海马溴化乙锭(EB)注射以诱导海马损伤。大鼠每 48 小时接受 ASA 和/或源自脂肪组织 MSC 的 CM 治疗,共治疗 16 天。进行行为测试(旷场试验、莫里斯水迷宫、新物体识别和被动回避)、氧化应激、脑源性神经营养因子(BDNF)和脑多巴胺神经营养因子(CDNF)表达的 Western blot 分析以及海马组织学研究。
EB 给药导致空间、识别和被动回避记忆受损,氧化应激加剧,BDNF/CDNF 表达减少,海马 CA1 区锥体神经元丢失。给予 ASA、CM 或两者联合减轻了这些海马损伤和认知缺陷,提高了 BDNF 和 CDNF 水平,并缓解了 EB 引起的 CA1 坏死。此外,与单独给予 ASA 相比,联合给予 ASA 和 CM 可显著改善空间记忆,表明可能存在协同作用。
ASA、脂肪组织来源 MSC 的 CM 及其联合治疗减轻海马损伤的能力突出了它们作为脑损伤神经保护策略的潜在治疗潜力。我们的发现提供了 ASA 和 CM 潜在协同作用的初步证据,值得进一步研究。